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Article

Monocyte Chemotactic Proteins (MCP) in Colorectal Adenomas Are Differently Expressed at the Transcriptional and Protein Levels: Implications for Colorectal Cancer Prevention

by
Jarosław Wierzbicki
1,*,
Artur Lipiński
2,
Iwona Bednarz-Misa
3,
Łukasz Lewandowski
3,
Katarzyna Neubauer
4,
Paulina Lewandowska
3 and
Małgorzata Krzystek-Korpacka
3,*
1
Department of Minimally Invasive Surgery and Proctology, Wroclaw Medical University, 50-556 Wroclaw, Poland
2
Department of Clinical Pathology, Wroclaw Medical University, 50-556 Wroclaw, Poland
3
Department of Medical Biochemistry, Wroclaw Medical University, 50-368 Wroclaw, Poland
4
Department of Gastroenterology and Hepatology, Wroclaw Medical University, 50-556 Wroclaw, Poland
*
Authors to whom correspondence should be addressed.
J. Clin. Med. 2021, 10(23), 5559; https://doi.org/10.3390/jcm10235559
Submission received: 18 October 2021 / Revised: 8 November 2021 / Accepted: 25 November 2021 / Published: 26 November 2021
(This article belongs to the Special Issue Novel Biomarkers and Therapeutic Targets for Human Cancers)
Browse Figures
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Abstract

:
The expression of monocyte chemotactic proteins (MCPs) in colorectal polyps and their suitability as targets for chemoprevention is unknown, although MCP expression and secretion can be modulated by non-steroidal inflammatory drugs. This study was designed to determine the expression patterns of MCP-1/CCL2, MCP-2/CCL8, and MCP-3/CCL7 at the protein (immunohistochemistry; n = 62) and transcriptional levels (RTqPCR; n = 173) in colorectal polyps with reference to the polyp malignancy potential. All chemokines were significantly upregulated in polyps at the protein level but downregulated at the transcriptional level by 1.4-(CCL2), 1.7-(CCL7), and 2.3-fold (CCL8). There was an inverse relation between the immunoreactivity toward chemokine proteins and the number of corresponding transcripts in polyps (CCL2 and CCL7) or in normal mucosa (CCL8). The downregulation of chemokine transcripts correlated with the presence of multiple polyps (CCL2 and CCL8), a larger polyp size (CCL2, CCL7, and CCL8), predominant villous growth patterns (CCL2, CCL7 and CCL8), and high-grade dysplasia (CCL2 and CCL8). In conclusion, MCP-1/CCL2, MCP-2/CCL8, and MCP-3/CCL7 chemokines are counter-regulated at the protein and transcriptional levels. Chemokine-directed chemopreventive strategies should therefore directly neutralize MCP proteins or target molecular pathways contributing to their enhanced translation or reduced degradation, rather than aiming at CCL2, CCL7 or CCL8 expression.

1. Introduction

Colorectal cancer (CRC) is one of the most common malignancies worldwide, the incidence of which has recently been reduced, owing to improved screening. Chemoprevention, which is using chemicals to prevent, delay, or reverse the carcinogenesis, is another intensively studied strategy for reducing CRC risk in high-risk people as well as the general population [1]. Patients with inflammatory bowel disease (IBD), encompassing Crohn’s disease and ulcerative colitis, are more likely to develop cancer, and the risk increases with increasing disease duration, extension, and severity, as well as the occurrence of primary sclerosing cholangitis or inflammatory pseudopolyps [2]. Most sporadic CRCs, however, develop from polyps via the classic adenoma-carcinoma sequence or, less commonly, the serrated polyp pathway [3]. This well-known and relatively slow progression makes CRC particularly open to chemoprevention. Therefore, a better understanding of the molecular profile of polyps as premalignant lesions and recognition of the features distinguishing those with high potential for malignancy is considered a prerequisite for developing effective surveillance and chemopreventive strategies [3].
Inflammation plays a well-established role in cancer development as a facilitator of tumor cell proliferation, survival, and migration and an enabler of cancer angiogenesis and metastasis [4]. While chronic inflammation is also a main trigger of neoplastic transformation in IBD patients [2], the contribution of inflammatory mediators to adenoma-carcinoma transition is less evident and poorly understood. Nonetheless, it has been increasingly recognized [5]. Pre-cancerous lesions have been shown to be infiltrated by immune cells in proportion to the dysplasia grade and adenoma size [6], implicating the involvement of chemokines. Consistently, chemokine decoy receptors—ACKR2 and 4—have been downregulated in colorectal adenomas, and their expression was inversely related with the malignancy potential [7]. Recent studies have shown a link between systemic inflammatory mediators, including macrophage-associated chemokines [8] and colorectal adenomas [9,10]. Moreover, non-steroidal anti-inflammatory drugs (NSAIDs) have been repeatedly shown to reduce the incidence and size of colorectal neoplasms [1,11,12,13,14] via cyclooxygenase/prostaglandin E2 pathway-dependent and independent mechanisms [15], further stressing the relevance of inflammation in colorectal carcinogenesis.
Macrophage-associated chemokines are gaining attention as potential targets for anti-neoplastic therapies [16]. Monocyte and macrophage chemotactic proteins (MCPs) belong to the C-C subfamily of chemokines and are expressed by epithelial, endothelial, stromal, and immune cells. They display activities that may support tumor growth both indirectly and directly, acting either in an autocrine or paracrine manner [17,18,19,20]. The expression of CCL2/MCP-1, an MCP protagonist, has been shown to increase along with an advancing CRC stage [21,22], and a close link between the chemokine and the invasion and metastasis [23] has been confirmed in functional studies [24]. However, depending on the chemokine, context, and type of recruited cells, MCP chemokines may also strengthen anti-tumor responses [17,18,19,20]. Accordingly, transfection with CCL7/MCP-3 hampered tumor growth and prevented metastasis in animal models of cancer [25,26].
The MCP chemokine status in colorectal adenomas is largely unknown but indicative of counter-regulation during normal mucosa-adenoma and adenoma-carcinoma transitions [27]. Our group has recently demonstrated that the expression of MCP chemokines can be modulated by novel NSAIDs belonging to the oxicam class (manuscript submitted). Therefore, this study was conducted to assess the suitability of MCP chemokines as targets for chemoprevention by determining the expression patterns of MCP-1/CCL2, MCP-2/CCL8, and MCP-3/CCL7 in colorectal polyps and the chemokine association with polyp potential for malignancy.

2. Materials and Methods

2.1. Immunohistochemistry (IHC)

2.1.1. Patients

Tissue samples of the large intestine lesions were routinely collected during endoscopic examination from 66 patients admitted into the Department of Minimally Invasive Surgery and Proctology of Wroclaw Medical University and evaluated by the Department of Clinical Pathology of Wroclaw Medical University. Following histopathological examination, based on hematoxylin-eosin staining (HE), two patients were diagnosed with celiac disease, one with adenocarcinoma, and one with inflammatory polyps, and they were therefore excluded from further examination. Detailed characteristics of the remaining patients are given in Table 1 (IHC cohort).
Patient-matched samples of macroscopically normal mucosa were collected 10–15 cm from the lesions and served as controls. Sample collection was approved by the medical ethics committees of Wroclaw Medical University (#KB-247/2018 from 24 April 2018).

