Circulating tumor cell markers for early detection and drug resistance assessment through liquid biopsy
- Priya Yadav 1, Saravanan Rajendrasozhan 2,3, Ramzi Hadj Lajimi 2,3, Raja Ramadevi Patel 3,4, Dominique Heymann 5,6,7, N Rajendra Prasad 1
- Priya Yadav 1, Saravanan Rajendrasozhan 2,3, Ramzi Hadj Lajimi 2,3
- 1Department of Biochemistry and Biotechnology, Annamalai University, Chidambaram, Tamil Nadu, India.
- 2Department of Chemistry, College of Science, University of Ha'il, Ha'il, Saudi Arabia.
- 3Medical and Diagnostic Research Centre, University of Ha'il, Ha'il, Saudi Arabia.
- 4Department of Biology, College of Science, University of Ha'il, Ha'il, Saudi Arabia.
- 5Nantes Université, CNRS, US2B, UMR 6286, Nantes, France.
- 6Institut de Cancérologie de l'Ouest, Tumor Heterogeneity and Precision Medecine Laboratory, Saint-Herblain, France.
- 7Medical School, University of Sheffield, Sheffield, United Kingdom.
- 0Department of Biochemistry and Biotechnology, Annamalai University, Chidambaram, Tamil Nadu, India.
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View abstract on PubMed
Summary
This summary is machine-generated.Circulating tumor cells (CTCs), particularly those undergoing epithelial-to-mesenchymal transition (EMT), are key indicators of cancer metastasis and drug resistance. Identifying EMT-specific markers on CTCs is vital for personalized cancer therapies.
Area Of Science
- Oncology
- Cell Biology
- Molecular Medicine
Background
- Circulating tumor cells (CTCs) are shed from primary tumors and disseminate through the bloodstream, offering insights into metastasis and treatment resistance.
- Epithelial-to-mesenchymal transition (EMT) is a critical process enabling CTCs' migration, invasiveness, and development of chemotherapy resistance.
- EMT involves loss of epithelial markers (e.g., EpCAM) and gain of mesenchymal markers (e.g., vimentin), regulated by transcription factors like Snail and Twist.
Purpose Of The Study
- To review the clinical significance of CTCs in understanding cancer metastasis and drug resistance.
- To highlight the role of EMT-derived CTCs in multidrug resistance (MDR).
- To discuss CTC-specific surface markers essential for isolation and enrichment, focusing on EMT-associated markers.
Main Methods
- Literature review focusing on CTCs, EMT, and cancer drug resistance.
- Analysis of common and specific cell surface markers used for CTC identification (e.g., EpCAM, CD44, CD24, cytokeratins, HER2/neu, vimentin).
- Discussion of immune-based isolation and enrichment techniques for CTCs.
Main Results
- CTCs provide critical data on tumor evolution, metastasis, and resistance mechanisms.
- EMT is strongly linked to increased CTC invasiveness and multidrug resistance.
- Various surface markers (EpCAM, vimentin, CD44, CD24, cytokeratins) are employed for CTC detection, with EMT-specific markers being particularly informative.
Conclusions
- Understanding CTCs, especially those undergoing EMT, is crucial for deciphering drug resistance.
- EMT-specific markers on CTCs hold significant potential for halting cancer progression.
- Targeting EMT-derived CTCs and their markers can pave the way for developing personalized cancer therapies.
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