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The current status of anti-GPCR drugs against different cancers
G protein coupled receptors (GPCRs) have emerged as the most potential target for a number of drug discovery programs ranging from control of blood pressure, diabetes, cure for genetic diseases to treatment of cancer. A panel of different ligands including hormones, peptides, ions and small molecule...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Xi'an Jiaotong University
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7775845/ https://www.ncbi.nlm.nih.gov/pubmed/33425448 http://dx.doi.org/10.1016/j.jpha.2020.01.001 |
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author | Usman, Sana Khawer, Maria Rafique, Shazia Naz, Zara Saleem, Komal |
author_facet | Usman, Sana Khawer, Maria Rafique, Shazia Naz, Zara Saleem, Komal |
author_sort | Usman, Sana |
collection | PubMed |
description | G protein coupled receptors (GPCRs) have emerged as the most potential target for a number of drug discovery programs ranging from control of blood pressure, diabetes, cure for genetic diseases to treatment of cancer. A panel of different ligands including hormones, peptides, ions and small molecules is responsible for activation of these receptors. Molecular genetics has identified key GPCRs, whose mutations or altered expressions are linked with tumorgenicity. In this review, we discussed recent advances regarding the involvement of GPCRs in the development of cancers and approaches to manipulating the mechanism behind GPCRs involved tumor growth and metastasis to treat different types of human cancer. This review provides an insight into the current scenario of GPCR-targeted therapy, progress to date and the challenges in the development of anticancer drugs. |
format | Online Article Text |
id | pubmed-7775845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Xi'an Jiaotong University |
record_format | MEDLINE/PubMed |
spelling | pubmed-77758452021-01-07 The current status of anti-GPCR drugs against different cancers Usman, Sana Khawer, Maria Rafique, Shazia Naz, Zara Saleem, Komal J Pharm Anal Review Paper G protein coupled receptors (GPCRs) have emerged as the most potential target for a number of drug discovery programs ranging from control of blood pressure, diabetes, cure for genetic diseases to treatment of cancer. A panel of different ligands including hormones, peptides, ions and small molecules is responsible for activation of these receptors. Molecular genetics has identified key GPCRs, whose mutations or altered expressions are linked with tumorgenicity. In this review, we discussed recent advances regarding the involvement of GPCRs in the development of cancers and approaches to manipulating the mechanism behind GPCRs involved tumor growth and metastasis to treat different types of human cancer. This review provides an insight into the current scenario of GPCR-targeted therapy, progress to date and the challenges in the development of anticancer drugs. Xi'an Jiaotong University 2020-12 2020-01-11 /pmc/articles/PMC7775845/ /pubmed/33425448 http://dx.doi.org/10.1016/j.jpha.2020.01.001 Text en © 2020 Xi'an Jiaotong University. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Paper Usman, Sana Khawer, Maria Rafique, Shazia Naz, Zara Saleem, Komal The current status of anti-GPCR drugs against different cancers |
title | The current status of anti-GPCR drugs against different cancers |
title_full | The current status of anti-GPCR drugs against different cancers |
title_fullStr | The current status of anti-GPCR drugs against different cancers |
title_full_unstemmed | The current status of anti-GPCR drugs against different cancers |
title_short | The current status of anti-GPCR drugs against different cancers |
title_sort | current status of anti-gpcr drugs against different cancers |
topic | Review Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7775845/ https://www.ncbi.nlm.nih.gov/pubmed/33425448 http://dx.doi.org/10.1016/j.jpha.2020.01.001 |
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