Oncoproteomics of hepatocellular carcinoma: from cancer markers' discovery to functional pathways

被引:44
作者
Sun, Stella
Lee, Nikki P. Y.
Poon, Ronnie T. P.
Fan, Sheung-Tat
He, Qing Y.
Lau, George K.
Luk, John M.
机构
[1] Univ Hong Kong, LKS Fac Med, Jockey Club Clin Res Ctr, Dept Surg, Pokfulam, Peoples R China
[2] Univ Hong Kong, LKS Fac Med, Jockey Club Clin Res Ctr, Canc Res Ctr, Pokfulam, Peoples R China
[3] Univ Hong Kong, LKS Fac Med, Jockey Club Clin Res Ctr, Dept Med, Pokfulam, Peoples R China
[4] Jinan Univ, Inst Life Hlth Engn, Guangzhou, Peoples R China
关键词
biomarkers; hepatocellular carcinoma; proteomics;
D O I
10.1111/j.1478-3231.2007.01533.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatocellular carcinoma (HCC) is a heterogeneous cancer with no promising treatment and remains one of the most prevailing and lethal malignancies in the world. Researchers in many biological areas now routinely identify and characterize protein markers by a mass spectrometry-based proteomic approach, a method that has been commonly used to discover diagnostic biomarkers for cancer detection. The proteomic research platforms span from the classical two-dimensional polyacrylamide gel electrophoresis (2-DE) to the latest Protein Chip or array technology, which are often integrated with the MALDI (matrix-assisted laser-desorption ionization), SELDI (surface-enhanced laser desorption/ionization) or tandem mass spectrometry (MS/MS). New advances on quantitative proteomic analysis (e.g. SILAC, ICAT, and ITRAQ) and multidimensional protein identification technology (MudPIT) have greatly enhanced the capability of proteomic methods to study the expressions, modifications and functions of protein markers. The present article reviews the latest proteomic development and discovery of biomarkers in HCC that may provide insights into the underlying mechanisms of hepatocarcinogenesis and the readiness of biomarkers for clinical uses.
引用
收藏
页码:1021 / 1038
页数:18
相关论文
共 125 条
[31]   Caught up in a Wnt storm: Wnt signaling in cancer [J].
Giles, RH ;
van Es, JH ;
Clevers, H .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2003, 1653 (01) :1-24
[32]  
Gonias Steven L., 2001, Frontiers in Bioscience, V6, pd1403, DOI 10.2741/Gonias
[33]  
Goshe Michael B., 2006, Briefings in Functional Genomics & Proteomics, V4, P363, DOI 10.1093/bfgp/eli007
[34]  
Haab B B, 2001, Curr Opin Drug Discov Devel, V4, P116
[35]   The hallmarks of cancer [J].
Hanahan, D ;
Weinberg, RA .
CELL, 2000, 100 (01) :57-70
[36]   Identification of soluble NH2-terminal fragment of glypican-3 as a serological marker for early-stage hepatocellular carcinoma [J].
Hippo, Y ;
Watanabe, K ;
Watanabe, A ;
Midorikawa, Y ;
Yamamoto, S ;
Ihara, S ;
Tokita, S ;
Iwanari, H ;
Ito, Y ;
Nakano, K ;
Nezu, J ;
Tsunoda, H ;
Yoshino, T ;
Ohizumi, I ;
Tsuchiya, M ;
Ohnishi, S ;
Makuuchi, M ;
Hamakubo, T ;
Kodama, T ;
Aburatani, H .
CANCER RESEARCH, 2004, 64 (07) :2418-2423
[37]  
HONG W-S, 1991, Journal of Korean Medical Science, V6, P206
[38]  
Hough CD, 2000, CANCER RES, V60, P6281
[39]   The Orbitrap: a new mass spectrometer [J].
Hu, QZ ;
Noll, RJ ;
Li, HY ;
Makarov, A ;
Hardman, M ;
Cooks, RG .
JOURNAL OF MASS SPECTROMETRY, 2005, 40 (04) :430-443
[40]   Diverse cellular transformation capability of overexpressed genes in human hepatocellular carcinoma [J].
Huang, JS ;
Chao, CC ;
Su, TL ;
Yeh, SH ;
Chen, DS ;
Chen, CT ;
Chen, PJ ;
Jou, YS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 315 (04) :950-958