SIRT6 Inhibits Anoikis of Colorectal Cancer Cells by Down-Regulating NDRG1

被引:2
|
作者
Li, Fengying [1 ,2 ]
Yu, Wentao [3 ]
Zhou, Xiaoling [3 ]
Hou, Jingyu [3 ]
Gao, Yunyi [3 ]
Zhang, Jun [2 ]
Gao, Xiangwei [1 ,3 ]
机构
[1] Zhejiang Univ, Sir Run Run Shaw Hosp, Sch Publ Hlth, Sch Med, Hangzhou 310058, Peoples R China
[2] Zhejiang Univ, Sir Run Run Shaw Hosp, Dept Clin Lab, Sch Med, Hangzhou 310016, Peoples R China
[3] Zhejiang Univ, Inst Environm Med, Sch Med, Hangzhou 310058, Peoples R China
基金
中国国家自然科学基金;
关键词
colorectal cancer; anoikis; SIRT6; epigenetic regulation; NDRG1; HISTONE DEACETYLASE SIRT6; HOMEOSTASIS; METASTASIS; SUPPRESSOR;
D O I
10.3390/ijms25115585
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Anoikis, a form of apoptosis resulting from the loss of cell-extracellular matrix interaction, is a significant barrier to cancer cell metastasis. However, the epigenetic regulation of this process remains to be explored. Here, we demonstrate that the histone deacetylase sirtuin 6 (SIRT6) plays a pivotal role in conferring anoikis resistance to colorectal cancer (CRC) cells. The protein level of SIRT6 is negatively correlated with anoikis in CRC cells. The overexpression of SIRT6 decreases while the knockdown of SIRT6 increases detachment-induced anoikis. Mechanistically, SIRT6 inhibits the transcription of N-myc downstream-regulated gene 1 (NDRG1), a negative regulator of the AKT signaling pathway. We observed the up-regulation of SIRT6 in advanced-stage CRC samples. Together, our findings unveil a novel epigenetic program regulating the anoikis of CRC cells.
引用
收藏
页数:13
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