Investigation the Role of Autophagy in Non-Small Cell Lung Cancer.

Asian Pac J Cancer Prev

Department of Genetics and Biotechnology, School of Biological Science, Varamin Pishva Branch, Islamic Azad University, Varamin, Iran.

Published: March 2021

AI Article Synopsis

  • Recent studies highlight the role of autophagy and microRNAs in lung cancer, particularly how specific microRNAs like miR-30d and miR-204-5p can suppress autophagy-related genes.
  • The research analyzed the expression levels of these microRNAs and their target genes in non-small cell lung cancer (NSCLC) patients, finding significant downregulation of miR-30d and miR-204-5p in tumor samples compared to normal tissues.
  • Results suggest that these microRNAs act as tumor suppressors while their target genes may function as oncogenes in NSCLC, indicating a need for further studies on their potential in lung cancer treatment.

Article Abstract

Objective: Recent studies have shown the role of autophagy in different types of cancer including lung cancer. MicroRNAs are considered as key factors in regulation of autophagy related genes. miR-30d, miR-204-5p and miR-20a are regulatory markers which can suppress the expression of beclin1, LC3, bcl2 and ULK1 as their target genes and they lead to decrement of autophagy in human cancer cells. Moreover, epigenetic modifications DNA methylation has been indicated in regulation of autophagy in different stages of cancer.

Methods: In this study, the expression levels of miR-30d, miR-204-5p and miR-20a as well as their target genes were analyzed in 30 non-small cell lung cancers (NSCLCs) patients sample and adjacent normal tissues by real-time qPCR. In addition, DNA methylation of beclin1, LC3, bcl2 and ULK1 genes were assessed by MS-HRM method.

Results: MiR-30d (p value= 0.01) and miR-204-5p (P=0.048) significantly down-regulated in tumor samples compared to normal adjacent tissues, while there was no significant change in expression level of miR-20a. On the other hand, target genes expression level was significantly increased in NSCLC tissues, however methylation pattern of the target gene promoters, did not show any significant alteration.

Conclusion: These results indicate roles for miR-30d, miR-204-5p as tumor suppressor genes as well as target genes as oncogenes in NSCLC patients. Although these factors may have a significant role in NSCLC progression, further studies are necessary to investigate the implications of these findings for treatment of lung cancer. 
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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286697PMC
http://dx.doi.org/10.31557/APJCP.2021.22.3.947DOI Listing

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