TY - JOUR
T1 - Cancer stem cell–associated miRNAs serve as prognostic biomarkers in colorectal cancer
AU - Toden, Shusuke
AU - Kunitoshi, Shigeyasu
AU - Cardenas, Jacob
AU - Gu, Jinghua
AU - Hutchins, Elizabeth
AU - Van Keuren-Jensen, Kendall
AU - Uetake, Hiroyuki
AU - Toiyama, Yuji
AU - Goel, Ajay
N1 - Publisher Copyright:
Copyright 2019, American Society for Clinical Investigation.
PY - 2019/3/21
Y1 - 2019/3/21
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85069817656&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85069817656&partnerID=8YFLogxK
U2 - 10.1172/jci.insight.125294
DO - 10.1172/jci.insight.125294
M3 - Article
C2 - 30895943
AN - SCOPUS:85069817656
SN - 2379-3708
VL - 4
JO - JCI Insight
JF - JCI Insight
IS - 6
M1 - e125294
ER -