MBIP promotes ESCC metastasis by activating MAPK pathway

被引:1
作者
Ma, Yanchun [1 ,2 ,4 ]
Hua, Yuyan [2 ]
Yin, Xiaojie [2 ]
Jiao, Ye [2 ]
Xu, Enwei [3 ]
Yan, Ting [1 ,2 ]
Yang, Jian [1 ,2 ]
Zhang, Ling [2 ]
机构
[1] Shanxi Med Univ, Translat Med Res Ctr, Taiyuan 030001, Shanxi, Peoples R China
[2] Shanxi Med Univ, Coll Basic Med, Dept Pathol, Taiyuan 030001, Shanxi, Peoples R China
[3] Shanxi Canc Hosp, Dept Pathol, Taiyuan 030001, Shanxi, Peoples R China
[4] Shanxi Med Univ, 56 Xinjian South Rd, Taiyuan 030001, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
MBIP; Esophageal squamous cell carcinoma; EMT; MAPK signaling pathway; ACETYLTRANSFERASE COMPLEX; CANCER; ATAC; JNK;
D O I
10.1016/j.cellsig.2024.111040
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
MBIP is a component of the Ada2A containing complex (ATAC) and has been identified as a susceptibility gene in several cancers. However, the role and molecular mechanism of MBIP in esophageal squamous cell carcinoma (ESCC) remain unclear. Our finding indicated that the expression level of MBIP in ESCC was higher than that in normal tissue (P < 0.05) based on the data from the Cancer Gene Atlas (TCGA) and Gene Expression Omnibus (GEO). Kaplan-Meier analysis showed that high MBIP expression was closely associated with deeper invasion and worse prognosis. Transwell assay and mouse xenograft assay demonstrated that MBIP overexpression promoted migration and invasion in vitro and in vivo, while MBIP knockdown played the opposite role. Furthermore, the results of RNA-seq, qRT-PCR, western blotting and rescue experiments revealed that MBIP promoted epithelialmesenchymal transition (EMT) via the phosphorylation JNK/p38 in ESCC. Our study indicates that MBIP plays a significant role in the prognosis and metastasis of ESCC, suggesting that MBIP might serve as an ESCC prognostic biomarker.
引用
收藏
页数:12
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