Abstract | BACKGROUND: Our previous studies suggested that deficient function of RUNX3 protein is causally related to development and progression of human gastric cancer. RUNX3 is mapped to 1p36, which is frequently deleted in hepatocellular carcinomas (HCC), therefore, these tumors were investigated for expression and copy number changes of RUNX3 and other Runt-related genes, RUNX1, RUNX2, and their co-factor CBFP. Similarly nearby uninvolved liver showing cirrhosis or normal histology was investigated in conjunction with various clinicopathological factors. MATERIALS AND METHODS: Copy number change and expression change of RUNX family genes in 35 hepatocellular carcinoma specimens and adjoining liver with cirrhosis (LC) or normal histology were estimated using quantitative reverse transcription polymerase chain reaction (RT-PCR) and in situ hybridization.
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Authors | Kouji Miyagawa, Chouhei Sakakura, Susumu Nakashima, Tetsuji Yoshikawa, Shuichi Kin, Yuenn Nakase, Kosei Ito, Hisakazu Yamagishi, Hiroshi Ida, Shujiro Yazumi, Tsutomu Chiba, Yoshiaki Ito, Akeo Hagiwara |
Journal | Anticancer research
(Anticancer Res)
2006 Sep-Oct
Vol. 26
Issue 5B
Pg. 3633-43
ISSN: 0250-7005 [Print] Greece |
PMID | 17094378
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Core Binding Factor Alpha 2 Subunit
- Core Binding Factor Alpha 3 Subunit
- Core Binding Factor alpha Subunits
- DNA Primers
- RUNX1 protein, human
- Runx3 protein, human
- core binding factor alpha
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Topics |
- Base Sequence
- Carcinoma, Hepatocellular
(genetics)
- Core Binding Factor Alpha 2 Subunit
(genetics)
- Core Binding Factor Alpha 3 Subunit
(genetics)
- Core Binding Factor alpha Subunits
(genetics)
- DNA Primers
- Down-Regulation
- Gene Deletion
- Humans
- In Situ Hybridization, Fluorescence
- Liver
(metabolism)
- Liver Cirrhosis
(genetics)
- Liver Neoplasms
(genetics)
- Molecular Sequence Data
- Reverse Transcriptase Polymerase Chain Reaction
- Sequence Homology, Nucleic Acid
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