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

Journal
Annals of the New York Academy of Sciences
Journal Volume
1271
Journal Issue
1
Pages
44-52
Date Issued
2012
Author(s)
Wang H.-C.
Pao J.
Lin S.-Y.
Sheen L.-Y.  
DOI
10.1111/j.1749-6632.2012.06743.x
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84867368272&doi=10.1111%2fj.1749-6632.2012.06743.x&partnerID=40&md5=4ec9eff31f5f3fdd624ba1b2c1d67d0a
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/413567
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84867368272&doi=10.1111%2fj.1749-6632.2012.06743.x&partnerID=40&md5=4ec9eff31f5f3fdd624ba1b2c1d67d0a
Abstract
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. ? 2012 New York Academy of Sciences.
Subjects
Allyl sulfides
Apoptosis
ER stress
Garlic
ROS
Skin cancer
SDGs

[SDGs]SDG3

Other Subjects
ajoene; allyl sulfide; apoptotic protease activating factor 1; benzo[a]pyrene; caspase 3; caspase 4; caspase 9; croton oil; dimethylbenz[a]anthracene; garlic oil; inhibitor of apoptosis protein; protein Bax; protein bcl 2; protein kinase B; protein p53; reactive oxygen metabolite; survivin; antineoplastic activity; apoptosis; article; cancer growth; cancer inhibition; cell adhesion; cell differentiation; cell migration; cell proliferation; cell survival; chromosome segregation; disulfide bond; DNA content; DNA damage; DNA repair; endoplasmic reticulum stress; G2 phase cell cycle checkpoint; in vitro study; melanoma metastasis; mitochondrial membrane potential; nonhuman; protein phosphorylation; skin cancer; skin carcinogenesis
Type
journal article
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j.1749-6632.2012.06743.x.pdf

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(MD5):d5aa3d1a3630c95b0dd44081682d344a

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