Determination of Chemical Irritation Potential Using a Defined Gene Signature Set on Tissue-Engineered Human Skin Equivalents.

CA, cinnamaldehyde CAP, capsaicin CON, control Co-DEA, cocamide diethanolamine Co-MEA, cocamide monoethanolamine H2O, water HDF, human dermal fibroblast HSE, human skin equivalent KC, keratinocyte LA, lactic acid LDA, linear discrimination analysis LDH, lactate dehydrogenase MMP, matrix metalloproteinase MP, methylparaben N-LA, neutralized lactic acid PCA, principal component analysis TEER, transepithelial electrical resistance

Journal

JID innovations : skin science from molecules to population health
ISSN: 2667-0267
Titre abrégé: JID Innov
Pays: Netherlands
ID NLM: 101776173

Informations de publication

Date de publication:
Jun 2021
Historique:
received: 11 01 2021
revised: 24 02 2021
accepted: 25 02 2021
entrez: 15 12 2021
pubmed: 16 12 2021
medline: 16 12 2021
Statut: epublish

Résumé

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 (

Identifiants

pubmed: 34909715
doi: 10.1016/j.xjidi.2021.100011
pii: S2667-0267(21)00011-4
pmc: PMC8659397
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100011

Informations de copyright

© 2021 The Authors.

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Auteurs

Amy L Harding (AL)

The School of Clinical Dentistry, The University of Sheffield, Sheffield, United Kingdom.

Craig Murdoch (C)

The School of Clinical Dentistry, The University of Sheffield, Sheffield, United Kingdom.

Simon Danby (S)

Sheffield Dermatology Research, Department of Infection, Immunity and Cardiovascular Disease, The Medical School, The University of Sheffield, Sheffield, United Kingdom.

Md Zobaer Hasan (MZ)

Safety Design Centre, Rohto Pharmaceutical Co, Ltd, Kyoto, Japan.

Hirofumi Nakanishi (H)

Safety Design Centre, Rohto Pharmaceutical Co, Ltd, Kyoto, Japan.

Tetsuo Furuno (T)

Safety Design Centre, Rohto Pharmaceutical Co, Ltd, Kyoto, Japan.

Sirwan Hadad (S)

Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, United Kingdom.

Robert Turner (R)

Research Software Engineering Sheffield, The University of Sheffield, Sheffield, United Kingdom.

Helen E Colley (HE)

The School of Clinical Dentistry, The University of Sheffield, Sheffield, United Kingdom.

Classifications MeSH