2.1.2. Sample Handling

Th collected tissue samples were preserved in 4% buffered formalin solution for 24–72 h and subsequently subjected to a dewatering process in a Tissue-Tek Xpress® x120 microwave tissue processor (Sakura Finetek, Alphen aan den Rijn, The Netherlands) using the Xpress Reagent set (Sakura Finetek; cat. No 7730). After being embedded in paraffin to create blocks, the tissue samples were sliced into 3-μm thick fragments.

2.1.3. IHC Procedure

The 3-μm thick tissue fragments were placed on a microscope slide with an additional adhesive surface. Cusabio Technology LLC (Houston, TX, USA) rabbit monoclonal anti-human antibodies directed against the corresponding chemokine were used for the immunohistochemical reactions, consisting of CCL2 Antibody (cat. No CSB-PA05865A0Rb), CCL7 Antibody (cat. No CSB-PA082817), and CCL8 Antibody (cat. No CSB-PA07629A0Rb).
The first stage was the dewaxing of tissue fragments using the PT Link system (Agilent Technologies Inc., Carpinteria, CA, USA) by boiling in a high-pH buffer at 97 °C. The next stage (i.e., antibody application) took place automatically using the Autostainer Plus Link platform (Agilent Technologies Inc.) according to the protocol provided by the antibodies’ manufacturer. The effects of all reactions were visualized with the EnVision FLEX set (Agilent Technologies Inc.; cat. No K800221-2) using a 3, 39-diaminobenzidine tetrahydrochloride (DAB) chromogen, which turned brown in the case of a positive reaction. Hematoxylin was used for counterstaining.
Photos were taken under an Olympus System BX51 microscope with a U0TV.63XC digital camera (Olympus Corporation, Tokyo, Japan).

2.1.4. IHC Scoring

In accordance with the characteristics of the antibodies used, a granular cytoplasmic reaction occurred in all cases. The basis for the assessment was a reaction in the cytoplasm of glandular epithelial cells, which forms the mucous membrane of the large intestine, as well as adenomas, regardless of their histological type.
The reaction results were classified as follows:
  • Score 0, a negative result: either no reaction occurred in the glandular epithelial cells, or it only occurred in the stromal area of the lesion or control tissue fragment;
  • Score 1, a weak positive result (+): such cases exhibited a weak cytoplasmic reaction (a low-intensity one), or the reaction did not encompass the entire lesion or control tissue fragment;
  • Score 2, a positive result (++): a strong cytoplasmic reaction encompassing the entire lesion or the entire control tissue epithelium.

2.2. Transcriptional Analysis (Reverse-Transcribed Quantitative Polymerase Chain Reaction (RTqPCR))

2.2.1. Patients

Paired samples of polyp and normal mucosa from 176 patients admitted to the Department of Minimally Invasive Surgery and Proctology or to the Department of Gastroenterology and Hepatology of Wroclaw Medical University were included in the current study (Medical Ethics Committees of Wroclaw Medical University approval #KB-247/2018 from 24 April 2018). Of those, 66 patients were common with the IHC cohort, and 3 of them were excluded from further analysis for the reasons stated previously (2 cases of celiac disease and 1 inflammatory polyp). The characteristics of the RTqPCR cohort are presented in Table 1.

2.2.2. Sample Handling

The tissue samples were rinsed with PBS, soaked in RNAlater (Ambion Inc., Austin TX, USA), and kept frozen at −80 °C until RNA extraction.

2.2.3. RNA Isolation, cDNA Synthesis, and Quantitative PCR (qPCR)

After thawing, the samples (up to 40 mg) were homogenized in Fastprep 24 Homogenizer (MP Biomedical, OH, USA) using ceramic spheres and a lysis buffer (PureLink™ RNA Mini Kit from Invitrogen, Thermo Fisher Scientific, Waltham, MA, USA) supplemented with β-mercaptoethanol (Sigma Aldrich, St. Luis, MO, USA) at 1:10 (v/v).
The total RNA was isolated using phenol-chloroform extraction and purified with a PureLink™ RNA Mini Kit (Invitrogen). On-column digestion with DNase (PureLink™ DNase Set (Invitrogen) was applied to avoid contamination with the genomic DNA. The RNA was quantified in the extract, and its purity as well as integrity were assessed with a NanoDrop 2000 spectrophotometer (Thermo-Fisher Scientific, Waltham, MA, USA) and LabChip microfluidic technology using the Experion platform and Experion RNA StdSens analysis kits (BioRad, Herkules CA, USA).
An iScript™ cDNA Synthesis Kit (BioRad, Herkules CA, USA) and C1000 thermocycler (BioRad) were used to reverse transcribe the obtained RNA (1000 ng per reaction).
The relative number of transcripts was determined by quantitative polymerase chain reactions (qPCRs) using the CFX96 Real-Time PCR system (BioRad, Herkules CA, USA) under the following cycling conditions: 30 s activation at 95 °C, 5 s denaturation at 95 °C, and annealing and extension for 5 s at 61 °C for 40 cycles. Product specificity was ensured by melting curve analysis (60–95 °C with fluorescent readings every 0.5 °C) and an electrophoresis in agarose with SYBR Green detection. The reaction mixture consisted of 10 nM forward and reverse target-specific primers (1 µL of each; Genomed, Warsaw, Poland), 2 × SsoFast EvaGreen® Supermix (10 µL; BioRad, Herkules CA, USA), a cDNA template (2 µL, diluted 1:5), and water up to 20 µL. The intron-spanning starter sequences were as follows: 5′-tctgtgcctgctgctcatag-3′ and 5′-acttgctgctggtgattcttc-3′ (CCL2 forward and reverse; product size: 155 bp); 5′-acagaaggaccaccagtagcca-3′ and 5′-ggtgcttcataaagtcctggacc-3′ (CCL7 forward and reverse; product size: 117 bp); 5′-tatccagaggctggagagctac-3′ and 5′-tggaatccctgacccatctctc-3′ (CCL8 forward and reverse; product size: 128 bp); 5′-ggcaaatgctggacccaacaca-3′ and 5′-tgctggtcttgccattcctgga-3′ (PPIA forward and reverse; product size: 161 bp); 5′-tcacaacaagcataccaagaagc-3′ and 5′-gtatccgatgtccacaatgtcaag-3′ (RPLP0 forward and reverse; product size: 263 bp); and 5′-tagattattctctgatttggtcgtattgg-3′ and 5′-gctcctggaagatggtgatgg-3′ (GAPDH forward and reverse; product size: 223 bp). Except for CCL2 and GAPDH, being designed using Beacon Designer Probe/Primer Design Software (BioRad) and validated in silico (Blast analysis), the starters’ sequences were proposed by OriGene (www.origene.com (accessed on 1 March 2021)).
The Cq values of the technical replicates were averaged prior to expression analysis. For each analyzed gene, the geometric mean of all Cq values was subtracted from the sample Cq, yielding ΔCq. The ΔCq values were then linearized by 2ΔCq conversion and normalized to the internal control: the geometric mean of PPIA and RPLP0 expression [28] or GAPDH expression. The resulting normalized relative quantity values were denoted NRQ [29] and subjected to statistical analysis.

