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SAGE Publications, Slas Discovery, 8(11), p. 977-984, 2006

DOI: 10.1177/1087057106292556

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Identification of Novel Keratinocyte Differentiation Modulating Compounds by High-Throughput Screening

Journal article published in 2006 by Masaru Honma, Mark Stubbs, Ian Collins, Paul Workman, Wynne Aherne, Fiona M. Watt ORCID
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

The authors have designed high-throughput screens to identify compounds that promote or inhibit terminal differentiation of primary human epidermal keratinocytes. Eleven known inhibitors of signaling pathways and approximately 4000 compounds of diverse structure were screened using an In-Cell Western system based on immunofluorescent staining of the terminal differentiation marker, involucrin. Staurosporine, a nonspecific protein kinase C inhibitor, and H89, a protein kinase A inhibitor, promoted expression of involucrin. Conversely, U0126, a MEK inhibitor, and SAHA or SBHA, 2 histone deacetylase inhibitors, reduced the expression of involucrin during calcium-induced stratification. In addition, the authors found 1 novel compound that induced keratinocyte differentiation and 2 novel compounds that were inhibitory to calcium-induced differentiation. The differentiation-inducing compound also inhibited growth of a human squamous cell carcinoma line by stimulating both differentiation and apoptosis. Because the compound affected the tumor cells at a lower concentration than primary keratinocytes, it may have potential as an antitumor therapy.