| Literature DB >> 30895943 |
Shusuke Toden1, Shigeyasu Kunitoshi1, Jacob Cardenas2, Jinghua Gu2, Elizabeth Hutchins3, Kendall Van Keuren-Jensen3, Hiroyuki Uetake4, Yuji Toiyama5, Ajay Goel1.
Abstract
Chemoresistance in cancer is linked to a subset of cancer cells termed "cancer stem cells" (CSCs), and in particular, those expressing the CD44 variant appear to represent a more aggressive disease phenotype. Herein, we demonstrate that CD44v6 represents a CSC population with increased resistance to chemotherapeutic agents, and its high expression is frequently associated with poor overall survival (OS) and disease-free survival (DFS) in patients with colorectal cancer (CRC). CD44v6+ cells showed elevated resistance to chemotherapeutic drugs and significantly high tumor initiation capacity. Inhibition of CD44v6 resulted in the attenuation of self-renewal capacity and resensitization to chemotherapeutic agents. Of note, miRNA profiling of CD44v6+ spheroid-derived CSCs identified a unique panel of miRNAs indicative of high self-renewal capacity. In particular, miR-1246 was overexpressed in CD44v6+ cells, and associated with poor OS and DFS in CRC patients. We demonstrate that CD44v6+ CSCs induced chemoresistance and enhance tumorigenicity in CRC cells, and this was in part orchestrated by a distinct panel of miRNAs with dysregulated profiles. These findings suggest that specific miRNAs could serve as therapeutic targets as well as promising prognostic biomarkers in patients with colorectal neoplasia.Entities:
Keywords: Cancer; Gastroenterology; Oncology
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Year: 2019 PMID: 30895943 PMCID: PMC6483002 DOI: 10.1172/jci.insight.125294
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708