Gene expression profiling of hepatitis B- and hepatitis C-related hepatocellular carcinoma using graphical Gaussian modeling
書誌事項
- 公開日
- 2013-04
- 資源種別
- journal article
- 権利情報
-
- https://www.elsevier.com/tdm/userlicense/1.0/
- https://www.elsevier.com/legal/tdmrep-license
- http://www.elsevier.com/open-access/userlicense/1.0/
- DOI
-
- 10.1016/j.ygeno.2013.02.007
- 公開者
- Elsevier BV
この論文をさがす
説明
Gene expression profiling of hepatocellular carcinoma (HCC) and background liver has been studied extensively; however, the relationship between the gene expression profiles of different lesions has not been assessed.We examined the expression profiles of 34 HCC specimens (17 hepatitis B virus [HBV]-related and 17 hepatitis C virus [HCV]-related) and 71 non-tumor liver specimens (36 chronic hepatitis B [CH-B] and 35 chronic hepatitis C [CH-C]) using an in-house cDNA microarray consisting of liver-predominant genes. Graphical Gaussian modeling (GGM) was applied to elucidate the interactions of gene clusters among the HCC and non-tumor lesions.In CH-B-related HCC, the expression of vascular endothelial growth factor-family signaling and regulation of T cell differentiation, apoptosis, and survival, as well as development-related genes was up-regulated. In CH-C-related HCC, the expression of ectodermal development and cell proliferation, wnt receptor signaling, cell adhesion, and defense response genes was also up-regulated. Many of the metabolism-related genes were down-regulated in both CH-B- and CH-C-related HCC. GGM analysis of the HCC and non-tumor lesions revealed that DNA damage response genes were associated with AP1 signaling in non-tumor lesions, which mediates the expression of many genes in CH-B-related HCC. In contrast, signal transducer and activator of transcription 1 and phosphatase and tensin homolog were associated with early growth response protein 1 signaling in non-tumor lesions, which potentially promotes angiogenesis, fibrogenesis, and tumorigenesis in CH-C-related HCC.Gene expression profiling of HCC and non-tumor lesions revealed the predisposing changes of gene expression in HCC. This approach has potential for the early diagnosis and possible prevention of HCC.
収録刊行物
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- Genomics
-
Genomics 101 (4), 238-248, 2013-04
Elsevier BV
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キーワード
- Adult
- Male
- Carcinoma, Hepatocellular
- Transcription, Genetic
- Normal Distribution
- Genetics
- Cell Adhesion
- Humans
- Wnt Signaling Pathway
- Aged
- Early Growth Response Protein 1
- Models, Genetic
- Vascular Endothelial Growth Factors
- Gene Expression Profiling
- Liver Neoplasms
- Middle Aged
- Hepatitis B
- Hepatitis C
- Gene Expression Regulation, Neoplastic
- STAT1 Transcription Factor
- Female
- DNA Damage
詳細情報 詳細情報について
-
- CRID
- 1360848657489358336
-
- ISSN
- 08887543
-
- PubMed
- 23485556
-
- 資料種別
- journal article
-
- データソース種別
-
- Crossref
- KAKEN
- OpenAIRE

