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8号染色体短臂、9号染色体短臂和14号染色体长臂杂合性缺失与非乳头状肾细胞癌的分期和分级相关。

Loss of heterozygosity at chromosomes 8p, 9p, and 14q is associated with stage and grade of non-papillary renal cell carcinomas.

作者信息

Schullerus D, Herbers J, Chudek J, Kanamaru H, Kovacs G

机构信息

Department of Urology, Ruprecht-Karls-University, Heidelberg, Germany.

出版信息

J Pathol. 1997 Oct;183(2):151-5. doi: 10.1002/(SICI)1096-9896(199710)183:2<151::AID-PATH928>3.0.CO;2-R.

Abstract

In this study, 105 non-papillary renal cell carcinomas (RCCs) have been examined for allelic loss at the chromosome 8p12-21.1, 9p21, and 14q24.2-qter regions, each by two highly polymorphic microsatellites. Loss of heterozygosity (LOH) was detected at both chromosome 8p and 9p in 33 per cent of the cases and at chromosome 14q in 45 per cent of the tumours. A correlation of variables such as size, grade, and stage of tumours with these specific genetic alterations showed that loss of chromosomes 8p and 9p, and especially loss of chromosome 14q regions, is significantly associated with a higher grade of tumour and the combined LOH at these chromosomal sites with advanced tumour stage. These genetic alterations did not show any correlation with the size of non-papillary RCCs. This study suggests that genetic markers at the above-mentioned chromosomal sites can predict the clinical outcome of non-papillary RCCs.

摘要

在本研究中,对105例非乳头状肾细胞癌(RCC)进行了检测,通过两个高度多态性微卫星分别检测8号染色体p12 - 21.1、9号染色体p21以及14号染色体q24.2 - qter区域的等位基因缺失情况。在33%的病例中检测到8号染色体p臂和9号染色体p臂杂合性缺失(LOH),在45%的肿瘤中检测到14号染色体q臂杂合性缺失。肿瘤的大小、分级和分期等变量与这些特定基因改变的相关性表明,8号染色体p臂和9号染色体p臂缺失,尤其是14号染色体q区域缺失,与肿瘤分级较高显著相关,并且这些染色体位点的联合杂合性缺失与肿瘤晚期相关。这些基因改变与非乳头状肾细胞癌的大小没有任何相关性。本研究表明,上述染色体位点的基因标志物可以预测非乳头状肾细胞癌的临床结局。

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