Oncogenic RAS Regulates Long Noncoding RNA Orilnc1 in Human Cancer

Document Type

Article

Publication Date

7-15-2017

Abstract

RAS and its downstream cascades transmit cellular signals, resulting in increased transcription of genes involved in cell growth and division. Protein-coding gene targets of RAS signaling have been characterized extensively, but long noncoding RNAs (lncRNA) regulated by these processes have not. Using a customdesigned lncRNA microarray, we identified the lncRNA Orilnc1 as a genetic target of RAS that is critical for RAS oncogenicity. Orilnc1 expression was regulated by RAS–RAF–MEK–ERK signaling via the transcription factor AP1. Orilnc1 was highly expressed in BRAF-mutant cancers, such as melanoma. Silencing of Orilnc1 blocked tumor cell proliferation and growth in vitro and in vivo. In addition, Orilnc1 blockade reduced expression of cyclin E1 and induced G1–S cell-cycle arrest in tumor cells. Taken together, our results identify Orilnc1 as a novel, nonprotein mediator of RAS/ RAF activation that may serve as a therapeutic target in RAS/RAF– driven cancers.

Identifier

85024133722 (Scopus)

Publication Title

Cancer Research

External Full Text Location

https://doi.org/10.1158/0008-5472.CAN-16-1768

e-ISSN

15387445

ISSN

00085472

PubMed ID

28473531

First Page

3745

Last Page

3757

Issue

14

Volume

77

Grant

P50CA174523

Fund Ref

National Cancer Institute

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