| Literature DB >> 25807371 |
Thilo Bracht1, Vincent Schweinsberg1, Martin Trippler2, Michael Kohl1, Maike Ahrens1, Juliet Padden1, Wael Naboulsi1, Katalin Barkovits1, Dominik A Megger1, Martin Eisenacher1, Christoph H Borchers3, Jörg F Schlaak2, Andreas-Claudius Hoffmann4, Frank Weber5, Hideo A Baba6, Helmut E Meyer1,7, Barbara Sitek1.
Abstract
Hepatic fibrosis and cirrhosis are major health problems worldwide. Until now, highly invasive biopsy remains the diagnostic gold standard despite many disadvantages. To develop noninvasive diagnostic assays for the assessment of liver fibrosis, it is urgently necessary to identify molecules that are robustly expressed in association with the disease. We analyzed biopsied tissue samples from 95 patients with HBV/HCV-associated hepatic fibrosis using three different quantification methods. We performed a label-free proteomics discovery study to identify novel disease-associated proteins using a subset of the cohort (n = 27). Subsequently, gene expression data from all available clinical samples were analyzed (n = 77). Finally, we performed a targeted proteomics approach, multiple reaction monitoring (MRM), to verify the disease-associated expression in samples independent from the discovery approach (n = 68). We identified fibulin-5 (FBLN5) as a novel protein expressed in relation to hepatic fibrosis. Furthermore, we confirmed the altered expression of microfibril-associated glycoprotein 4 (MFAP4), lumican (LUM), and collagen alpha-1(XIV) chain (COL14A1) in association to hepatic fibrosis. To our knowledge, no tissue-based quantitative proteomics study for hepatic fibrosis has been performed using a cohort of comparable size. By this means, we add substantial evidence for the disease-related expression of the proteins examined in this study.Entities:
Keywords: MFAP4; cirrhosis; fibrosis; fibulin-5; hepatic fibrosis; label-free proteomics; liver; lumican; multiple reaction monitoring; selected reaction monitoring
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Year: 2015 PMID: 25807371 DOI: 10.1021/acs.jproteome.5b00053
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466