Cargando…
Discovery of Promising Inhibitors of Epidermal Growth Factor Receptor (EGFR), Human Epidermal Growth Factor Receptor 2 (HER2), Estrogen Receptor (ER), and Phosphatidylinositol-3-kinase a (PI3Ka) for Personalized Breast Cancer Treatment
Despite the rapid developments and advancements to improve treatments, Breast cancer remains one of the deadliest health challenges and the most frequently diagnosed tumor. One of the major problems with treatment is the unique difference that each cancerous cell exhibits. As a result, treatment of...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9536107/ https://www.ncbi.nlm.nih.gov/pubmed/36213305 http://dx.doi.org/10.1177/11769351221127862 |
_version_ | 1784802920425848832 |
---|---|
author | Akinnusi, Precious A Olubode, Samuel O Adebesin, Ayomide O Nana, Toluwani A Shodehinde, Sidiqat A |
author_facet | Akinnusi, Precious A Olubode, Samuel O Adebesin, Ayomide O Nana, Toluwani A Shodehinde, Sidiqat A |
author_sort | Akinnusi, Precious A |
collection | PubMed |
description | Despite the rapid developments and advancements to improve treatments, Breast cancer remains one of the deadliest health challenges and the most frequently diagnosed tumor. One of the major problems with treatment is the unique difference that each cancerous cell exhibits. As a result, treatment of breast cancer has now become more personalized based on the specific features of the tumor such as overexpression of growth factor receptors (Epidermal growth factor receptor (EGFR), Human Epidermal Growth Factor Receptor 2 (HER2)), hormone receptors (Human Estrogen receptor alpha (ER)) and kinases involved in pivotal signaling associated with growth (Phosphatidylinositol 3-kinase (PI3K)). Several chemotherapeutic agents have been developed to curb the menace, but the associated adverse drug effects cannot be overlooked. To this end, this study employed a molecular modeling approach to identify novel compounds of natural origin that can potentially antagonize the receptors (mentioned above) associated with the pathophysiology of breast cancer and at the same time pose very little or no side effects. The results of the molecular model of biological interactions between a library of 118 anthocyanins and the binding pockets of the protein targets identified 5 compounds (Pelargonin, Delphinidin 3-O-rutinoside, Malvin, Cyanidin-3-(6-acetylglucoside), and Peonidin 3-O-rutinoside) with good binding affinities to the protein targets. Further MM-GBSA calculations returned high binding energies. The specific molecular interactions between the compounds and the targets were analyzed and reported herein. Also, all the compounds exhibited good pharmacokinetic profiles and are therefore recommended for further analyses as they could be explored as new treatment options for a broad range and personalized breast cancer treatments. |
format | Online Article Text |
id | pubmed-9536107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-95361072022-10-07 Discovery of Promising Inhibitors of Epidermal Growth Factor Receptor (EGFR), Human Epidermal Growth Factor Receptor 2 (HER2), Estrogen Receptor (ER), and Phosphatidylinositol-3-kinase a (PI3Ka) for Personalized Breast Cancer Treatment Akinnusi, Precious A Olubode, Samuel O Adebesin, Ayomide O Nana, Toluwani A Shodehinde, Sidiqat A Cancer Inform Original Research Despite the rapid developments and advancements to improve treatments, Breast cancer remains one of the deadliest health challenges and the most frequently diagnosed tumor. One of the major problems with treatment is the unique difference that each cancerous cell exhibits. As a result, treatment of breast cancer has now become more personalized based on the specific features of the tumor such as overexpression of growth factor receptors (Epidermal growth factor receptor (EGFR), Human Epidermal Growth Factor Receptor 2 (HER2)), hormone receptors (Human Estrogen receptor alpha (ER)) and kinases involved in pivotal signaling associated with growth (Phosphatidylinositol 3-kinase (PI3K)). Several chemotherapeutic agents have been developed to curb the menace, but the associated adverse drug effects cannot be overlooked. To this end, this study employed a