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(C-A)n微卫星重复序列D7S522是人类原发性乳腺癌中最常缺失的区域。

(C-A)n microsatellite repeat D7S522 is the most commonly deleted region in human primary breast cancer.

作者信息

Zenklusen J C, Bièche I, Lidereau R, Conti C J

机构信息

University of Texas M. D. Anderson Cancer Center Science Park-Research Division, Smithville 78957.

出版信息

Proc Natl Acad Sci U S A. 1994 Dec 6;91(25):12155-8. doi: 10.1073/pnas.91.25.12155.

Abstract

Loss of heterozygosity in human chromosome 7q was studied to determine the location of a putative tumor suppressor gene. Twenty-six of 31 cases studied presented loss of heterozygosity at one or more loci on chromosome 7q. Eighty-three percent loss of heterozygosity (in 11 informative cases) was detected by using the (C-A)n microsatellite repeat marker D7S522 at 7q31.1-7q31.2. These results suggest that a tumor suppressor gene relevant to the development of breast cancer is present in the 7q31.1-7q31.2 region, confirming our previous evidence for a tumor suppressor gene in this chromosome and frequent deletions of the long arm in human primary breast cancers.

摘要

为确定一个假定的肿瘤抑制基因的位置,对人类7号染色体长臂(7q)杂合性缺失进行了研究。在研究的31例病例中,有26例在7q染色体的一个或多个位点出现杂合性缺失。通过使用位于7q31.1 - 7q31.2的(C - A)n微卫星重复标记D7S522,在11例信息充分的病例中检测到83%的杂合性缺失。这些结果表明,与乳腺癌发生相关的一个肿瘤抑制基因存在于7q31.1 - 7q31.2区域,证实了我们之前关于该染色体上存在肿瘤抑制基因以及人类原发性乳腺癌中7号染色体长臂频繁缺失的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b05/45395/8bb1655e4bd5/pnas01147-0397-a.jpg

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