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Article

Connexin 43 Expression as Biomarker of Oral Squamous Cell Carcinoma and Its Association with Human Papillomavirus 16 and 18

by
Jose Roberto Gutierrez-Camacho
,
Lorena Avila-Carrasco
*,
Idalia Garza-Veloz
,
Joel Monárrez-Espino
,
Maria Calixta Martinez-Vazquez
,
Roxana Araujo-Espino
,
Perla M. Trejo-Ortiz
,
Rosa B. Martinez-Flores
,
Reinaldo Gurrola-Carlos
,
Lorena Troncoso-Vazquez
and
Margarita L. Martinez-Fierro
*
Doctorate in Sciences with Orientation in Molecular Medicine, Academic Unit of Human Medicine and Health Sciences, Universidad Autónoma de Zacatecas, Zacatecas 98160, Mexico
*
Authors to whom correspondence should be addressed.
Int. J. Mol. Sci. 2025, 26(3), 1232; https://doi.org/10.3390/ijms26031232
Submission received: 19 December 2024 / Revised: 23 January 2025 / Accepted: 28 January 2025 / Published: 30 January 2025

Abstract

Oral squamous cell carcinoma (OSCC) is the main form of head and neck cancer. Gap junctions (GJs) are communication channels involved in cell proliferation control; they consist of hemichannels formed by connexin (Cx) proteins. The abnormal expression/function of Cx43 has been associated with tumor progression. Also, some human papillomaviruses (HPVs) have been linked to squamous cell cancer. Therefore, this study aimed at assessing Cx43 as a potential OSCC biomarker and exploring its association with histopathological differentiation and HPV infection. OSCC samples were inspected using hematoxylin and eosin staining, and Cx43 expression and HPV 16/18 were tested by immunofluorescence. Pearson correlation tests, ANOVA, and Kaplan–Meier curves were used in the analysis. Samples from 39 patients with OSCC were studied. Most had well-differentiated histology and 61.5% were HPV+. Cx43 expression was significantly associated with HPV infection (p = 0.047), differentiation (p < 0.001), and survival (p = 0.009), and HPV positivity was also associated with the degree of differentiation (p = 0.012). Cx43 shows potential as a prognostic biomarker for OSCC. Lower Cx43 expression, correlated with poorer differentiation, is associated with an unfavorable prognosis. Further studies are needed to confirm its clinical utility.
Keywords: Connexin 43; oral squamous cell carcinoma; human papillomaviruses Connexin 43; oral squamous cell carcinoma; human papillomaviruses

Share and Cite

MDPI and ACS Style

Gutierrez-Camacho, J.R.; Avila-Carrasco, L.; Garza-Veloz, I.; Monárrez-Espino, J.; Martinez-Vazquez, M.C.; Araujo-Espino, R.; Trejo-Ortiz, P.M.; Martinez-Flores, R.B.; Gurrola-Carlos, R.; Troncoso-Vazquez, L.; et al. Connexin 43 Expression as Biomarker of Oral Squamous Cell Carcinoma and Its Association with Human Papillomavirus 16 and 18. Int. J. Mol. Sci. 2025, 26, 1232. https://doi.org/10.3390/ijms26031232

AMA Style

Gutierrez-Camacho JR, Avila-Carrasco L, Garza-Veloz I, Monárrez-Espino J, Martinez-Vazquez MC, Araujo-Espino R, Trejo-Ortiz PM, Martinez-Flores RB, Gurrola-Carlos R, Troncoso-Vazquez L, et al. Connexin 43 Expression as Biomarker of Oral Squamous Cell Carcinoma and Its Association with Human Papillomavirus 16 and 18. International Journal of Molecular Sciences. 2025; 26(3):1232. https://doi.org/10.3390/ijms26031232

Chicago/Turabian Style

Gutierrez-Camacho, Jose Roberto, Lorena Avila-Carrasco, Idalia Garza-Veloz, Joel Monárrez-Espino, Maria Calixta Martinez-Vazquez, Roxana Araujo-Espino, Perla M. Trejo-Ortiz, Rosa B. Martinez-Flores, Reinaldo Gurrola-Carlos, Lorena Troncoso-Vazquez, and et al. 2025. "Connexin 43 Expression as Biomarker of Oral Squamous Cell Carcinoma and Its Association with Human Papillomavirus 16 and 18" International Journal of Molecular Sciences 26, no. 3: 1232. https://doi.org/10.3390/ijms26031232

APA Style

Gutierrez-Camacho, J. R., Avila-Carrasco, L., Garza-Veloz, I., Monárrez-Espino, J., Martinez-Vazquez, M. C., Araujo-Espino, R., Trejo-Ortiz, P. M., Martinez-Flores, R. B., Gurrola-Carlos, R., Troncoso-Vazquez, L., & Martinez-Fierro, M. L. (2025). Connexin 43 Expression as Biomarker of Oral Squamous Cell Carcinoma and Its Association with Human Papillomavirus 16 and 18. International Journal of Molecular Sciences, 26(3), 1232. https://doi.org/10.3390/ijms26031232

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