Identification of differentially expressed genes in small and non-small cell lung cancer based on meta-analysis of

Nitesh Shriwash1, Prithvi Singh2, Shweta Arora3

  • 1Department of Computer Science, Faculty of Natural Science, Jamia Millia Islamia, New Delhi, 110025, India.

Heliyon
|July 25, 2019
PubMed

Insights

This study analyzed gene expression in Non-Small-Cell Lung Cancer (NSCLC) and Small-Cell Lung Cancer (SCLC) to find key differences. Researchers identified potential therapeutic targets for lung cancer treatment.

Area of Science:

  • Oncology
  • Genomics
  • Bioinformatics

Background:

  • Lung cancer has a low survival rate globally, with early detection and chemoresistance being major challenges.
  • Lung cancer is classified into Non-Small-Cell Lung Cancer (NSCLC, 85%) and Small-Cell Lung Cancer (SCLC, 15%).
  • Understanding gene expression differences is crucial for developing effective lung cancer therapies.

Purpose of the Study:

  • To identify Differentially Expressed Genes (DEGs) in NSCLC and SCLC subtypes.
  • To compare gene expression profiles between cancer subtypes and normal lung tissue.
  • To uncover potential therapeutic targets through overlapping gene analysis.

Main Methods:

  • Utilized meta-analysis on two public datasets from the Omnibus database.
  • Analyzed gene expression in 50 NSCLC, 31 SCLC, and 48 normal lung tissue samples.
  • Applied Benjamini-Hochberg method for p-value adjustment and constructed a Protein-Protein Interaction (PPI) network.

Main Results:

  • Identified 440 overexpressed and 489 underexpressed genes in NSCLC.
  • Identified 489 overexpressed and 525 underexpressed genes in SCLC.
  • Discovered overlapping DEGs and constructed a PPI network highlighting TRIM29, ANK3, CSTA, FGG, and AGR2 as key candidates.

Conclusions:

  • The identified overlapping genes, particularly TRIM29, ANK3, CSTA, FGG, and AGR2, represent potential therapeutic targets.
  • Gene expression analysis provides insights into NSCLC and SCLC heterogeneity.
  • Further research into these candidate genes could lead to novel lung cancer treatments.

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