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Chinese Journal of Hepatic Surgery(Electronic Edition) ›› 2020, Vol. 09 ›› Issue (06): 602-608. doi: 10.3877/cma.j.issn.2095-3232.2020.06.022

Special Issue:

• Basic Research • Previous Articles     Next Articles

Expression of IGFBP in hepatocellular carcinoma based on bioinformatics study and its prognostic value

Bin Dai1, Zaixing Wang2(), Dandan Ma3, Weidong Jin3, Zhiyong Zhang3, Desheng Wang4,()   

  1. 1. Department of Hepatobiliary Surgery, Wuhan No.1 Hospital, Wuhan 430022, China
    2. Department of General Surgery, Taikang Tongji (Wuhan) Hospital, Wuhan 430000, China
    3. Department of General Surgery, General Hospital of Central Theater Command of Chinese People's Liberation Army, Wuhan 430070, China
    4. Department of Hepatobiliary, Pancreatic and Splenic Surgery, Xijing Hospital of Air Force Medical University, Xi'an 710032, China
  • Received:2020-08-03 Online:2020-12-10 Published:2020-12-10
  • Contact: Zaixing Wang, Desheng Wang

Abstract:

Objective

To explore the expression level and prognostic value of insulin-like growth factor binding protein (IGFBP) family members in hepatocellular carcinoma (HCC) by bioinformatics analysis.

Methods

The expression levels of IGFBP family members in HCC were analyzed by GEPIA online analysis. The relationship between IGFBP and clinical prognosis was assessed by Kaplan-Meier survival curve. The changes of IGFBP genes in HCC patients were observed by cBioPortal for Cancer Genomics. IGFBP-related gene network was constructed by GeneMANIA. Gene ontology (GO) enrichment analysis was performed by Metascape database.

Results

GEPIA online analysis showed that the relative expression of IGFBP3 mRNA in HCC was significantly lower than that in normal liver tissues (P<0.05). The expression of IGFBP3 was significantly correlated with the pathological stage of HCC (F=5.52, P<0.05). Kaplan-Meier survival analysis demonstrated that the expression levels of IGFBP3 and IGFBP4 mRNA were significantly associated with poor prognosis (HR=1.50, 0.43; P<0.05). cBioPortal analysis revealed that genetic changes of IGFBP in HCC including mutation, fusion, amplification, deep deletion and multiple changes, among which mutation, amplification and deep deletion were the most common changes. The genetic changes of IGFBPs were ranged from 0 to 1%. GeneMANIA analysis identified 20 genes were closely correlated with IGFBPs. GO enrichment analysis found that IGFBP was mainly expressed in the signaling pathways related to growth and cell movement.

Conclusions

Bioinformatics-based study demonstrates that IGFBP3 is abnormally expressed in HCC tissues, which is associated with clinical prognosis of HCC patients. IGFBP3 might serve as a biomarker for clinical prognosis anda potential therapeutic target in HCC patients.

Key words: Carcinoma, hepatocellular, Insulin-like growth factor binding proteins, Prognosis, Computational biology

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