The Role of miR-486-5p on CSCs Phenotypes in Colorectal Cancer
Metadatos
Mostrar el registro completo del ítemAutor
Etzi, Federica; Griñán Lisón, Carmen; Fenu, Grazia; González Titos, Aitor; Pisano, Andrea; Farace, Cristiano; Sabalic, Angela; Picon-Ruiz, Manuel; Marchal Corrales, Juan Antonio; Madeddu, Roberto Beniamino GublielmoEditorial
MDPI
Materia
colorectal cancer spheres cancer stem cells
Fecha
2024-12-19Referencia bibliográfica
Etzi, F. et. al. Cancers 2024, 16, 4237. [https://doi.org/10.3390/cancers16244237]
Patrocinador
MCIN/AEI/10.13039/501100011033/FEDER “Una manera de hacer Europa”: RTI2018.101309B-C22; The Chair “Doctors Galera-Requena in cancer stem cell research” (CMC-CTS963); Junta de Andalucía, Plan Andaluz de Investigación, Desarrollo e Innovación (grant POSTDOC_21_638 to C.G.-L.)Resumen
Background: Colorectal cancer (CRC) is the third diagnosed cancer worldwide. Forty-four
percent of metastatic colorectal cancer patients were diagnosed at an early stage. Despite curative
resection, approximately 40% of patients will develop metastases within a few years. Previous studies
indicate the presence of cancer stem cells (CSCs) and their contribution to CRC progression and
metastasis. miRNAs deregulation plays a role in CSCs formation and in tumor development. In
light of previous studies, we investigated the role of miR-486-5p to understand its role in CSC better.
Methods: The expression of miR-486-5p was assessed in adherent cells and spheres generated from
two CRC cell lines to observe the difference in expression in CSC-enriched spheroids. Afterward,
we overexpressed and underexpressed this miRNA in adherent and sphere cultures through the
transfection of a miR-486-5p mimic and a mimic inhibitor. Results: The results demonstrated that
miR-486-5p exhibited a notable downregulation in CSC models, and its overexpression led to a
significant decrease in colony size. Conclusions: In this study, we confirmed that miR-486-5p plays
an oncosuppressive role in CRC, thereby advancing our understanding of the role of this microRNA
in the CSC phenotype.