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Apatinib as targeted therapy for sarcoma
Sarcomas are a group of malignant tumors originating from mesenchymal tissue with a variety of cell subtypes. Despite several major treatment breakthroughs, standard treatment using surgery, radiation, and chemotherapy has failed to improve overall survival. Therefore, there is an urgent need to exp...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5966248/ https://www.ncbi.nlm.nih.gov/pubmed/29849960 http://dx.doi.org/10.18632/oncotarget.24647 |
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author | Li, Feng Liao, Zhichao Zhang, Chao Zhao, Jun Xing, Ruwei Teng, Sheng Zhang, Jin Yang, Yun Yang, Jilong |
author_facet | Li, Feng Liao, Zhichao Zhang, Chao Zhao, Jun Xing, Ruwei Teng, Sheng Zhang, Jin Yang, Yun Yang, Jilong |
author_sort | Li, Feng |
collection | PubMed |
description | Sarcomas are a group of malignant tumors originating from mesenchymal tissue with a variety of cell subtypes. Despite several major treatment breakthroughs, standard treatment using surgery, radiation, and chemotherapy has failed to improve overall survival. Therefore, there is an urgent need to explore new strategies and innovative therapies to further improve the survival rates of patients with sarcomas. Pathological angiogenesis has an important role in the growth and metastasis of tumors. Vascular endothelial growth factor (VEGF) and vascular endothelial growth factor receptors (VEGFRs) play a central role in tumor angiogenesis and represent potential targets for anticancer therapy. As a novel targeted therapy, especially with regard to angiogenesis, apatinib is a new type of small molecule tyrosine kinase inhibitor that selectively targets VEGFR-2 and has shown encouraging anticancer activity in a wide range of malignancies, including gastric cancer, non-small cell lung cancer, breast cancer, hepatocellular carcinoma, and sarcomas. In this review, we summarize the preclinical and clinical data for apatinib, focusing primarily on its use in the treatment of sarcomas. |
format | Online Article Text |
id | pubmed-5966248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-59662482018-05-30 Apatinib as targeted therapy for sarcoma Li, Feng Liao, Zhichao Zhang, Chao Zhao, Jun Xing, Ruwei Teng, Sheng Zhang, Jin Yang, Yun Yang, Jilong Oncotarget Review Sarcomas are a group of malignant tumors originating from mesenchymal tissue with a variety of cell subtypes. Despite several major treatment breakthroughs, standard treatment using surgery, radiation, and chemotherapy has failed to improve overall survival. Therefore, there is an urgent need to explore new strategies and innovative therapies to further improve the survival rates of patients with sarcomas. Pathological angiogenesis has an important role in the growth and metastasis of tumors. Vascular endothelial growth factor (VEGF) and vascular endothelial growth factor receptors (VEGFRs) play a central role in tumor angiogenesis and represent potential targets for anticancer therapy. As a novel targeted therapy, especially with regard to angiogenesis, apatinib is a new type of small molecule tyrosine kinase inhibitor that selectively targets VEGFR-2 and has shown encouraging anticancer activity in a wide range of malignancies, including gastric cancer, non-small cell lung cancer, breast cancer, hepatocellular carcinoma, and sarcomas. In this review, we summarize the preclinical and clinical data for apatinib, focusing primarily on its use in the treatment of sarcomas. Impact Journals LLC 2018-05-11 /pmc/articles/PMC5966248/ /pubmed/29849960 http://dx.doi.org/10.18632/oncotarget.24647 Text en Copyright: © 2018 Li et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Review Li, Feng Liao, Zhichao Zhang, Chao Zhao, Jun Xing, Ruwei Teng, Sheng Zhang, Jin Yang, Yun Yang, Jilong Apatinib as targeted therapy for sarcoma |
title | Apatinib as targeted therapy for sarcoma |
title_full | Apatinib as targeted therapy for sarcoma |
title_fullStr | Apatinib as targeted therapy for sarcoma |
title_full_unstemmed | Apatinib as targeted therapy for sarcoma |
title_short | Apatinib as targeted therapy for sarcoma |
title_sort | apatinib as targeted therapy for sarcoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5966248/ https://www.ncbi.nlm.nih.gov/pubmed/29849960 http://dx.doi.org/10.18632/oncotarget.24647 |
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