Nkx2.8 promotes chemosensitivity in bladder urothelial carcinoma via transcriptional repression of MDR1

被引:3
|
作者
Zhou, Zhaohui [1 ,2 ,3 ]
Xiong, Longbin [1 ,2 ,3 ]
Wu, Zeshen [1 ,2 ,3 ,4 ]
Jiang, Lijuan [1 ,2 ,3 ]
Li, Yonghong [1 ,2 ,3 ]
Li, Zhiyong [1 ,2 ,3 ]
Peng, Yulu [1 ,2 ,3 ]
Ning, Kang [1 ,2 ,3 ]
Zou, Xiangpeng [1 ,2 ,3 ]
Liu, Zefu [1 ,2 ,3 ]
Wang, Jun [1 ,2 ,3 ]
Li, Zhen [1 ,2 ,3 ]
Zhou, Fangjian [1 ,2 ,3 ]
Liu, Zhuowei [1 ,2 ,3 ]
Zhang, Zhiling [1 ,2 ,3 ]
Yu, Chunping [1 ,2 ,3 ]
机构
[1] Sun Yat Sen Univ, Canc Ctr, Dept Urol, Guangzhou, Peoples R China
[2] State Key Lab Oncol Southern China, Guangzhou, Peoples R China
[3] Collaborat Innovat Ctr Canc Med, Guangzhou, Peoples R China
[4] Huazhong Univ Sci & Technol, Union Shenzhen Hosp, Nanshan Hosp, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
MULTIDRUG-RESISTANCE; P-GLYCOPROTEIN; NEOADJUVANT CHEMOTHERAPY; CANCER; METHOTREXATE; VINBLASTINE; CISPLATIN; TUMOR; DNA; CHEMORESISTANCE;
D O I
10.1038/s41419-022-04947-x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Multidrug resistance gene 1 (MDR1), a key factor contributing to drug insensitivity, has been associated with treatment failure and poor prognoses in various cancers, including bladder urothelial carcinoma (UC). Here we show that positive Nkx2.8 expression was associated with better prognosis of UC patients received chemotherapy. Patients with positive Nkx2.8 expression had promising prognosis from adjuvant chemotherapy. Enforced expression of Nkx2.8 promotes drug sensitivity of UC cells. Mechanistic investigations showed that Nkx2.8 negatively regulated expression of MDR1 by binds directly to the MDR1 promoter and transcriptionally represses MDR1 expression. P-gp inhibitor reversed chemosensitivity inhibition by Nkx2.8 scilencing. In clinical UC specimens, expression of Nkx2.8 inversely correlated with P-gp expression, and UC patients with Nkx2.8 positivity and low P-gp expression displayed the best prognosis. Our findings uncovered a new mechanism of chemosensitivity in UC cells and proposing Nkx2.8-MDR1 axis as a novel candidate target for therapeutic intervention of UC.
引用
收藏
页数:11
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