AI Article Synopsis

  • Lung cancer is the leading cause of cancer deaths worldwide, divided into small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC), with the latter often diagnosed too late for effective treatment.
  • A study focused on identifying important microRNAs (miRNAs) involved in NSCLC carcinogenesis, revealing 12 differentially expressed miRNAs (DEMs) that could serve as potential biomarkers for better diagnosis and prognosis.
  • The research highlighted four key miRNAs and nine associated genes, suggesting their potential to improve prognosis and diagnosis of lung cancer, while also predicting relevant transcription factors for further studies.

Article Abstract

Lung cancer is the major cause of cancer-associated deaths across the world in both men and women. Lung cancer consists of two major clinicopathological categories, i.e., small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC). Lack of diagnosis of NSCLC at an early stage in addition to poor prognosis results in ineffective treatment, thus, biomarkers for appropriate diagnosis and exact prognosis of NSCLC need urgent attention. The proposed study aimed to reveal essential microRNAs (miRNAs) involved in the carcinogenesis of NSCLC that probably could act as potential biomarkers. The NSCLC-associated expression datasets revealed 12 differentially expressed miRNAs (DEMs). MiRNA-mRNA network identified key miRNAs and their associated genes, for which functional enrichment analysis was applied. Further, survival and validation analysis for key genes was performed and consequently transcription factors (TFs) were predicted. We obtained twelve miRNAs as common DEMs after assessment of all datasets. Further, four key miRNAs and nine key genes were extracted from significant modules based on the centrality approach. The key genes and miRNAs reported in our study might provide some information for potential biomarkers profitable to increased prognosis and diagnosis of lung cancer.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9317345PMC
http://dx.doi.org/10.3390/genes13071174DOI Listing

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