Cargando…

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,...

Descripción completa

Detalles Bibliográficos
Autores principales: McDonald, Sierra J., VanderVeen, Brandon N., Velazquez, Kandy T., Enos, Reilly T., Fairman, Ciaran M., Cardaci, Thomas D., Fan, Daping, Murphy, E. Angela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
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
_version_ 1784628998429474816
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
work_keys_str_mv AT mcdonaldsierraj therapeuticpotentialofemodinforgastrointestinalcancers
AT vanderveenbrandonn therapeuticpotentialofemodinforgastrointestinalcancers
AT velazquezkandyt therapeuticpotentialofemodinforgastrointestinalcancers
AT enosreillyt therapeuticpotentialofemodinforgastrointestinalcancers
AT fairmanciaranm therapeuticpotentialofemodinforgastrointestinalcancers
AT cardacithomasd therapeuticpotentialofemodinforgastrointestinalcancers
AT fandaping therapeuticpotentialofemodinforgastrointestinalcancers
AT murphyeangela therapeuticpotentialofemodinforgastrointestinalcancers