The lncRNA SLNCR1 Mediates Melanoma Invasion through a Conserved SRA1-like Region.

Cell Rep
Authors
Abstract

Long non-coding RNAs (lncRNAs) have been implicated in numerous physiological processes and diseases, most notably cancers. However, little is known about the mechanism of many functional lncRNAs. We identified an abundantly expressed lncRNA associated with decreased melanoma patient survival. Increased expression of this lncRNA, SLNCR1, mediates melanoma invasion through a highly conserved sequence similar to that of the lncRNA SRA1. Using a sensitive technique we term RATA (RNA-associated transcription factor array), we show that the brain-specific homeobox protein 3a (Brn3a) and the androgen receptor (AR) bind within and adjacent to SLNCR1's conserved region, respectively. SLNCR1, AR, and Brn3a are specifically required for transcriptional activation of matrix metalloproteinase 9 (MMP9) and increased melanoma invasion. Our observations directly link AR to melanoma invasion, possibly explaining why males experience more melanoma metastases and have an overall lower survival in comparison to females.

Year of Publication
2016
Journal
Cell Rep
Volume
15
Issue
9
Pages
2025-37
Date Published
2016 May 31
ISSN
2211-1247
URL
DOI
10.1016/j.celrep.2016.04.018
PubMed ID
27210747
PubMed Central ID
PMC4889529
Links
Grant list
R01 CA140986 / CA / NCI NIH HHS / United States
R01 CA185151 / CA / NCI NIH HHS / United States
T32 AI007386 / AI / NIAID NIH HHS / United States