2.3. Data Analysis

All statistical analyses were conducted using MedCalc® Statistical Software version 20.011 (MedCalc Software Ltd., Ostend, Belgium). The level of statistical significance was set at ≤0.05, and all calculated p values were two-sided.
The distribution of data and homogeneity of variances were tested prior to the analyses using the Kolmogorov–Smirnov test and Levene test, respectively. The expression data, following log transformation, were analyzed using a t-test for the paired samples and a t-test for the independent samples with Welch correction in case of unequal variances or one-way ANOVA (multigroup comparisons) with Student–Newman–Keuls post hoc analysis. The IHC data were analyzed with the Wilcoxon test. Frequency analysis was conducted with a chi-squared test and correlation analysis with Pearson moment (r) or Spearman rank (ρ) correlation. The contingency coefficient (C) was calculated to express association for the categorical data. The stepwise method of linear multivariate regression was applied to identify the independent predictors of the dependent variable, with variables entered into the regression model if p < 0.05 and removed if p > 0.1.

3. Results

3.1. Expression of MCP Chemokines at the Protein Level

3.1.1. MCP Proteins in Colorectal Adenomas

Protein expression between the normal and polyp tissue was compared in 62 patients. Regarding MCP-1/CCL2, 8.1% of patients had lower protein expression in the polyps than the corresponding normal tissue, 40.3% had comparable expression levels, and 51.6% had higher MCP-1/CCL2 expression in the polyps than the matching normal tissue. Pairwise comparison showed significant MCP-1/CCL2 overexpression in the polyps (p = 0.0002). Photos representing various immunoreactivities of the polyps toward MCP-1/CCL2 are presented in Figure 1.
Regarding MCP-3/CCL7, 8.1% of patients had lower protein expression in the polyps than the corresponding normal tissue, 58.1% had comparable expression levels, and 33.9% had higher MCP-3/CCL7 expression in the polyps than the matching normal tissue. Still, pairwise comparison showed significant MCP-3/CCL7 overexpression in the polyps (p = 0.003). There were no polyp samples negative for MCP-3/CCL7 in the tested cohort. Photos representing immunoreactivity scores of one and two toward MCP-3/CCL7 are presented in Figure 2.
Regarding MCP-2/CCL8, 6.5% of patients had lower protein expression in the polyps than the corresponding normal tissue, 40.3% had comparable expression levels, and 53.2% had higher MCP-2/CCL8 expression in the polyps than the matching normal tissue. The pairwise comparison showed significant MCP-2/CCL8 overexpression in the polyps (p < 0.0001). Photos representing various immunoreactivities of the polyps toward MCP-2/CCL8 are presented in Figure 3.

3.1.2. MCP Association with the Anatomical Site and Pathological Findings

MCP-1/CCL2, MCP-3/CCL7, and MCP-2/CCL8 protein expression in the polyps was not associated with the polyp histology or grade of dysplasia. The exception was MCP-1/CCL2, for which low immunoreactivity was significantly associated with low-grade dysplasia and higher immunoreactivity with high-grade dysplasia (Table 2). The polyp size and its anatomical location had no effect on MCP-1/CCL2, MCP-3/CCL7, or MCP-2/CCL8 protein expression in the neoplasm (Table 2).
The change in expression between the normal and neoplastic mucosa (decreased, unaffected, or increased) with reference to the histological type, dysplasia grade, size, and anatomical location did not show significant associations, except for MCP-3/CCL7 and the anatomical site. Higher MCP-3/CCL7 immunoreactivity in the polyps than the adjacent mucosa was more likely to accompany left-sided polyps, and no change in immunoreactivity was more likely for the right-sided polyps (contingency coefficient (C) = 0.372, p = 0.041).
The immunoreactivity for MCP-1/CCL2 in the polyps positively correlated with that for MCP-2/CCL8 (ρ = 0.46, p = 0.0001), while MCP-1/CCL2′s correlation with MCP-3/CCL7 was weak and borderline significant (ρ = 0.25, p = 0.047), and that between MCP-3/CCL7 and MCP-2/CCL8 was non-significant (ρ = 0.25, p = 0.053).

3.2. Expression of MCP Chemokines at the Transcriptional Level

3.2.1. MCP Transcripts in Colorectal Adenomas

CCL2, CCL7, and CCL8 mRNA expression was analyzed against GAPDH or the geometric mean of a pair of normalizers: PPIA and RPLP0. Regardless the normalization strategy, the average CCL2, CCL7, and CCL8 expression was lower in the polyps than the normal mucosa and significantly lower in the case of CCL7 and CCL8 (Table 3).
As these results contradicted those obtained for the MCP proteins, an additional 110 patient-matched pairs of polyp and normal mucosa samples were analyzed by RTqPCR. Like for the IHC cohort alone, CCL2, CCL7, and CCL8 were downregulated in the polyps compared with the normal mucosa, and the degree of downregulation was similar between the smaller and larger cohorts and between the normalizers (Table 3).
Further analyses were conducted on the enlarged cohort (n = 173) using PPIA/RPLP0 as normalizers.

3.2.2. Effect of the Polyp Size on the Expression of MCP Chemokines (mRNA)

The fold change in CCL2, CCL7, and CCL8 expression was significantly affected by the polyp size. CCL2 expression was downregulated solely in the largest polyps (by 2.7-fold). In the case of CCL7 (3.1-fold) and CCL8 (4-fold), the downregulation was more marked in the larger polyps than the smaller polyps. Detailed analysis showed that gene expression was non-significantly higher in the normal mucosa of the patients with the largest polyps while being significantly lower in their polyps (by 2.1-fold for CCL2 and CCL7 and 2.7-fold for CCL8) (Figure 4).

3.2.3. Effect of the Polyp Type on the Expression of MCP Chemokines (mRNA)

The polyp type had a significant impact on the fold change in CCL2, CCL7, and CCL8 expression. For CCL2 and CCL8, it was the highest and indicative of gene upregulation (by 1.8- and 1.5-fold, respectively) in the polyp compared with the corresponding normal mucosa in hyperplastic polyps and the lowest in adenocarcinoma in the polyp, being indicative of gene downregulation in the polyp compared with the normal mucosa (by 11.1- and 16.7-fold, respectively). The fold change in CCL2, CCL7, and CCL8 expression decreased gradually along with an increasing villous component in the adenomas. CCL2 was upregulated in the tubular adenomas by 1.4-fold compared with the normal tissue but downregulated in the tubulo-villous and villous adenomas by 1.4- and 5.9-fold, respectively. CCL7 expression in the tubular adenomas was comparable to normal tissue but downregulated in the tubulo-villous and villous adenomas by 2.0- and 5.3-fold, respectively. CCL8 was already downregulated in the tubular adenomas (by 1.5-fold) but more markedly so in the tubulo-villous and villous adenomas, in which CCL8 was downregulated by 2.4- and 8.3-fold, respectively (Figure 5).
Detailed analysis of the gene expression patterns in the normal mucosa and polyps showed that the CCL2, CCL7, and CCL8 expression in the normal tissue was comparable and not affected by the polyp type, contrary to gene expression in the polyps. CCL2, CCL7, and CCL8 expression was the highest in the hyperplastic polyps and lower in the adenomas, in which it gradually decreased along with an increasing villous component. The polyp expression of CCL2 and CCL8 (but not CCL7) was the lowest in the adenocarcinomas (Figure 5).

3.2.4. Effect of the Dysplasia Grade on the Expression of MCP Chemokines (mRNA)

CCL2, CCL7 and CCL8 expression tended to decrease in the polyps compared with the normal tissue, though more markedly in the case of adenomas with high-grade dysplasia. CCL2 expression in the adenomas with high-grade dysplasia was significantly decreased compared with the adenomas with low-grade dysplasia (by 2.8-fold). Likewise, CCL8 expression was lower by 2.2-fold (Figure 6).

