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Cytotoxicity patterns of arsenic trioxide exposure on HaCaT keratinocytes
Author(s) -
Raphael D. Isokpehi,
Udensi,
Cohly,
Graham-Evans,
C. Paul Rogers
Publication year - 2011
Publication title -
clinical cosmetic and investigational dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.73
H-Index - 35
ISSN - 1178-7015
DOI - 10.2147/ccid.s24677
Subject(s) - hacat , arsenic trioxide , keratinocyte , arsenic , epidermis (zoology) , chemistry , viability assay , psoriasis , immunology , pharmacology , andrology , medicine , physiology , in vitro , biochemistry , anatomy , organic chemistry
Arsenic is a ubiquitous environmental toxicant, and abnormalities of the skin are the most common outcomes of long-term, low-dose, chronic arsenic exposure. If the balance between keratinocyte proliferation, differentiation, and death is perturbed, pathologic changes of the epidermis may result, including psoriasis, atopic dermatitis, and certain forms of ichthyosis. Therefore, research investigations using in vitro human epidermal cells could help elucidate cellular and molecular processes in keratinocytes affected by arsenic. Data from such investigations could also provide the basis for developing cosmetic intervention for skin diseases caused by arsenic.

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