Targeting BMI-1-mediated epithelial-mesenchymal transition to inhibit colorectal cancer liver metastasis.
- Author:
Zhiyao XU
1
;
Zhuha ZHOU
2
;
Jing ZHANG
1
;
Feichao XUAN
3
;
Mengjing FAN
1
;
Difan ZHOU
3
;
Zhenyu LIUYANG
3
;
Ximei MA
3
;
Yiyang HONG
1
;
Yihong WANG
4
;
Sherven SHARMA
5
;
Qinghua DONG
1
;
Guanyu WANG
3
Author Information
- Publication Type:Journal Article
- Keywords: AKT; ANOVA, One-way analysis of variance; BMI-1; CRC, colorectal cancer; CRCLM, colorectal cancer liver metastasis; Colorectal cancer; EMT, epithelial–mesenchymal transition; Epithelial–mesenchymal transition; GSK-3β; HDACi, histone deacetylase inhibitor; HE, hematoxylin and eosin; IHC, immunohistochemistry; LNM, lymph node metastasis; Liver metastasis; NaB, sodium butyrate; PBS, phosphate buffered solution; PcG, polycomb-group; Snail; Sodium butyrate; TCGA, Cancer Genome Atlas; qPCR, real time polymerase chain reaction
- From: Acta Pharmaceutica Sinica B 2021;11(5):1274-1285
- CountryChina
- Language:English
- Abstract: Liver is the most common metastatic site for colorectal cancer (CRC), there is no satisfied approach to treat CRC liver metastasis (CRCLM). Here, we investigated the role of a polycomb protein BMI-1 in CRCLM. Immunohistochemical analysis showed that BMI-1 expression in liver metastases was upregulated and associated with T4 stage, invasion depth and right-sided primary tumor. Knockdown