3.2.5. Effect of the Number of Polyps on the Expression of MCP Chemokines (mRNA)

Based on the number of polyps and their character (protruding or flat lesions), patients were classified as having single, multiple, or carpet-like polyps. Only polyp CCL2 expression was significantly affected by the number of polyps; it was significantly lower in patients with multiple lesions than those with single polyps (by 2.3-fold). In turn, CCL8 expression in normal mucosa tended to be higher in patients with multiple polyps, resulting in more pronounced downregulation (5-fold in the case of multiple lesions and 1.9-fold in the case of single polyps) (Figure 7).

3.2.6. Association of Cumulative Risk of Adenoma-to-Adenocarcinoma Transformation with the Expression of MCP Chemokines (mRNA)

As the risk of adenoma transformation to adenocarcinoma is higher in the case of larger and multiple polyps and those with dominant villous growth patterns and high-grade dysplasia, we summarized those risk factors by calculating a cumulative risk factor. To ensure the same weight for all risk factors, three categorical variables such as tubular, tubulo-villous, and villous adenomas or <10 mm, 10–19 mm, and ≥20 mm adenomas were assigned scores of 1, 1.5, and 2, respectively, and two categorical variables such as low- and high-grade dysplasia or single and multiple adenomas were assigned scores of 1 and 2, respectively.
Both the fold change in expression of CCL2, CCL7, and CCL8 and gene expression in adenoma were inversely correlated with a cumulative risk of transformation. The strongest association was noted for adenoma expression of CCL2. In the case of CCL7, its expression concomitantly decreased in adenoma and increased in macroscopically normal tissue (Table 4).

3.2.7. Effect of the Anatomical Subsite on the Expression of MCP Chemokines (mRNA)

The anatomical subsite significantly affected the fold change in CCL2, CCL7, and CCL8 expression. The rectal polyps downregulated CCL2 and CCL7 by 3.1-fold and CCL8 by 5.3-fold, while gene downregulation in the colonic polyps was absent or less substantial. Detailed analysis of the gene expression in the polyp and normal mucosa showed that the polyp expression tended to be lower in the case of the rectal location (significantly so for CCL8) while being relatively higher in normal mucosa (Figure 8).
A polyp location in the rectum was significantly associated with a high grade of dysplasia (p = 0.004), prevalence of the villous component (p = 0.001), and the polyp size (p = 0.0001). Therefore, to verify the effect of the polyp sublocation on chemokine expression and discern the independent predictors of CCL2, CCL7, and CCL8 expression in colorectal adenomas, a multivariate analysis was conducted.

3.2.8. Multivariate Analysis

A stepwise method was applied to co-analyze the effect of the dysplasia grade, adenoma growth pattern, adenoma size, number of polyps, and subsite and patient’s age and sex on CCL2, CCL7, and CCL7 expression in colorectal adenomas.
Of those variables, CCL2 expression was independently associated with the grade of dysplasia, growth pattern, number of adenomas, and patient’s age, which together explained 22% of the variability in gene expression. All associations were inverse; that is, CCL2 expression in colorectal adenomas decreased along with the increasing number of polyps, and the patient’s age and was lower in adenomas with high grades of dysplasia and dominant villous components. The effect of the dysplasia grade was the strongest, and that of age was the weakest (Table 5).
Of the examined variables, CCL7 expression in colorectal adenomas was affected solely by the growth pattern, which explained 8% of the variability in gene expression. CCL7 decreased along with an increasing villous component (Table 5).
CCL8 was significantly affected by the dysplasia grade and growth pattern, which explained 10% of the variability in gene expression. CCL8 expression decreased along with an increasing villous component and was lower in adenomas with high-grade dysplasia (Table 5).

3.2.9. Interrelationship between the Expression of MCP Chemokines

There was a positive correlation between CCL2, CCL7, and CCL8 in the normal mucosa and polyps, with the correlation between CCL2 and CCL8 being equally strong, while those between CCL2 and CCL7 and between CCL7 and CCL8 were stronger in the polyps than the normal tissue (Table 6).

3.3. Interrelationship between the Expression of MCP Chemokines at the Protein and Transcriptional Levels

CCL2 and CCL7 mRNA expression was inversely related with the CCL2 and CCL7 immunoreactivity score in the polyps, as indicated by the lower NRQ values accompanying score 1 compared with score 0 (CCL2) or score 2 compared with score 1 (CCL7). CCL8 mRNA expression decreased along with increasing CCL8 immunoreactivity, which was non-significant in the polyps but significant in the adjacent normal tissue (Figure 9).

