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家族性乳腺癌和卵巢癌中17q12 - 21区域的等位基因缺失涉及野生型染色体。

Allele losses in the region 17q12-21 in familial breast and ovarian cancer involve the wild-type chromosome.

作者信息

Smith S A, Easton D F, Evans D G, Ponder B A

机构信息

Department of Pathology, University of Cambridge, UK.

出版信息

Nat Genet. 1992 Oct;2(2):128-31. doi: 10.1038/ng1092-128.

Abstract

A predisposing gene for breast and ovarian cancer has recently been mapped to chromosome 17q12-21. If this gene is a tumour suppressor gene, allele losses would be expected in the tumours of affected family members and the losses should affect the wild-type chromosome, reflecting the need for inactivation of the wild-type allele at the predisposing locus. In four multiple case breast-ovarian cancer families, we have found that in each of nine tumours which showed allele losses, the losses were from the wild-type chromosome. This suggests that the putative 'breast-ovarian' cancer gene is indeed a tumour suppressor gene.

摘要

一种乳腺癌和卵巢癌的易感基因最近已被定位到17号染色体的12 - 21区域。如果该基因是一个肿瘤抑制基因,那么在受影响家庭成员的肿瘤中预计会出现等位基因缺失,并且这些缺失应该会影响野生型染色体,这反映了在易感位点使野生型等位基因失活的必要性。在四个有多例乳腺癌 - 卵巢癌患者的家族中,我们发现,在九个显示等位基因缺失的肿瘤中,每个肿瘤的缺失都来自野生型染色体。这表明推测的“乳腺癌 - 卵巢癌”基因确实是一个肿瘤抑制基因。

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