» Articles » PMID: 29163834

Prognostic Value of C-Met Overexpression in Hepatocellular Carcinoma: a Meta-analysis and Review

Overview
Journal Oncotarget
Specialty Oncology
Date 2017 Nov 23
PMID 29163834
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

The overexpression of c-Met protein has been detected in hepatocellular carcinoma (HCC). However, its prognostic impact remains uncertain. We performed this meta-analysis to evaluate the prognostic value of c-Met overexpression in patients who underwent curative surgical resection for HCC. A systematic computerized search of the electronic databases was carried out. From 5 studies, 1,408 patients who underwent surgical resection for HCC were included in the meta-analysis. Compared with patients with HCC having low c-Met expression, patients with c-Met-high tumor showed significantly worse relapse-free survival (hazard ratio = 1.26 [95% confidence interval, 1.02-1.56], = 0.03) and overall survival (hazard ratio = 1.16 [95% confidence interval, 1.03-1.31], = 0.01). In conclusion, our meta-analysis indicates that c-Met overexpression is a significant adverse prognostic factor for recurrence and survival in patients who underwent surgical resection for HCC.

Citing Articles

Identification of basement membrane-related prognostic model associated with the immune microenvironment and synthetic therapy response in pancreatic cancer: integrated bioinformatics analysis and clinical validation.

Zhang B, Chen X, Song H, Gao X, Ma S, Ji H J Cancer. 2024; 15(19):6273-6298.

PMID: 39513120 PMC: 11540510. DOI: 10.7150/jca.100891.


New pyrazolopyridine and pyrazolothiazole-based compounds as anti-proliferative agents targeting c-Met kinase inhibition: design, synthesis, biological evaluation, and computational studies.

Alamshany Z, Algamdi E, Othman I, Anwar M, Nossier E RSC Adv. 2023; 13(19):12889-12905.

PMID: 37114032 PMC: 10128108. DOI: 10.1039/d3ra01931d.


Predictive Biomarkers for Immune-Checkpoint Inhibitor Treatment Response in Patients with Hepatocellular Carcinoma.

Ji J, Ha S, Lee D, Sankar K, Koltsova E, Abou-Alfa G Int J Mol Sci. 2023; 24(8).

PMID: 37108802 PMC: 10144688. DOI: 10.3390/ijms24087640.


Resistance to Antiangiogenic Therapy in Hepatocellular Carcinoma: From Molecular Mechanisms to Clinical Impact.

Federico P, Giunta E, Tufo A, Tovoli F, Petrillo A, Daniele B Cancers (Basel). 2022; 14(24).

PMID: 36551730 PMC: 9776845. DOI: 10.3390/cancers14246245.


MET Signaling Pathways, Resistance Mechanisms, and Opportunities for Target Therapies.

Rivas S, Marin A, Samtani S, Gonzalez-Feliu E, Armisen R Int J Mol Sci. 2022; 23(22).

PMID: 36430388 PMC: 9697723. DOI: 10.3390/ijms232213898.


References
1.
Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M . Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 2014; 136(5):E359-86. DOI: 10.1002/ijc.29210. View

2.
Sterne J, Sutton A, Ioannidis J, Terrin N, Jones D, Lau J . Recommendations for examining and interpreting funnel plot asymmetry in meta-analyses of randomised controlled trials. BMJ. 2011; 343:d4002. DOI: 10.1136/bmj.d4002. View

3.
Santoro A, Rimassa L, Borbath I, Daniele B, Salvagni S, Van Laethem J . Tivantinib for second-line treatment of advanced hepatocellular carcinoma: a randomised, placebo-controlled phase 2 study. Lancet Oncol. 2012; 14(1):55-63. DOI: 10.1016/S1470-2045(12)70490-4. View

4.
Cheng A, Kang Y, Lin D, Park J, Kudo M, Qin S . Sunitinib versus sorafenib in advanced hepatocellular cancer: results of a randomized phase III trial. J Clin Oncol. 2013; 31(32):4067-75. DOI: 10.1200/JCO.2012.45.8372. View

5.
Wang Z, Liang P, Dong B, Yu X, Yu D . Prognostic factors and recurrence of small hepatocellular carcinoma after hepatic resection or microwave ablation: a retrospective study. J Gastrointest Surg. 2007; 12(2):327-37. DOI: 10.1007/s11605-007-0310-0. View