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                <identifier>oai:data.mendeley.com/vzr4snpdb4.1</identifier>
                <datestamp>2025-08-11T15:43:52Z</datestamp>
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    <dc:creator>Kemp, Michael</dc:creator>
    <dc:title>SR8278 inhibits cell proliferation independent of REV-ERB</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>SR8278 has been reported to be an antagonist of the REV-ERB proteins. In this work, we treated HaCaT cells with SR8278 and used RNA-seq to identify genes that were significantly altered by treatment. Genes involved in cell proliferation and the G1/S phase transition were a major group of altered genes. We confirmed the RNA-seq results with RT-qPCR and western blotting. Furthermore, SR8278 treatment slowed the growth of HaCaT and other cell lines. Using CRISPR/Cas9 genome editing, we generated REV-ERB alpha, REV-ERB beta, and REV-ERB alpha/beta double-knockout HaCaT cells and found that SR8278&apos;s effects were independent of REV-ERB. The data include those generated by RT-qPCR, western blotting, and cell viability assays.</dc:description>
    <dc:subject>Pharmacology</dc:subject>
    <dc:subject>Nuclear Receptor</dc:subject>
    <dc:subject>Transcription Factor</dc:subject>
    <dc:subject>Small Molecule</dc:subject>
    <dc:subject>Keratinocyte</dc:subject>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/vzr4snpdb4.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/vzr4snpdb4.1</dc:identifier>
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    <dc:date>2025-08-11T15:43:52Z</dc:date>
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