Literature DB >> 9144901

Molecular and immunopathology studies of oncogenes and tumor-suppressor genes in bladder cancer.

C Cordon-Cardo1, J Sheinfeld.   

Abstract

Target genes implicated in cellular transformation and tumor progression have been divided into two categories: proto-oncogenes (that when activated become dominant events characterized by gain of function) and tumor-suppressor genes (recessive events characterized by the loss of function). Alterations in proto-oncogenes and tumor-suppressor genes seem equally prevalent among human cancers. Multiple mutations appear to be required to conform the malignant phenotype. It is therefore conceivable that cancer be viewed fundamentally as a genetic disease entailing inherited (also called germ-line) and/or acquired (also termed somatic) mutations of genes in these two categories. Molecular studies of bladder neoplasms have identified a series of nonrandom genetic alterations affecting a particular set of oncogenes and tumor-suppressor genes. Because the modality of therapy for patients with bladder neoplasms primarily depends on morphological evaluation and clinical staging, the diagnosis carries significant consequences. However, it is well known that morphologically similar tumors presenting in any assigned stage may behave in radically different fashions, which seriously hampers the physician's ability accurately to predict clinical behavior in a given case. Recent studies have shown that inactivation of certain tumor-suppressor genes, such as RB and TP53, occur in bladder tumors that have a more aggressive clinical outcome and poor prognosis. In the present paper we review the molecular abnormalities associated with these dominant and recessive genes in bladder cancer and discuss the potential clinical use of their detection. The implementation of objective predictive assays to identify these alterations in clinical material will enhance our ability to assess tumor biological activities and to design effective treatment regimens. The need now is to translate this newly developed scientific knowledge into diagnostic and therapeutic strategies, which in turn will enhance the quality of life and prolong the survival of patients with bladder cancer.

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Year:  1997        PMID: 9144901     DOI: 10.1007/bf02201982

Source DB:  PubMed          Journal:  World J Urol        ISSN: 0724-4983            Impact factor:   4.226


  69 in total

1.  Ha-ras codon 12 mutation in papillary tumors of the urinary-bladder - a retrospective study.

Authors:  A Ooi; F Herz; S Ii; C Cordoncardo; Y Fradet; B Mayall
Journal:  Int J Oncol       Date:  1994-01       Impact factor: 5.650

2.  Clinical implications of the expression of epidermal growth factor receptors in human transitional cell carcinoma.

Authors:  E M Messing
Journal:  Cancer Res       Date:  1990-04-15       Impact factor: 12.701

3.  Amplification of a gene encoding a p53-associated protein in human sarcomas.

Authors:  J D Oliner; K W Kinzler; P S Meltzer; D L George; B Vogelstein
Journal:  Nature       Date:  1992-07-02       Impact factor: 49.962

4.  Genetic alterations in bladder cancer.

Authors:  G Dalbagni; J Presti; V Reuter; W R Fair; C Cordon-Cardo
Journal:  Lancet       Date:  1993-08-21       Impact factor: 79.321

5.  An immunohistologic evaluation of C-erbB-2 gene product in patients with urinary bladder carcinoma.

Authors:  K Sato; M Moriyama; S Mori; M Saito; T Watanuki; K Terada; E Okuhara; T Akiyama; K Toyoshima; T Yamamoto
Journal:  Cancer       Date:  1992-11-15       Impact factor: 6.860

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

Authors:  Y C Tsai; P W Nichols; A L Hiti; Z Williams; D G Skinner; P A Jones
Journal:  Cancer Res       Date:  1990-01-01       Impact factor: 12.701

7.  Association of P53 nuclear overexpression and tumor progression in carcinoma in situ of the bladder.

Authors:  A S Sarkis; G Dalbagni; C Cordon-Cardo; J Melamed; Z F Zhang; J Sheinfeld; W R Fair; H W Herr; V E Reuter
Journal:  J Urol       Date:  1994-08       Impact factor: 7.450

8.  Epidermal-growth-factor receptors in human bladder cancer: comparison of invasive and superficial tumours.

Authors:  D E Neal; C Marsh; M K Bennett; P D Abel; R R Hall; J R Sainsbury; A L Harris
Journal:  Lancet       Date:  1985-02-16       Impact factor: 79.321

9.  Over-expression of p53 nuclear oncoprotein in transitional-cell bladder cancer and its prognostic value.

Authors:  P K Lipponen
Journal:  Int J Cancer       Date:  1993-02-01       Impact factor: 7.396

10.  Nuclear overexpression of p53 protein in transitional cell bladder carcinoma: a marker for disease progression.

Authors:  A S Sarkis; G Dalbagni; C Cordon-Cardo; Z F Zhang; J Sheinfeld; W R Fair; H W Herr; V E Reuter
Journal:  J Natl Cancer Inst       Date:  1993-01-06       Impact factor: 13.506

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  2 in total

1.  Urinary bladder transitional cell carcinogenesis is associated with down-regulation of NF1 tumor suppressor gene in vivo and in vitro.

Authors:  V Aaltonen; P J Boström; K O Söderström; O Hirvonen; J Tuukkanen; M Nurmi; M Laato; J Peltonen
Journal:  Am J Pathol       Date:  1999-03       Impact factor: 4.307

Review 2.  Molecular Oncology of Bladder Cancer from Inception to Modern Perspective.

Authors:  Soum D Lokeshwar; Maite Lopez; Semih Sarcan; Karina Aguilar; Daley S Morera; Devin M Shaheen; Bal L Lokeshwar; Vinata B Lokeshwar
Journal:  Cancers (Basel)       Date:  2022-05-24       Impact factor: 6.575

  2 in total

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