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家族性和散发性脊索瘤中的一个肿瘤抑制基因座定位于1p36。

A tumor suppressor locus in familial and sporadic chordoma maps to 1p36.

作者信息

Miozzo M, Dalprà L, Riva P, Volontà M, Macciardi F, Pericotti S, Tibiletti M G, Cerati M, Rohde K, Larizza L, Fuhrman Conti A M

机构信息

Department of Biology and Genetics, Medical Faculty, University of Milan, Milan, Italy.

出版信息

Int J Cancer. 2000 Jul 1;87(1):68-72.

Abstract

Previous cytogenetic/FISH data have demonstrated 1p36 deletions in a relapsing familial clivus chordoma developed by a patient who has 2 daughters, respectively affected with childhood astrocytoma and clivus chordoma. Using an approach that combined the LOH (loss of heterozygosity) study of the father chordoma and the daughter astrocytoma and a segregation analysis from parents to sibs using 17 CA-repeats spanning 1p36.32-1p36.11, we mapped the cancer susceptibility locus in this family to the 1p36 region. The LOH and haplotype information was elaborated using a pairwise linkage analysis that gave a maximum lod score of 1.2. Additional LOH data relating to 6 sporadic chordomas allowed us to define an SRO (the smallest region of overlapping loss) of about 25 cM from D1S2845 (1p36.31) to D1S2728 (1p36.13). Our overall findings converge on mapping to 1p36 a tumor-suppressor gene involved in familial and sporadic chordoma.

摘要

先前的细胞遗传学/荧光原位杂交(FISH)数据显示,一名患有脊索瘤的患者复发的家族性斜坡脊索瘤存在1p36缺失,该患者有两个女儿,分别患有儿童星形细胞瘤和斜坡脊索瘤。我们采用了一种方法,将父亲脊索瘤和女儿星形细胞瘤的杂合性缺失(LOH)研究与使用跨越1p36.32 - 1p36.11的17个CA重复序列从父母到同胞的分离分析相结合,从而将这个家族中的癌症易感基因座定位到1p36区域。通过成对连锁分析阐述了LOH和单倍型信息,该分析给出的最大对数优势分数为1.2。另外6例散发性脊索瘤的LOH数据使我们能够确定一个约25厘摩的最小重叠缺失区域(SRO),范围从D1S2845(1p36.31)到D1S2728(1p36.13)。我们的总体研究结果集中在将一个与家族性和散发性脊索瘤相关的肿瘤抑制基因定位到1p36。

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