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Novel Drugs with High Efficacy against Tumor Angiogenesis
Angiogenesis is involved in physiological and pathological processes in the body. Tumor angiogenesis is a key factor associated with tumor growth, progression, and metastasis. Therefore, there is great interest in developing antiangiogenic strategies. Hypoxia is the basic initiating factor of tumor...
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/PMC9267017/ https://www.ncbi.nlm.nih.gov/pubmed/35805939 http://dx.doi.org/10.3390/ijms23136934 |
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author | Qi, Shiyu Deng, Shoulong Lian, Zhengxing Yu, Kun |
author_facet | Qi, Shiyu Deng, Shoulong Lian, Zhengxing Yu, Kun |
author_sort | Qi, Shiyu |
collection | PubMed |
description | Angiogenesis is involved in physiological and pathological processes in the body. Tumor angiogenesis is a key factor associated with tumor growth, progression, and metastasis. Therefore, there is great interest in developing antiangiogenic strategies. Hypoxia is the basic initiating factor of tumor angiogenesis, which leads to the increase of vascular endothelial growth factor (VEGF), angiopoietin (Ang), hypoxia-inducible factor (HIF-1), etc. in hypoxic cells. The pathways of VEGF and Ang are considered to be critical steps in tumor angiogenesis. A number of antiangiogenic drugs targeting VEGF/VEGFR (VEGF receptor) or ANG/Tie2, or both, are currently being used for cancer treatment, or are still in various stages of clinical development or preclinical evaluation. This article aims to review the mechanisms of angiogenesis and tumor angiogenesis and to focus on new drugs and strategies for the treatment of antiangiogenesis. However, antitumor angiogenic drugs alone may not be sufficient to eradicate tumors. The molecular chaperone heat shock protein 90 (HSP90) is considered a promising molecular target. The VEGFR system and its downstream signaling molecules depend on the function of HSP90. This article also briefly introduces the role of HSP90 in angiogenesis and some HSP90 inhibitors. |
format | Online Article Text |
id | pubmed-9267017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92670172022-07-09 Novel Drugs with High Efficacy against Tumor Angiogenesis Qi, Shiyu Deng, Shoulong Lian, Zhengxing Yu, Kun Int J Mol Sci Review Angiogenesis is involved in physiological and pathological processes in the body. Tumor angiogenesis is a key factor associated with tumor growth, progression, and metastasis. Therefore, there is great interest in developing antiangiogenic strategies. Hypoxia is the basic initiating factor of tumor angiogenesis, which leads to the increase of vascular endothelial growth factor (VEGF), angiopoietin (Ang), hypoxia-inducible factor (HIF-1), etc. in hypoxic cells. The pathways of VEGF and Ang are considered to be critical steps in tumor angiogenesis. A number of antiangiogenic drugs targeting VEGF/VEGFR (VEGF receptor) or ANG/Tie2, or both, are currently being used for cancer treatment, or are still in various stages of clinical development or preclinical evaluation. This article aims to review the mechanisms of angiogenesis and tumor angiogenesis and to focus on new drugs and strategies for the treatment of antiangiogenesis. However, antitumor angiogenic drugs alone may not be sufficient to eradicate tumors. The molecular chaperone heat shock protein 90 (HSP90) is considered a promising molecular target. The VEGFR system and its downstream signaling molecules depend on the function of HSP90. This article also briefly introduces the role of HSP90 in angiogenesis and some HSP90 inhibitors. MDPI 2022-06-22 /pmc/articles/PMC9267017/ /pubmed/35805939 http://dx.doi.org/10.3390/ijms23136934 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 Qi, Shiyu Deng, Shoulong Lian, Zhengxing Yu, Kun Novel Drugs with High Efficacy against Tumor Angiogenesis |
title | Novel Drugs with High Efficacy against Tumor Angiogenesis |
title_full | Novel Drugs with High Efficacy against Tumor Angiogenesis |
title_fullStr | Novel Drugs with High Efficacy against Tumor Angiogenesis |
title_full_unstemmed | Novel Drugs with High Efficacy against Tumor Angiogenesis |
title_short | Novel Drugs with High Efficacy against Tumor Angiogenesis |
title_sort | novel drugs with high efficacy against tumor angiogenesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9267017/ https://www.ncbi.nlm.nih.gov/pubmed/35805939 http://dx.doi.org/10.3390/ijms23136934 |
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