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The oncogenic role of circPVT1 in head and neck squamous cell carcinoma is mediated through the mutant p53/YAP/TEAD transcription-competent complex

Authors :
Sabrina Strano
Maria Ferraiuolo
Giovanni Blandino
Lorena Verduci
Andrea Sacconi
Jlenia Vitale
Giuseppe Macino
Nikolaus Rajewsky
Teresa Colombo
Federica Ganci
Paola Paci
Source :
Genome Biology, Genome biology, 18 (2017). doi:10.1186/s13059-017-1368-y, info:cnr-pdr/source/autori:Verduci L.; Ferraiuolo M.; Sacconi A.; Ganci F.; Vitale J.; Colombo T.; Paci P.; Strano S.; Macino G.; Rajewsky N.; Blandino G./titolo:The oncogenic role of circPVT1 in head and neck squamous cell carcinoma is mediated through the mutant p53%2FYAP%2FTEAD transcription-competent complex/doi:10.1186%2Fs13059-017-1368-y/rivista:Genome biology (Print)/anno:2017/pagina_da:/pagina_a:/intervallo_pagine:/volume:18, Genome Biology, Vol 18, Iss 1, Pp 1-24 (2017)
Publication Year :
2017
Publisher :
Springer Science and Business Media LLC, 2017.

Abstract

Background Circular RNAs are a class of endogenous RNAs with various functions in eukaryotic cells. Worthy of note, circular RNAs play a critical role in cancer. Currently, nothing is known about their role in head and neck squamous cell carcinoma (HNSCC). The identification of circular RNAs in HNSCC might become useful for diagnostic and therapeutic strategies in HNSCC. Results Using samples from 115 HNSCC patients, we find that circPVT1 is over-expressed in tumors compared to matched non-tumoral tissues, with particular enrichment in patients with TP53 mutations. circPVT1 up- and down-regulation determine, respectively, an increase and a reduction of the malignant phenotype in HNSCC cell lines. We show that circPVT1 expression is transcriptionally enhanced by the mut-p53/YAP/TEAD complex. circPVT1 acts as an oncogene modulating the expression of miR-497-5p and genes involved in the control of cell proliferation. Conclusions This study shows the oncogenic role of circPVT1 in HNSCC, extending current knowledge about the role of circular RNAs in cancer. Electronic supplementary material The online version of this article (doi:10.1186/s13059-017-1368-y) contains supplementary material, which is available to authorized users.

Details

ISSN :
1474760X
Volume :
18
Database :
OpenAIRE
Journal :
Genome Biology
Accession number :
edsair.doi.dedup.....d344f022e5d98d1a7f192c8f3d1b9387
Full Text :
https://doi.org/10.1186/s13059-017-1368-y