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乳腺癌中17号染色体短臂上的等位基因缺失。

Allele loss on short arm of chromosome 17 in breast cancers.

作者信息

Mackay J, Steel C M, Elder P A, Forrest A P, Evans H J

机构信息

MRC Human Genetics Unit, Western General Hospital, Edinburgh.

出版信息

Lancet. 1988 Dec 17;2(8625):1384-5. doi: 10.1016/s0140-6736(88)90584-3.

Abstract

Tumour and blood leucocyte DNA from a consecutive series of patients with primary breast cancer was probed to detect deletions at six polymorphic loci in tumour tissue. The highest frequency of allele loss (61%) was found with the probe YNZ22, which detects a sequence on the short arm of chromosome 17 (at p13.3). The previously reported loss of alleles at the Harvey ras locus (11p14) in about 20% of breast tumours was confirmed. The putative breast tumour suppressor gene on 17p may be the same as that already noted for colon and lung cancers and it is suggested that deletion of this gene is one of a cumulative series of lesions involving genetic changes in the evolution of breast cancer. The findings identify chromosome 17p as a candidate region for linkage studies in breast cancer families.

摘要

对一系列原发性乳腺癌患者的肿瘤和血液白细胞DNA进行检测,以探测肿瘤组织中六个多态性位点的缺失情况。使用检测17号染色体短臂(p13.3处)序列的探针YNZ22时,发现等位基因缺失的频率最高(61%)。此前报道约20%的乳腺肿瘤中哈维ras基因座(11p14)存在等位基因缺失,这一情况得到了证实。17号染色体短臂上推测的乳腺肿瘤抑制基因可能与结肠癌和肺癌中已发现的相同,有人提出该基因的缺失是乳腺癌发展过程中涉及基因改变的一系列累积性病变之一。这些发现确定17号染色体短臂是乳腺癌家族连锁研究的一个候选区域。

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