Distinct areas of allelic loss on chromosomal regions 10p and 10q in human prostate cancer

Cancer Research

Volumn 56, Issue 10, 1996, Pages 2263-2267

  Trybus, Tanya M ^a   Burgess, Ann C ^b   Wojno, Kirk J ^a,b   Glover, Thomas W ^b   Macoska, Jill A ^a,b  

^a UNIVERSITY OF MICHIGAN   (United States)

^b UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CANCER INVASION; CARCINOGENESIS; CHROMOSOME 10P; CHROMOSOME LOSS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE LOCATION; HUMAN; HUMAN CELL; MALE; METASTASIS POTENTIAL; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROGNOSIS; PROSTATE CANCER; TUMOR SUPPRESSOR GENE;

ALLELES; CHROMOSOMES, HUMAN, PAIR 10; ETHNIC GROUPS; GENE DELETION; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; NEOPLASM STAGING; POLYMERASE CHAIN REACTION; PROSTATIC NEOPLASMS; TUMOR CELLS, CULTURED;

EID: 0029975245     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (23)

1. Alkin, N. B , and Baker, M C. Chromosome study of five cancers of the prostate. Hum. Genet., 70: 359-364, 1985.
2. Lundgren, R., Mandahl, N., Heim, S., Limon, J., Henrikson, H., and Mitelman, F. Cytogenetic analysis of 57 primary prostatic adenocarcinomas. Genes Chromosomes & Cancer, 4: 16-24, 1992.
3. Arps, S., Rodewald, A., Schmalenberger, B., Carl, P., Bressel, M., and Kastendieck, H Cytogenetic survey of 32 cancers of the prostate. Cancer Genet. Cytogenet., 66: 93-99, 1993
4. Carter, B S., Ewing, C. M., Ward, W S , Treiger, B F., Aalders, T W., Schalken, J. A., Epstein, J I., and Isaacs, W B Allelic loss of chromosomes 16q and 10q in human prostate cancer. Proc Natl. Acad. Sci. USA, 87: 8751-8755, 1990
5. Bergerheim, U. S. R., Kunimi, K., Collins, V. P , and Ekman, P. Deletion mapping of chromosomes 8, 10 and 16 in human prostatic carcinoma Genes Chromosomes & Cancer, 3: 215-220, 1991.
6. Macoska, J. A., Micale, M. A., Sakr, W. A., Benson, P D., and Wolman, S. R. Extensive genetic alterations in prostate cancer revealed by dual PCR and FISH analysis. Genes Chromosomes & Cancer, 8: 88-97, 1993.
7. Sakr, W. A., Macoska, J. A., Benson, P. D., Grignon, D. J., Wolman, S. R., Pontes, J. E., and Crissman, J D. Allelic loss in locally metastatic, multisampled prostate cancer. Cancer Res., 54. 3273-3277, 1994.
8. Phillips, S. M. A , Morton, D. G., Lee, S. J., Wallace, D M A., and Neoptolemos, J. P. Loss of heteozygosity of the retinoblastoma and adenomatous polyposis susceptibility gene loci and in chromosomes 10p, 10q and 16q in human prostate cancer. Br. J. Urol., 73: 390-395, 1994
9. Gray, I. C , Phillipa, S. M. A., Lee, S. J., Neoptolemos, J. P., Weissenbach, J , and Spurr, N. K. Loss of the chromosomal region 10q23-25 in prostate cancer. Cancer Res., 55: 4800-4803, 1995.
10. Wolman, S. R , Macoska, J. A , Micale, M. A., and Sakr, W. A. An approach to definition of genetic alterations in prostate cancer. Diag. Mol. Pathol., 1: 192-199, 1992.
11. Macoska, J. A., Trybus, T. M., Benson, P. D., Sakr, W. A , Grignon, D J., Wojno, K. D., Pietruk, T., and Powell, I. J. Evidence for three tumor suppressor gene loci on chromosome 8p in human prostate cancer Cancer Res., 55: 5390-5395, 1995.
12. Meltzer, P. S., Guan, X-Y., Burgess, A., and Trent, J. M. Rapid generation of region specific probes by chromosome microdissection and their application. Nat. Genet., 1. 24-28, 1992.
13. Klever, M., Grond-Ginsbach, C , Scherthan, H., and Schroeder-Kurth, T M. Chromosomal in situ suppression hybridization after Giemsa banding Hum. Genet., 86: 484-486, 1991.
14. Stecik, P. A., Ligon, A. H., Cheong, P., Yung, W. K. A., and Pershouse M A. Two tumor suppressive loci on chromosome 10 involved in human glioblastomas. Genes Chromosomes & Cancer, 12: 255-261, 1995
15. von Deimling, A , von Ammon, K., Schoenfeld, D., Wiestler, O D., Seizinger, B. R., and Louis, D. N Subsets of glioblastoma multiforme defined by molecular genetic analysis. Brain Pathol., 3: 19-26, 1993.
16. Bello, M. J , de Campos, J. M., Kusak, M. E , Vaquero, J., Sarasa, J. L., Pestana, A , and Rey, J. A Molecular analysis of genomic abnormalities in human gliomas. Cancer Genet. Cytogenet., 73: 122-129, 1944.
17. Brothman, A R., Peehl, D. M., Patel, A. M., and McNeal, J. E. Frequency and pattern of karyotypic abnormalities in human prostate cancer. Cancer Res., 50: 3795-3803, 1990.
18. Simon, D., Hener, S., Satyaswaroop, P. G , Farber, M., and Noumoff, J. S. Is chromosome 10 a primary chromosomal abnormality in endometrial adenocarcinoma? Cancer Genet Cytogenet., 47: 155-162, 1990.
19. Fults, D , and Pedone, C. Deletion mapping of the long arm of chromosome 10 in glioblastoma multiforme Genes Chromosomes & Cancer, 7: 173-177, 1993.
20. Nihei, N., Ichikawa, T., Kawana, Y., Kuramochi, H., Kugo, H., Oshimura, M., Killary, A M , Rinker-Schaeffer, C. W., Barret, J. C., Isaacs, J. T., and Shimazaki, J. Localization of metastasis suppressor gene(s) for rat prostatic cancer to the long arm of human chromosome 10. Genes Chromosomes & Cancer, 14: 112-119, 1995.
21. Baretton, G. B., Valina, C., Vogt, T., Schniderbanger, K., Diebold, J., and Lohrs, U. Interphase cytogenetic analysis of prostatic carcinomas by use of nonisotopic in situ hybridization Cancer Res., 54: 4472-4480, 1994.
22. Visakorpi, T , Hyytinen, E., Kallioniemi, A., Isola, J., and Kallioniemi, O-T. Sensitive detection of chromosome copy number aberrations in prostate cancer by fluorescence in situ hybridization. Am. J. Pathol., 145: 624-630, 1994.
23. Brown, J. A., Alcarez, A , Takahashi, S., Persons, D. I., Lieber, I. M., and Jenkins, R. B. Chromosomal aneusomies detected by fluorescent in situ hybridization analysis in clinically localized prostate carcinoma. J. Urol., 152: 1157-1162, 1994.