Source:http://linkedlifedata.com/resource/pubmed/id/17126992
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2007-4-11
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pubmed:abstractText |
Widespread DNA copy number alterations are well recognized in hepatocellular carcinoma (HCC), although the affected genes expression remained largely undefined. In this study, we performed genome-wide analysis on HCC to examine the relationship between gene copy number and corresponding transcriptional changes. To ensure analysis on a homogenous population of tumor cells, integrative analysis of array-based CGH and expression profilings was performed on 20 HCC cell lines using a 19,200-element cDNA microarray platform. Further validation studies were carried out on a large series of primary HCC tumors and paired adjacent non-malignant liver to ascertain finding. Correlative analyses highlighted 31 candidate genes that manifested both copy gains and gene up-regulations (R2>0.5; p<0.05). Of interest was over-expressed paternally expressed 10 (PEG10) resided within the chromosome region 7q21 that has been implicated in the progression of HCC. Quantitative PCR and qRT-PCR studies verified concurrent genomic gains and over-expression of PEG10 in HCC cell lines and primary tumors (34/40 cases; 85%). In addition, qRT-PCR demonstrated a significant progressive trend of increasing PEG10 expressions from the putative pre-malignant adjacent livers to early resectable HCC tumors, and to late inoperable HCCs (p=0.007). In summary, the present study demonstrated the usefulness of integrated genomic and expression profilings in identifying candidate genes within regions of genomic alteration. Our results also suggested that PEG10 may be a potential biomarker in the progressive development of HCC, and that genomic gain represents one of the major mechanisms in the induction of PEG10 over-expressions.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0304-3835
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
8
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pubmed:volume |
250
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
284-91
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pubmed:meshHeading |
pubmed-meshheading:17126992-Base Sequence,
pubmed-meshheading:17126992-Carcinoma, Hepatocellular,
pubmed-meshheading:17126992-Cell Line, Tumor,
pubmed-meshheading:17126992-DNA Primers,
pubmed-meshheading:17126992-Disease Progression,
pubmed-meshheading:17126992-Gene Expression Profiling,
pubmed-meshheading:17126992-Humans,
pubmed-meshheading:17126992-Liver Neoplasms,
pubmed-meshheading:17126992-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:17126992-Proteins,
pubmed-meshheading:17126992-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:17126992-Tumor Markers, Biological
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pubmed:year |
2007
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pubmed:articleTitle |
Identification of PEG10 as a progression related biomarker for hepatocellular carcinoma.
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pubmed:affiliation |
Department of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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