4. Discussion

There is growing interest in inflammatory mediators as potential targets for CRC chemoprevention, evoked by the efficacy of aspirin and non-aspirin NSAIDs at reducing the incidence, number, and size of neoplasm evidenced in animal models of colorectal carcinogenesis as well as human studies (reviewed in [1]). Apart from interfering with the COX/PGE2 pathway, NSAIDs are believed to act by affecting other tumor-promoting signaling pathways, altering the gut microbiome, and disrupting the inflammatory microenvironment (reviewed in [15]). Among other effects, NSAIDs can modulate the expression of MCP chemokines (manuscript submitted). The key representative, MCP-1/CCL2, has previously been demonstrated to be upregulated in CRC at the local [21,22] and systemic levels [30] and induce the proliferation [31] and epithelial-mesenchymal transition of tumor cells [19]. Moreover, circulating MCP-1 has been indicated as a prognosticator of increased CRC risk [32] and a component of cytokine panels differentiating CRC patients from those with high-risk conditions such as IBD and adenomas [33]. However, data on MCP-1/CCL2 expression in colorectal adenomas are limited, not allowing confirmation of the chemokine potential as a target for chemoprevention. Only recently, comparative RNAseq analysis of the colorectal transcriptome of patient-matched (n = 5) samples of normal mucosa, adenomas, and adenocarcinomas has shown that CCL2 expression is significantly upregulated in tumors compared with adenomas but downregulated in adenomas compared with normal mucosa [27]. The results presented in the current study corroborate observations regarding adenomas on a larger set of samples, indicating a similar level of downregulation. They also link a magnitude of downregulation with a polyp’s potential for malignancy. The risk of transformation into carcinoma is higher in patients with multiple polyps and in the case of larger lesions. For adenomas, this depends on the dysplasia grade as well as the contribution of the villous growth pattern. Large, predominantly villous adenomas with high-grade dysplasia are referred to as “advanced adenomas” [34]. Hyperplastic polyps, in turn, are representatives of serrated polyps [3] and have previously been considered innocuous [34]. However, recent evidence indicates that they may progress to serrated adenomas and then cancer over time [3]. Here, we showed that CCL2 expression in polyps and the polyp-to-normal expression ratio were lower in patients with large and multiple polyps and adenomas with a dominant villous growth pattern and high-grade dysplasia. Moreover, the dysplasia grade, growth pattern, and number of polyps were, together with the patient’s age, independent predictors of CCL2 expression. Likewise, CCL7 and CCL8 expression was downregulated in polyps compared with the patient-matched normal mucosa, the most pronounced example being in the case of CCL8, both herein and in the RNAseq analysis of Hong et al. [27]. Their expression in the polyp and expression rate mimicked the CCL2 patterns; they were lower in the larger polyps and adenomas with a higher grade of dysplasia and decreased with the increasing contribution of the villous growth pattern. CCL8 expression was also significantly lower in patients with multiple polyps. A dominant villous growth pattern for both CCL7 and CCL8 and high-grade dysplasia for CCL8 were independent predictors of chemokine expression, although their contributions to the expression variability were rather low and indicative of the presence of other effectors which were not evaluated in the current study. The CCL2, CCL7, and CCL8 expression seemed to depend on the polyp location, as the lowest expression ratios were observed for the rectal polyps. However, as indicated by the results of the multivariate analysis, the neoplasm location lost significance when co-examined with the histopathological findings.
The role of MCP-2/CCL8 and MCP-3/CCL7 in colorectal carcinogenesis and cancer progression is less studied and clear. Clinical studies have linked MCP-3/CCL7 overexpression with liver metastasis [35], while cell culture studies have demonstrated MCP-3 to promote cancer cell proliferation in addition to enhancing their migratory and invasive properties [36]. MCP-3 also displays immunomodulatory properties and facilitates tumor growth by attracting monocytes and promoting their phenotypic transformation to tumor-associated macrophages, but it can also contribute to tumor infiltration with tumor-suppressing subsets of T lymphocyte and dendritic cells [37]. Accordingly, CCL7 transfection has inhibited the growth of primary tumors and prevented metastasis [25,26]. In osteosarcoma [38] and melanoma [39], high CCL8 expression has been a good prognosticator and correlated with tumor infiltration with CD8+ T cells and M1 macrophages [38], while in animal models, MCP-2/CCL8 negatively affected the proliferation of melanoma cells and reduced the number of liver metastases [40]. On the other hand, CCL8 has been found to facilitate the progression of glioblastoma by promoting invasion and stemness [41], pancreatic ductal adenocarcinoma by stimulating proliferation and invasiveness [42], and breast and lung cancer by recruiting Tregs into metastatic sites [16]. Corroborating its pro-tumorigenic character, overexpression of CCL8 in breast and endometrial cancer has been predictive of poor prognoses [43]. Regarding CRC, MCP-2/CCL8 derived from cancer-associated fibroblasts have been shown to stimulate the proliferation of cancer cells [31], while MCP-2/CCL8 and MCP-3/CCL7 derived from tumor-associated macrophages attract anti-tumor CD4+ and CD8+ T cells [44].
Intriguingly, all MCP proteins were upregulated in the polyps compared with the patient-matched normal mucosa, although their corresponding transcripts demonstrated unanimous downregulation. As the results of transcriptional analysis depend on genes used as normalizers, we used several internal controls, namely the most popular (GAPDH), the pair of genes previously found to be stably expressed in colorectal cancer (PPIA and RPLP0) [28], and RN18S1, which all yielded consistent results. As mentioned earlier, chemokine downregulation in the paired analysis of adenoma and normal mucosa from five patients was also noted in the study by Hong et al. [27]. Here, we demonstrated that gene expression was inversely correlated with immunoreactivity toward chemokine proteins. There are several possible explanations for the observed counter-regulation of CCL2, CCL7, and CCL8 transcripts and MCP-1, MCP-3, and MCP-2 proteins. First, different fragments of polyps were analyzed in the transcriptomic and protein analysis, and while IHC semi-quantitatively detected the MCP content solely in the epithelial cells, the relative transcript number was determined fully quantitatively but in tissue fragments that were heterogenous and unspecified in terms of cellular composition. Secondly, there might be an expression gradient formed across the longitudinal section of the polyp resembling an expression gradient formed by MCP-2/CCL8 in breast cancer, with an increasing chemokine concentration from the neoplastic epithelium via stroma to the periphery [45]. The prolonged half-life of MCP proteins and possible feedback inhibition is yet another plausible explanation for the observed discrepancy supported by our recent findings regarding polyp expression of heat shock proteins (HSP)-70 and 90 (manuscript submitted) and atypical chemokine receptors [7]. The HSPs play a role in carcinogenesis as chaperones of cancer-promoting proteins including MCP, protecting them from degradation and thus increasing their longevity, leading to accumulation [46,47]. Indeed, we have found HSPA1 (HSP70) and HSP90AA1 expression in patients with polyps to be upregulated and positively correlated with the dysplasia grade and villous component. We have also observed a downregulation of the decoy chemokine receptors ACKR2 and ACKR4 [7], which are involved in scavenging chemokines and directing them to degradation [48]. Lower expression of ACKRs would therefore translate into reduced chemokine turnover and further contribute to their accumulation. Like for the analyzed chemokines, ACKR downregulation has been the greatest in adenomas with the highest malignancy potential. Moreover, a recent study by Smit et al. [49] indicated that mutations in the APC, TP53, KRAS, and SMAD4 genes, all characteristics for colorectal adenoma-carcinoma transition, are associated with enhanced global translational capacity, which may, at least in part, counterbalance the reduced transcription observed here.

5. Conclusions

Colorectal polyps are characterized by a significantly higher content of MCP-1, MCP-2, and MCP-3 proteins but a lower number of the respective CCL2, CCL7, and CCL8 transcripts, the downregulation of which is more pronounced in polyps with greater potential for malignancy. Considering a discrepancy between mRNA and protein expression, which an enhanced translational capacity and reduced protein degradation might contribute to, chemopreventive strategies directed against chemokine proteins or molecules contributing to their accumulation, such as HSPs and ACKRs, or components of the translational machinery, rather than targeting chemokine gene expression, should be considered.

Author Contributions

Conceptualization, J.W. and M.K.-K.; methodology, J.W., A.L., and M.K.-K.; formal analysis, J.W., A.L., K.N., and M.K.-K.; investigation, A.L., I.B.-M., Ł.L., P.L., and M.K-.K.; resources, J.W., K.N., and M.K.-K.; data curation, J.W.; writing, J.W., A.L., and M.K.-K.; writing—review and editing, J.W., K.N., and M.K.-K.; visualization, A.L. and M.K.-K.; supervision, M.K.-K.; project administration, M.K.-K.; funding acquisition, K.N. and M.K.-K. All authors have read and agreed to the published version of the manuscript.

Funding

This research was financed by Wroclaw Medical University (SUB.A040.21.012).

Institutional Review Board Statement

Sample collection was approved by the medical ethics committees of Wroclaw Medical University (#KB-247/2018 from 24 April 2018).

