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Determination of Chemical Irritation Potential Using a Defined Gene Signature Set on Tissue-Engineered Human Skin Equivalents.
Harding, Amy L; Murdoch, Craig; Danby, Simon; Hasan, Md Zobaer; Nakanishi, Hirofumi; Furuno, Tetsuo; Hadad, Sirwan; Turner, Robert; Colley, Helen E.
Afiliação
  • Harding AL; The School of Clinical Dentistry, The University of Sheffield, Sheffield, United Kingdom.
  • Murdoch C; The School of Clinical Dentistry, The University of Sheffield, Sheffield, United Kingdom.
  • Danby S; Sheffield Dermatology Research, Department of Infection, Immunity and Cardiovascular Disease, The Medical School, The University of Sheffield, Sheffield, United Kingdom.
  • Hasan MZ; Safety Design Centre, Rohto Pharmaceutical Co, Ltd, Kyoto, Japan.
  • Nakanishi H; Safety Design Centre, Rohto Pharmaceutical Co, Ltd, Kyoto, Japan.
  • Furuno T; Safety Design Centre, Rohto Pharmaceutical Co, Ltd, Kyoto, Japan.
  • Hadad S; Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, United Kingdom.
  • Turner R; Research Software Engineering Sheffield, The University of Sheffield, Sheffield, United Kingdom.
  • Colley HE; The School of Clinical Dentistry, The University of Sheffield, Sheffield, United Kingdom.
JID Innov ; 1(2): 100011, 2021 Jun.
Article em En | MEDLINE | ID: mdl-34909715
ABSTRACT
There are no physical or visual manifestations that define skin sensitivity or irritation; a subjective diagnosis is made on the basis of the evaluation of clinical presentations, including burning, prickling, erythema, and itching. Adverse skin reaction in response to topically applied products is common and can limit the use of dermatological or cosmetic products. The purpose of this study was to evaluate the use of human skin equivalents based on immortalized skin keratinocytes and evaluate the potential of a 22-gene panel in combination with multivariate analysis to discriminate between chemicals known to act as irritants and those that do not. Test compounds were applied topically to full-thickness human skin equivalent or human ex vivo skin and gene signatures determined for known irritants and nonirritants. Principle component analysis showed the discriminatory potential of the 22-gene panel. Linear discrimination analysis, performed to further refine the gene set for a more high-throughput analysis, identified a putative seven-gene panel (IL-6, PTGS2, ATF3, TRPV3, MAP3K8, HMGB2, and matrix metalloproteinase gene MMP-3) that could distinguish potential irritants from nonirritants. These data offer promise as an in vitro prediction tool, although analysis of a large chemical test set is required to further evaluate the system.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article