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Molecular mechanisms of garlic-derived allyl sulfides in the inhibition of skin cancer progression

Skin cancer is a serious concern whose incidence is increasing at an alarming rate. Allyl sulfides—i.e., sulfur metabolites in garlic oil—have been demonstrated to have anticancer activity against several cancer types, although the mechanisms underlying these effects remain enigmatic. Our previous s...

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Autores principales: Wang, Hsiao-Chi, Pao, Jung, Lin, Shuw-Yuan, Sheen, Lee-Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Inc 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499657/
https://www.ncbi.nlm.nih.gov/pubmed/23050963
http://dx.doi.org/10.1111/j.1749-6632.2012.06743.x
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author Wang, Hsiao-Chi
Pao, Jung
Lin, Shuw-Yuan
Sheen, Lee-Yan
author_facet Wang, Hsiao-Chi
Pao, Jung
Lin, Shuw-Yuan
Sheen, Lee-Yan
author_sort Wang, Hsiao-Chi
collection PubMed
description Skin cancer is a serious concern whose incidence is increasing at an alarming rate. Allyl sulfides—i.e., sulfur metabolites in garlic oil—have been demonstrated to have anticancer activity against several cancer types, although the mechanisms underlying these effects remain enigmatic. Our previous study showed that diallyl trisulfide (DATS) is more potent than mono- and disulfides against skin cancer. DATS inhibits cell growth of human melanoma A375 cells and basal cell carcinoma (BCC) cells by increasing the levels of intracellular reactive oxygen species (ROS) and DNA damage and by inducing G2/M arrest, endoplasmic reticulum (ER) stress, and mitochondria-mediated apoptosis, including the caspase-dependent and -independent pathways. This short review focuses on the molecular mechanisms of garlic-derived allyl sulfides on skin cancer prevention.
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spelling pubmed-34996572012-11-20 Molecular mechanisms of garlic-derived allyl sulfides in the inhibition of skin cancer progression Wang, Hsiao-Chi Pao, Jung Lin, Shuw-Yuan Sheen, Lee-Yan Ann N Y Acad Sci Original Articles Skin cancer is a serious concern whose incidence is increasing at an alarming rate. Allyl sulfides—i.e., sulfur metabolites in garlic oil—have been demonstrated to have anticancer activity against several cancer types, although the mechanisms underlying these effects remain enigmatic. Our previous study showed that diallyl trisulfide (DATS) is more potent than mono- and disulfides against skin cancer. DATS inhibits cell growth of human melanoma A375 cells and basal cell carcinoma (BCC) cells by increasing the levels of intracellular reactive oxygen species (ROS) and DNA damage and by inducing G2/M arrest, endoplasmic reticulum (ER) stress, and mitochondria-mediated apoptosis, including the caspase-dependent and -independent pathways. This short review focuses on the molecular mechanisms of garlic-derived allyl sulfides on skin cancer prevention. Blackwell Publishing Inc 2012-10 2012-10-10 /pmc/articles/PMC3499657/ /pubmed/23050963 http://dx.doi.org/10.1111/j.1749-6632.2012.06743.x Text en © 2012 New York Academy of Sciences. http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Articles
Wang, Hsiao-Chi
Pao, Jung
Lin, Shuw-Yuan
Sheen, Lee-Yan
Molecular mechanisms of garlic-derived allyl sulfides in the inhibition of skin cancer progression
title Molecular mechanisms of garlic-derived allyl sulfides in the inhibition of skin cancer progression
title_full Molecular mechanisms of garlic-derived allyl sulfides in the inhibition of skin cancer progression
title_fullStr Molecular mechanisms of garlic-derived allyl sulfides in the inhibition of skin cancer progression
title_full_unstemmed Molecular mechanisms of garlic-derived allyl sulfides in the inhibition of skin cancer progression
title_short Molecular mechanisms of garlic-derived allyl sulfides in the inhibition of skin cancer progression
title_sort molecular mechanisms of garlic-derived allyl sulfides in the inhibition of skin cancer progression
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499657/
https://www.ncbi.nlm.nih.gov/pubmed/23050963
http://dx.doi.org/10.1111/j.1749-6632.2012.06743.x
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