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Epigenetic mechanisms in cancer: push and pull between kneaded erasers and fate writers

Research concerning the epigenome over the years has systematically and sequentially shown substantial development and we have moved from global inhibition of modifications of the epigenome toward identification and targeted therapy against tumor-specific epigenetic mechanisms. In accordance with th...

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Autores principales: Farooqi, Ammad Ahmad, Tang, Jen-Yang, Li, Ruei-Nian, Ismail, Muhammad, Chang, Yung-Ting, Shu, Chih-Wen, Yuan, Shyng-Shiou F, Liu, Jing-Ru, Mansoor, Qaisar, Huang, Chih-Jen, Chang, Hsueh-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4425311/
https://www.ncbi.nlm.nih.gov/pubmed/25995628
http://dx.doi.org/10.2147/IJN.S82527
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author Farooqi, Ammad Ahmad
Tang, Jen-Yang
Li, Ruei-Nian
Ismail, Muhammad
Chang, Yung-Ting
Shu, Chih-Wen
Yuan, Shyng-Shiou F
Liu, Jing-Ru
Mansoor, Qaisar
Huang, Chih-Jen
Chang, Hsueh-Wei
author_facet Farooqi, Ammad Ahmad
Tang, Jen-Yang
Li, Ruei-Nian
Ismail, Muhammad
Chang, Yung-Ting
Shu, Chih-Wen
Yuan, Shyng-Shiou F
Liu, Jing-Ru
Mansoor, Qaisar
Huang, Chih-Jen
Chang, Hsueh-Wei
author_sort Farooqi, Ammad Ahmad
collection PubMed
description Research concerning the epigenome over the years has systematically and sequentially shown substantial development and we have moved from global inhibition of modifications of the epigenome toward identification and targeted therapy against tumor-specific epigenetic mechanisms. In accordance with this approach, several drugs with epigenetically modulating activity have received considerable attention and appreciation, and recently emerging scientific evidence is uncovering details of their mode of action. High-throughput technologies have considerably improved our existing understanding of tumor suppressors, oncogenes, and signaling pathways that are key drivers of cancer. In this review, we summarize the general epigenetic mechanisms in cancer, including: the post-translational modification of DNA methyltransferase and its mediated inactivation of Ras association domain family 1 isoform A, Sonic hedgehog signaling, Wnt signaling, Notch signaling, transforming growth factor signaling, and natural products with epigenetic modification ability. Moreover, we introduce the importance of nanomedicine for delivery of natural products with modulating ability to epigenetic machinery in cancer cells. Such in-depth and comprehensive knowledge regarding epigenetic dysregulation will be helpful in the upcoming era of molecular genomic pathology for both detection and treatment of cancer. Epigenetic information will also be helpful when nanotherapy is used for epigenetic modification.
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spelling pubmed-44253112015-05-20 Epigenetic mechanisms in cancer: push and pull between kneaded erasers and fate writers Farooqi, Ammad Ahmad Tang, Jen-Yang Li, Ruei-Nian Ismail, Muhammad Chang, Yung-Ting Shu, Chih-Wen Yuan, Shyng-Shiou F Liu, Jing-Ru Mansoor, Qaisar Huang, Chih-Jen Chang, Hsueh-Wei Int J Nanomedicine Review Research concerning the epigenome over the years has systematically and sequentially shown substantial development and we have moved from global inhibition of modifications of the epigenome toward identification and targeted therapy against tumor-specific epigenetic mechanisms. In accordance with this approach, several drugs with epigenetically modulating activity have received considerable attention and appreciation, and recently emerging scientific evidence is uncovering details of their mode of action. High-throughput technologies have considerably improved our existing understanding of tumor suppressors, oncogenes, and signaling pathways that are key drivers of cancer. In this review, we summarize the general epigenetic mechanisms in cancer, including: the post-translational modification of DNA methyltransferase and its mediated inactivation of Ras association domain family 1 isoform A, Sonic hedgehog signaling, Wnt signaling, Notch signaling, transforming growth factor signaling, and natural products with epigenetic modification ability. Moreover, we introduce the importance of nanomedicine for delivery of natural products with modulating ability to epigenetic machinery in cancer cells. Such in-depth and comprehensive knowledge regarding epigenetic dysregulation will be helpful in the upcoming era of molecular genomic pathology for both detection and treatment of cancer. Epigenetic information will also be helpful when nanotherapy is used for epigenetic modification. Dove Medical Press 2015-04-24 /pmc/articles/PMC4425311/ /pubmed/25995628 http://dx.doi.org/10.2147/IJN.S82527 Text en © 2015 Farooqi et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Farooqi, Ammad Ahmad
Tang, Jen-Yang
Li, Ruei-Nian
Ismail, Muhammad
Chang, Yung-Ting
Shu, Chih-Wen
Yuan, Shyng-Shiou F
Liu, Jing-Ru
Mansoor, Qaisar
Huang, Chih-Jen
Chang, Hsueh-Wei
Epigenetic mechanisms in cancer: push and pull between kneaded erasers and fate writers
title Epigenetic mechanisms in cancer: push and pull between kneaded erasers and fate writers
title_full Epigenetic mechanisms in cancer: push and pull between kneaded erasers and fate writers
title_fullStr Epigenetic mechanisms in cancer: push and pull between kneaded erasers and fate writers
title_full_unstemmed Epigenetic mechanisms in cancer: push and pull between kneaded erasers and fate writers
title_short Epigenetic mechanisms in cancer: push and pull between kneaded erasers and fate writers
title_sort epigenetic mechanisms in cancer: push and pull between kneaded erasers and fate writers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4425311/
https://www.ncbi.nlm.nih.gov/pubmed/25995628
http://dx.doi.org/10.2147/IJN.S82527
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