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人类膀胱癌中9号、11号和17号染色体的等位基因缺失。

Allelic losses of chromosomes 9, 11, and 17 in human bladder cancer.

作者信息

Tsai Y C, Nichols P W, Hiti A L, Williams Z, Skinner D G, Jones P A

机构信息

Urologic Cancer Research Laboratory, Kenneth Norris Jr. Comprehensive Cancer Center, University of Southern California School of Medicine, Los Angeles 90033.

出版信息

Cancer Res. 1990 Jan 1;50(1):44-7.

PMID:2293558
Abstract

Twenty-five human bladder tumors were examined for loss of heterozygosity of markers on chromosomes 6p, 9q, 11p, 14q, and 17p. These studies show that all of the markers were reduced to homozygosity in at least some of the tumors. They also confirmed earlier studies by Fearon et al. [Nature (Lond.), 318: 377-380, 1985] that approximately 40% of bladder tumors were reduced to homozygosity for markers on chromosome 11p. However, the greatest frequency of allelic loss was seen for chromosomes 9q (67% of informative cases) and 17p (63% of informative cases) with both chromosomes being lost concordantly in 10 out of 20 informative tumors. Allelic loss of chromosome 9q has not been previously observed with other human cancers; however, deletions of 17p have been reported in breast, lung, and colorectal carcinomas. The data raise the interesting possibility that allelic losses of specific chromosomes might be a feature of cancer in a particular differentiated cell type whereas loss of other chromosomes harboring more generally acting tumor suppressor genes might be a common feature of human cancers.

摘要

对25例人类膀胱肿瘤进行了6号染色体短臂(6p)、9号染色体长臂(9q)、11号染色体短臂(11p)、14号染色体长臂(14q)和17号染色体短臂(17p)上标记杂合性缺失的检测。这些研究表明,至少在部分肿瘤中,所有标记均呈现纯合性。它们还证实了Fearon等人[《自然》(伦敦),318: 377 - 380,1985]早期的研究,即约40%的膀胱肿瘤11号染色体短臂上的标记呈现纯合性。然而,等位基因缺失频率最高的是9号染色体长臂(信息充分病例中的67%)和17号染色体短臂(信息充分病例中的63%),在20例信息充分的肿瘤中有10例这两条染色体同时缺失。9号染色体长臂的等位基因缺失在其他人类癌症中此前未见报道;不过,17号染色体短臂的缺失在乳腺癌、肺癌和结直肠癌中已有报道。这些数据提出了一个有趣的可能性,即特定染色体的等位基因缺失可能是特定分化细胞类型癌症的一个特征,而携带更具普遍作用的肿瘤抑制基因的其他染色体的缺失可能是人类癌症的一个共同特征

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