Simon R, Bürger H, Brinkschmidt C, Böcker W, Hertle L, Terpe H J
Gerhard-Domagk-Institute of Pathology, University of Münster, Germany.
J Pathol. 1998 Aug;185(4):345-51. doi: 10.1002/(SICI)1096-9896(199808)185:4<345::AID-PATH109>3.0.CO;2-0.
Non-invasive and invasive papillary transitional cell carcinomas of stages pTa and pT1 represent the first steps of tumour progression in bladder cancer. In order to analyse different chromosomal alterations of pTa and pT1 superficial bladder cancer, 46 tumour specimens were examined by comparative genomic hybridization (CGH). Losses of chromosome 9 material (11/20) and gains of chromosome 17 material (6/20) were frequently found in pTa tumours. Stage pT1 tumours were characterized by gains of chromosome 1q (14/26; including amplification at 1q21-q24 in three cases) and chromosome 17 material (15/26), as well as by losses of 11p (15/26) and 11q (13/26). Other loci frequently showing losses in pT1 tumours were 2q (9/26), 4q (10/26), 5q (9/26), 8p (10/26), 9p (9/26), 9q (12/26), 10q (8/26), 17p (7/26), and 18q (8/26). Amplifications were detected at 8q21/22, 5q21, 7q36, 10p14, 10p12, 10q25, 12q12, and 12q14. The most striking differences between grade 2 pTa and pT1 tumours were gains of 1q (P < 0.01) and losses at 2q (P < 0.025), 10q (P < 0.05), 11p (P < 0.01), 11q (P < 0.01), and 17p (P < 0.05), as well as the total number of aberrations (pTa grade 2: 4.1; pT1 grade 2: 8.6 aberrations per tumour). These data show characteristic chromosomal aberrations associated with invasion in superficial bladder cancer.
pTa期和pT1期的非侵袭性和侵袭性乳头状移行细胞癌是膀胱癌肿瘤进展的第一步。为了分析pTa期和pT1期浅表性膀胱癌的不同染色体改变,采用比较基因组杂交(CGH)技术检测了46例肿瘤标本。pTa期肿瘤中经常发现9号染色体物质缺失(11/20)和17号染色体物质增加(6/20)。pT1期肿瘤的特征是1号染色体增加(14/26;包括3例1q21 - q24扩增)和17号染色体物质增加(15/26),以及11p缺失(15/26)和11q缺失(13/26)。pT1期肿瘤中其他经常出现缺失的位点有2q(9/26)、4q(10/26)、5q(9/26)、8p(10/26)、9p(9/26)、9q(12/26)、10q(8/26)、17p(7/26)和18q(8/26)。在8q21/22、5q21、7q36、10p14、10p12、10q25、12q12和12q14检测到扩增。2级pTa期和pT1期肿瘤最显著的差异是1号染色体增加(P < 0.01)以及2q(P < 0.025)、10q(P < 0.05)、11p(P < 0.01)、11q(P < 0.01)和17p(P < 0.05)缺失,以及畸变总数(2级pTa期:每个肿瘤4.1个畸变;2级pT1期:每个肿瘤8.6个畸变)。这些数据显示了浅表性膀胱癌中与侵袭相关的特征性染色体畸变。