학술논문

Comprehensive functional profiling of long non-coding RNAs through a novel pan-cancer integration approach and modular analysis of their protein-coding gene association networks
Document Type
Report
Source
BMC Genomics. June 3, 2019, Vol. 20 Issue 1
Subject
Usage
Research
Extracellular matrix -- Research
Transforming growth factors -- Research
DNA sequencing -- Usage
Gene expression -- Research
Stem cells
Genetic research
Biochemistry
Genes
Criminal investigation
Cancer
Cancer genetics
Tumors
Contract manufacturing
Novels
Language
English
ISSN
1471-2164
Abstract
Author(s): Kevin Walters[sup.1] , Radmir Sarsenov[sup.2] , Wen Siong Too[sup.2] , Roseanna K. Hare[sup.3] , Ian C. Paterson[sup.4] , Daniel W. Lambert[sup.5] , Stephen Brown[sup.2] and James R. Bradford[sup.6,7] Background [...]
Background Long non-coding RNAs (lncRNAs) are emerging as crucial regulators of cellular processes in diseases such as cancer, although the functions of most remain poorly understood. To address this, here we apply a novel strategy to integrate gene expression profiles across 32 cancer types, and cluster human lncRNAs based on their pan-cancer protein-coding gene associations. By doing so, we derive 16 lncRNA modules whose unique properties allow simultaneous inference of function, disease specificity and regulation for over 800 lncRNAs. Results Remarkably, modules could be grouped into just four functional themes: transcription regulation, immunological, extracellular, and neurological, with module generation frequently driven by lncRNA tissue specificity. Notably, three modules associated with the extracellular matrix represented potential networks of lncRNAs regulating key events in tumour progression. These included a tumour-specific signature of 33 lncRNAs that may play a role in inducing epithelial-mesenchymal transition through modulation of TGF[beta] signalling, and two stromal-specific modules comprising 26 lncRNAs linked to a tumour suppressive microenvironment and 12 lncRNAs related to cancer-associated fibroblasts. One member of the 12-lncRNA signature was experimentally supported by siRNA knockdown, which resulted in attenuated differentiation of quiescent fibroblasts to a cancer-associated phenotype. Conclusions Overall, the study provides a unique pan-cancer perspective on the lncRNA functional landscape, acting as a global source of novel hypotheses on lncRNA contribution to tumour progression. Keywords: lncRNA, Functional profiling, Genes networks, Cancer, Epithelial-mesenchymal transition, Extracellular matrix, Tumour microenvironment