No AccessJournal of UrologyInvestigative Urology1 Aug 1995Increased p53 Protein Does Not Correlate to p53 Gene Mutations in Microdissected Human Testicular Germ Cell Tumors Noah S. Schenkman, Isabell A. Sesterhenn, Lucille Washington, Yue Ao Tong, Christopher M. Weghorst, Gregory S. Buzard, Shiv Srivastava, and Judd W.* Moul Noah S. SchenkmanNoah S. Schenkman More articles by this author , Isabell A. SesterhennIsabell A. Sesterhenn More articles by this author , Lucille WashingtonLucille Washington More articles by this author , Yue Ao TongYue Ao Tong More articles by this author , Christopher M. WeghorstChristopher M. Weghorst More articles by this author , Gregory S. BuzardGregory S. Buzard More articles by this author , Shiv SrivastavaShiv Srivastava More articles by this author , and Judd W.* MoulJudd W.* Moul More articles by this author View All Author Informationhttps://doi.org/10.1016/S0022-5347(01)67122-2AboutFull TextPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail Abstract Purpose: To determine if primary testicular germ cell tumors that overexpress p53 tumor suppressor gene protein have p53 gene mutations. Materials and Methods: We examined 30 primary testicular tissues from 26 patients representing two groups. Group one consisted of eleven cases (6 nonseminomatous germ cell tumors and 5 seminomas) in which tissue samples for DNA analysis were microdissected from paraffin block regions with elevated immunohistochemical staining for p53 protein. Group two consisted of 19 testis tumor tissues which had been fresh frozen and were chosen to correspond to archival tissue specimens exhibiting elevated levels of p53 protein. The DNA was extracted from these tissues and subjected to exon specific amplification by polymerase chain reaction (PCR) and cold single-strand conformation polymorphism (Cold SSCP) analysis. Results: In these cases with elevated p53 protein, no p53 gene exon 5-8 mutations were detected except 1 seminoma with a codon 140 silent mutation (no protein alteration). Conclusions: Testicular tumors appear to exhibit elevated levels of wild-type p53 protein, the significance of which is yet to be elucidated. References 1 : Germ cell tumors of testis: prognostic factors and results. Eur. Urol.1990; 18: 242. Google Scholar 2 : Neoplasms of the testis. In: Campbell's Urology. 6th edition. Edited by . Philadelphia: W. B. Sanders Co.1992: 1222. Google Scholar 3 : Treatment of testicular cancer: a new and improved model. J. Clin. Oncol.1990; 8: 1777. Google Scholar 4 : Pitfalls in the management of testicular cancer patients and complications of therapy. In: Urology Annual. Edited by . New York: Norton1992: 161. Google Scholar 5 : Molecular biology of testicular cancer. In: Problems in Urology. Edited by . Phildelphia: Lippincott, vol. 8, no. 11994: 1. Google Scholar 6 : Clinical implications of p53 tumor-suppressor gene. N. Engl. J. Med.1993; 329: 1318. Google Scholar 7 : p53 protein alterations in human testicular cancer including pre-invasive intratubular germ-cell neoplasia. Int. J. Cancer1991; 49: 196. Google Scholar 8 : Evidence of wild and mutant type p53 in human germ cell tumors by histochemical staining. Tumordiagn. Ther.1992; 13: 213. Google Scholar 9 : Mutations of the p53 gene do not occur in testis cancer. Cancer Res.1993; 53: 3574. Google Scholar 10 : p53 gene mutations in Chinese human testicular seminoma. J. Urol.1993; 150: 884. Google Scholar 11 : No germline p53 mutations detected in familial and bilateral testicular cancer. Genes Chromosom. Cancer1993; 6: 92. Google Scholar 12 : p53 mutant gene expression in archival material of mature teratome of the testis. J. Urol., abstract1993; 149: 310A. Google Scholar 13 : The relationship of p53 PCNA and S-phase in nonseminomatous germ cell tumors. Lab Invest., abstract1993; 68: A71. Google Scholar 14 : Immunohistologic characterization of tumor proliferation and p53 expression in nonseminomatous germ cell tumors. Lab. Invest., abstract1993; 68: 69. Google Scholar 15 : Mutations of the p53 gene are not detectable in human testicular tumors. Mod. Pathol.1994; 7: 435. Google Scholar 16 : Identification of frequent p53 gene alterations in testicular cancer by in situ molecular genetic and immunohistochemical analysis. J. Urol., abstract1994; 151: 408A. Google Scholar 17 : Immunohistochemical expression of p53 tumor suppressor gene protein in adult germ testis tumors: clinical correlation in stage 1 disease. J. Urol.1994; 152: 418. Abstract, Google Scholar 18 : Frequent detection of codon 877 mutation in the androgen receptor gene in advanced prostate cancer. Cancer Res.1994; 54: 2861. Google Scholar 19 : Infrequent ras oncogene mutations in human prostate cancer. Prostate1992; 20: 327. Google Scholar 20 : Cold SSCP: a simple, rapid and non-radioactive method for optimized single-strand conformation allomorphism analyses. Nucleic Acids Res.1993; 21: 3637. Google Scholar 21 Heidenberg, H., Sesterhenn, I. A., Gaddipati, J., Weghorst, C., Buzard, G. S., Moul, J. W. and Srivastava, S.: Alterations of tumor suppressor gene p53 in a high fraction of treatment resistant prostate cancer. J. Urol., in press. Google Scholar 22 : Amplification of a gene encoding a p53 associated protein in human sarcomas. Nature1992; 358: 80. Google Scholar 23 : p53 mutations in breast cancer. Cancer Res.1992; 52: 5291. Google Scholar 24 : Two distinct mechanisms alter p53 in breast cancer: mutation and nuclear exclusion. Proc. Natl. Acad. Sci. U.S.A.1992; 89: 7262. Google Scholar 25 : Mutational hotspots due to sunlight in the p53 gene of nonmelanoma skin cancers. Proc. Natl. Acad. Sci. U.S.A.1993; 90: 4216. Google Scholar 26 : Mutation of p53 in primary biopsy material and cell lines from Hodgkins disease. Proc. Natl. Acad. Sci. U.S.A.1993; 90: 2817. Google Scholar 27 : p53 immunohistochemistry in malignant fibrous histiocytomas and other mesenchymal tumors. J. Pathol.1992; 168: 29. Google Scholar 28 : p53 mutations in human lymphoid malignancies: association with Burkitt lymphoma and chronic lymphocytic leukemia. Proc. Natl. Acad. Sci. U.S.A.1991; 88: 5413. Google Scholar 29 : p53 mutations and immunohistochemistry in AIDs-related lymphomas. Blood1993; 82: 920. Google Scholar 30 : High levels of p53 protein expression do not correlate with p53 gene mutations in CD30 (Ki-1) positive anaplastic large cell lymphoma. Am. J. Pathol.1993; 143: 1. Google Scholar 31 : Post-thymic T cell lymphomas frequently overexpress p53 protein but infrequently exhibit p53 gene mutations. Am. J. Pathol.1994; 144: 573. Google Scholar 32 : p53 protein expression in non-neoplastic lesions and benign and malignant neoplasms of soft tissue. Histopathology1993; 22: 45. Google Scholar 33 : Quantitation and characterization of a species-specific and embryo stage-dependent 55-kilodalton phosphoprotein also present in cells transformed by simian virus 40. Proc. Natl. Acad. Sci. U.S.A.1981; 78: 6953. Google Scholar 34 : Regulation of the p53 tumor antigen in teratocarcinoma cells and their differentiated progeny. Mol. Cell. Biol.1982; 2: 443. Google Scholar 35 : Cellular oncogenes in human teratocarcinoma cell lines. Int. J. Androl.1990; 13: 377. Google Scholar 36 : The phosphoprotein p53 is down-regulated post-transcriptionally during embryogenesis in vertebrates. Biochem. Biophys. Acta1988; 950: 395. Google Scholar 37 : Testicular tissue-specific expression of the p53 suppressor gene. Devel. Biol.1993; 156: 107. Google Scholar 38 Lutzker, S. and Levine, A.: The regulation of p53 pf transcriptional activity in testicular teratocarcinomas (abstract). Fifth Meeting on the Molecular Basis of Cancer, Frederick, Maryland, June 1994. Google Scholar 39 : Germ-line transmission of a mutated p53 gene in cancerprone family with Li-Fraumeni syndrome. Nature1990; 348: 747. Google Scholar Urology Service, Department of Surgery, Walter Reed Army Medical Center, Washington, D.C., the Center for Prostate Disease Research, Uniformed Services University of the Health Sciences, Bethesda, Maryland, the Armed Forces Institute of Pathology, Washington, D.C., the Laboratory of Comparative Carcinogenesis, N.C.I., F.C.R.D.C., Frederick, Maryland and B.C.D.P., PRI/Dyn Corporation, Frederick, Maryland.© 1995 by American Urological Association, Inc.FiguresReferencesRelatedDetailsCited byMoul J (2018) Molecular Genetics of Testicular CancerJournal of Urology, VOL. 157, NO. 5, (1552-1553), Online publication date: 1-May-1997.Sandberg A, Meloni A and Suijkerbuijk R (2018) Reviews of Chromosome Studies in Urological Tumors. III. Cytogenetics and Genes in Testicular TumorsJournal of Urology, VOL. 155, NO. 5, (1531-1556), Online publication date: 1-May-1996. Volume 154 Issue 2 August 1995 Page: 617-621 Advertisement Copyright & Permissions© 1995 by American Urological Association, Inc.Metrics Author Information Noah S. Schenkman More articles by this author Isabell A. Sesterhenn More articles by this author Lucille Washington More articles by this author Yue Ao Tong More articles by this author Christopher M. Weghorst More articles by this author Gregory S. Buzard More articles by this author Shiv Srivastava More articles by this author Judd W.* Moul More articles by this author Expand All Advertisement PDF downloadLoading ...
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