CBX2 Deletion Suppresses Growth and Metastasis of Colorectal Cancer by Mettl3-p38/ERK MAPK Signalling Pathway

被引:9
作者
Sun, Rui [1 ]
Tu, Xucan [1 ]
Chan, Shixin [1 ]
Wang, Xu [1 ]
Ji, Yizhong [1 ]
Wang, Zhenglin [1 ]
Yu, Zhen [1 ]
Zuo, Xiaomin [1 ]
Zhang, Qing [2 ]
Chen, Jiajie [4 ]
Han, Qijun [1 ]
Wang, Ming [1 ]
Zhao, Hu [1 ]
Zhang, Huabing [2 ,3 ]
Chen, Wei [1 ]
机构
[1] Anhui Med Univ, Affiliated Hosp 1, Dept Gen Surg, Hefei 230032, Anhui, Peoples R China
[2] Anhui Med Univ, Metab Dis Res Ctr, Sch Basic Med, Dept Biochem & Mol Biol, Hefei 230032, Peoples R China
[3] Anhui Prov Inst Translat Med, Hefei 230032, Peoples R China
[4] Anhui Med Univ, Affiliated Hosp 1, Dept Dermatol, Hefei 230032, Peoples R China
基金
中国国家自然科学基金;
关键词
CBX2; METTL3; MAPK signal pathway; proliferation; metastasis; liver metastasis; METTL3; PROLIFERATION; KINASE; APOPTOSIS; MIGRATION; PROTEINS; FAMILY;
D O I
10.7150/jca.92633
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Colorectal cancer (CRC) seriously endangers human health owing to its high morbidity and mortality. Previous studies have suggested that high expression of CBX2 may be associated with poor prognosis in CRC patients. However, its functional role in CRC remains to be elucidated. Herein, we found that CBX2 overexpression in colorectal cancer tissue compared with adjacent tissues. Additionally, forest maps and the nomogram model indicated that elevated CBX2 expression was an independent prognostic factor in CRC. Moreover, we confirmed that the deletion of CBX2 markedly suppressed the proliferation and migration of CRC cells in vitro and in vivo. Furthermore, downregulation of CBX2 promotes CRC cell apoptosis and hinders the cell cycle. Mechanistically, our data demonstrated that deletion of CBX2 inhibited the MAPK signaling pathway by regulating the protein levels of Mettl3. In conclusion, our study demonstrated that CBX2 is a vital tumor suppressor in CRC and could be a promising anti-cancer therapeutic target.
引用
收藏
页码:2123 / 2136
页数:14
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