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PIK3R3 inhibits cell senescence through p53/p21 signaling

Cellular senescence is a stress response of human cells that removes potentially harmful cells by initiating cell cycle arrest. Inducing senescence of tumor cells may be an effective tumor-inhibiting strategy. In this study we found that PIK3R3 could inhibit the cell senescence of colorectal cancer...

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Detalles Bibliográficos
Autores principales: Chen, Qianzhi, Sun, Xuling, Luo, Xuelai, Wang, Jing, Hu, Junbo, Feng, Yongdong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519147/
https://www.ncbi.nlm.nih.gov/pubmed/32973127
http://dx.doi.org/10.1038/s41419-020-02921-z
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author Chen, Qianzhi
Sun, Xuling
Luo, Xuelai
Wang, Jing
Hu, Junbo
Feng, Yongdong
author_facet Chen, Qianzhi
Sun, Xuling
Luo, Xuelai
Wang, Jing
Hu, Junbo
Feng, Yongdong
author_sort Chen, Qianzhi
collection PubMed
description Cellular senescence is a stress response of human cells that removes potentially harmful cells by initiating cell cycle arrest. Inducing senescence of tumor cells may be an effective tumor-inhibiting strategy. In this study we found that PIK3R3 could inhibit the cell senescence of colorectal cancer cells and promote cell proliferation through the p53/p21 signal pathway. PIK3R3 could bind to p53 and inhibit the binding of p53 to the p21 gene promoter region, and thus affecting the transcriptional activity of p21 gene. Our study has provided new evidence of the role of PIK3R3 in p53 regulation and inhibition of PIK3R3 may be one of the potential targets of tumor therapy.
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spelling pubmed-75191472020-10-14 PIK3R3 inhibits cell senescence through p53/p21 signaling Chen, Qianzhi Sun, Xuling Luo, Xuelai Wang, Jing Hu, Junbo Feng, Yongdong Cell Death Dis Article Cellular senescence is a stress response of human cells that removes potentially harmful cells by initiating cell cycle arrest. Inducing senescence of tumor cells may be an effective tumor-inhibiting strategy. In this study we found that PIK3R3 could inhibit the cell senescence of colorectal cancer cells and promote cell proliferation through the p53/p21 signal pathway. PIK3R3 could bind to p53 and inhibit the binding of p53 to the p21 gene promoter region, and thus affecting the transcriptional activity of p21 gene. Our study has provided new evidence of the role of PIK3R3 in p53 regulation and inhibition of PIK3R3 may be one of the potential targets of tumor therapy. Nature Publishing Group UK 2020-09-24 /pmc/articles/PMC7519147/ /pubmed/32973127 http://dx.doi.org/10.1038/s41419-020-02921-z 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
Chen, Qianzhi
Sun, Xuling
Luo, Xuelai
Wang, Jing
Hu, Junbo
Feng, Yongdong
PIK3R3 inhibits cell senescence through p53/p21 signaling
title PIK3R3 inhibits cell senescence through p53/p21 signaling
title_full PIK3R3 inhibits cell senescence through p53/p21 signaling
title_fullStr PIK3R3 inhibits cell senescence through p53/p21 signaling
title_full_unstemmed PIK3R3 inhibits cell senescence through p53/p21 signaling
title_short PIK3R3 inhibits cell senescence through p53/p21 signaling
title_sort pik3r3 inhibits cell senescence through p53/p21 signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519147/
https://www.ncbi.nlm.nih.gov/pubmed/32973127
http://dx.doi.org/10.1038/s41419-020-02921-z
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