Liquid Biopsy: Latest Insights into the Biological Significance of Circulating Tumor Cells

A special issue of Biomedicines (ISSN 2227-9059). This special issue belongs to the section "Molecular and Translational Medicine".

Deadline for manuscript submissions: closed (15 August 2024) | Viewed by 1058

Special Issue Editor


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Guest Editor
Department of Radiological, Oncological and Pathological Sciences, Sapienza-University of Rome, 00161 Rome, Italy
Interests: precision medicine; liquid biopsy; CTC; ctDNA; breast cancer; personalized treatment
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Special Issue Information

Dear Colleagues,

Described by Thomas Ashworth in 1869 for the first time, circulating tumor cells (CTCs) represent one of the most important biomarkers in the field of liquid biopsy. Being passively and actively shed by primary tumor or secondary metastases, CTCs play a major role in the metastatic cascade, contributing to metastasis formation. Despite massive efforts being spent to refine and improve the isolation and analysis of these cells, only a single application has been introduced into clinical practice to date, concerning the prognostic value of CTC counts. Indeed, methodological limitations have hampered the study of the biological significance of these cells, which remain elusive. However, during the last few years, we witnessed constant technical progress that led to more accurate insights into the biology of CTCs. As emerged from recent scientific works, CTCs can exhibit different phenotypes and structural features, overcoming their original definition and adding multiple layers of complexity in the interpretation of these events, which require deeper investigations. In this context, a new classification is extremely desirable to correctly acknowledge the different types of tumor cells found in the blood of cancer patients.

Under these premises, we are pleased to invite you to contribute to this Special Issue with original research articles and reviews, focused on new biological insights into the nature of circulating tumor cells in different tumor types. Topics of interest may include (but are not limited to) the following:

  • New biological features of circulating tumor cells;
  • Structural characteristics of circulating tumor cells;
  • Structural/phenotypical-based classifications of circulating tumor cells;
  • The impact of these newly identified CTC characteristics on the clinical decision-making process.

We look forward to receiving your manuscripts.

Dr. Valentina Magri
Guest Editor

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Keywords

  • liquid biopsy
  • circulating tumor cells
  • tumor biomarkers
  • cancer
  • clinical decision-making process
  • biology

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Published Papers (1 paper)

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Research

11 pages, 886 KiB  
Article
Blood Extracellular Vesicles Beyond Circulating Tumour Cells: A Valuable Risk Stratification Biomarker in High-Risk Non-Muscle-Invasive Bladder Cancer Patients
by Valentina Magri, Luca Marino, Francesco Del Giudice, Michela De Meo, Marco Siringo, Ettore De Berardinis, Orietta Gandini, Daniele Santini, Chiara Nicolazzo and Paola Gazzaniga
Biomedicines 2024, 12(10), 2359; https://doi.org/10.3390/biomedicines12102359 - 16 Oct 2024
Viewed by 737
Abstract
Non-muscle-invasive bladder cancer (NMIBC) prognosis varies significantly due to the biological and clinical heterogeneity. High-risk stage T1-G3, comprising 15–20% of NMIBCs, involves the lamina propria and is associated with higher rates of recurrence, progression, and cancer-specific mortality. In the present study, we have [...] Read more.
Non-muscle-invasive bladder cancer (NMIBC) prognosis varies significantly due to the biological and clinical heterogeneity. High-risk stage T1-G3, comprising 15–20% of NMIBCs, involves the lamina propria and is associated with higher rates of recurrence, progression, and cancer-specific mortality. In the present study, we have evaluated the enumeration of tumour-derived extracellular vesicles (tdEVs) and circulating tumour cells (CTCs) in high-risk NMIBC patients and their correlation with survival outcomes such as time to progression (TTP), and cancer-specific survival (CSS). Eighty-three high-risk T1-G3 NMIBC patients treated between September 2010 and January 2013 were included. Blood samples were collected before a transurethral resection of the bladder (TURB) and analysed using the CellSearch® system. The presence of at least one CTC was associated with a shorter TTP and CSS. Extending follow-up to 120 months and incorporating automated tdEV evaluation using ACCEPT software demonstrated that tdEV count may additionally stratify patient risk. Combining tdEVs and CTCs improves risk stratification for NMIBC progression, suggesting that tdEVs could be valuable biomarkers for prognosis and disease monitoring. Further research is needed to confirm these findings and establish the clinical significance of tdEVs in early-stage cancers. Full article
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