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17p13和9p21区域遗传事件的分析支持多灶性复发性膀胱癌主要为单克隆起源。

Analysis of genetic events in 17p13 and 9p21 regions supports predominant monoclonal origin of multifocal and recurrent bladder cancer.

作者信息

Trkova Marie, Babjuk Marko, Duskova Jaroslava, Benesova-Minarikova Lucie, Soukup Viktor, Mares Jaroslav, Minarik Marek, Sedlacek Zdenek

机构信息

Institute of Biology and Medical Genetics, Charles University Second Medical School, V uvalu 84, 15006 Prague, Czech Republic.

出版信息

Cancer Lett. 2006 Oct 8;242(1):68-76. doi: 10.1016/j.canlet.2005.10.036. Epub 2005 Dec 15.

Abstract

Clonality was tested in 86 tumours from 25 patients with recurrent and multifocal superficial bladder transitional cell carcinomas (TCCs) using the analysis of TP53 mutations and of LOH in the 17p13 and 9p21 regions. Tumours from the majority of individuals showed either absence or presence of the same TP53 mutation and/or an identical LOH pattern, with the same allele lost in all tumours. Only two pairs of tumours from two patients had discordant findings, which were incompatible with monoclonality. Therefore, our results rather support the monoclonal model of development of highly recurrent superficial bladder TCCs.

摘要

运用对TP53突变以及17p13和9p21区域杂合性缺失(LOH)的分析,对25例复发性多灶性浅表性膀胱移行细胞癌(TCC)患者的86个肿瘤进行了克隆性检测。大多数个体的肿瘤显示不存在或存在相同的TP53突变和/或相同的LOH模式,所有肿瘤中丢失的是相同的等位基因。只有两名患者的两对肿瘤有不一致的结果,这与单克隆性不相符。因此,我们的结果更支持高度复发性浅表性膀胱TCC的单克隆发展模型。

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