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Integrated Analysis of Prognostic Gene Expression Profiles from Hepatitis B Virus-Positive Hepatocellular Carcinoma and Adjacent Liver Tissue

Authors
Kim, Bu-YeoSuh, Kyung-SukLee, Je-GeunWoo, Seon RangPark, In-ChulPark, Sun-HooHan, Chul JuKim, Sang-BumJeong, Sook-HyangYeom, Young IlYang, Suk-JinKim, Chang-MinCho, Su JinYoo, Young DoCho, Myung-HaingJang, Ja JuneChoi, Dong WookLee, Kee-Ho
Issue Date
7월-2012
Publisher
SPRINGER
Keywords
THERAPEUTIC TARGETS; CANCER; CLASSIFICATION; PREDICTION; SURVIVAL; RECURRENCE; HYPERMETHYLATION; IDENTIFICATION; MICROARRAY; SUPPRESSOR
Citation
ANNALS OF SURGICAL ONCOLOGY, v.19, pp.S328 - S338
Indexed
SCIE
SCOPUS
Journal Title
ANNALS OF SURGICAL ONCOLOGY
Volume
19
Start Page
S328
End Page
S338
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/108104
DOI
10.1245/s10434-011-1709-0
ISSN
1068-9265
Abstract
Background. The tissue environment in the region of hepatocellular carcinoma (HCC) influences both vascular invasion and recurrence. Thus, HCC patient prognosis depends on the characteristics not only of the tumor but also those of adjacent surrounding liver tissue. Materials and Methods. Expression profiles of both tumor and adjacent liver tissue following curative resection were measured to discriminate 56 hepatitis B virus-positive HCC patients into subgroups based on survival risk. This approach was further tested in 40 patients. Results. Expression profiles of both tumor and adjacent liver tissue successfully discriminated 56 training samples into 2 subgroups, those at low-or high-risk for survival and recurrence. However, the prognostic gene set selected for tumor tissue was quite different from that for adjacent tissues. This variation in prognostic genes resulted in a change in allocation of patients within each low-or highrisk group. Combination of survival subgroups from tumor and adjacent liver tissue significantly improved the prediction of prognostic outcome. This integrative approach was confirmed to be effective in a further 40 test patients. A clinicopathological study showed that survival subgroups divided by tumor and adjacent liver tissue gene expression were also statistically associated with UICC stage and extent of cell differentiation, respectively. Conclusions. Variation in gene expression during the nontumor stage as well as the tumor stage may affect the prognosis of HCC patients, and integration of the gene expression profiles of HCC and adjacent liver tissue increases discriminatory effectiveness between patient groups, predicting clinical outcomes with enhanced statistical reliability.
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