Protein Profiling in Hepatocellular Carcinoma by Label-Free Quantitative Proteomics in Two West African Populations

被引:17
|
作者
Fye, Haddy K. S. [1 ,4 ]
Wright-Drakesmith, Cynthia [1 ]
Kramer, Holger B. [1 ]
Camey, Suzi [2 ,3 ,6 ]
da Costa, Andre Nogueira [2 ,3 ]
Jeng, Adam [4 ]
Bah, Alasana [4 ]
Kirk, Gregory D. [5 ]
Sharif, Mohamed I. F. [7 ]
Ladep, Nimzing G. [7 ]
Okeke, Edith [9 ]
Hainaut, Pierre [2 ,3 ,8 ]
Taylor-Robinson, Simon D. [7 ]
Kessler, Benedikt M. [1 ]
Mendy, Maimuna E. [2 ,3 ,4 ]
机构
[1] Univ Oxford, Nuffield Dept Med, Oxford, Oxfordshire, England
[2] Int Agcy Res Canc, Lab Serv, F-69372 Lyon, France
[3] Int Agcy Res Canc, Biobank Grp, F-69372 Lyon, France
[4] Gambia Labs, MRC Unit UK, Dept Dis Control & Eliminat, Banjul, Gambia
[5] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[6] Univ Fed Rio Grande do Sul, Dept Estatist, Inst Matemat, BR-90046900 Rio Grande, Brazil
[7] Imperial Coll London, Dept Med, Liver Unit, Div Diabet Endocrinol & Metab, London, England
[8] Int Prevent Res Inst, Lyon, France
[9] Univ Jos, Teaching Hosp, Jos, Plateau State, Nigeria
来源
PLOS ONE | 2013年 / 8卷 / 07期
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
CHRONIC HEPATITIS-B; GLOBAL CANCER STATISTICS; HUMAN LIVER-CANCER; ALPHA-FETOPROTEIN; VIRUS-DNA; DIETARY AFLATOXINS; SERUM MARKERS; BIOMARKERS; RISK; IDENTIFICATION;
D O I
10.1371/journal.pone.0068381
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Hepatocellular Carcinoma is the third most common cause of cancer related death worldwide, often diagnosed by measuring serum AFP; a poor performance stand-alone biomarker. With the aim of improving on this, our study focuses on plasma proteins identified by Mass Spectrometry in order to investigate and validate differences seen in the respective proteomes of controls and subjects with LC and HCC. Methods: Mass Spectrometry analysis using liquid chromatography electro spray ionization quadrupole time-of-flight was conducted on 339 subjects using a pooled expression profiling approach. ELISA assays were performed on four significantly differentially expressed proteins to validate their expression profiles in subjects from the Gambia and a pilot group from Nigeria. Results from this were collated for statistical multiplexing using logistic regression analysis. Results: Twenty-six proteins were identified as differentially expressed between the three subject groups. Direct measurements of four; hemopexin, alpha-1-antitrypsin, apolipoprotein A1 and complement component 3 confirmed their change in abundance in LC and HCC versus control patients. These trends were independently replicated in the pilot validation subjects from Nigeria. The statistical multiplexing of these proteins demonstrated performance comparable to or greater than ALT in identifying liver cirrhosis or carcinogenesis. This exercise also proposed preliminary cut offs with achievable sensitivity, specificity and AUC statistics greater than reported AFP averages. Conclusions: The validated changes of expression in these proteins have the potential for development into high-performance tests usable in the diagnosis and or monitoring of HCC and LC patients. The identification of sustained expression trends strengthens the suggestion of these four proteins as worthy candidates for further investigation in the context of liver disease. The statistical combinations also provide a novel inroad of analyses able to propose definitive cutoffs and combinations for evaluation of performance.
引用
收藏
页数:13
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