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肾细胞癌的细胞遗传学分析:与肿瘤侵袭性的相关性

Cytogenetic analysis in renal cell carcinoma: correlation with tumor aggressiveness.

作者信息

Weaver D J, Michalski K, Miles J

机构信息

Department of Surgery, University of Missouri Medical Center.

出版信息

Cancer Res. 1988 May 15;48(10):2887-9.

PMID:3359445
Abstract

Twenty-eight tissue specimens from 26 patients with renal cell carcinoma were subjected to cytogenetic analysis using a newly developed combined method of enzymatic technique and short term tissue culture. Of the 28 tumor samples studied, 21 were chromosomally abnormal. Four (including two oncocytomas) were normal, and three did not grow in tissue culture. Of the 21 tumors with abnormal chromosomes, the most frequent abnormality was either trisomy or tetrasomy of chromosome 7 (18 of 21 tumors). In four of these tumors, trisomy 7 was the only visible abnormality. Ten tumors contained abnormalities of chromosome 3. Three showed a previously reported chromosome 3 interstitial deletion, five were hyperdiploid, and two revealed a monosomy 3. Of these 10 patients, six have had disease progression, compared to one of the 16 remaining patients without an abnormal chromosome 3. These data suggest that abnormalities of chromosome 7 represent a primary abnormality, and that when these abnormalities are present in association with abnormalities involving chromosome 3, they may correlate with a more aggressive clinical course and a corresponding higher stage of disease at diagnosis.

摘要

采用一种新开发的酶技术与短期组织培养相结合的方法,对26例肾细胞癌患者的28个组织标本进行了细胞遗传学分析。在所研究的28个肿瘤样本中,21个存在染色体异常。4个(包括2个嗜酸细胞瘤)正常,3个在组织培养中未生长。在21个染色体异常的肿瘤中,最常见的异常是7号染色体三体或四体(21个肿瘤中有18个)。在其中4个肿瘤中,7号染色体三体是唯一可见的异常。10个肿瘤存在3号染色体异常。3个显示先前报道的3号染色体间质缺失,5个为超二倍体,2个显示3号染色体单体。在这10例患者中,6例出现疾病进展,而其余16例3号染色体无异常的患者中有1例出现疾病进展。这些数据表明,7号染色体异常代表一种原发性异常,当这些异常与涉及3号染色体的异常同时存在时,它们可能与更具侵袭性的临床病程以及诊断时相应更高的疾病分期相关。

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