Informed Consent Statement

This study was conducted in accordance with the Helsinki Declaration of 1975, as revised in 1983, and written informed consent has been obtained from all patients.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Immunohistochemical analysis of MCP-1/CCL2 protein expression in colorectal adenomas: (a) negative reaction, with no reaction in the glandular epithelial cells or it only occurring in the stromal area of the lesion; (b) a weak cytoplasmic reaction, or the reaction did not encompass the entire lesion (score 1; +); and (c) a strong cytoplasmic reaction encompassing the entire lesion (score 2; ++). The tissue slides were incubated with rabbit anti-human MCP-1/CCL2 antibodies with a DAB chromogen, stained brown in the case of a positive reaction and counterstained with hematoxylin. All the photos were taken at 200×.
Figure 1. Immunohistochemical analysis of MCP-1/CCL2 protein expression in colorectal adenomas: (a) negative reaction, with no reaction in the glandular epithelial cells or it only occurring in the stromal area of the lesion; (b) a weak cytoplasmic reaction, or the reaction did not encompass the entire lesion (score 1; +); and (c) a strong cytoplasmic reaction encompassing the entire lesion (score 2; ++). The tissue slides were incubated with rabbit anti-human MCP-1/CCL2 antibodies with a DAB chromogen, stained brown in the case of a positive reaction and counterstained with hematoxylin. All the photos were taken at 200×.
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Figure 2. Immunohistochemical analysis of MCP-3/CCL7 protein expression in colorectal adenomas: (a) a weak cytoplasmic reaction, or the reaction did not encompass the entire lesion (score 1; +) and (b) a strong cytoplasmic reaction encompassing the entire lesion (score 2; ++). There were no polyp samples negative for MCP-3/CCL7 in the tested cohort. The tissue slides were incubated with rabbit anti-human MCP-3/CCL7 antibodies with a DAB chromogen, stained brown in the case of a positive reaction and counterstained with hematoxylin. All the photos were taken at 200×.
Figure 2. Immunohistochemical analysis of MCP-3/CCL7 protein expression in colorectal adenomas: (a) a weak cytoplasmic reaction, or the reaction did not encompass the entire lesion (score 1; +) and (b) a strong cytoplasmic reaction encompassing the entire lesion (score 2; ++). There were no polyp samples negative for MCP-3/CCL7 in the tested cohort. The tissue slides were incubated with rabbit anti-human MCP-3/CCL7 antibodies with a DAB chromogen, stained brown in the case of a positive reaction and counterstained with hematoxylin. All the photos were taken at 200×.
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Figure 3. Immunohistochemical analysis of MCP-2/CCL8 protein expression in colorectal adenomas: (a) negative reaction, showing either no reaction in the glandular epithelial cells or it only occurring in the stromal area of the lesion; (b) a weak cytoplasmic reaction, or the reaction did not encompass the entire lesion (score 1; +); and (c) a strong cytoplasmic reaction encompassing the entire lesion (score 2; ++). The tissue slides were incubated with rabbit anti-human MCP-2/CCL8 antibodies with a DAB chromogen, stained brown in the case of a positive reaction and counterstained with hematoxylin. All the photos were taken at 200×.
Figure 3. Immunohistochemical analysis of MCP-2/CCL8 protein expression in colorectal adenomas: (a) negative reaction, showing either no reaction in the glandular epithelial cells or it only occurring in the stromal area of the lesion; (b) a weak cytoplasmic reaction, or the reaction did not encompass the entire lesion (score 1; +); and (c) a strong cytoplasmic reaction encompassing the entire lesion (score 2; ++). The tissue slides were incubated with rabbit anti-human MCP-2/CCL8 antibodies with a DAB chromogen, stained brown in the case of a positive reaction and counterstained with hematoxylin. All the photos were taken at 200×.
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Figure 4. Effect of polyp size on the expression (mRNA) of MCP chemokines in patients with colorectal polyps: (a) fold change (FC) in CCL2 expression between the polyp and normal mucosa (P/N); (b) CCL2 expression in a polyp; (c) CCL2 expression in normal tissue; (d) fold change (FC) in CCL7 expression between the polyp and normal mucosa (P/N); (e) CCL7 expression in a polyp; (f) CCL7 expression in normal tissue; (g) fold change (FC) in CCL8 expression between the polyp and normal mucosa (P/N); (h) CCL8 expression in a polyp; (i) CCL8 expression in normal tissue. Data analyzed as logarithms using one-way ANOVA with a Student–Newman–Keuls post hoc test and presented as means with 95% confidence intervals (red squares with whiskers and numbers below the dot plots). Significant (p < 0.05) differences between groups (identified in post hoc analysis) are indicated by the same symbol type (*, ^). NRQ: normalized relative quantity.
Figure 4. Effect of polyp size on the expression (mRNA) of MCP chemokines in patients with colorectal polyps: (a) fold change (FC) in CCL2 expression between the polyp and normal mucosa (P/N); (b) CCL2 expression in a polyp; (c) CCL2 expression in normal tissue; (d) fold change (FC) in CCL7 expression between the polyp and normal mucosa (P/N); (e) CCL7 expression in a polyp; (f) CCL7 expression in normal tissue; (g) fold change (FC) in CCL8 expression between the polyp and normal mucosa (P/N); (h) CCL8 expression in a polyp; (i) CCL8 expression in normal tissue. Data analyzed as logarithms using one-way ANOVA with a Student–Newman–Keuls post hoc test and presented as means with 95% confidence intervals (red squares with whiskers and numbers below the dot plots). Significant (p < 0.05) differences between groups (identified in post hoc analysis) are indicated by the same symbol type (*, ^). NRQ: normalized relative quantity.
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Figure 5. Effect of the polyp type on the expression (mRNA) of MCP chemokines in patients with colorectal polyps: (a) fold change (FC) in CCL2 expression between the polyp and normal mucosa (P/N); (b) CCL2 expression in a polyp; (c) CCL2 expression in normal tissue; (d) fold change (FC) in CCL7 expression between the polyp and normal mucosa (P/N); (e) CCL7 expression in a polyp; (f) CCL7 expression in normal tissue; (g) fold change (FC) in CCL8 expression between the polyp and normal mucosa (P/N); (h) CCL8 expression in a polyp; (i) CCL8 expression in normal tissue. Data analyzed as logarithms using one-way ANOVA with a Student–Newman–Keuls post hoc test and presented as means with 95% confidence intervals (red squares with whiskers and numbers below dot plots). Significant (p < 0.05) differences between groups (identified in post hoc analysis) are indicated by the same symbol type (*, ^, <, +, #). NRQ: normalized relative quantity; H: hyperplastic polyps; T: tubular adenomas; T-V: tubulo-villous adenomas; V: villous adenomas; A: adenocarcinoma in a polyp.
Figure 5. Effect of the polyp type on the expression (mRNA) of MCP chemokines in patients with colorectal polyps: (a) fold change (FC) in CCL2 expression between the polyp and normal mucosa (P/N); (b) CCL2 expression in a polyp; (c) CCL2 expression in normal tissue; (d) fold change (FC) in CCL7 expression between the polyp and normal mucosa (P/N); (e) CCL7 expression in a polyp; (f) CCL7 expression in normal tissue; (g) fold change (FC) in CCL8 expression between the polyp and normal mucosa (P/N); (h) CCL8 expression in a polyp; (i) CCL8 expression in normal tissue. Data analyzed as logarithms using one-way ANOVA with a Student–Newman–Keuls post hoc test and presented as means with 95% confidence intervals (red squares with whiskers and numbers below dot plots). Significant (p < 0.05) differences between groups (identified in post hoc analysis) are indicated by the same symbol type (*, ^, <, +, #). NRQ: normalized relative quantity; H: hyperplastic polyps; T: tubular adenomas; T-V: tubulo-villous adenomas; V: villous adenomas; A: adenocarcinoma in a polyp.
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Figure 6. Effect of the dysplasia grade on the expression (mRNA) of MCP chemokines in patients with colorectal polyps: (a) fold change (FC) in CCL2 expression between the polyp and normal mucosa (P/N); (b) CCL2 expression in a polyp; (c) CCL2 expression in normal tissue; (d) fold change (FC) in CCL7 expression between the polyp and normal mucosa (P/N); (e) CCL7 expression in a polyp; (f) CCL7 expression in normal tissue; (g) fold change (FC) in CCL8 expression between the polyp and normal mucosa (P/N); (h) CCL8 expression in a polyp; (i) CCL8 expression in normal tissue. Data analyzed as logarithms using a t-test for independent samples with Welch correction in the case of unequal variances and presented as means with 95% confidence intervals (red squares with whiskers and numbers below dot plots). NRQ: normalized relative quantity; LGD: low-grade dysplasia; HGD: high-grade dysplasia.
Figure 6. Effect of the dysplasia grade on the expression (mRNA) of MCP chemokines in patients with colorectal polyps: (a) fold change (FC) in CCL2 expression between the polyp and normal mucosa (P/N); (b) CCL2 expression in a polyp; (c) CCL2 expression in normal tissue; (d) fold change (FC) in CCL7 expression between the polyp and normal mucosa (P/N); (e) CCL7 expression in a polyp; (f) CCL7 expression in normal tissue; (g) fold change (FC) in CCL8 expression between the polyp and normal mucosa (P/N); (h) CCL8 expression in a polyp; (i) CCL8 expression in normal tissue. Data analyzed as logarithms using a t-test for independent samples with Welch correction in the case of unequal variances and presented as means with 95% confidence intervals (red squares with whiskers and numbers below dot plots). NRQ: normalized relative quantity; LGD: low-grade dysplasia; HGD: high-grade dysplasia.
