| Home > Publications database > The MYB-related transcription factor MYPOP acts as a selective regulator of cancer cell growth. |
| Journal Article | DKFZ-2026-01187 |
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2026
Springer Nature
London
Abstract: The MYB-related transcription factor and partner of profilin (MYPOP or p42POP) is a ubiquitously expressed yet understudied protein recently identified as a restriction factor of oncogenic human papillomaviruses (HPV) and proposed tumor suppressor. Here we show that in HPV-transformed cervical cancer cells, MYPOP induces alterations in cell morphology, silences viral and cellular oncogenes including E6 and MYC, and stimulates the release of the cancer-killing cytokine interleukin-24. Transcriptomic and live-cell analyses reveal a rapid G1/S-phase arrest followed by loss of viable cervical cancer cells and induction of apoptosis. Moreover, MYPOP expression is broadly diminished across multiple human cancers, and its re-expression by both DNA- and mRNA-gene transfer markedly suppresses tumor cell proliferation while sparing normal epidermal keratinocytes. Similarly, murine Mypop inhibits mouse cancer cell growth. Collectively, our findings identify MYPOP as a selective suppressor of tumor cell proliferation across species in vitro and point to its potential relevance for future therapeutic investigation.
Keyword(s): Humans (MeSH) ; Cell Proliferation (MeSH) ; Animals (MeSH) ; Mice (MeSH) ; Female (MeSH) ; Cell Line, Tumor (MeSH) ; Gene Expression Regulation, Neoplastic (MeSH) ; Uterine Cervical Neoplasms: metabolism (MeSH) ; Uterine Cervical Neoplasms: genetics (MeSH) ; Uterine Cervical Neoplasms: pathology (MeSH) ; Uterine Cervical Neoplasms: virology (MeSH) ; Transcription Factors: metabolism (MeSH) ; Transcription Factors: genetics (MeSH) ; Apoptosis (MeSH) ; Transcription Factors
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