2009
DOI: 10.1021/pr8009275
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Differential Proteomic Analysis of Subfractioned Human Hepatocellular Carcinoma Tissues

Abstract: To discover new potential biomarkers of HCC, we used 2-DE gel separation and MALDI-TOF-MS analysis of partially enriched nuclear fractions from liver biopsies of 20 different patients. We obtained a proteomic map of subfractioned liver samples including about 200 common protein spots, among which identified components corresponded to expression products of 52 different genes. A differential analysis of proteins from tumoral and control tissues revealed a significant change in the expression level of 16 protein… Show more

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Cited by 14 publications
(12 citation statements)
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References 118 publications
(187 reference statements)
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“…at sub‐pathological doses, is of particular importance. It is a current procedure allowing for the identification of biomarkers 10–15 and making possible human studies that otherwise could not be carried out at overtly toxic exposures 16.…”
Section: Environmental Proteomicsmentioning
confidence: 99%
“…at sub‐pathological doses, is of particular importance. It is a current procedure allowing for the identification of biomarkers 10–15 and making possible human studies that otherwise could not be carried out at overtly toxic exposures 16.…”
Section: Environmental Proteomicsmentioning
confidence: 99%
“…a-Fetoprotein (AFP), as the most widely used tumor marker in clinical practice, is not an effective marker for hepatocellular carcinoma diagnosis due to its poor sensitivity and low specificity (4)(5)(6). To explore more sensitive and specific markers for early and accurate diagnosis of hepatocellular carcinoma, there have been a number of previous investigations on gene expression, miRNA profiles, and protein expression of hepatocellular carcinoma (7)(8)(9)(10)(11)(12). Recently, metabolomics investigations have provided a new angle for biomarker discovery.…”
Section: Introductionmentioning
confidence: 99%
“…HCC pathogenesis is quite complicated and is basically triggered by chromosomal aberrations, epigenetic abnormalities and changes in gene expression. At the molecular level, the onset and progression of HCC has been observed to be mechanistically linked to the differential expression of genes (Feitelson et al, ; Lee & Thorgeirsson, ; Lleonart et al, ; Wang et al, ; Sharma, Vouros, & Glick, ), deregulation of protein expression (Cui et al, ; Codarin et al, ; Corona et al, ; D'Alessandro, Meyer, & Klingmuller, ), particular RNA modifications (Santamaría et al, ; Yang et al, ) and, markedly, metabolic perturbations (Xue et al, ; Patterson et al, ; Budhu et al, ; Wang et al, ) (Fig. ).…”
Section: Assignments Of Omics Technologies To Hcc Pathogenesismentioning
confidence: 99%
“…Mass spectrometry‐based proteomics strategy is capable of identifying the differentially expressed proteins from a large validated protein database, that together. The combination of with genetic/transcriptomic/metabolomics and bioinformatics identification and integration of these multiple ‘omics can determine the functional significance of proteins and biochemical pathways responsible for as HCC pathogenesis, as well as other diseases (Cui et al, ; Codarin et al, ; Gstaiger & Aebersold, ; Corona et al, ; Lee et al, ).…”
Section: Proteomic Snapshot Of the Molecular Signature Of Hccmentioning
confidence: 99%