Wnt信号通路
癌症研究
结直肠癌
自噬
小干扰RNA
化学
癌症
癌细胞
信号转导
细胞生物学
生物
细胞培养
细胞凋亡
医学
内科学
生物化学
转染
遗传学
作者
Kun Zhou,Jae Eun Cheong,Subrahmanian Tarakkad Krishnaji,Aram Ghalali,Haojie Fu,Lufei Sui,Catherine Alix‐Panabières,Laure Cayrefourcq,Diane R. Bielenberg,Lijun Sun,Bruce R. Zetter
标识
DOI:10.1158/1535-7163.mct-21-0801
摘要
Abstract We have synthesized an oxetane derivative of the benzimidazole compound mebendazole (OBD9) with enhanced solubility and strong anticancer activity in multiple types of cancer cells, especially colorectal cancer. In this report, we provide evidence that OBD9 suppresses colorectal cancer growth by interfering with the Wnt signaling pathway, a main driver of cell growth in colorectal cancer. Specifically, we find that OBD9 induces autophagic degradation of TNIK (traf2 and Nck-interacting kinase), which promotes T-cell factor-4 (TCF4)/beta-catenin–mediated gene expression. Thus, OBD9 as a TNIK inhibitor blocks Wnt/beta-catenin signaling at the final step of transcriptional activation. We suggest that OBD9 provides a potential novel autophagy-mediated, Wnt-damping therapeutic strategy for the treatment of colorectal cancer.
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