A genome screen of multiplex sibships with prostate cancer

Brian K. Suarez, Jennifer Lin, James K. Burmester, Karl W. Broman, James L. Weber, Tarit K. Banerjee, Katrina A B Goddard, John S. Witte, Robert C. Elston, William J. Catalona*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

130 Scopus citations


Analysis of a genome screen of 504 brothers with prostate cancer (CaP) who were from 230 multiplex sibships identified five regions with nominally positive linkage signals, on chromosomes 2q, 12p, 15q, 16p, and 16q. The strongest signal in these data is found on chromosome 16q, between markers D16S515 and D16S3040, a region suspected to contain a tumor-suppressor gene. On the basis of findings from previous genome screens of families with CaP, three preplanned subanalyses were carried out, in the hope of increasing the subgroup homogeneity. Subgroups were formed by dividing the sibships into a group with a positive family history (FH+) that met criteria for 'hereditary' CaP (n = 111) versus those which did not meet the criteria (n = 119) and by dividing the families into those with a mean onset age below the median (n = 115) versus those with a mean onset age above the median (n = 115). A separate subanalysis was carried out for families with a history of breast cancer (CaB+ [n = 53]). Analyses of these subgroups revealed a number of potentially important differences in regions that were nonsignificant when all the families were analyzed together. In particular, the subgroup without a positive family history (FH-) had a signal in a region that is proximal to the putative site of the HPC1 locus on chromosome 1, whereas the late-age-at- onset group had a signal on 4q. The CaB+ subgroup revealed a strong linkage signal at 1p35.1.

Original languageEnglish (US)
Pages (from-to)933-944
Number of pages12
JournalAmerican journal of human genetics
Issue number3
StatePublished - 2000

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)


Dive into the research topics of 'A genome screen of multiplex sibships with prostate cancer'. Together they form a unique fingerprint.

Cite this