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Tubeimoside-1 inhibits the growth and invasion of colorectal cancer cells through the Wnt/β-catenin signaling pathway

机译:Tubeimoside-1通过Wnt /β-catenin信号通路抑制大肠癌细胞的生长和侵袭

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摘要

Tubeimoside-1 (TBMS1) is considered to have anti-tumor properties. However, the role of TBMS1 on human colorectal cancer (CRC) is still unclear. Therefore, in this study, we investigated the role of TBMS1 on human CRC and explored the underlying mechanism. The cell proliferation of CRC cells was detected by MTT assay. Cell migration and invasion were assessed by Boyden chamber assay, and the involvement of molecular mechanisms was examined by western blot. In this study, we found that TBMS1 inhibited the proliferation, migration/invasion of CRC cells, and it reduced β-catenin expression in CRC cells. Furthermore, overexpression of β-catenin rescued TBMS1-induced proliferation and invasion inhibition, and knockdown of β-catenin potentiated TBMS1-induced proliferation and invasion inhibition. Taken together, our results demonstrate that TBMS1 inhibited CRC cell proliferation and invasion via suppressing the Wnt/β-catenin signaling pathway. Therefore, TBMS1 may represent a chemopreventive and/or therapeutic agent in the prevention of CRC.
机译:Tubeimoside-1(TBMS1)被认为具有抗肿瘤特性。但是,TBMS1在人类大肠癌(CRC)中的作用仍不清楚。因此,在这项研究中,我们调查了TBMS1对人CRC的作用并探讨了其潜在机制。通过MTT法检测CRC细胞的增殖。通过博登室测定法评估细胞迁移和侵袭,并通过蛋白质印迹法检查分子机制的参与。在这项研究中,我们发现TBMS1抑制CRC细胞的增殖,迁移/侵袭,并降低CRC细胞中β-catenin的表达。此外,β-catenin的过表达挽救了TBMS1诱导的增殖和侵袭抑制,而敲低β-catenin增强了TBMS1诱导的增殖和侵袭抑制。两者合计,我们的结果表明TBMS1通过抑制Wnt /β-catenin信号通路抑制CRC细胞的增殖和侵袭。因此,TBMS1可以代表预防CRC的化学预防剂和/或治疗剂。

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