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
相关论文
共 47 条
[41]   Identification of differentially expressed genes in hepatocellular carcinoma with cDNA microarrays [J].
Shirota, Y ;
Kaneko, S ;
Honda, M ;
Kawai, HF ;
Kobayashi, K .
HEPATOLOGY, 2001, 33 (04) :832-840
[42]   Molecular prognostication of liver cancer: End of the beginning [J].
Thorgeirsson, SS ;
Lee, JS ;
Grisham, JW .
JOURNAL OF HEPATOLOGY, 2006, 44 (04) :798-805
[43]   Missing value estimation methods for DNA microarrays [J].
Troyanskaya, O ;
Cantor, M ;
Sherlock, G ;
Brown, P ;
Hastie, T ;
Tibshirani, R ;
Botstein, D ;
Altman, RB .
BIOINFORMATICS, 2001, 17 (06) :520-525
[44]   Significance analysis of microarrays applied to the ionizing radiation response [J].
Tusher, VG ;
Tibshirani, R ;
Chu, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (09) :5116-5121
[45]   A gene-expression signature as a predictor of survival in breast cancer. [J].
van de Vijver, MJ ;
He, YD ;
van 't Veer, LJ ;
Dai, H ;
Hart, AAM ;
Voskuil, DW ;
Schreiber, GJ ;
Peterse, JL ;
Roberts, C ;
Marton, MJ ;
Parrish, M ;
Atsma, D ;
Witteveen, A ;
Glas, A ;
Delahaye, L ;
van der Velde, T ;
Bartelink, H ;
Rodenhuis, S ;
Rutgers, ET ;
Friend, SH ;
Bernards, R .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (25) :1999-2009
[46]   Metallothionein - overexpression as a highly significant prognostic factor in melanoma: a prospective study on 1270 patients [J].
Weinlich, G ;
Eisendle, K ;
Hassler, E ;
Baltaci, M ;
Fritsch, PO ;
Zelger, B .
BRITISH JOURNAL OF CANCER, 2006, 94 (06) :835-841
[47]   Promoter hypermethylation of DLC-1, a candidate tumor suppressor gene, in several common human cancers [J].
Yuan, BZ ;
Durkin, ME ;
Popescu, NC .
CANCER GENETICS AND CYTOGENETICS, 2003, 140 (02) :113-117