American Association for Cancer Research
Browse

Supplementary Figures 1-5 from Identification of a Cholangiocarcinoma-Like Gene Expression Trait in Hepatocellular Carcinoma

Download (768.68 kB)
journal contribution
posted on 2023-03-30, 20:06 authored by Hyun Goo Woo, Jeong-Hoon Lee, Jung-Hwan Yoon, Chung Yong Kim, Hyo-Suk Lee, Ja June Jang, Nam-Joon Yi, Kyung-Suk Suh, Kuhn Uk Lee, Eun Sung Park, Snorri S. Thorgeirsson, Yoon Jun Kim
Supplementary Figures 1-5 from Identification of a Cholangiocarcinoma-Like Gene Expression Trait in Hepatocellular Carcinoma

History

ARTICLE ABSTRACT

Hepatocellular carcinoma (HCC) and cholangiocarcinoma (CC) are the major adult liver cancers. The existence of combined hepatocellular-cholangiocarcinoma (CHC), a histopathologic intermediate form between HCC and CC, suggests phenotypic overlap between these tumors. Here, we applied an integrative oncogenomic approach to address the clinical and functional implications of the overlapping phenotype between these tumors. By performing gene expression profiling of human HCC, CHC, and CC, we identified a novel HCC subtype, i.e., cholangiocarcinoma-like HCC (CLHCC), which expressed cholangiocarcinoma-like traits (CC signature). Similar to CC and CHC, CLHCC showed an aggressive phenotype with shorter recurrence-free and overall survival. In addition, we found that CLHCC coexpressed embryonic stem cell–like expression traits (ES signature) suggesting its derivation from bipotent hepatic progenitor cells. By comparing the expression of CC signature with previous ES-like, hepatoblast-like, or proliferation-related traits, we observed that the prognostic value of the CC signatures was independent of the expression of those signatures. In conclusion, we suggest that the acquisition of cholangiocarcinoma-like expression traits plays a critical role in the heterogeneous progression of HCC. Cancer Res; 70(8); 3034–41. ©2010 AACR.

Usage metrics

    Cancer Research

    Licence

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC