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Transcriptional profiling in hepatoblastomas using high-density oligonucleotide DNA array.

Abstract
Hepatoblastoma is a common hepatic tumor in children. Although evidence regarding cytogenetic and molecular genetic alterations in hepatoblastomas has been reported, the molecular events affecting the biologic characteristics of this tumor, including alterations of the gene expression profile, are largely unknown. To identify genes differentially expressed between nondiseased liver (NDL) and hepatoblastoma tumor (HBT), we analyzed the gene expression profile in 14 NDL and 16 HBT samples using a high-density oligonucleotide DNA array. Using Mann-Whitney U test followed by the k-nearest neighbor algorithm, we identified 26 genes (predictor genes) that were able to assign unknown samples derived from NDL and HBT to either the NDL group or HBT group with 100% accuracy. Using a cross-validation approach, we confirmed that the k-nearest neighbor algorithm assigned the particular samples derived from NDL and HBT to either the NDL or HBT group with 93.3% (28/30 samples) accuracy. In the 26 predictor genes, we found alteration of the expression of genes regulating cell division (NAP1L1, STMN1, CCNG2, and CDC7L1) and tumor cell growth (IGF2 and IGFBP4) in HBT. Four predictor genes (ETV3, TPR, CD34, and NR1I3) were also found to be mapped to the chromosomal region 1q21 approximately q32, which has been reported to be frequently involved in the development of hepatoblastoma. The findings obtained in this study suggest that alteration of the expression of some genes regulating cell division and tumor cell growth may be characteristics of the gene expression profile in HBT, and that alteration of the expression of the four predictor genes mapped to chromosomal region 1q21 approximately q32 may also contribute to the differences in gene expression profile between NDL and HBT.
AuthorsToshihito Nagata, Yasuo Takahashi, Yukimoto Ishii, Satoshi Asai, Yayoi Nishida, Akiko Murata, Tsugumichi Koshinaga, Masahiro Fukuzawa, Minoru Hamazaki, Keiko Asami, Etsuro Ito, Hitoshi Ikeda, Hideo Takamatsu, Kenichi Koike, Atsushi Kikuta, Minoru Kuroiwa, Arata Watanabe, Yoshiyuki Kosaka, Hiroo Fujita, Munenori Miyake, Hideo Mugishima
JournalCancer genetics and cytogenetics (Cancer Genet Cytogenet) Vol. 145 Issue 2 Pg. 152-60 (Sep 2003) ISSN: 0165-4608 [Print] United States
PMID12935928 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Constitutive Androstane Receptor
  • NR1I3 protein, human
  • Insulin-Like Growth Factor II
Topics
  • Child
  • Child, Preschool
  • Chromosome Mapping
  • Constitutive Androstane Receptor
  • Female
  • Gene Expression Profiling
  • Hepatoblastoma (genetics, physiopathology)
  • Humans
  • Infant
  • Infant, Newborn
  • Insulin-Like Growth Factor II (metabolism)
  • Male
  • Oligonucleotide Array Sequence Analysis
  • Phylogeny

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