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Rac1, A Potential Target for Tumor Therapy

RAS-related C3 botulinum toxin substrate 1 (Rac.1) is one of the important members of Rho GTPases. It is well known that Rac1 is a cytoskeleton regulation protein that regulates cell adhesion, morphology, and movement. Rac1 is highly expressed in different types of tumors, which is related to poor p...

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Autores principales: Liang, Jiaxin, Oyang, Linda, Rao, Shan, Han, Yaqian, Luo, Xia, Yi, Pin, Lin, Jinguan, Xia, Longzheng, Hu, Jiaqi, Tan, Shiming, Tang, Lu, Pan, Qing, Tang, Yanyan, Zhou, Yujuan, Liao, Qianjin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165220/
https://www.ncbi.nlm.nih.gov/pubmed/34079763
http://dx.doi.org/10.3389/fonc.2021.674426
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author Liang, Jiaxin
Oyang, Linda
Rao, Shan
Han, Yaqian
Luo, Xia
Yi, Pin
Lin, Jinguan
Xia, Longzheng
Hu, Jiaqi
Tan, Shiming
Tang, Lu
Pan, Qing
Tang, Yanyan
Zhou, Yujuan
Liao, Qianjin
author_facet Liang, Jiaxin
Oyang, Linda
Rao, Shan
Han, Yaqian
Luo, Xia
Yi, Pin
Lin, Jinguan
Xia, Longzheng
Hu, Jiaqi
Tan, Shiming
Tang, Lu
Pan, Qing
Tang, Yanyan
Zhou, Yujuan
Liao, Qianjin
author_sort Liang, Jiaxin
collection PubMed
description RAS-related C3 botulinum toxin substrate 1 (Rac.1) is one of the important members of Rho GTPases. It is well known that Rac1 is a cytoskeleton regulation protein that regulates cell adhesion, morphology, and movement. Rac1 is highly expressed in different types of tumors, which is related to poor prognosis. Studies have shown that Rac1 not only participates in the tumor cell cycle, apoptosis, proliferation, invasion, migration and angiogenesis, but also participates in the regulation of tumor stem cell, thus promoting the occurrence of tumors. Rac1 also plays a key role in anti-tumor therapy and participates in immune escape mediated by the tumor microenvironment. In addition, the good prospects of Rac1 inhibitors in cancer prevention and treatment are exciting. Therefore, Rac1 is considered as a potential target for the prevention and treatment of cancer. The necessity and importance of Rac1 are obvious, but it still needs further study.
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spelling pubmed-81652202021-06-01 Rac1, A Potential Target for Tumor Therapy Liang, Jiaxin Oyang, Linda Rao, Shan Han, Yaqian Luo, Xia Yi, Pin Lin, Jinguan Xia, Longzheng Hu, Jiaqi Tan, Shiming Tang, Lu Pan, Qing Tang, Yanyan Zhou, Yujuan Liao, Qianjin Front Oncol Oncology RAS-related C3 botulinum toxin substrate 1 (Rac.1) is one of the important members of Rho GTPases. It is well known that Rac1 is a cytoskeleton regulation protein that regulates cell adhesion, morphology, and movement. Rac1 is highly expressed in different types of tumors, which is related to poor prognosis. Studies have shown that Rac1 not only participates in the tumor cell cycle, apoptosis, proliferation, invasion, migration and angiogenesis, but also participates in the regulation of tumor stem cell, thus promoting the occurrence of tumors. Rac1 also plays a key role in anti-tumor therapy and participates in immune escape mediated by the tumor microenvironment. In addition, the good prospects of Rac1 inhibitors in cancer prevention and treatment are exciting. Therefore, Rac1 is considered as a potential target for the prevention and treatment of cancer. The necessity and importance of Rac1 are obvious, but it still needs further study. Frontiers Media S.A. 2021-05-17 /pmc/articles/PMC8165220/ /pubmed/34079763 http://dx.doi.org/10.3389/fonc.2021.674426 Text en Copyright © 2021 Liang, Oyang, Rao, Han, Luo, Yi, Lin, Xia, Hu, Tan, Tang, Pan, Tang, Zhou and Liao 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
Liang, Jiaxin
Oyang, Linda
Rao, Shan
Han, Yaqian
Luo, Xia
Yi, Pin
Lin, Jinguan
Xia, Longzheng
Hu, Jiaqi
Tan, Shiming
Tang, Lu
Pan, Qing
Tang, Yanyan
Zhou, Yujuan
Liao, Qianjin
Rac1, A Potential Target for Tumor Therapy
title Rac1, A Potential Target for Tumor Therapy
title_full Rac1, A Potential Target for Tumor Therapy
title_fullStr Rac1, A Potential Target for Tumor Therapy
title_full_unstemmed Rac1, A Potential Target for Tumor Therapy
title_short Rac1, A Potential Target for Tumor Therapy
title_sort rac1, a potential target for tumor therapy
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165220/
https://www.ncbi.nlm.nih.gov/pubmed/34079763
http://dx.doi.org/10.3389/fonc.2021.674426
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