Chromosomal changes in uroepithelial carcinomas.

Imad Fadl-Elmula
{"title":"Chromosomal changes in uroepithelial carcinomas.","authors":"Imad Fadl-Elmula","doi":"10.1186/1475-9268-4-1","DOIUrl":null,"url":null,"abstract":"<p><p>This article reviews and summarizes chromosomal changes responsible for the initiation and progression of uroepithelial carcinomas. Characterization of these alterations may lead to a better understanding of the genetic mechanisms and open the door for molecular markers that can be used for better diagnosis and prognosis of the disease. Such information might even help in designing new therapeutic strategies geared towards prevention of tumor recurrences and more aggressive approach in progression-prone cases. The revision of 205 cases of uroepithelial carcinomas reported with abnormal karyotypes showed karyotypic profile characterized by nonrandom chromosomal aberrations varying from one or few changes in low-grade and early stage tumors to massively rearranged karyotypes in muscle invasive ones. In general, the karyotypic profile was dominated by losses of chromosomal material seen as loss of entire chromosome and/or deletions of genetic materials. Rearrangements of chromosome 9 resulting in loss of material from 9p, 9q, or of the entire chromosome were the most frequent cytogenetic alterations, seen in 45% of the cases. Whereas loss of material from chromosome arms 1p, 8p, and 11p, and gains of chromosome 7, and chromosome arm 1q, and 8q seem to be an early, but secondary, changes appearing in superficial and well differentiated tumors, the formation of an isochromosome for 5p and loss of material from 17p are associated with more aggressive tumor phenotypes. Upper urinary tract TCCs have identical karyotypic profile to that of bladder TCCs, indicating the same pathogenetic mechanisms are at work in both locales. Intratumor cytogenetic heterogeneity was not seen except in a few post-radiation uroepithelial carcinomas in which distinct karyotypic and clonal pattern were characterized by massive intratumor heterogeneity (cytogenetic polyclonality) with near-diploid clones and simple balanced and/or unbalanced translocations. In the vast majority of cases strong correlation between the tumors grade/stage and karyotypic complexity was seen, indicating that progressive accumulation of acquired genetic alterations is the driving force behind multistep bladder TCC carcinogenesis. Although most of these cytogenetic alterations have been identified for many years, the molecular consequences and relevant cancer genes of these alterations have not yet been identified. However, loss of TSG(s) from chromosome 9 seems to be the primary and important event(s) in uroepithelial carcinogenesis.</p>","PeriodicalId":84415,"journal":{"name":"Cell & chromosome","volume":"4 ","pages":"1"},"PeriodicalIF":0.0000,"publicationDate":"2005-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/1475-9268-4-1","citationCount":"63","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell & chromosome","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/1475-9268-4-1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 63

Abstract

This article reviews and summarizes chromosomal changes responsible for the initiation and progression of uroepithelial carcinomas. Characterization of these alterations may lead to a better understanding of the genetic mechanisms and open the door for molecular markers that can be used for better diagnosis and prognosis of the disease. Such information might even help in designing new therapeutic strategies geared towards prevention of tumor recurrences and more aggressive approach in progression-prone cases. The revision of 205 cases of uroepithelial carcinomas reported with abnormal karyotypes showed karyotypic profile characterized by nonrandom chromosomal aberrations varying from one or few changes in low-grade and early stage tumors to massively rearranged karyotypes in muscle invasive ones. In general, the karyotypic profile was dominated by losses of chromosomal material seen as loss of entire chromosome and/or deletions of genetic materials. Rearrangements of chromosome 9 resulting in loss of material from 9p, 9q, or of the entire chromosome were the most frequent cytogenetic alterations, seen in 45% of the cases. Whereas loss of material from chromosome arms 1p, 8p, and 11p, and gains of chromosome 7, and chromosome arm 1q, and 8q seem to be an early, but secondary, changes appearing in superficial and well differentiated tumors, the formation of an isochromosome for 5p and loss of material from 17p are associated with more aggressive tumor phenotypes. Upper urinary tract TCCs have identical karyotypic profile to that of bladder TCCs, indicating the same pathogenetic mechanisms are at work in both locales. Intratumor cytogenetic heterogeneity was not seen except in a few post-radiation uroepithelial carcinomas in which distinct karyotypic and clonal pattern were characterized by massive intratumor heterogeneity (cytogenetic polyclonality) with near-diploid clones and simple balanced and/or unbalanced translocations. In the vast majority of cases strong correlation between the tumors grade/stage and karyotypic complexity was seen, indicating that progressive accumulation of acquired genetic alterations is the driving force behind multistep bladder TCC carcinogenesis. Although most of these cytogenetic alterations have been identified for many years, the molecular consequences and relevant cancer genes of these alterations have not yet been identified. However, loss of TSG(s) from chromosome 9 seems to be the primary and important event(s) in uroepithelial carcinogenesis.

Abstract Image

Abstract Image

Abstract Image

尿上皮癌的染色体改变。
本文综述了尿上皮癌发生和发展的染色体变化。这些改变的特征可能会导致更好地了解遗传机制,并为分子标记打开大门,可用于更好地诊断和预后疾病。这些信息甚至可能有助于设计新的治疗策略,以预防肿瘤复发,并在进展倾向的病例中采用更积极的方法。对205例泌尿上皮癌核型异常病例的修正显示,其核型特征为非随机染色体畸变,从低级别和早期肿瘤的一个或几个变化到肌肉侵袭性肿瘤的大量重排核型。总的来说,核型特征主要是染色体物质的损失,被视为整个染色体的损失和/或遗传物质的缺失。9号染色体重排导致9p、9q或整个染色体的物质丢失是最常见的细胞遗传学改变,占45%。尽管染色体臂1p、8p和11p的物质丢失,以及染色体臂7、1q和8q的获得似乎是早期的继发性变化,出现在浅表和分化良好的肿瘤中,但5p同工染色体的形成和17p同工染色体的物质丢失与更具侵袭性的肿瘤表型相关。上尿路tcc与膀胱tcc具有相同的核型特征,这表明在这两个部位有相同的发病机制。肿瘤内细胞遗传学异质性未见,除了在少数放射后尿上皮癌中,其独特的核型和克隆模式以大量肿瘤内异质性(细胞遗传学多克隆)为特征,具有近二倍体克隆和简单的平衡和/或不平衡易位。在绝大多数病例中,肿瘤分级/分期与核型复杂性之间存在很强的相关性,表明获得性遗传改变的渐进式积累是膀胱TCC多阶段癌变的驱动力。尽管这些细胞遗传学改变中的大多数已经被发现多年,但这些改变的分子后果和相关的癌症基因尚未被确定。然而,9号染色体上TSG的缺失似乎是尿上皮癌发生的主要和重要事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信