m6A demethylase ALKBH5 suppression contributes to esophageal squamous cell carcinoma progression

被引:0
|
作者
Xiao, Dong [1 ,2 ,3 ,5 ]
Fang, Ting-Xiao [4 ]
Lei, Ye [1 ,2 ,3 ]
Xiao, Sheng-Jun [6 ]
Xia, Jia-Wei [7 ]
Lin, Tao-Yan [3 ,8 ]
Li, Yong-Long [1 ,2 ,3 ]
Zhai, Jian-Xue [4 ]
Li, Xiao-Yan [1 ,2 ]
Huang, Shi-Hao [3 ]
Jia, Jun-Shuang [3 ]
Tian, Yu-Guang [1 ,2 ]
Lin, Xiao-Lin [3 ]
Cai, Kai-Can [4 ]
Sun, Yan [9 ]
机构
[1] Southern Med Univ, Lab Anim Ctr, Guangzhou 510515, Peoples R China
[2] Guangzhou Southern Med Lab Anim Sci & Tech Co Ltd, Guangzhou 510515, Peoples R China
[3] Southern Med Univ, Sch Basic Med Sci, Canc Res Inst, Guangzhou Key Lab Tumor Immunol Res, Guangzhou 510515, Peoples R China
[4] Southern Med Univ, Nanfang Hosp, Dept Thorac Surg, Guangzhou 510515, Peoples R China
[5] Southern Med Univ, Natl Demonstrat Ctr Expt Educ Basic Med Sci, Guangzhou 510515, Peoples R China
[6] Guilin Med Univ, Affiliated Hosp 2, Dept Pathol, Guilin 541199, Peoples R China
[7] Dali Univ, Peoples Hosp Kunming 3, Affiliated Hosp 6, Kunming 650041, Yunnan, Peoples R China
[8] Southern Med Univ, Nanfang Hosp, Dept Pharm, Guangzhou 510515, Peoples R China
[9] Sun Yat Sen Univ, Zhongshan Sch Med, Guangzhou 510080, Peoples R China
来源
AGING-US | 2021年 / 13卷 / 17期
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
esophageal squamous cell carcinoma; m(6)A RNA modification; ALKBH5; cell proliferation; tumorigenicity; MESSENGER-RNA; PROMOTES PROLIFERATION; POOR-PROGNOSIS; EXPRESSION; STEM; METHYLATION; INVASION; METTL3; N-6-METHYLADENOSINE; DIFFERENTIATION;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Esophageal squamous cell carcinoma (ESCC) is a highly malignant gastrointestinal cancer with a high recurrence rate and poor prognosis. Although N-6-methyladenosine (m(6)A), the most abundant epitranscriptomic modification of mRNAs, has been implicated in several cancers, little is known about its participation in ESCC progression. We found reduced expression of ALKBH5, an m(6)A demethylase, in ESCC tissue specimens with a more pronounced effect in T3-T4, N1-N3, clinical stages III-IV, and histological grade III tumors, suggesting its involvement in advanced stages of ESCC. Exogenous expression of ALKBH5 inhibited the in vitro proliferation of ESCC cells, whereas depletion of endogenous ALKBH5 markedly enhanced ESCC cell proliferation in vitro. This suggests ALKBH5 exerts anti-proliferative effects on ESCC growth. Furthermore, ALKBH5 overexpression suppressed tumor growth of Eca-109 cells in nude mice; conversely, depletion of endogenous ALKBH5 accelerated tumor growth of TE-13 cells in vivo. The growth-inhibitory effects of ALKBH5 overexpression are partly attributed to a G1-phase arrest. In addition, ALKBH5 overexpression reduced the in vitro migration and invasion of ESCC cells. Altogether, our findings demonstrate that the loss of ALKBH5 expression contributes to ESCC malignancy.
引用
收藏
页码:21497 / 21512
页数:16
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