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A study of deregulated MMR pathways and anticancer potential of curcuma derivatives using computational approach

Plant derived products have steadily gained momentum in treatment of cancer over the past decades. Curcuma and its derivatives, in particular, have diverse medicinal properties including anticancer potential with proven safety as supported by numerous in vivo and in vitro studies. A defective Mis-Ma...

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Autores principales: Bhattacharya, Priyanjali, Patel, Trupti N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115291/
https://www.ncbi.nlm.nih.gov/pubmed/33980898
http://dx.doi.org/10.1038/s41598-021-89282-5
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author Bhattacharya, Priyanjali
Patel, Trupti N.
author_facet Bhattacharya, Priyanjali
Patel, Trupti N.
author_sort Bhattacharya, Priyanjali
collection PubMed
description Plant derived products have steadily gained momentum in treatment of cancer over the past decades. Curcuma and its derivatives, in particular, have diverse medicinal properties including anticancer potential with proven safety as supported by numerous in vivo and in vitro studies. A defective Mis-Match Repair (MMR) is implicated in solid tumors but its role in haematologic malignancies is not keenly studied and the current literature suggests that it is limited. Nonetheless, there are multiple pathways interjecting the mismatch repair proteins in haematologic cancers that may have a direct or indirect implication in progression of the disease. Here, through computational analysis, we target proteins that are involved in rewiring of multiple signaling cascades via altered expression in cancer using various curcuma derivatives (Curcuma longa L. and Curcuma caesia Roxb.) which in turn, profoundly controls MMR protein function. These biomolecules were screened to identify their efficacy on selected targets (in blood-related cancers); aberrations of which adversely impacted mismatch repair machinery. The study revealed that of the 536 compounds screened, six of them may have the potential to regulate the expression of identified targets and thus revive the MMR function preventing genomic instability. These results reveal that there may be potential plant derived biomolecules that may have anticancer properties against the tumors driven by deregulated MMR-pathways.
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spelling pubmed-81152912021-05-14 A study of deregulated MMR pathways and anticancer potential of curcuma derivatives using computational approach Bhattacharya, Priyanjali Patel, Trupti N. Sci Rep Article Plant derived products have steadily gained momentum in treatment of cancer over the past decades. Curcuma and its derivatives, in particular, have diverse medicinal properties including anticancer potential with proven safety as supported by numerous in vivo and in vitro studies. A defective Mis-Match Repair (MMR) is implicated in solid tumors but its role in haematologic malignancies is not keenly studied and the current literature suggests that it is limited. Nonetheless, there are multiple pathways interjecting the mismatch repair proteins in haematologic cancers that may have a direct or indirect implication in progression of the disease. Here, through computational analysis, we target proteins that are involved in rewiring of multiple signaling cascades via altered expression in cancer using various curcuma derivatives (Curcuma longa L. and Curcuma caesia Roxb.) which in turn, profoundly controls MMR protein function. These biomolecules were screened to identify their efficacy on selected targets (in blood-related cancers); aberrations of which adversely impacted mismatch repair machinery. The study revealed that of the 536 compounds screened, six of them may have the potential to regulate the expression of identified targets and thus revive the MMR function preventing genomic instability. These results reveal that there may be potential plant derived biomolecules that may have anticancer properties against the tumors driven by deregulated MMR-pathways. Nature Publishing Group UK 2021-05-12 /pmc/articles/PMC8115291/ /pubmed/33980898 http://dx.doi.org/10.1038/s41598-021-89282-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bhattacharya, Priyanjali
Patel, Trupti N.
A study of deregulated MMR pathways and anticancer potential of curcuma derivatives using computational approach
title A study of deregulated MMR pathways and anticancer potential of curcuma derivatives using computational approach
title_full A study of deregulated MMR pathways and anticancer potential of curcuma derivatives using computational approach
title_fullStr A study of deregulated MMR pathways and anticancer potential of curcuma derivatives using computational approach
title_full_unstemmed A study of deregulated MMR pathways and anticancer potential of curcuma derivatives using computational approach
title_short A study of deregulated MMR pathways and anticancer potential of curcuma derivatives using computational approach
title_sort study of deregulated mmr pathways and anticancer potential of curcuma derivatives using computational approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115291/
https://www.ncbi.nlm.nih.gov/pubmed/33980898
http://dx.doi.org/10.1038/s41598-021-89282-5
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