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Figure 7. Effect of the number of polyps on the expression (mRNA) of MCP chemokines in patients with colorectal polyps: (a) fold change (FC) in CCL2 expression between the polyp and normal mucosa (P/N); (b) CCL2 expression in a polyp; (c) CCL2 expression in normal tissue; (d) fold change (FC) in CCL7 expression between the polyp and normal mucosa (P/N); (e) CCL7 expression in a polyp; (f) CCL7 expression in normal tissue; (g) fold change (FC) in CCL8 expression between the polyp and normal mucosa (P/N); (h) CCL8 expression in a polyp; (i) CCL8 expression in normal tissue. Data analyzed as logarithms using one-way ANOVA with a Student–Newman–Keuls post hoc test and presented as means with 95% confidence intervals (red squares with whiskers and numbers below dot plots). Significant (p < 0.05) differences between groups (identified in post hoc analysis) are indicated by an asterisk (*). NRQ: normalized relative quantity.
Figure 7. Effect of the number of polyps on the expression (mRNA) of MCP chemokines in patients with colorectal polyps: (a) fold change (FC) in CCL2 expression between the polyp and normal mucosa (P/N); (b) CCL2 expression in a polyp; (c) CCL2 expression in normal tissue; (d) fold change (FC) in CCL7 expression between the polyp and normal mucosa (P/N); (e) CCL7 expression in a polyp; (f) CCL7 expression in normal tissue; (g) fold change (FC) in CCL8 expression between the polyp and normal mucosa (P/N); (h) CCL8 expression in a polyp; (i) CCL8 expression in normal tissue. Data analyzed as logarithms using one-way ANOVA with a Student–Newman–Keuls post hoc test and presented as means with 95% confidence intervals (red squares with whiskers and numbers below dot plots). Significant (p < 0.05) differences between groups (identified in post hoc analysis) are indicated by an asterisk (*). NRQ: normalized relative quantity.
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Figure 8. Effect of the anatomical subsite on the expression (mRNA) of MCP chemokines in patients with colorectal polyps: (a) fold change (FC) in CCL2 expression between the polyp and normal mucosa (P/N); (b) CCL2 expression in a polyp; (c) CCL2 expression in normal tissue; (d) fold change (FC) in CCL7 expression between the polyp and normal mucosa (P/N); (e) CCL7 expression in a polyp; (f) CCL7 expression in normal tissue; (g) fold change (FC) in CCL8 expression between the polyp and normal mucosa (P/N); (h) CCL8 expression in a polyp; (i) CCL8 expression in normal tissue. Data analyzed as logarithms using one-way ANOVA with a Student–Newman–Keuls post hoc test and presented as means with 95% confidence intervals (red squares with whiskers and numbers below dot plots). Significant (p < 0.05) differences between groups (identified in post hoc analysis) are indicated by the same symbol type (*, ^). NRQ: normalized relative quantity.
Figure 8. Effect of the anatomical subsite on the expression (mRNA) of MCP chemokines in patients with colorectal polyps: (a) fold change (FC) in CCL2 expression between the polyp and normal mucosa (P/N); (b) CCL2 expression in a polyp; (c) CCL2 expression in normal tissue; (d) fold change (FC) in CCL7 expression between the polyp and normal mucosa (P/N); (e) CCL7 expression in a polyp; (f) CCL7 expression in normal tissue; (g) fold change (FC) in CCL8 expression between the polyp and normal mucosa (P/N); (h) CCL8 expression in a polyp; (i) CCL8 expression in normal tissue. Data analyzed as logarithms using one-way ANOVA with a Student–Newman–Keuls post hoc test and presented as means with 95% confidence intervals (red squares with whiskers and numbers below dot plots). Significant (p < 0.05) differences between groups (identified in post hoc analysis) are indicated by the same symbol type (*, ^). NRQ: normalized relative quantity.
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Figure 9. Correlation between the expression of MCP chemokines at the transcriptional and protein levels: (a) CCL2 in polyps; (b) CCL7 in polyps; (c) CCL8 in polyps; (d) CCL2 in normal mucosa; (e) CCL7 in normal mucosa; and (f) CCL8 in normal mucosa. Data analyzed as logarithms using one-way ANOVA with a Student–Newman–Keuls post hoc test and presented as means with 95% confidence intervals (red squares with whiskers and numbers below dot plots). Significant (p < 0.05) differences between groups (identified in post hoc analysis) are indicated by the same symbol type (*, ^). NRQ: normalized relative quantity.
Figure 9. Correlation between the expression of MCP chemokines at the transcriptional and protein levels: (a) CCL2 in polyps; (b) CCL7 in polyps; (c) CCL8 in polyps; (d) CCL2 in normal mucosa; (e) CCL7 in normal mucosa; and (f) CCL8 in normal mucosa. Data analyzed as logarithms using one-way ANOVA with a Student–Newman–Keuls post hoc test and presented as means with 95% confidence intervals (red squares with whiskers and numbers below dot plots). Significant (p < 0.05) differences between groups (identified in post hoc analysis) are indicated by the same symbol type (*, ^). NRQ: normalized relative quantity.
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Table
Table 1. Characteristics of patients with colorectal polyps.
Table 1. Characteristics of patients with colorectal polyps.
ParameterIHC CohortRTqPCR Cohort
n62173
Sex distribution (F/M), n27/3578/95
Age (years), mean (95%CI)62.9 (60.2–65.7)65.3 (63.6–67.0)
Polyp histology, n
hyperplastic polyps411
tubular adenoma2337
tubulo-villous adenoma29107
villous adenoma613
adenocarcinoma in the polyp(1)5
Grade of dysplasia, n
low55128
high329
Polyp size, n
<10 mm1939
10–19 mm2475
≥20 mm1958
Polyp location, n
right colon1290
left colon3538
rectum1545
Number of polyps, n
single60129
multiple (≥2)236
carpet-like lesions07
n: number of observations; F/M: female-to-male ratio; yrs.: years; CI: confidence interval; IHC: immunohistochemistry; RTqPCR: reverse-transcribed quantitative (real-time) polymerase chain reaction (transcriptomic analysis).
Table
Table 2. Association of polyp CCL2, CCL7, and CCL8 expression with polyp characteristics.
Table 2. Association of polyp CCL2, CCL7, and CCL8 expression with polyp characteristics.
PathologyCCL2 Immunoreactivity Score 0/1/2, nCCL7 Immunoreactivity Score 0/1/2, nCCL8 Immunoreactivity Score 0/1/2, n
Histology:p = 0.956 1p = 0.212 1p = 0.600 1
  hyperplastic0/4/00/0/40/3/1
  tubular8/10/50/7/164/8/11
  tubulo-villous10/15/40/5/247/14/8
  villous2/3/10/0/62/2/2
Dysplasia:p = 0.033p = 0.368p = 0.547
  low grade20/27/80/12/4313/22/20
  high grade0/1/20/0/30/2/1
Size:p = 0.429p = 0.260p = 0.267
  <10 mm8/7/40/6/136/5/8
  10–19 mm8/12/40/3/215/13/6
  ≥20 mm4/13/20/3/162/9/8
Anatomical site:p = 0.769p = 0.837p = 0.842
  right colon3/7/20/3/93/4/5
  left colon11/17/70/6/296/16/13
  rectum6/8/10/3/124/7/4
n: number of observations. 1 Analyzed for adenomas (without hyperplastic polyps). Data analyzed using a chi-squared test.
Table
Table 3. CCL2, CCL7, and CCL8 expression in colorectal adenomas.
Table 3. CCL2, CCL7, and CCL8 expression in colorectal adenomas.
Patients from IHC Cohort, n = 62Patients from Whole RTqPCR Cohort, n = 173
PPIA/RPLP0GAPDHPPIA/RPLP0GAPDH
CCL2↓1.2, p = 0.209↓1.2, p = 0.245↓1.4, p = 0.037↓1.5, p = 0.066
CCL7↓1.5, p = 0.012↓1.5, p = 0.032↓1.7, p = 0.0001↓1.9, p = 0.005
CCL8↓2.0, p < 0.001↓2.0, p = 0.002↓2.3, p < 0.0001↓2.5, p = 0.0001
Data presented as a fold change in expression in the polyps compared with the patient-matched normal mucosa, with ↓ indicating a downregulation. Data were analyzed as logarithms using a t-test for paired samples. IHC: immunohistochemistry; RTqPCR: reverse-transcribed quantitative (real-time) polymerase chain reaction; n: group size.
Table
Table 4. Effect of cumulative risk of adenoma-to-adenocarcinoma transformation on expression of MCP chemokines.
Table 4. Effect of cumulative risk of adenoma-to-adenocarcinoma transformation on expression of MCP chemokines.
GeneFC (P/N)Polyp (p)Normal (n)
CCL2−0.32, p = 0.0001−0.46, p < 0.0001ns
CCL7−0.36, p < 0.0001−0.32, p = 0.00010.18, p = 0.032
CCL8−0.25, p = 0.003−0.30, p < 0.001ns
Data presented as Spearman correlation coefficients (ρ). FC: fold change; ns: non-significant (p > 0.05).
Table
Table 5. Regression models explaining expression of MCP chemokines in colorectal adenomas.
Table 5. Regression models explaining expression of MCP chemokines in colorectal adenomas.
Dependent
Variable		Explanatory
Variables		Regression
Coefficient (β), p		rpVIFR2; ANOVA
CCL2 (log)(constant)1.88 R2 = 0.22; F = 9.63,
p < 0.0001
dysplasia grade−0.41, p = 0.003−0.251.10
number of polyps−0.16, p = 0.017−0.201.02
growth pattern−0.27, p = 0.004−0.241.10
patient’s age−0.01, p = 0.011−0.211.02
CCL7 (log)(constant)0.36 R2 = 0.08; F = 12.0,
p < 0.001
growth pattern−0.29, p < 0.001−0.291
CCL8 (log)(constant)0.65 R2 = 0.10; F = 7.97,
p < 0.001
dysplasia grade−0.33, p = 0.027−0.191.10
growth pattern−0.25, p = 0.013−0.211.10
Data were analyzed using the stepwise method of linear multivariate regression. The adenoma size (as a continuous variable), number of polyps (as a continuous variable), growth pattern (tubular adenomas coded as 1, tubulo-villous as 2, and villous as 3), grade of dysplasia (low-grade dysplasia coded as 1 and high grade as 2), and anatomical subsite (rectum coded as 1 and colon coded as 0) as well as the patient’s age and sex (male coded as 1 and female as 0) were entered into the analysis. Results are presented as regression coefficients β together with a corresponding p value, partial correlation coefficient (rp), and variance inflation factor (VIF; multicollinearity indicator) for each explanatory variable retained in the regression model and as the model’s coefficient of determination (R2) together with ANOVA results (F statistics and p value).
Table
Table 6. Interrelationship between CCL2, CCL7, and CCL8 expression.
Table 6. Interrelationship between CCL2, CCL7, and CCL8 expression.
GeneFC (P/N)Polyp (p)Normal (n)
CCL7CCL8CCL7CCL8CCL7CCL8
CCL20.48 10.63 10.52 10.54 10.31 10.55 1
CCL7 0.63 1 0.66 1 0.48 1
Data analyzed as logarithms and presented as Pearson moment correlation coefficients (r). 1 p ≤ 0.0001. FC: fold change.
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Wierzbicki, J.; Lipiński, A.; Bednarz-Misa, I.; Lewandowski, Ł.; Neubauer, K.; Lewandowska, P.; Krzystek-Korpacka, M. Monocyte Chemotactic Proteins (MCP) in Colorectal Adenomas Are Differently Expressed at the Transcriptional and Protein Levels: Implications for Colorectal Cancer Prevention. J. Clin. Med. 2021, 10, 5559. https://doi.org/10.3390/jcm10235559

