This study is a linkage analysis of families with human prostate cancer. Papers published in Science (1996), Nature Genetics (1998) have shown evidence of prostate cancer susceptibility genes in regions of chromosome 1 and chromosome X. These results have been followed up by intensive linkage analyses of additional families to markers in these regions and in other regions that showed some mild evidence of linkage in the initial genome scan. Families have been obtained and genotyped from several regions of the United States, Finland, Iceland and Sweden. Dr. Bailey-Wilson's group is involved in the analyses of the Finnish and Icelandic data and the African-American data. Papers were previously published in Clinical Cancer Research (2000) showing strong evidence for the chromosome X locus but limited evidence for the chromosome 1 locus in our Finnish data. Another paper was published in Human Genetics (2000) detailing the linkage results in the Icelandic data. Efforts are underway to develop additional family resources for this project. These investigators have joined the International Prostate Cancer Genetics Consortium (ICPCG) to try to localize prostate cancer loci more rapidly, and a meta-analysis paper from this consortium describing the evidence for linkage to the chromosome 1 locus in a very large combined dataset was published previously. In the current fiscal year, our group identified mutations in the ribonuclease-L (RNASEL) gene as being the locus in our chromosome 1 linkage region causing increased risk to prostate cancer. We also found evidence that mutations in the macrophage scavenger receptor 1 gene plays a role in prostate cancer risk. Several papers have been published with these results. We also published the results of segregation analyses of breast and prostate cancer. The ICPCG consortium is currently performing meta-analyses of two other regions that have been implicated as regions of susceptibility loci in prostate cancer. Dr. Bailey-Wilson is in charge of the Chromosome X meta-analysis. This work will be ongoing. Association analyses have also been performed on additional marker data from Finland, Iceland and the U.S. A manuscript is currently being prepared. A linkage genome-wide scan of families from Finland, Sweden, and the U.S., including a significant number of African-American families from the African American Hereditary Prostate Cancer Consortium, of which Dr. Bailey-Wilson is a member, is ongoing in this fiscal year and will continue into the next year. A paper is in press detailing the results of this genome wide scan in the Finnish families. Analyses of the other datasets and of fine mapping data for the Finnish dataset will be ongoing into the next fiscal year. We also plan to continue with follow-up of candidate regions identified in the Finnish and African-American genome wide scans.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Intramural Research (Z01)
Project #
1Z01HG000107-07
Application #
6830087
Study Section
(IDRB)
Project Start
Project End
Budget Start
Budget End
Support Year
7
Fiscal Year
2003
Total Cost
Indirect Cost
Name
Human Genome Research
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Gillanders, Elizabeth M; Xu, Jianfeng; Chang, Bao-li et al. (2004) Combined genome-wide scan for prostate cancer susceptibility genes. J Natl Cancer Inst 96:1240-7
Carpten, J; Nupponen, N; Isaacs, S et al. (2002) Germline mutations in the ribonuclease L gene in families showing linkage with HPC1. Nat Genet 30:181-4
Ho, Gloria Y F; Knapp, Michael; Freije, Diha et al. (2002) Transmission/disequilibrium tests of androgen receptor and glutathione S-transferase pi variants in prostate cancer families. Int J Cancer 98:938-42
Rokman, Annika; Ikonen, Tarja; Seppala, Eija H et al. (2002) Germline alterations of the RNASEL gene, a candidate HPC1 gene at 1q25, in patients and families with prostate cancer. Am J Hum Genet 70:1299-304
Baffoe-Bonnie, Agnes B; Kiemeney, Lambertus A L M; Beaty, Terri H et al. (2002) Segregation analysis of 389 Icelandic pedigrees with Breast and prostate cancer. Genet Epidemiol 23:349-63
Xu, Jianfeng; Zheng, S Lilly; Komiya, Akira et al. (2002) Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk. Nat Genet 32:321-5
Stephan, Dietrich A; Howell, Gareth R; Teslovich, Tanya M et al. (2002) Physical and transcript map of the hereditary prostate cancer region at xq27. Genomics 79:41-50
Powell, I J; Carpten, J; Dunston, G et al. (2001) African-American heredity prostate cancer study: a model for genetic research. J Natl Med Assoc 93:120-3
Verhage, B A; Baffoe-Bonnie, A B; Baglietto, L et al. (2001) Autosomal dominant inheritance of prostate cancer: a confirmatory study. Urology 57:97-101
Powell, I J; Carpten, J; Dunston, G et al. (2001) African-American heredity prostate cancer study: a model for genetic research. J Natl Med Assoc 93:25S-28S

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