Circulating markers of biliary malignancy: opportunities in proteomics?

被引:86
作者
Bonney, Glenn K. [1 ,2 ]
Craven, Rachel A. [1 ]
Prasad, Raj [2 ]
Melcher, Alan F. [1 ]
Selby, Peter J. [1 ]
Banks, Rosamonde E. [1 ]
机构
[1] St James Univ Hosp, Canc Res UK Clin Ctr, Leeds LS9 7TF, W Yorkshire, England
[2] St James Univ Hosp, Liver Transplant Unit, Leeds LS9 7TF, W Yorkshire, England
关键词
D O I
10.1016/S1470-2045(08)70027-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Cholangiocarcinoma, a primary liver tumour that arises from biliary epithelial cells, is increasing in incidence and has poor prognosis. Diagnosis is difficult, particularly in patients with primary sclerosing cholangitis, who are at risk of developing the disease. Timely diagnosis is essential because surgical resection in early disease remains the only cure. The lack of a sensitive and specific early diagnostic marker and of alternative treatments are the main reasons why patients have limited survival. The use of proteomic-based approaches, which analyse the physiological or pathological complement of proteins (ie, the proteome) in cells, tissues, or biological fluids, has received substantial interest in biomarker discovery. Proteomics complements genomic studies and examines functional end-units quantitatively and qualitatively, including post-translational modifications which might vary with disease and might have key roles in protein function or localisation. Major advances in technology and bioinformatics have enhanced proteomic studies, resulting in increased understanding of the pathogenesis of many diseases and in biomarker discovery with effective use of tissues, cell lines, and biological fluids. We review the current status and promise of proteomic-based approaches in biomarker discovery for cholangiocarcinoma.
引用
收藏
页码:149 / 158
页数:10
相关论文
共 71 条
[1]
Mass spectrometry-based proteomics [J].
Aebersold, R ;
Mann, M .
NATURE, 2003, 422 (6928) :198-207
[2]
The utility of keratin 903 as a new prognostic marker in mass-forming-type intrahepatic cholangiocarcinorna [J].
Aishima, S ;
Asayama, Y ;
Taguchi, K ;
Sugimachi, K ;
Shirabe, K ;
Shimada, M ;
Sugimachi, K ;
Tsuneyoshi, M .
MODERN PATHOLOGY, 2002, 15 (11) :1181-1190
[3]
The human plasma proteome - A nonredundant list developed by combination of four separate sources [J].
Anderson, NL ;
Polanski, M ;
Pieper, R ;
Gatlin, T ;
Tirumalai, RS ;
Conrads, TP ;
Veenstra, TD ;
Adkins, JN ;
Pounds, JG ;
Fagan, R ;
Lobley, A .
MOLECULAR & CELLULAR PROTEOMICS, 2004, 3 (04) :311-326
[4]
Influences of blood sample processing on low-molecular-weight proteome identified by surface-enhanced laser desorption/ionization mass spectrometry [J].
Banks, RE ;
Stanley, AJ ;
Cairns, DA ;
Barrett, JH ;
Clarke, P ;
Thompson, D ;
Selby, PJ .
CLINICAL CHEMISTRY, 2005, 51 (09) :1637-1649
[5]
The proteins and the formation of gallstones [J].
Binette, JP ;
Binette, MB .
CLINICA CHIMICA ACTA, 2000, 296 (1-2) :59-69
[6]
Chen CY, 2003, HEPATO-GASTROENTEROL, V50, P924
[7]
Craven RA, 2002, METHOD ENZYMOL, V356, P33
[8]
Proteomic analysis of primary cell lines identifies protein changes present in renal cell carcinoma [J].
Craven, Rachel A. ;
Stanley, Anthea J. ;
Hanrahan, Sarah ;
Dods, James ;
Unwin, Richard ;
Totty, Nick ;
Hamden, Patricia ;
Eardley, Ian ;
Selby, Peter J. ;
Banks, Rosamonde E. .
PROTEOMICS, 2006, 6 (09) :2853-2864
[9]
Movement of a novel serum tumour marker, RCAS1, in patients with biliary diseases [J].
Enjoji, M ;
Yamaguchi, K ;
Nakamuta, M ;
Nakashima, M ;
Kotoh, K ;
Tanaka, M ;
Nawata, H ;
Watanabe, T .
DIGESTIVE AND LIVER DISEASE, 2004, 36 (09) :622-627
[10]
Fiorentino M, 2001, CLIN CANCER RES, V7, P3994