AMA Style

Wierzbicki J, Lipiński A, Bednarz-Misa I, Lewandowski Ł, Neubauer K, Lewandowska P, Krzystek-Korpacka M. Monocyte Chemotactic Proteins (MCP) in Colorectal Adenomas Are Differently Expressed at the Transcriptional and Protein Levels: Implications for Colorectal Cancer Prevention. Journal of Clinical Medicine. 2021; 10(23):5559. https://doi.org/10.3390/jcm10235559

Chicago/Turabian Style

Wierzbicki, Jarosław, Artur Lipiński, Iwona Bednarz-Misa, Łukasz Lewandowski, Katarzyna Neubauer, Paulina Lewandowska, and Małgorzata Krzystek-Korpacka. 2021. "Monocyte Chemotactic Proteins (MCP) in Colorectal Adenomas Are Differently Expressed at the Transcriptional and Protein Levels: Implications for Colorectal Cancer Prevention" Journal of Clinical Medicine 10, no. 23: 5559. https://doi.org/10.3390/jcm10235559

APA Style

Wierzbicki, J., Lipiński, A., Bednarz-Misa, I., Lewandowski, Ł., Neubauer, K., Lewandowska, P., & Krzystek-Korpacka, M. (2021). Monocyte Chemotactic Proteins (MCP) in Colorectal Adenomas Are Differently Expressed at the Transcriptional and Protein Levels: Implications for Colorectal Cancer Prevention. Journal of Clinical Medicine, 10(23), 5559. https://doi.org/10.3390/jcm10235559

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