Genes associated with progression and recurrence of hepatocellular carcinoma in hepatitis C patients waiting and undergoing liver transplantation: Preliminary results

被引:26
作者
Mas, Valeria R.
Fisher, Robert A.
Archer, Kellie J.
Yanek, Kenneth C.
Williams, Bridgette
Dumur, Catherine I.
Maluf, Daniel G.
机构
[1] Virginia Commonwealth Univ, Dept Surg, Div Transplantat, Richmond, VA 23284 USA
[2] Virginia Commonwealth Univ, Dept Pathol, Richmond, VA 23284 USA
[3] Virginia Commonwealth Univ, Dept Biostat, Richmond, VA 23284 USA
[4] Virginia Commonwealth Univ, Ctr Study Biol Complex, Richmond, VA 23284 USA
关键词
liver transplantation; hepatocellular carcinoma; gene expression analysis;
D O I
10.1097/01.tp.0000258643.05294.0b
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Liver transplantation (LT) represents a curative treatment for small hepatocellular carcinoma (HCC). Potentially curable higher-stage HCC patients are denied LT due to the lack of cancer markers that predict progression and recurrence. Methods. Thirty-eight candidates for LT with hepatitis C virus (HCV) cirrhosis and HCC were studied. Gene expression (Gexp) analysis of tumor samples was performed using microarrays. Results. Twenty patients underwent transplantation, 13 progressed while waiting for transplantation, 4 are alive awaiting transplantation, and 1 died without progression while waiting for LT. Differences in GExp among patients who underwent LT or did not progress (n=25) versus those whose disease progressed while waiting for LT (n=13) were assessed. Thus, 54 probe sets (Pset) were significantly differentially expressed. Among LT patients, 10 Psets were differentially expressed between LT patients with the same explanted stage that recurred (n=5) versus LT patients who did not recur (n=5). Ninety-eight Psets were significantly associated with survival at the alpha=0.005 level. Conclusions. Here, we have identified genes associated with HCC progression in HCV-HCC patients awaiting LT transplantation. A limited number of genes were related to overall survival and cancer-free survival after LT. Incorporation of these molecular markers could help to improve organ allocation for HCV-HCC patients.
引用
收藏
页码:973 / 981
页数:9
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