APA
Galindo-Pumarino, C. & Collado, M. & Castillo, María Encarnación & Barquín, J. & Romio, E. & Larriba, M.J. & Muñoz de Mier, G.J & Carrato, A. & de la Pinta, C. & Pena, C. (2022-07 ) .SNAI1-expressing fibroblasts and derived-extracellular matrix as mediators of drug resistance in colorectal cancer patients.
ISO 690
Galindo-Pumarino, C. & Collado, M. & Castillo, María Encarnación & Barquín, J. & Romio, E. & Larriba, M.J. & Muñoz de Mier, G.J & Carrato, A. & de la Pinta, C. & Pena, C.. 2022-07 .SNAI1-expressing fibroblasts and derived-extracellular matrix as mediators of drug resistance in colorectal cancer patients.
https://hdl.handle.net/20.500.12080/39546
Resumen:
of colorectal cancer (CRC) patients. Cancer-Associated Fibroblasts (CAFs) are the main producers and remodelers
of the extracellular matrix (ECM), which is directly involved in drug resistance mechanisms. Primary Normal
Fibroblasts (NFs) and CAFs and cell lines (fibroblasts and tumor cells), were used to generate ECM and to identify
its role in the oxaliplatin and cetuximab chemoresistance processes of CRC cells mediated by SNAI1-expressing
fibroblasts. Matrices generated by Snai1 KO MEFs (Knockout Mouse Embryonic Fibroblasts) confer less resistance
on oxaliplatin and cetuximab than wild-type MEF-derived matrices. Similarly, matrices derived from CAFs cause
greater survival of colorectal cancer cells than NF-derived matrices, in a similar way to Snai1 expression levels. In
addition, Snail1 expression in fibroblasts regulates drug resistance and metabolism gene expression in tumor cells
mediated by ECM. Finally, a series of 531 patients (TCGA) with CRC was used to assess the role of SNAI1
expression in patients' prognosis indicating an association between tumor SNAI1 expression and overall survival
in colon cancer patients but not in rectal cancer patients. SNAI1 expression in CRC cancer patients, together with
in vitro experimentation, suggests the possible use of SNAI1 expression in tumor-associated fibroblasts as a
predictive biomarker of response to oxaliplatin and cetuximab treatments in patients with CRC.