We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
Investigating the role of prognostic mitophagy-related genes in non-small cell cancer pathogenesis via multiomics and network-based approach.
- Authors
Singh, Prithvi; Tabassum, Gulnaz; Masood, Mohammad; Anwar, Saleha; Syed, Mansoor Ali; Dev, Kapil; Hassan, Md. Imtaiyaz; Haque, Mohammad Mahfuzul; Dohare, Ravins; Singh, Indrakant Kumar
- Abstract
As one of the most prevalent malignancies, lung cancer displays considerable biological variability in both molecular and clinical characteristics. Lung cancer is broadly categorized into small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC) with the latter being most prevalent. The primary histological subtypes of NSCLC are lung adenocarcinoma (LUAD) and lung squamous cell carcinoma (LUSC). In the present work, we primarily extracted mRNA count data from a publicly accessible database followed by differentially expressed genes (DEGs) and differentially expressed mitophagy-related genes (DEMRGs) identification in case of both LUAD and LUSC cohorts. Next, we identified important DEMRGs via clustering approach followed by enrichment, survival, and mutational analyses. Lastly, the finalized prognostic biomarker was validated using wet-lab experimentations. Primarily, we obtained 986 and 1714 DEGs across LUAD and LUSC cohorts. Only 7 DEMRGs from both cohorts had significant membership values as indicated by the clustering analysis. Most significant pathway, Gene Ontology (GO)-biological process (BP), GO-molecular function (MF), GO-cellular compartment (CC) terms were macroautophagy, GTP metabolic process, magnesium ion binding, mitochondrial outer membrane. Among all, only TDRKH reported significant overall survival (OS) and 14% amplification across LUAD patients. Lastly, we validated TDRKH via immunohistochemistry (IHC) and semi-quantitative polymerase chain reaction (PCR). In conclusion, our findings advocate for the exploration of TDRKH and their genetic alterations in precision oncology therapeutic approaches for LUAD, emphasizing the potential for target-driven therapy and early diagnostics.
- Subjects
SMALL cell lung cancer; NON-small-cell lung carcinoma; SQUAMOUS cell carcinoma; GENE expression; LUNG cancer
- Publication
3 Biotech, 2024, Vol 14, Issue 11, p1
- ISSN
2190-572X
- Publication type
Academic Journal
- DOI
10.1007/s13205-024-04127-y