Evidence for a prostate cancer-susceptibility locus on chromosome 20

American Journal of Human Genetics

Volumn 67, Issue 1, 2000, Pages 82-91

  Berry, Rebecca ^a   Schroeder, Jennifer J ^a   French, Amy J ^a   McDonnell, Shannon K ^a   Peterson, Brett J ^a   Cunningham, Julie M ^a   Thibodeau, Stephen N ^a   Schaid, Daniel J ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CANCER SUSCEPTIBILITY; CHROMOSOME 20Q; CONTROLLED STUDY; GENE LOCUS; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PROSTATE CANCER;

EID: 0033910573     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302994     Document Type: Article

References (47)

1. Berry R, Schaid DJ, Smith JR, French AJ, Schroeder JJ, McDonnell SK, Peterson BJ, et al (2000) Linkage analyses at the chromosome 1 loci 1q24-25 (HPC1), 1q42.2-43 (PCAP), and 1p36 (CAPB) in families with hereditary prostate cancer. Am J Hum Genet 66:539-546
2. Berthon P, Valeri A, Cohen-Akenine A, Drelon E, Paiss T, Wohr G, Latil A, et al (1998) Predisposing gene for early-onset prostate cancer, localized on chromosome 1q42.2-43. Am J Hum Genet 62:1416-1424
3. Bockmuhl U, Petersen S, Schmidt S, Wolf G, Jahnke V, Dietel M, Petersen I (1997) Patterns of chromosomal alterations in metastasizing and nonmetastasizing primary head and neck carcinomas. Cancer Res 57:5213-5216
4. Cannon, L, Bishop, DT, Skolnick M, Hunt S, Lyon JL, Smart CR (1982) Genetic epidemiology of prostate cancer in the Utah Mormon genealogy. Cancer Surv 1:47-69
5. Carter BS, Beaty TH, Steinberg GD, Childs B, Walsh PC (1992) Mendelian inheritance of familial prostate cancer. Proc Natl Acad Sci USA 89:3367-3371
6. Carter BS, Carter H, Isaacs JT (1990) Epidemiologic evidence regarding predisposing factors to prostate cancer. Prostate 16:187-197
7. Cooney KA, McCarthy JD, Lange E, Huang L, Miesfeldt S, Montie JE, Oesterling JE, et al (1997) Prostate cancer susceptibility locus on chromosome 1q: a confirmatory study. J Natl Cancer Inst 89:955-959
8. Cox NJ, Frigge M, Nicolae DL, Concannon P, Hanis CL, Bell GI, Kong A (1999) Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans. Nat Genet 21:213-215
9. Eeles RA, Durocher F, Edwards S, Teare D, Badzioch M, Hamoudi R, Gill S, et al (1998) Linkage analyses of chromosome 1q markers in 136 prostate cancer families. Am J Hum Genet 62:653-658
10. Ellis NA, Groden J, Ye TZ, Straughen J, Lennon DJ, Ciocci S, Proytcheva M, et al (1995) The Bloom's syndrome gene product is homologous to RecQ helicases. Cell 83:655-666
11. Gibbs M, Chakrabarti L, Stanford JL, Goode EL, Kolb S, Schuster EF, Buckley VA, et al (1999a) Analysis of chromosome 1q42.2-43 in 152 families with high risk of prostate cancer. Am J Hum Genet 64:1087-1095
12. Gibbs M, Stanford JL, McIndoe RA, Jarvik GP, Kolb S, Goode EL, Chakrabarti L, et al (1999b) Evidence for a rare prostate cancer-susceptibility locus at chromosome 1p36. Am J Hum Genet 64:776-787
13. Goldgar DE, Easton DF, Cannon-Albright LA, Skolnick MH (1994) Systematic population-based assessment of cancer risk in first-degree relatives of cancer probands. J Natl Cancer Inst 86:1600-1608
14. Gray MD, Shen JC, Kamath-Loeb AS, Blank A, Sopher BL, Martin GM, Oshima J, et al (1997) The Werner syndrome protein is a DNA helicase. Nat Genet 17:100-103
15. Grönberg H, Xu J, Smith JR, Carpten JD, Isaacs SD, Freije D, Bova GS, et al (1997) Early age at diagnosis in families providing evidence of linkage to the hereditary prostate cancer locus (HPC1) on chromosome 1. Cancer Res 57: 4707-4709
16. Hall JG (1990) Genomic imprinting: review and relevance to human diseases. Am J Hum Genet 46:857-873
17. Hayward BE , Moran V, Strain L, Bonthron DT (1998) Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally and biallelically derived proteins. Proc Natl Acad Sci USA 95:15475-15480
18. Hsieh C-L, Oakley-Girvan I, Gallagher RP, Wu AH, Kolonel LN, Teh C-Z, Halpern J, et al (1997) Re: Prostate cancer susceptibility locus on chromosome 1q: a confirmatory study. J Natl Cancer Inst 89:1893-1894
19. Iwabuchi H, Sakamoto M, Sakunaga H, Ma YY, Carcangiu ML, Pinkel D, Yang-Feng TL, et al (1995) Genetic analysis of benign, low-grade, and high-grade ovarian tumors. Cancer Res 55:6172-6180
20. Kallioniemi A, Kallioniemi OP, Piper J, