Literature DB >> 29428551

Detection of Bladder Cancer in Urine Sediments by a Novel Multicolor Fluorescence In Situ Hybridization (Quartet) Test.

Shizhen Zhang1, Yan Wang1, Jolanta Bondaruk1, Tadeusz Majewski1, Hui Yao2, Sangkyou Lee1, June Goo Lee1, David Cogdell1, Yair Lotan3, Colin Dinney4, Peng Wei2, Keith Baggerly2, Bogdan Czerniak5.   

Abstract

BACKGROUND: Bladder cancer is among the common human malignancies that show a heavy mutational load and copy number variations of numerous chromosomes, which makes them a target for diagnostic explorations.
OBJECTIVE: We aimed to design a multicolor fluorescence in situ hybridization (FISH) test referred to as the quartet test for the detection of bladder cancer in urine. DESIGN, SETTING, AND PARTICIPANTS: We performed genome-wide copy number variation analysis on cohorts from the University of Texas MD Anderson Cancer Center (n=40) and The Cancer Genome Atlas (n=129), and identified the most frequently amplified chromosomal regions. These data were used to select four of the amplified regions to design a multicolor FISH test, referred to as the quartet test. Assay validation was performed on urine samples from 98 patients with bladder cancer: 56 with low-grade papillary, 42 with high-grade invasive disease, and 48 benign controls. INTERVENTION: The quartet test can be used in clinical practice for noninvasive detection of bladder cancer. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: We initially analyzed samples using a fraction of abnormal cell scores and then by the quantitative score, which included not only the proportion of cells with abnormal copy numbers, but also the proportion of cells with numbers of altered copies and degree of amplification. We used receiver operator characteristic (ROC) curves to identify cutoff values for the scores at which performances of sensitivity and specificity were maximized. RESULTS AND LIMITATIONS: The copy number status assessed by probes detected in voided urine reflected the amplification status of the primary tumor. An ROC curve summarizing the proportion of assayed cells with any abnormal copy numbers gave specificity of 93.8% and sensitivity of 78.6% using the proportion of cells with abnormal copy numbers. The quantitative score giving extra weight to cells with multiple simultaneous amplifications provided 95.8% specificity and 76.8% sensitivity. Both percentage of abnormal cells and quantitative scores were highly effective for assessing the grade of the tumor. The full spectrum of potential clinical applications was not explored in the current study, and further validation studies are needed.
CONCLUSIONS: The quartet test shows promising specificity and sensitivity results, but it requires validation on a larger multi-institutional cohort of samples. PATIENT
SUMMARY: The quartet test can be used for noninvasive detection of bladder cancer in voided urine. It can also be used to assess the grade of the tumor and tumor recurrence as well as post-treatment effects.
Copyright © 2018 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Bladder tumor; Copy number variation; Fluorescence in situ hybridization

Year:  2018        PMID: 29428551      PMCID: PMC6081265          DOI: 10.1016/j.euf.2018.01.017

Source DB:  PubMed          Journal:  Eur Urol Focus        ISSN: 2405-4569


  35 in total

1.  Automation of fluorescence in situ hybridization pretreatment: a comparative study of different sample types.

Authors:  K Jacobson; A Thompson; G Browne; C Shasserre; S A Seelig; W King
Journal:  Mol Diagn       Date:  2000-09

Review 2.  Focus on bladder cancer.

Authors:  Colin P N Dinney; David J McConkey; Randall E Millikan; Xifeng Wu; Menashe Bar-Eli; Liana Adam; Ashish M Kamat; Arlene O Siefker-Radtke; Tomasz Tuziak; Anita L Sabichi; H Barton Grossman; William F Benedict; Bogdan Czerniak
Journal:  Cancer Cell       Date:  2004-08       Impact factor: 31.743

Review 3.  Aneuploidy in bladder cancers: the utility of fluorescent in situ hybridization in clinical practice.

