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DEPDC1B is a tumor promotor in development of bladder cancer through targeting SHC1
Bladder cancer is one of the most commonly diagnosed malignant tumors in the urinary system and causes a massive cancer-related death. DEPDC1B is a DEP domain-containing protein that has been found to be associated with a variety of human cancers. This study aimed to explore the role and mechanism o...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7672062/ https://www.ncbi.nlm.nih.gov/pubmed/33203836 http://dx.doi.org/10.1038/s41419-020-03190-6 |
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author | Lai, Chin-Hui Xu, Kexin Zhou, Jianhua Wang, Mingrui Zhang, Weiyu Liu, Xianhui Xiong, Jie Wang, Tao Wang, Qi Wang, Huanrui Xu, Tao Hu, Hao |
author_facet | Lai, Chin-Hui Xu, Kexin Zhou, Jianhua Wang, Mingrui Zhang, Weiyu Liu, Xianhui Xiong, Jie Wang, Tao Wang, Qi Wang, Huanrui Xu, Tao Hu, Hao |
author_sort | Lai, Chin-Hui |
collection | PubMed |
description | Bladder cancer is one of the most commonly diagnosed malignant tumors in the urinary system and causes a massive cancer-related death. DEPDC1B is a DEP domain-containing protein that has been found to be associated with a variety of human cancers. This study aimed to explore the role and mechanism of DEPDC1B in the development of bladder cancer. The analysis of clinical specimens revealed the upregulated expression of DEPDC1B in bladder cancer, which was positively related to tumor grade. In vitro and in vivo studies showed that DEPDC1B knockdown could inhibit the growth of bladder cancer cells or xenografts in mice. The suppression of bladder cancer by DEPDC1B was executed through inhibiting cell proliferation, cell migration, and promoting cell apoptosis. Moreover, a mechanistic study found that SHC1 may be an important route through which DEPDC1B regulates the development of bladder cancer. Knockdown of SHC1 in DEPDC1B-overexpressed cancer cells could abolish the promotion effects induced by DEPDC1B. In conclusion, DEPDC1B was identified as a key regulator in the development of bladder cancer, which may be used as a potential therapeutic target in the treatment of bladder cancer. |
format | Online Article Text |
id | pubmed-7672062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76720622020-11-20 DEPDC1B is a tumor promotor in development of bladder cancer through targeting SHC1 Lai, Chin-Hui Xu, Kexin Zhou, Jianhua Wang, Mingrui Zhang, Weiyu Liu, Xianhui Xiong, Jie Wang, Tao Wang, Qi Wang, Huanrui Xu, Tao Hu, Hao Cell Death Dis Article Bladder cancer is one of the most commonly diagnosed malignant tumors in the urinary system and causes a massive cancer-related death. DEPDC1B is a DEP domain-containing protein that has been found to be associated with a variety of human cancers. This study aimed to explore the role and mechanism of DEPDC1B in the development of bladder cancer. The analysis of clinical specimens revealed the upregulated expression of DEPDC1B in bladder cancer, which was positively related to tumor grade. In vitro and in vivo studies showed that DEPDC1B knockdown could inhibit the growth of bladder cancer cells or xenografts in mice. The suppression of bladder cancer by DEPDC1B was executed through inhibiting cell proliferation, cell migration, and promoting cell apoptosis. Moreover, a mechanistic study found that SHC1 may be an important route through which DEPDC1B regulates the development of bladder cancer. Knockdown of SHC1 in DEPDC1B-overexpressed cancer cells could abolish the promotion effects induced by DEPDC1B. In conclusion, DEPDC1B was identified as a key regulator in the development of bladder cancer, which may be used as a potential therapeutic target in the treatment of bladder cancer. Nature Publishing Group UK 2020-11-17 /pmc/articles/PMC7672062/ /pubmed/33203836 http://dx.doi.org/10.1038/s41419-020-03190-6 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Lai, Chin-Hui Xu, Kexin Zhou, Jianhua Wang, Mingrui Zhang, Weiyu Liu, Xianhui Xiong, Jie Wang, Tao Wang, Qi Wang, Huanrui Xu, Tao Hu, Hao DEPDC1B is a tumor promotor in development of bladder cancer through targeting SHC1 |
title | DEPDC1B is a tumor promotor in development of bladder cancer through targeting SHC1 |
title_full | DEPDC1B is a tumor promotor in development of bladder cancer through targeting SHC1 |
title_fullStr | DEPDC1B is a tumor promotor in development of bladder cancer through targeting SHC1 |
title_full_unstemmed | DEPDC1B is a tumor promotor in development of bladder cancer through targeting SHC1 |
title_short | DEPDC1B is a tumor promotor in development of bladder cancer through targeting SHC1 |
title_sort | depdc1b is a tumor promotor in development of bladder cancer through targeting shc1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7672062/ https://www.ncbi.nlm.nih.gov/pubmed/33203836 http://dx.doi.org/10.1038/s41419-020-03190-6 |
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