PHF19 mediated regulation of proliferation and invasiveness in prostate cancer cells

Payal Jain, Cecilia Ballare, Enrique Blanco, Pedro Vizan, Luciano Di Croce

Producción científica: Artículo en revista indizadaArtículorevisión exhaustiva

19 Citas (Scopus)

Resumen

The Polycomb-like protein PHF19/PCL3 associates with PRC2 and mediates its recruitment to chromatin in embryonic stem cells. PHF19 is also overexpressed in many cancers. However, neither PHF19 targets nor misregulated pathways involving PHF19 are known. Here, we investigate the role of PHF19 in prostate cancer cells. We find that PHF19 interacts with PRC2 and binds to PRC2 targets on chromatin. PHF19 target genes are involved in proliferation, differentiation, angiogenesis, and extracellular matrix organization. Depletion of PHF19 triggers an increase in MTF2/PCL2 chromatin recruitment, with a genome-wide gain in PRC2 occupancy and H3K27me3 deposition. Transcriptome analysis shows that PHF19 loss promotes deregulation of key genes involved in growth, metastasis, invasion, and of factors that stimulate blood vessels formation. Consistent with this, PHF19 silencing reduces cell proliferation, while promotes invasive growth and angiogenesis. Our findings reveal a role for PHF19 in controlling the balance between cell proliferation and invasiveness in prostate cancer.

Idioma originalInglés
Número de artículoe51373
PublicacióneLife
Volumen9
DOI
EstadoPublicada - mar 2020
Publicado de forma externa

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