molecular modeling approach to identify novel compounds of natural origin that can potentially antagonize the receptors (mentioned above) associated with the pathophysiology of breast cancer and at the same time pose very little or no side effects. The results of the molecular model of biological interactions between a library of 118 anthocyanins and the binding pockets of the protein targets identified 5 compounds (Pelargonin, Delphinidin 3-O-rutinoside, Malvin, Cyanidin-3-(6-acetylglucoside), and Peonidin 3-O-rutinoside) with good binding affinities to the protein targets. Further MM-GBSA calculations returned high binding energies. The specific molecular interactions between the compounds and the targets were analyzed and reported herein. Also, all the compounds exhibited good pharmacokinetic profiles and are therefore recommended for further analyses as they could be explored as new treatment options for a broad range and personalized breast cancer treatments. SAGE Publications 2022-10-04 /pmc/articles/PMC9536107/ /pubmed/36213305 http://dx.doi.org/10.1177/11769351221127862 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Akinnusi, Precious A Olubode, Samuel O Adebesin, Ayomide O Nana, Toluwani A Shodehinde, Sidiqat A Discovery of Promising Inhibitors of Epidermal Growth Factor Receptor (EGFR), Human Epidermal Growth Factor Receptor 2 (HER2), Estrogen Receptor (ER), and Phosphatidylinositol-3-kinase a (PI3Ka) for Personalized Breast Cancer Treatment |
title | Discovery of Promising Inhibitors of Epidermal Growth Factor Receptor (EGFR), Human Epidermal Growth Factor Receptor 2 (HER2), Estrogen Receptor (ER), and Phosphatidylinositol-3-kinase a (PI3Ka) for Personalized Breast Cancer Treatment |
title_full | Discovery of Promising Inhibitors of Epidermal Growth Factor Receptor (EGFR), Human Epidermal Growth Factor Receptor 2 (HER2), Estrogen Receptor (ER), and Phosphatidylinositol-3-kinase a (PI3Ka) for Personalized Breast Cancer Treatment |
title_fullStr | Discovery of Promising Inhibitors of Epidermal Growth Factor Receptor (EGFR), Human Epidermal Growth Factor Receptor 2 (HER2), Estrogen Receptor (ER), and Phosphatidylinositol-3-kinase a (PI3Ka) for Personalized Breast Cancer Treatment |
title_full_unstemmed | Discovery of Promising Inhibitors of Epidermal Growth Factor Receptor (EGFR), Human Epidermal Growth Factor Receptor 2 (HER2), Estrogen Receptor (ER), and Phosphatidylinositol-3-kinase a (PI3Ka) for Personalized Breast Cancer Treatment |
title_short | Discovery of Promising Inhibitors of Epidermal Growth Factor Receptor (EGFR), Human Epidermal Growth Factor Receptor 2 (HER2), Estrogen Receptor (ER), and Phosphatidylinositol-3-kinase a (PI3Ka) for Personalized Breast Cancer Treatment |
title_sort | discovery of promising inhibitors of epidermal growth factor receptor (egfr), human epidermal growth factor receptor 2 (her2), estrogen receptor (er), and phosphatidylinositol-3-kinase a (pi3ka) for personalized breast cancer treatment |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9536107/ https://www.ncbi.nlm.nih.gov/pubmed/36213305 http://dx.doi.org/10.1177/11769351221127862 |
work_keys_str_mv | AT akinnusipreciousa discoveryofpromisinginhibitorsofepidermalgrowthfactorreceptoregfrhumanepidermalgrowthfactorreceptor2her2estrogenreceptorerandphosphatidylinositol3kinaseapi3kaforpersonalizedbreastcancertreatment AT olubodesamuelo discoveryofpromisinginhibitorsofepidermalgrowthfactorreceptoregfrhumanepidermalgrowthfactorreceptor2her2estrogenreceptorerandphosphatidylinositol3kinaseapi3kaforpersonalizedbreastcancertreatment AT adebesinayomideo discoveryofpromisinginhibitorsofepidermalgrowthfactorreceptoregfrhumanepidermalgrowthfactorreceptor2her2estrogenreceptorerandphosphatidylinositol3kinaseapi3kaforpersonalizedbreastcancertreatment AT nanatoluwania discoveryofpromisinginhibitorsofepidermalgrowthfactorreceptoregfrhumanepidermalgrowthfactorreceptor2her2estrogenreceptorerandphosphatidylinositol3kinaseapi3kaforpersonalizedbreastcancertreatment AT shodehindesidiqata discoveryofpromisinginhibitorsofepidermalgrowthfactorreceptoregfrhumanepidermalgrowthfactorreceptor2her2estrogenreceptorerandphosphatidylinositol3kinaseapi3kaforpersonalizedbreastcancertreatment |