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Authors = Clarisse S. Muenyi

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Open AccessReview Arsenic Disruption of DNA Damage Responses—Potential Role in Carcinogenesis and Chemotherapy
Biomolecules 2015, 5(4), 2184-2193; doi:10.3390/biom5042184
Received: 14 August 2015 / Revised: 6 September 2015 / Accepted: 9 September 2015 / Published: 24 September 2015
Cited by 3 | Viewed by 1324 | PDF Full-text (426 KB) | HTML Full-text | XML Full-text
Abstract
Arsenic is a Class I human carcinogen and is widespread in the environment. Chronic arsenic exposure causes cancer in skin, lung and bladder, as well as in other organs. Paradoxically, arsenic also is a potent chemotherapeutic against acute promyelocytic leukemia and can potentiate
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Arsenic is a Class I human carcinogen and is widespread in the environment. Chronic arsenic exposure causes cancer in skin, lung and bladder, as well as in other organs. Paradoxically, arsenic also is a potent chemotherapeutic against acute promyelocytic leukemia and can potentiate the cytotoxic effects of DNA damaging chemotherapeutics, such as cisplatin, in vitro. Arsenic has long been implicated in DNA repair inhibition, cell cycle disruption, and ubiquitination dysregulation, all negatively impacting the DNA damage response and potentially contributing to both the carcinogenic and chemotherapeutic potential of arsenic. Recent studies have provided mechanistic insights into how arsenic interferes with these processes including disruption of zinc fingers and suppression of gene expression. This review discusses these effects of arsenic with a view toward understanding the impact on the DNA damage response. Full article
(This article belongs to the Special Issue DNA Damage Response)
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