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Pan-Cancer Analysis and Drug Formulation for GPR139 and GPR142
GPR (G protein receptor) 139 and 142 are novel foundling GPCRs (G protein-coupled receptors) in the class “A” of the GPCRs family and are suitable targets for various biological conditions. To engage these targets, validated pharmacophores and 3D QSAR (Quantitative structure-activity relationship) m...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933564/ https://www.ncbi.nlm.nih.gov/pubmed/33679382 http://dx.doi.org/10.3389/fphar.2020.521245 |
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author | Kaushik, Aman Chandra Mehmood, Aamir Dai, Xiaofeng Wei, Dong-Qing |
author_facet | Kaushik, Aman Chandra Mehmood, Aamir Dai, Xiaofeng Wei, Dong-Qing |
author_sort | Kaushik, Aman Chandra |
collection | PubMed |
description | GPR (G protein receptor) 139 and 142 are novel foundling GPCRs (G protein-coupled receptors) in the class “A” of the GPCRs family and are suitable targets for various biological conditions. To engage these targets, validated pharmacophores and 3D QSAR (Quantitative structure-activity relationship) models are widely used because of their direct fingerprinting capability of the target and an overall accuracy. The current work initially analyzes GPR139 and GPR142 for its genomic alteration via tumor samples. Next to that, the pharmacophore is developed to scan the 3D database for such compounds that can lead to potential agonists. As a result, several compounds have been considered, showing satisfactory performance and a strong association with the target. Additionally, it is gripping to know that the obtained compounds were observed to be responsible for triggering pan-cancer. This suggests the possible role of novel GPR139 and GPR142 as the substances for initiating a physiological response to handle the condition incurred as a result of cancer. |
format | Online Article Text |
id | pubmed-7933564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79335642021-03-06 Pan-Cancer Analysis and Drug Formulation for GPR139 and GPR142 Kaushik, Aman Chandra Mehmood, Aamir Dai, Xiaofeng Wei, Dong-Qing Front Pharmacol Pharmacology GPR (G protein receptor) 139 and 142 are novel foundling GPCRs (G protein-coupled receptors) in the class “A” of the GPCRs family and are suitable targets for various biological conditions. To engage these targets, validated pharmacophores and 3D QSAR (Quantitative structure-activity relationship) models are widely used because of their direct fingerprinting capability of the target and an overall accuracy. The current work initially analyzes GPR139 and GPR142 for its genomic alteration via tumor samples. Next to that, the pharmacophore is developed to scan the 3D database for such compounds that can lead to potential agonists. As a result, several compounds have been considered, showing satisfactory performance and a strong association with the target. Additionally, it is gripping to know that the obtained compounds were observed to be responsible for triggering pan-cancer. This suggests the possible role of novel GPR139 and GPR142 as the substances for initiating a physiological response to handle the condition incurred as a result of cancer. Frontiers Media S.A. 2021-02-19 /pmc/articles/PMC7933564/ /pubmed/33679382 http://dx.doi.org/10.3389/fphar.2020.521245 Text en Copyright © 2021 Kaushik, Mehmood, Dai and Wei. http://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 | Pharmacology Kaushik, Aman Chandra Mehmood, Aamir Dai, Xiaofeng Wei, Dong-Qing Pan-Cancer Analysis and Drug Formulation for GPR139 and GPR142 |
title | Pan-Cancer Analysis and Drug Formulation for GPR139 and GPR142 |
title_full | Pan-Cancer Analysis and Drug Formulation for GPR139 and GPR142 |
title_fullStr | Pan-Cancer Analysis and Drug Formulation for GPR139 and GPR142 |
title_full_unstemmed | Pan-Cancer Analysis and Drug Formulation for GPR139 and GPR142 |
title_short | Pan-Cancer Analysis and Drug Formulation for GPR139 and GPR142 |
title_sort | pan-cancer analysis and drug formulation for gpr139 and gpr142 |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933564/ https://www.ncbi.nlm.nih.gov/pubmed/33679382 http://dx.doi.org/10.3389/fphar.2020.521245 |
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