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MiR-497-5p inhibits cell proliferation and metastasis in hepatocellular carcinoma by targeting insulin-like growth factor 1

  • Guo shu Xu
  • , Zi wei Li
  • , Zhi Ping Huang
  • , F. Charles Brunicardi
  • , Fu Jia
  • , Chao Song
  • , Hai jian Zou
  • , Rui fen Sun

Research output: Contribution to journalArticlepeer-review

30 Scopus citations

Abstract

Background: MicroRNAs (miRNAs) play an important regulatory role in carcinogenesis and cancer progression. Aberrant expression of miR-497-5p has been reported in various human malignancies. However, the role of miR-497-5p in hepatocellular carcinoma (HCC) remains unclear. Results: In this study, we found that miR-497-5p was downregulated in HCC tissues. The low level of miR-497-5p in HCC tumors was correlated with aggressive clinicopathological characteristics and predicted poor prognosis in HCC patients. The overexpression of miR-497-5p significantly inhibited HCC cell proliferation, colony formation, and metastasis in vitro and vivo. Bioinformatics analysis further identified insulin-like growth factor 1 (IGF1) as a novel target of miR-497-5p in HCC cells. Conclusion: Our study suggested that miR-497-5p regulates HCC cell survival, partially through downregulation of IGF1. Therefore, the miR-497-5p/IGF1 axis might serve as a novel therapeutic target in patients with HCC.

Original languageEnglish
Article numbere00860
JournalMolecular Genetics and Genomic Medicine
Volume7
Issue number10
DOIs
StatePublished - Oct 1 2019

Keywords

  • IGF1
  • biomarker
  • hepatocellular carcinoma
  • miR-497-5p
  • proliferation

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