| Literature DB >> 30117276 |
Janine Regneri1, Barbara Klotz1, Brigitta Wilde1, Verena A Kottler1, Michael Hausmann1, Susanne Kneitz1, Martina Regensburger1, Katja Maurus2, Ralph Götz3, Yuan Lu4, Ronald B Walter4, Amaury Herpin5, Manfred Schartl1,6,7.
Abstract
In humans, the CDKN2A locus encodes two transcripts, INK4A and ARF. Inactivation of either one by mutations or epigenetic changes is a frequent signature of malignant melanoma and one of the most relevant entry points for melanomagenesis. To analyze whether cdkn2ab, the fish ortholog of CDKN2A, has a similar function as its human counterpart, we studied its action in fish models for human melanoma. Overexpression of cdkn2ab in a Xiphophorus melanoma cell line led to decreased proliferation and induction of a senescence-like phenotype, indicating a melanoma-suppressive function analogous to mammals. Coexpression of Xiphophorus cdkn2ab in medaka transgenic for the mitfa:xmrk melanoma-inducing gene resulted in full suppression of melanoma development, whereas CRISPR/Cas9 knockout of cdkn2ab resulted in strongly enhanced tumor growth. In summary, this provides the first functional evidence that cdkn2ab acts as a potent tumor suppressor gene in fish melanoma models.Entities:
Keywords: zzm321990xmrkzzm321990; cell cycle regulation; nevi; p16/INK4A; senescence
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Year: 2018 PMID: 30117276 PMCID: PMC6377863 DOI: 10.1111/pcmr.12729
Source DB: PubMed Journal: Pigment Cell Melanoma Res ISSN: 1755-1471 Impact factor: 4.693