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pubmed-article:18266055pubmed:abstractTextPrevious studies indicated that region 11.2 of the long arm of chromosome 22 (22q11.2) might be a locus encoding a tumor suppressor gene, since its deletion is a recurrent genetic characteristic of aggressive pediatric cancer. This region is found in the human immunodeficiency virus integrase interactor 1 (hSNF5/INI1) gene. To investigate whether the hSNF5/INI1 gene is involved in leukemogenesis, mutation analysis of the hSNF5/INI1 gene was performed in the present study using 5 hematopoietic cell lines, acute myeloid leukemia (AML) specimen and normal control. We found two single nucleotide polymorphisms at the hSNF5/INI1 gene in exon 4 and exon 9. The results of this study suggest that the hSNF5/INI1 gene does not play an important role in the leukemogenesis of AML.lld:pubmed
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pubmed-article:18266055pubmed:authorpubmed-author:SuYu-ChiehYClld:pubmed
pubmed-article:18266055pubmed:authorpubmed-author:ChangYa-TingY...lld:pubmed
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pubmed-article:18266055pubmed:authorpubmed-author:ChenChao-BinC...lld:pubmed
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pubmed-article:18266055pubmed:pagination172-5lld:pubmed
pubmed-article:18266055pubmed:dateRevised2008-12-29lld:pubmed
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pubmed-article:18266055pubmed:year2008lld:pubmed
pubmed-article:18266055pubmed:articleTitlehSNF5 /INI1 mutation analysis in acute myeloid leukemia.lld:pubmed
pubmed-article:18266055pubmed:affiliationDivision of Hematology-Oncology, Department of Internal Medicine, Buddhist Dalin TzuChi General Hospital, Chiayi County, Taiwan. hepatoma@ms3.hinet.netlld:pubmed
pubmed-article:18266055pubmed:publicationTypeJournal Articlelld:pubmed
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