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Mutation of the MXI1 gene in prostate cancer.

作者信息

Eagle L R, Yin X, Brothman A R, Williams B J, Atkin N B, Prochownik E V

机构信息

Department of Pediatrics, Children's Hospital of Pittsburgh, Pennsylvania 15213, USA.

出版信息

Nat Genet. 1995 Mar;9(3):249-55. doi: 10.1038/ng0395-249.

DOI:10.1038/ng0395-249
PMID:7773287
Abstract

The Mxi1 protein negatively regulates Myc oncoprotein activity and thus potentially serves a tumour suppressor function. MXI1 maps to chromosome 10q24-q25, a region that is deleted in some cases of prostate cancer. We have detected mutations in the retained MXI1 alleles in four primary prostate tumours with 10q24-q25 deletions. Two tumours contained inactivating mutations, whereas two others contained the identical missense mutation. Fluorescence in situ hybridization also demonstrated loss of one MXI1 allele in an additional tumour lacking chromosome 10 abnormalities. MXI1 thus displays allelic loss and mutation in some cases of prostate cancer that may contribute to the pathogenesis or neoplastic evolution of this common malignancy.

摘要

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Mutation of the MXI1 gene in prostate cancer.
Nat Genet. 1995 Mar;9(3):249-55. doi: 10.1038/ng0395-249.
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Localization of the human Mxi1 transcription factor gene (MXI1) to chromosome 10q24-q25.人类Mxi1转录因子基因(MXI1)定位于染色体10q24 - q25。
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Mapping of two genes encoding members of a distinct subfamily of MAX interacting proteins: MAD to human chromosome 2 and mouse chromosome 6, and MXI1 to human chromosome 10 and mouse chromosome 19.两个编码MAX相互作用蛋白不同亚家族成员的基因定位:MAD定位于人类2号染色体和小鼠6号染色体,MXI1定位于人类10号染色体和小鼠19号染色体。
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MXI1, a putative tumor suppressor gene, suppresses growth of human glioblastoma cells.MXI1是一种假定的肿瘤抑制基因,可抑制人胶质母细胞瘤细胞的生长。
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