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ALDH1: A potential therapeutic target for cancer stem cells in solid tumors

Solid tumors can be divided into benign solid tumors and solid malignant tumors in the academic community, among which malignant solid tumors are called cancers. Cancer is the second leading cause of death in the world, and the global incidence of cancer is increasing yearly New cancer patients in C...

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Autores principales: Wei, Yaolu, Li, Yan, Chen, Yenan, Liu, Pei, Huang, Sheng, Zhang, Yuping, Sun, Yanling, Wu, Zhe, Hu, Meichun, Wu, Qian, Wu, Hongnian, Liu, Fuxing, She, Tonghui, Ning, Zhifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650078/
https://www.ncbi.nlm.nih.gov/pubmed/36387165
http://dx.doi.org/10.3389/fonc.2022.1026278
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author Wei, Yaolu
Li, Yan
Chen, Yenan
Liu, Pei
Huang, Sheng
Zhang, Yuping
Sun, Yanling
Wu, Zhe
Hu, Meichun
Wu, Qian
Wu, Hongnian
Liu, Fuxing
She, Tonghui
Ning, Zhifeng
author_facet Wei, Yaolu
Li, Yan
Chen, Yenan
Liu, Pei
Huang, Sheng
Zhang, Yuping
Sun, Yanling
Wu, Zhe
Hu, Meichun
Wu, Qian
Wu, Hongnian
Liu, Fuxing
She, Tonghui
Ning, Zhifeng
author_sort Wei, Yaolu
collection PubMed
description Solid tumors can be divided into benign solid tumors and solid malignant tumors in the academic community, among which malignant solid tumors are called cancers. Cancer is the second leading cause of death in the world, and the global incidence of cancer is increasing yearly New cancer patients in China are always the first. After the concept of stem cells was introduced in the tumor community, the CSC markers represented by ALDH1 have been widely studied due to their strong CSC cell characteristics and potential to be the driving force of tumor metastasis. In the research results in the past five years, it has been found that ALDH1 is highly expressed in various solid cancers such as breast cancer, lung cancer, colorectal cancer, liver cancer, gastric cancer, cervical cancer, esophageal cancer, ovarian cancer, head,and neck cancer. ALDH1 can activate and transform various pathways (such as the USP28/MYC signaling pathway, ALDH1A1/HIF-1α/VEGF axis, wnt/β-catenin signaling pathway), as well as change the intracellular pH value to promote formation and maintenance, resulting in drug resistance in tumors. By targeting and inhibiting ALDH1 in tumor stem cells, it can enhance the sensitivity of drugs and inhibit the proliferation, differentiation, and metastasis of solid tumor stem cells to some extent. This review discusses the relationship and pathway of ALDH1 with various solid tumors. It proposes that ALDH1 may serve as a diagnosis and therapeutic target for CSC, providing new insights and new strategies for reliable tumor treatment.
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spelling pubmed-96500782022-11-15 ALDH1: A potential therapeutic target for cancer stem cells in solid tumors Wei, Yaolu Li, Yan Chen, Yenan Liu, Pei Huang, Sheng Zhang, Yuping Sun, Yanling Wu, Zhe Hu, Meichun Wu, Qian Wu, Hongnian Liu, Fuxing She, Tonghui Ning, Zhifeng Front Oncol Oncology Solid tumors can be divided into benign solid tumors and solid malignant tumors in the academic community, among which malignant solid tumors are called cancers. Cancer is the second leading cause of death in the world, and the global incidence of cancer is increasing yearly New cancer patients in China are always the first. After the concept of stem cells was introduced in the tumor community, the CSC markers represented by ALDH1 have been widely studied due to their strong CSC cell characteristics and potential to be the driving force of tumor metastasis. In the research results in the past five years, it has been found that ALDH1 is highly expressed in various solid cancers such as breast cancer, lung cancer, colorectal cancer, liver cancer, gastric cancer, cervical cancer, esophageal cancer, ovarian cancer, head,and neck cancer. ALDH1 can activate and transform various pathways (such as the USP28/MYC signaling pathway, ALDH1A1/HIF-1α/VEGF axis, wnt/β-catenin signaling pathway), as well as change the intracellular pH value to promote formation and maintenance, resulting in drug resistance in tumors. By targeting and inhibiting ALDH1 in tumor stem cells, it can enhance the sensitivity of drugs and inhibit the proliferation, differentiation, and metastasis of solid tumor stem cells to some extent. This review discusses the relationship and pathway of ALDH1 with various solid tumors. It proposes that ALDH1 may serve as a diagnosis and therapeutic target for CSC, providing new insights and new strategies for reliable tumor treatment. Frontiers Media S.A. 2022-10-28 /pmc/articles/PMC9650078/ /pubmed/36387165 http://dx.doi.org/10.3389/fonc.2022.1026278 Text en Copyright © 2022 Wei, Li, Chen, Liu, Huang, Zhang, Sun, Wu, Hu, Wu, Wu, Liu, She and Ning https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Wei, Yaolu
Li, Yan
Chen, Yenan
Liu, Pei
Huang, Sheng
Zhang, Yuping
Sun, Yanling
Wu, Zhe
Hu, Meichun
Wu, Qian
Wu, Hongnian
Liu, Fuxing
She, Tonghui
Ning, Zhifeng
ALDH1: A potential therapeutic target for cancer stem cells in solid tumors
title ALDH1: A potential therapeutic target for cancer stem cells in solid tumors
title_full ALDH1: A potential therapeutic target for cancer stem cells in solid tumors
title_fullStr ALDH1: A potential therapeutic target for cancer stem cells in solid tumors
title_full_unstemmed ALDH1: A potential therapeutic target for cancer stem cells in solid tumors
title_short ALDH1: A potential therapeutic target for cancer stem cells in solid tumors
title_sort aldh1: a potential therapeutic target for cancer stem cells in solid tumors
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650078/
https://www.ncbi.nlm.nih.gov/pubmed/36387165
http://dx.doi.org/10.3389/fonc.2022.1026278
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