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血管紧张素Ⅱ及其受体与恶性肿瘤关系的研究进展

Angiotensin AngⅡ, a linear small peptide, which is composed of eight amino acids, is the main effectors of renin-angiotensin systen (Renin-angiotensin system, RAS). AngⅡ, a main biopolypeptide of the RAS, has important pathophysiologic in effects participating in cardiac hypertrophy, vascular cell p...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5972952/
https://www.ncbi.nlm.nih.gov/pubmed/27666553
http://dx.doi.org/10.3779/j.issn.1009-3419.2016.09.10
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description Angiotensin AngⅡ, a linear small peptide, which is composed of eight amino acids, is the main effectors of renin-angiotensin systen (Renin-angiotensin system, RAS). AngⅡ, a main biopolypeptide of the RAS, has important pathophysiologic in effects participating in cardiac hypertrophy, vascular cell proproliferation, inflammation and tissue remodeling through G-protein-coupled receptors. In recent years, Ang Ⅱ can promote tumor cell proliferation, tumor vessel formation and inhibit the differentiation of the tumor cells. This suggests that inhibit the production of AngⅡ or block its effect is expected to become a new measure for the treatment of malignant tumors. This article reviews the advances in research on the relationship between AngⅡ and its receptor and malignant tumor in recent years.
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spelling pubmed-59729522018-07-06 血管紧张素Ⅱ及其受体与恶性肿瘤关系的研究进展 Zhongguo Fei Ai Za Zhi 综述 Angiotensin AngⅡ, a linear small peptide, which is composed of eight amino acids, is the main effectors of renin-angiotensin systen (Renin-angiotensin system, RAS). AngⅡ, a main biopolypeptide of the RAS, has important pathophysiologic in effects participating in cardiac hypertrophy, vascular cell proproliferation, inflammation and tissue remodeling through G-protein-coupled receptors. In recent years, Ang Ⅱ can promote tumor cell proliferation, tumor vessel formation and inhibit the differentiation of the tumor cells. This suggests that inhibit the production of AngⅡ or block its effect is expected to become a new measure for the treatment of malignant tumors. This article reviews the advances in research on the relationship between AngⅡ and its receptor and malignant tumor in recent years. 中国肺癌杂志编辑部 2016-09-20 /pmc/articles/PMC5972952/ /pubmed/27666553 http://dx.doi.org/10.3779/j.issn.1009-3419.2016.09.10 Text en 版权所有©《中国肺癌杂志》编辑部2016 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/
spellingShingle 综述
血管紧张素Ⅱ及其受体与恶性肿瘤关系的研究进展
title 血管紧张素Ⅱ及其受体与恶性肿瘤关系的研究进展
title_full 血管紧张素Ⅱ及其受体与恶性肿瘤关系的研究进展
title_fullStr 血管紧张素Ⅱ及其受体与恶性肿瘤关系的研究进展
title_full_unstemmed 血管紧张素Ⅱ及其受体与恶性肿瘤关系的研究进展
title_short 血管紧张素Ⅱ及其受体与恶性肿瘤关系的研究进展
title_sort 血管紧张素ⅱ及其受体与恶性肿瘤关系的研究进展
topic 综述
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5972952/
https://www.ncbi.nlm.nih.gov/pubmed/27666553
http://dx.doi.org/10.3779/j.issn.1009-3419.2016.09.10
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