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Quantitative proteomic analysis in HCV-induced HCC reveals sets of proteins with potential significance for racial disparity
被引:22
作者:

Dillon, Simon T.
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Harvard Univ, Sch Med, BIDMC, Boston, MA USA Harvard Univ, Sch Med, BIDMC, Boston, MA USA

Bhasin, Manoj K.
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Harvard Univ, Sch Med, BIDMC, Boston, MA USA Harvard Univ, Sch Med, BIDMC, Boston, MA USA

Feng, Xiaoxing
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Washington State Univ, Dept Pharmaceut Sci, Pullman, WA 99164 USA Harvard Univ, Sch Med, BIDMC, Boston, MA USA

Koh, David W.
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Washington State Univ, Dept Pharmaceut Sci, Pullman, WA 99164 USA Harvard Univ, Sch Med, BIDMC, Boston, MA USA

Daoud, Sayed S.
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机构:
Washington State Univ, Dept Pharmaceut Sci, Pullman, WA 99164 USA Harvard Univ, Sch Med, BIDMC, Boston, MA USA
机构:
[1] Harvard Univ, Sch Med, BIDMC, Boston, MA USA
[2] Washington State Univ, Dept Pharmaceut Sci, Pullman, WA 99164 USA
关键词:
Hepatocellular carcinoma;
Hepatitis C;
Tissue proteomics;
Isobaric tags for relative and absolute quantification (iTRAQ);
Cancer racial disparity;
CHRONIC HEPATITIS-C;
HEPATOCELLULAR-CARCINOMA;
AFRICAN-AMERICANS;
LIVER-DISEASE;
CANCER;
EXPRESSION;
GENE;
HNF4-ALPHA;
CELLS;
CORE;
D O I:
10.1186/1479-5876-11-239
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Background: The incidence and mortality of hepatitis C virus (HCV)-induced hepatocellular carcinoma (HCC) is higher in African Americans (AA) than other racial/ethnic groups in the U.S., but the reasons for this disparity are unknown. There is an urgent need for the discovery of novel molecular signatures for HCV disease progression to understand the underlying biological basis for this cancer rate disparity to improve the clinical outcome. Methods: We performed differential proteomics with isobaric labeling tags for relative and absolute quantitation (iTRAQ) and MS/MS analysis to identify proteins differentially expressed in cirrhotic (CIR) and HCC as compared to normal tissues of Caucasian American (CA) patients. The raw data were analyzed using the ProteinPilot v3.0. Searches were performed against all known sequences populating the Swiss-Prot, Refseq, and TrEMBL databases. Quality control analyses were accomplished using pairwise correlation plots, boxplots, principal component analysis, and unsupervised hierarchical clustering. Supervised analysis was carried out to identify differentially expressed proteins. Candidates were validated in independent cohorts of CA and AA tissues by qRT-PCR or Western blotting. Results: A total of 238 unique proteins were identified. Of those, around 15% were differentially expressed between normal, CIR & HCC groups. Target validation demonstrates racially distinct alteration in the expression of certain proteins. For example, the mRNA expression levels of transferrin (TF) were 2 and18-fold higher in CIR and HCC in AA as compared to CA. Similarly; the expression of Apolipoprotein A1 (APOA1) was 7-fold higher in HCC of AA. This increase was mirrored in the protein expression levels. Interestingly, the level of hepatocyte nuclear factor4 alpha (HNF4 alpha) protein was down regulated in AA, whereas repression of transcription is seen more in CA compared to AA. These data suggest that racial disparities in HCC could be a consequence of differential dysregulation of HNF4 alpha transcriptional activity. Conclusion: This study identifies novel molecular signatures in HCV-induced HCC using iTRAQ-based tissue proteomics. The proteins identified will further enhance a molecular explanation to the biochemical mechanism(s) that may play a role in HCC racial disparities.
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MOLECULAR MEDICINE REPORTS,
2010, 3 (04)
:589-596

Chen, Xiao-Li
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Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 2, Dept Pathol, Xian 710004, Shaanxi, Peoples R China Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 2, Dept Pathol, Xian 710004, Shaanxi, Peoples R China

Zhou, Le
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Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 2, Dept Neurosurg, Xian 710004, Shaanxi, Peoples R China Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 2, Dept Pathol, Xian 710004, Shaanxi, Peoples R China

Yang, Jun
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Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 2, Dept Pathol, Xian 710004, Shaanxi, Peoples R China Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 2, Dept Pathol, Xian 710004, Shaanxi, Peoples R China

Shen, Fu-Kun
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Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 2, Dept Pathol, Xian 710004, Shaanxi, Peoples R China Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 2, Dept Pathol, Xian 710004, Shaanxi, Peoples R China

Zhao, Shi-Ping
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Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 2, Dept Pathol, Xian 710004, Shaanxi, Peoples R China Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 2, Dept Pathol, Xian 710004, Shaanxi, Peoples R China

Wang, Yi-Li
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Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 2, Dept Pathol, Xian 710004, Shaanxi, Peoples R China
Xi An Jiao Tong Univ, Inst Canc Res, Natl Adm Educ, Key Lab Biomed Informat Engn, Xian 710061, Shaanxi, Peoples R China Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 2, Dept Pathol, Xian 710004, Shaanxi, Peoples R China