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Therapeutic Potential of Emodin for Gastrointestinal Cancers
Gastrointestinal (GI) cancers cause one-third of all cancer-related deaths worldwide. Natural compounds are emerging as alternative or adjuvant cancer therapies given their distinct advantage of manipulating multiple pathways to both suppress tumor growth and alleviate cancer comorbidities; however,...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8738880/ https://www.ncbi.nlm.nih.gov/pubmed/34984952 http://dx.doi.org/10.1177/15347354211067469 |
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author | McDonald, Sierra J. VanderVeen, Brandon N. Velazquez, Kandy T. Enos, Reilly T. Fairman, Ciaran M. Cardaci, Thomas D. Fan, Daping Murphy, E. Angela |
author_facet | McDonald, Sierra J. VanderVeen, Brandon N. Velazquez, Kandy T. Enos, Reilly T. Fairman, Ciaran M. Cardaci, Thomas D. Fan, Daping Murphy, E. Angela |
author_sort | McDonald, Sierra J. |
collection | PubMed |
description | Gastrointestinal (GI) cancers cause one-third of all cancer-related deaths worldwide. Natural compounds are emerging as alternative or adjuvant cancer therapies given their distinct advantage of manipulating multiple pathways to both suppress tumor growth and alleviate cancer comorbidities; however, concerns regarding efficacy, bioavailability, and safety are barriers to their development for clinical use. Emodin (1,3,8-trihydroxy-6-methylanthraquinone), a Chinese herb-derived anthraquinone, has been shown to exert anti-tumor effects in colon, liver, and pancreatic cancers. While the mechanisms underlying emodin’s tumoricidal effects continue to be unearthed, recent evidence highlights a role for mitochondrial mediated apoptosis, modulated stress and inflammatory signaling pathways, and blunted angiogenesis. The goals of this review are to (1) highlight emodin’s anti-cancer properties within GI cancers, (2) discuss the known anti-cancer mechanisms of action of emodin, (3) address emodin’s potential as a treatment complementary to standard chemotherapeutics, (4) assess the efficacy and bioavailability of emodin derivatives as they relate to cancer, and (5) evaluate the safety of emodin. |
format | Online Article Text |
id | pubmed-8738880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-87388802022-01-08 Therapeutic Potential of Emodin for Gastrointestinal Cancers McDonald, Sierra J. VanderVeen, Brandon N. Velazquez, Kandy T. Enos, Reilly T. Fairman, Ciaran M. Cardaci, Thomas D. Fan, Daping Murphy, E. Angela Integr Cancer Ther Review Article Gastrointestinal (GI) cancers cause one-third of all cancer-related deaths worldwide. Natural compounds are emerging as alternative or adjuvant cancer therapies given their distinct advantage of manipulating multiple pathways to both suppress tumor growth and alleviate cancer comorbidities; however, concerns regarding efficacy, bioavailability, and safety are barriers to their development for clinical use. Emodin (1,3,8-trihydroxy-6-methylanthraquinone), a Chinese herb-derived anthraquinone, has been shown to exert anti-tumor effects in colon, liver, and pancreatic cancers. While the mechanisms underlying emodin’s tumoricidal effects continue to be unearthed, recent evidence highlights a role for mitochondrial mediated apoptosis, modulated stress and inflammatory signaling pathways, and blunted angiogenesis. The goals of this review are to (1) highlight emodin’s anti-cancer properties within GI cancers, (2) discuss the known anti-cancer mechanisms of action of emodin, (3) address emodin’s potential as a treatment complementary to standard chemotherapeutics, (4) assess the efficacy and bioavailability of emodin derivatives as they relate to cancer, and (5) evaluate the safety of emodin. SAGE Publications 2022-01-05 /pmc/articles/PMC8738880/ /pubmed/34984952 http://dx.doi.org/10.1177/15347354211067469 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 pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Article McDonald, Sierra J. VanderVeen, Brandon N. Velazquez, Kandy T. Enos, Reilly T. Fairman, Ciaran M. Cardaci, Thomas D. Fan, Daping Murphy, E. Angela Therapeutic Potential of Emodin for Gastrointestinal Cancers |
title | Therapeutic Potential of Emodin for Gastrointestinal Cancers |
title_full | Therapeutic Potential of Emodin for Gastrointestinal Cancers |
title_fullStr | Therapeutic Potential of Emodin for Gastrointestinal Cancers |
title_full_unstemmed | Therapeutic Potential of Emodin for Gastrointestinal Cancers |
title_short | Therapeutic Potential of Emodin for Gastrointestinal Cancers |
title_sort | therapeutic potential of emodin for gastrointestinal cancers |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8738880/ https://www.ncbi.nlm.nih.gov/pubmed/34984952 http://dx.doi.org/10.1177/15347354211067469 |
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