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Anti-cancer activity of C. cainito leaves explained using its compounds docked with p53
Extensive research on the mutant P53 protein has identified its pivotal role in anti-apoptosis mechanisms, drug resistance, and cancer progression in OSCC. The mass spectrum revealed the pharmacologically significant bioactive compounds reported for the first time in C cainito. Molecular docking inv...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Biomedical Informatics
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465767/ https://www.ncbi.nlm.nih.gov/pubmed/37654835 http://dx.doi.org/10.6026/97320630018870 |
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author | Prabhu, Yesudass Antony Balalakshmi, Chinnasamy Vijayasarathy, Muthu Kumar, Kumar Praveen Shanmughavel, Piramanayagam Kavitha, Samiappan |
author_facet | Prabhu, Yesudass Antony Balalakshmi, Chinnasamy Vijayasarathy, Muthu Kumar, Kumar Praveen Shanmughavel, Piramanayagam Kavitha, Samiappan |
author_sort | Prabhu, Yesudass Antony |
collection | PubMed |
description | Extensive research on the mutant P53 protein has identified its pivotal role in anti-apoptosis mechanisms, drug resistance, and cancer progression in OSCC. The mass spectrum revealed the pharmacologically significant bioactive compounds reported for the first time in C cainito. Molecular docking investigation has identified four potential new P53 inhibitors compared with the standard P53 inhibitors. Hence, this analysis reinforces the likelihood of anti-cancer activities in C. cainito leaves. |
format | Online Article Text |
id | pubmed-10465767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Biomedical Informatics |
record_format | MEDLINE/PubMed |
spelling | pubmed-104657672023-08-31 Anti-cancer activity of C. cainito leaves explained using its compounds docked with p53 Prabhu, Yesudass Antony Balalakshmi, Chinnasamy Vijayasarathy, Muthu Kumar, Kumar Praveen Shanmughavel, Piramanayagam Kavitha, Samiappan Bioinformation Research Article Extensive research on the mutant P53 protein has identified its pivotal role in anti-apoptosis mechanisms, drug resistance, and cancer progression in OSCC. The mass spectrum revealed the pharmacologically significant bioactive compounds reported for the first time in C cainito. Molecular docking investigation has identified four potential new P53 inhibitors compared with the standard P53 inhibitors. Hence, this analysis reinforces the likelihood of anti-cancer activities in C. cainito leaves. Biomedical Informatics 2022-10-31 /pmc/articles/PMC10465767/ /pubmed/37654835 http://dx.doi.org/10.6026/97320630018870 Text en © 2022 Biomedical Informatics https://creativecommons.org/licenses/by/3.0/This is an Open Access article which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. This is distributed under the terms of the Creative Commons Attribution License. |
spellingShingle | Research Article Prabhu, Yesudass Antony Balalakshmi, Chinnasamy Vijayasarathy, Muthu Kumar, Kumar Praveen Shanmughavel, Piramanayagam Kavitha, Samiappan Anti-cancer activity of C. cainito leaves explained using its compounds docked with p53 |
title | Anti-cancer activity of C. cainito leaves explained using its compounds docked with p53 |
title_full | Anti-cancer activity of C. cainito leaves explained using its compounds docked with p53 |
title_fullStr | Anti-cancer activity of C. cainito leaves explained using its compounds docked with p53 |
title_full_unstemmed | Anti-cancer activity of C. cainito leaves explained using its compounds docked with p53 |
title_short | Anti-cancer activity of C. cainito leaves explained using its compounds docked with p53 |
title_sort | anti-cancer activity of c. cainito leaves explained using its compounds docked with p53 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465767/ https://www.ncbi.nlm.nih.gov/pubmed/37654835 http://dx.doi.org/10.6026/97320630018870 |
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