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通过荧光原位杂交检测p53缺失作为尿路上皮肿瘤的遗传标志物

p53 deletion as a genetic marker in urothelial tumor by fluorescence in situ hybridization.

作者信息

Matsuyama H, Pan Y, Mahdy E A, Malmström P U, Hedrum A, Uhlen M, Busch C, Hirano T, Auer G, Tribukait B

机构信息

Department of Urology, Karolinska Hospital, Stockholm, Sweden.

出版信息

Cancer Res. 1994 Dec 1;54(23):6057-60.

PMID:7954445
Abstract

In order to investigate the significance of p53 deletion, 42 specimens of transitional cell carcinoma were analyzed by interphase cytogenetics with a fluorescence in situ hybridization technique and compared with clinicopathological and cytochemical parameters. In total, 27 (64%) and 16 (38%) specimens demonstrated p53 deletion and overexpression, respectively. The p53 deletion was significantly correlated with grade (P < 0.01), stage (P < 0.05), S-phase fraction (P < 0.05), and DNA ploidy (P < 0.01), while p53 overexpression correlated only with grade (P < 0.05). The close correlation of p53 deletion with clinicopathological parameters suggests p53 deletion to be of clinical importance to indicate the malignant potential of human urothelial tumors.

摘要

为了研究p53缺失的意义,采用荧光原位杂交技术通过间期细胞遗传学分析了42例移行细胞癌标本,并与临床病理和细胞化学参数进行比较。总共27例(64%)和16例(38%)标本分别显示p53缺失和过表达。p53缺失与分级(P<0.01)、分期(P<0.05)、S期分数(P<0.05)和DNA倍体(P<0.01)显著相关,而p53过表达仅与分级相关(P<0.05)。p53缺失与临床病理参数的密切相关性表明p53缺失对于指示人类尿路上皮肿瘤的恶性潜能具有临床重要性。

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