Authors:  John L Phillips; Ingrid C Richardson
Journal:  BJU Int       Date:  2006-07       Impact factor: 5.588

4.  Aberrant promoter methylation profile of bladder cancer and its relationship to clinicopathological features.

Authors:  R Maruyama; S Toyooka; K O Toyooka; K Harada; A K Virmani; S Zöchbauer-Müller; A J Farinas; F Vakar-Lopez; J D Minna; A Sagalowsky; B Czerniak; A F Gazdar
Journal:  Cancer Res       Date:  2001-12-15       Impact factor: 12.701

5.  Frequent genetic alterations in flat urothelial hyperplasias and concomitant papillary bladder cancer as detected by CGH, LOH, and FISH analyses.

Authors:  E C Obermann; K Junker; R Stoehr; W Dietmaier; D Zaak; J Schubert; F Hofstaedter; R Knuechel; A Hartmann
Journal:  J Pathol       Date:  2003-01       Impact factor: 7.996

6.  The development of a multitarget, multicolor fluorescence in situ hybridization assay for the detection of urothelial carcinoma in urine.

Authors:  I A Sokolova; K C Halling; R B Jenkins; H M Burkhardt; R G Meyer; S A Seelig; W King
Journal:  J Mol Diagn       Date:  2000-08       Impact factor: 5.568

7.  Genetic modeling of human urinary bladder carcinogenesis.

Authors:  B Czerniak; L Li; V Chaturvedi; J Y Ro; D A Johnston; S Hodges; W F Benedict
Journal:  Genes Chromosomes Cancer       Date:  2000-04       Impact factor: 5.006

8.  Chromosomal abnormalities in macroscopically normal urothelium in patients with bladder pT1 and pT2a urothelial carcinoma: a fluorescence in situ hybridization study and correlation with histologic features.

Authors:  Roberta Mazzucchelli; Francesca Barbisan; Daniela Stramazzotti; Rodolfo Montironi; Antonio Lopez-Beltran; Marina Scarpelli
Journal:  Anal Quant Cytol Histol       Date:  2005-06       Impact factor: 0.302

9.  Understanding the development of human bladder cancer by using a whole-organ genomic mapping strategy.

Authors:  Tadeusz Majewski; Sangkyou Lee; Joon Jeong; Dong-Sup Yoon; Andrzej Kram; Mi-Sook Kim; Tomasz Tuziak; Jolanta Bondaruk; Sooyong Lee; Weon-Seo Park; Kuang S Tang; Woonbok Chung; Lanlan Shen; Saira S Ahmed; Dennis A Johnston; H Barton Grossman; Colin P Dinney; Jain-Hua Zhou; R Alan Harris; Carrie Snyder; Slawomir Filipek; Steven A Narod; Patrice Watson; Henry T Lynch; Adi Gazdar; Menashe Bar-Eli; Xifeng F Wu; David J McConkey; Keith Baggerly; Jean-Pierre Issa; William F Benedict; Steven E Scherer; Bogdan Czerniak
Journal:  Lab Invest       Date:  2008-05-05       Impact factor: 5.662

10.  Forerunner genes contiguous to RB1 contribute to the development of in situ neoplasia.

Authors:  Sangkyou Lee; Joon Jeong; Tadeusz Majewski; Steven E Scherer; Mi-Sook Kim; Tomasz Tuziak; Kuang S Tang; Keith Baggerly; Herbert Barton Grossman; Jain-Hua Zhou; Lanlan Shen; Jolanta Bondaruk; Saira S Ahmed; Susmita Samanta; Philippe Spiess; Xifeng Wu; Slawomir Filipek; David McConkey; Menashe Bar-Eli; Jean-Pierre Issa; William F Benedict; Bogdan Czerniak
Journal:  Proc Natl Acad Sci U S A       Date:  2007-08-16       Impact factor: 11.205

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  1 in total

1.  Low-Coverage Sequencing of Urine Sediment DNA for Detection of Copy Number Aberrations in Bladder Cancer.

Authors:  Yun-Xi Cai; Xu Yang; Ya-Wen Xu; Sheng Lin; Shan-Wen Zhu; Dong-Mei Fan; Min Zhao; Yuan-Bin Zhang; Xue-Xi Yang; Xin Li
Journal:  Cancer Manag Res       Date:  2021-02-26       Impact factor: 3.989

  1 in total

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