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Expression of c-Met in Primary and Recurrent Hepatocellular Carcinoma.

Authors :
Asaoka Y
Tateishi R
Hayashi A
Ushiku T
Shibahara J
Kinoshita J
Ouchi Y
Koike M
Fukayama M
Shiina S
Koike K
Source :
Oncology [Oncology] 2020; Vol. 98 (3), pp. 186-194. Date of Electronic Publication: 2019 Dec 17.
Publication Year :
2020

Abstract

Background: The clinical course of hepatocellular carcinoma (HCC) is complicated, because it often recurs and shows multiple lesions, some of which progress to a more malignant form, shortening the life of the patient. The hepatocyte growth factor receptor c-Met has been shown to play an important role in the pathogenesis of HCC, but the influence of c-Met expression on the clinical course of HCC remains to be fully elucidated.<br />Methods: We randomly selected and included 600 tumor specimens obtained from the primary and recurrent lesions of 319 HCC cases between 1995 and 2007. The expression of c-Met was determined by immunohistochemistry using archived formalin-fixed paraffin-embedded samples. We analyzed the correlation between c-Met expression and clinical parameters, including survival. In addition, we examined c-Met expression in the malignant transition of HCC in all cases including recurrent lesions.<br />Results: Survival analysis using the multivariate Cox proportional-regression model revealed that the prognosis was significantly better in the primary cases with high c-Met expression than in those with low c-Met expression (hazard ratio 0.159, 95% confidence interval 0.065-0.391; p < 0.001). During the course of recurrence, some cases with high c-Met expression returned to low c-Met expression. Among 40 cases with high c-Met expression, 29 survived more than 2 years after detecting the high c-Met expression.<br />Conclusion: High expression of c-Met may be a prognostic factor for a good, rather than a poor, HCC prognosis. The involvement of c-Met expression in the malignant transition of recurrent HCC is obscure.<br /> (© 2019 S. Karger AG, Basel.)

Details

Language :
English
ISSN :
1423-0232
Volume :
98
Issue :
3
Database :
MEDLINE
Journal :
Oncology
Publication Type :
Academic Journal
Accession number :
31846974
Full Text :
https://doi.org/10.1159/000504806