A mutant KRAS-induced factor REG4 promotes cancer stem cell properties via Wnt/β-catenin signaling

被引:41
作者
Hwang, Jeong-Ha [1 ,2 ,3 ]
Yoon, Junyong [1 ,2 ]
Cho, Yong-Hee [1 ,2 ]
Cha, Pu-Hyeon [1 ,2 ]
Park, Jong-Chan [1 ,2 ]
Choi, Kang-Yell [1 ,2 ,4 ]
机构
[1] Yonsei Univ, Translat Res Ctr Prot Funct Control, Seoul, South Korea
[2] Yonsei Univ, Coll Life Sci & Biotechnol, Dept Biotechnol, Seoul, South Korea
[3] Yonsei Univ, Dept Biomat Sci & Engn, Seoul, South Korea
[4] CK Biotechnol Inc, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
KRAS mutation; APC mutation; REG4; cancer stem cells; colorectal cancer; Wnt; beta-catenin signaling; GENE-EXPRESSION; BETA-CATENIN; COLON; RAS; MUTATIONS; MODEL; APC; METASTASIS; PATHWAY; ADENOMA;
D O I
10.1002/ijc.32728
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mutant KRAS provides a driving force for enhancement of cancer stem cells (CSCs) characteristics contributing transformation of colorectal cancer (CRC) cells harboring adenomatous polyposis coli (APC) mutations. Here, we identified the factors mediating the promotion of CSCs properties induced by KRAS mutation through microarray analyses of genes specifically induced in CRC spheroids harboring both KRAS and APC mutations. Among them, REG4 was identified as a key factor since CRISPR/Cas9-mediated knockout of REG4 most significantly affected the stem cell characteristics in which CSCs markers were effectively suppressed. We show that REG4 mediates promotion of CSCs properties via Wnt/beta-catenin signaling in various in vitro studies including tumor organoid systems. Furthermore, expression patterns of CSCs markers and REG4 correlated in intestinal tumors from Apc(min/+)/Kras(G12D)LA2 mice and in CRC patient tissues harboring both KRAS and APC mutations. The role of REG4 in the tumor-initiating capacity accompanied by enhancement of CSCs characteristics was also revealed by NSG mice xenograft system. Collectively, our study highlights the importance of REG4 in promoting CSCs properties induced by KRAS mutation, and provides a new therapeutic strategy for CRC harboring both APC and KRAS mutations.
引用
收藏
页码:2877 / 2890
页数:14
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