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Role of STAT3 and NRF2 in Tumors: Potential Targets for Antitumor Therapy
Signal transducer and activator of transcription 3 (STAT3) and nuclear factor erythroid-derived 2-like 2 (NRF2, also known as NFE2L2), are two of the most complicated transcription regulators, which participate in a variety of physiological processes. Numerous studies have shown that they are overac...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9781355/ https://www.ncbi.nlm.nih.gov/pubmed/36557902 http://dx.doi.org/10.3390/molecules27248768 |
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author | Tian, Yanjun Liu, Haiqing Wang, Mengwei Wang, Ruihao Yi, Guandong Zhang, Meng Chen, Ruijiao |
author_facet | Tian, Yanjun Liu, Haiqing Wang, Mengwei Wang, Ruihao Yi, Guandong Zhang, Meng Chen, Ruijiao |
author_sort | Tian, Yanjun |
collection | PubMed |
description | Signal transducer and activator of transcription 3 (STAT3) and nuclear factor erythroid-derived 2-like 2 (NRF2, also known as NFE2L2), are two of the most complicated transcription regulators, which participate in a variety of physiological processes. Numerous studies have shown that they are overactivated in multiple types of tumors. Interestingly, STAT3 and NRF2 can also interact with each other to regulate tumor progression. Hence, these two important transcription factors are considered key targets for developing a new class of antitumor drugs. This review summarizes the pivotal roles of the two transcription regulators and their interactions in the tumor microenvironment to identify potential antitumor drug targets and, ultimately, improve patients’ health and survival. |
format | Online Article Text |
id | pubmed-9781355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97813552022-12-24 Role of STAT3 and NRF2 in Tumors: Potential Targets for Antitumor Therapy Tian, Yanjun Liu, Haiqing Wang, Mengwei Wang, Ruihao Yi, Guandong Zhang, Meng Chen, Ruijiao Molecules Review Signal transducer and activator of transcription 3 (STAT3) and nuclear factor erythroid-derived 2-like 2 (NRF2, also known as NFE2L2), are two of the most complicated transcription regulators, which participate in a variety of physiological processes. Numerous studies have shown that they are overactivated in multiple types of tumors. Interestingly, STAT3 and NRF2 can also interact with each other to regulate tumor progression. Hence, these two important transcription factors are considered key targets for developing a new class of antitumor drugs. This review summarizes the pivotal roles of the two transcription regulators and their interactions in the tumor microenvironment to identify potential antitumor drug targets and, ultimately, improve patients’ health and survival. MDPI 2022-12-10 /pmc/articles/PMC9781355/ /pubmed/36557902 http://dx.doi.org/10.3390/molecules27248768 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Tian, Yanjun Liu, Haiqing Wang, Mengwei Wang, Ruihao Yi, Guandong Zhang, Meng Chen, Ruijiao Role of STAT3 and NRF2 in Tumors: Potential Targets for Antitumor Therapy |
title | Role of STAT3 and NRF2 in Tumors: Potential Targets for Antitumor Therapy |
title_full | Role of STAT3 and NRF2 in Tumors: Potential Targets for Antitumor Therapy |
title_fullStr | Role of STAT3 and NRF2 in Tumors: Potential Targets for Antitumor Therapy |
title_full_unstemmed | Role of STAT3 and NRF2 in Tumors: Potential Targets for Antitumor Therapy |
title_short | Role of STAT3 and NRF2 in Tumors: Potential Targets for Antitumor Therapy |
title_sort | role of stat3 and nrf2 in tumors: potential targets for antitumor therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9781355/ https://www.ncbi.nlm.nih.gov/pubmed/36557902 http://dx.doi.org/10.3390/molecules27248768 |
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