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8号染色体p12 - p22区域不存在家族性乳腺癌易感基因的证据。

Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22.

作者信息

Rahman N, Teare M D, Seal S, Renard H, Mangion J, Cour C, Thompson D, Shugart Y, Eccles D, Devilee P, Meijers H, Nathanson K L, Neuhausen S L, Weber B, Chang-Claude J, Easton D F, Goldgar D, Stratton M R

机构信息

Section of Cancer Genetics, ICR, Sutton, SM2 5NG, UK.

出版信息

Oncogene. 2000 Aug 24;19(36):4170-3. doi: 10.1038/sj.onc.1203735.

Abstract

Several recent studies indicate that the majority of families with five or fewer cases of breast cancer and no cases of ovarian cancer are not due to BRCA1 or BRCA2. It has been proposed that a further breast cancer susceptibility gene that may account for some of these families is located on chromosome 8p12-p22. We have identified 31 site-specific breast cancer families that have a greater than 80% posterior probability of being due to genes other than BRCA1 or BRCA2. These families have been examined for linkage to 8p12-p22 using markers flanking the putative location of the gene. The overall multi-point LOD score is strongly negative across the whole 44 cM. The individual multi-point LOD score is negative in 23 families and only exceeds 0.5 in a single family (with a multi-point LOD score of 1.22). The maximum heterogeneity LOD score was 0.03 at marker D8S136 with estimated proportion linked (alpha) of 3% (95% CI 0 - 30%). These data do not lend support to the hypothesis that chromosome 8p12-p22 harbours a familial breast cancer susceptibility gene. Oncogene (2000) 19, 4170 - 4173

摘要

最近的几项研究表明,大多数乳腺癌病例数为五例或更少且无卵巢癌病例的家族并非由BRCA1或BRCA2基因所致。有人提出,可能导致其中一些家族发病的另一种乳腺癌易感基因位于8号染色体的p12 - p22区域。我们已经确定了31个位点特异性乳腺癌家族,这些家族因BRCA1或BRCA2以外的基因导致发病的后验概率大于80%。利用该基因假定位置两侧的标记,对这些家族进行了与8p12 - p22区域的连锁分析。在整个44厘摩的区域内,总体多点对数优势分数呈强负值。23个家族的个体多点对数优势分数为负值,只有一个家族的分数超过0.5(多点对数优势分数为1.22)。在标记D8S136处,最大异质性对数优势分数为0.03,估计连锁比例(α)为3%(95%可信区间0 - 30%)。这些数据不支持8号染色体p12 - p22区域存在家族性乳腺癌易感基因这一假说。《癌基因》(2000年)第19卷,4170 - 4173页

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