Back to Search Start Over

Long non-coding RNA signatures in non-small cell lung cancer and their clinicopathological significance.

Authors :
Kahraman, Demet Tasdemir
Bozgeyik, Esra
Guven, Hulya
Guler, Semih
Saglam, Ebru
Cangi, Sibel
Oztuzcu, Serdar
Bozgeyik, Ibrahim
Isik, Ahmet Ferudun
Source :
Pathology - Research & Practice. Jan2024, Vol. 253, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

Lung cancer is the most common type of cancer in our country and worldwide, and it is a leading cause of cancer-related deaths. According to the latest global cancer statistics, lung cancer was identified as the second most common type of cancer, and the leading cause of cancer-related deaths. Long non-coding RNAs (lncRNAs) are a highly heterogeneous class of RNA molecules sharing many characteristics with mRNAs, except for the protein-coding potential. Accumulating mass of evidence suggest that lncRNAs play key regulatory roles during the multistep formation of human cancers including lung cancer. In previous studies, it has been shown that many lncRNA molecules play significant roles in the formation and progression of lung cancer. However, there are still numerous lncRNA molecules in lung cancer whose roles remain unknown. Accordingly, here we sought to ascertain the diagnostic and prognostic value of lncRNAs by analyzing the expression profiles of THRIL, NEAT1, and LOC105376095 in lung cancer. Remarkably, NEAT1 and LOC105376095 but not THRIL were identified to be differentially expressed in tissues of lung tumors. More importantly, LOC105376095, a yet uncharacterized lncRNA molecule, was significantly associated with the disease severity. Collectively, NEAT1 and LOC105376095 hold promise as potential diagnostic and prognostic biomarkers for lung cancer, presenting opportunities for targeted therapeutic interventions in the future. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03440338
Volume :
253
Database :
Academic Search Index
Journal :
Pathology - Research & Practice
Publication Type :
Academic Journal
Accession number :
174873221
Full Text :
https://doi.org/10.1016/j.prp.2023.154946