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

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...

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Autores principales: Zhou, Zhaohui, Xiong, Longbin, Wu, Zeshen, Jiang, Lijuan, Li, Yonghong, Li, Zhiyong, Peng, Yulu, Ning, Kang, Zou, Xiangpeng, Liu, Zefu, Wang, Jun, Li, Zhen, Zhou, Fangjian, Liu, Zhuowei, Zhang, Zhiling, Yu, Chunping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130207/
https://www.ncbi.nlm.nih.gov/pubmed/35610207
http://dx.doi.org/10.1038/s41419-022-04947-x
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author Zhou, Zhaohui
Xiong, Longbin
Wu, Zeshen
Jiang, Lijuan
Li, Yonghong
Li, Zhiyong
Peng, Yulu
Ning, Kang
Zou, Xiangpeng
Liu, Zefu
Wang, Jun
Li, Zhen
Zhou, Fangjian
Liu, Zhuowei
Zhang, Zhiling
Yu, Chunping
author_facet Zhou, Zhaohui
Xiong, Longbin
Wu, Zeshen
Jiang, Lijuan
Li, Yonghong
Li, Zhiyong
Peng, Yulu
Ning, Kang
Zou, Xiangpeng
Liu, Zefu
Wang, Jun
Li, Zhen
Zhou, Fangjian
Liu, Zhuowei
Zhang, Zhiling
Yu, Chunping
author_sort Zhou, Zhaohui
collection PubMed
description 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.
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spelling pubmed-91302072022-05-26 Nkx2.8 promotes chemosensitivity in bladder urothelial carcinoma via transcriptional repression of MDR1 Zhou, Zhaohui Xiong, Longbin Wu, Zeshen Jiang, Lijuan Li, Yonghong Li, Zhiyong Peng, Yulu Ning, Kang Zou, Xiangpeng Liu, Zefu Wang, Jun Li, Zhen Zhou, Fangjian Liu, Zhuowei Zhang, Zhiling Yu, Chunping Cell Death Dis Article 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. Nature Publishing Group UK 2022-05-24 /pmc/articles/PMC9130207/ /pubmed/35610207 http://dx.doi.org/10.1038/s41419-022-04947-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhou, Zhaohui
Xiong, Longbin
Wu, Zeshen
Jiang, Lijuan
Li, Yonghong
Li, Zhiyong
Peng, Yulu
Ning, Kang
Zou, Xiangpeng
Liu, Zefu
Wang, Jun
Li, Zhen
Zhou, Fangjian
Liu, Zhuowei
Zhang, Zhiling
Yu, Chunping
Nkx2.8 promotes chemosensitivity in bladder urothelial carcinoma via transcriptional repression of MDR1
title Nkx2.8 promotes chemosensitivity in bladder urothelial carcinoma via transcriptional repression of MDR1
title_full Nkx2.8 promotes chemosensitivity in bladder urothelial carcinoma via transcriptional repression of MDR1
title_fullStr Nkx2.8 promotes chemosensitivity in bladder urothelial carcinoma via transcriptional repression of MDR1
title_full_unstemmed Nkx2.8 promotes chemosensitivity in bladder urothelial carcinoma via transcriptional repression of MDR1
title_short Nkx2.8 promotes chemosensitivity in bladder urothelial carcinoma via transcriptional repression of MDR1
title_sort nkx2.8 promotes chemosensitivity in bladder urothelial carcinoma via transcriptional repression of mdr1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130207/
https://www.ncbi.nlm.nih.gov/pubmed/35610207
http://dx.doi.org/10.1038/s41419-022-04947-x
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