Serum KL-6 as a novel tumor marker for hepatocellular carcinoma in hepatitis C virus infected patients

The up-regulation of MUC1 protein is associated with malignant phenotype of cancer. We investigated the significance of KL-6, one of the MUC1 antigens, as a tumor marker in hepatitis C virus positive hepatocellular carcinoma (HCC). Serum KL-6 was determined in 203 patients with chronic hepatitis (CH...

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Veröffentlicht in:Hepatology research 2005-11, Vol.33 (3), p.250-257
Hauptverfasser: Kurosaki, Masayuki, Izumi, Namiki, Onuki, Yuko, Nishimura, Yuki, Ueda, Ken, Tsuchiya, Kaoru, Nakanishi, Hiroyuki, Kitamura, Takatoshi, Asahina, Yasuhiro, Uchihara, Masakatsu, Miyake, Shozo
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Sprache:eng
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Zusammenfassung:The up-regulation of MUC1 protein is associated with malignant phenotype of cancer. We investigated the significance of KL-6, one of the MUC1 antigens, as a tumor marker in hepatitis C virus positive hepatocellular carcinoma (HCC). Serum KL-6 was determined in 203 patients with chronic hepatitis (CH), 47 patients with liver cirrhosis (LC) and 78 patients with HCC. KL-6 was higher in HCC compared to non-HCC ( p = 0.0005) and was higher in patients with multiple HCC nodules compared to a single nodule ( p = 0.02). There was no correlation between KL-6 and existent tumor markers for HCC such as alpha-fetoprotein, lens culinaris agglutinin-reactive alpha-fetoprotein or des-gamma-carboxyprothrombin. In the prospective analysis, the cumulative incidence of HCC was significantly greater in CH and LC patients with high initial KL-6 (above 400 U/ml) compared to the others ( p = 0.02). Moreover, in the prospective observation of 25 patients whose HCC was completely cured by radiofrequency ablation therapy, the cumulative incidence of distant recurrences was significantly greater in patients with high initial KL-6 compared to the others ( p = 0.005). These results suggest that serum KL-6 could be a novel tumor marker in the diagnosis and the prediction of prognosis of HCC that may have additive value to the existent markers.
ISSN:1386-6346
1872-034X
DOI:10.1016/j.hepres.2005.06.011