YEATS2 regulates the activation of TAK1/NF-κB pathway and is critical for pancreatic ductal adenocarcinoma cell survival

被引:7
|
作者
Sheng, Hao [1 ,2 ,3 ]
Zheng, Fang [1 ]
Lan, Tian [1 ]
Chen, Hang-fei [4 ]
Xu, Chun-yi [4 ]
Wang, Si-wei [1 ]
Weng, Yuan-yuan [1 ,5 ]
Xu, Li-feng [1 ]
Zhang, Feng [1 ,3 ,4 ]
机构
[1] Wenzhou Med Univ, Quzhou Peoples Hosp, Quzhou Affiliated Hosp, Core Facil, Quzhou 324000, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 2, Jiande Branch, Sch Med, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, Hangzhou, Peoples R China
[4] Zhejiang Chinese Med Univ, Hangzhou, Peoples R China
[5] Wenzhou Med Univ, Quzhou Peoples Hosp, Dept Clin Lab, Quzhou Affiliated Hosp, Quzhou, Peoples R China
关键词
YEATS2; NF-kappa B; TAK1; Pancreatic ductal adenocarcinoma; Histone acetylation; NF-KAPPA-B; KINASE KINASE KINASE; TAK1; GROWTH; PHOSPHORYLATION; COMPLEX; CANCER; INFLAMMATION; EXPRESSION; BINDING;
D O I
10.1007/s10565-021-09671-4
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The prognosis of pancreatic ductal adenocarcinoma (PDAC) is poor despite diagnostic progress and new chemotherapeutic regimens. Constitutive activation of NF-kappa B is frequently observed in PDAC. In this study, we found that YEATS2, a scaffolding protein of ATAC complex, was highly expressed in human PDAC. Depletion of YEATS2 reduced the growth, survival, and tumorigenesis of PDAC cells. The binding of YEATS2 is crucial for maintaining TAK1 activation and NF-kappa B transcriptional activity. Of importance, our results reveal that YEATS2 promotes NF-kappa B transcriptional activity through modulating TAK1 abundance and directly interacting with NF-kappa B as a co-transcriptional factor.
引用
收藏
页码:1 / 16
页数:16
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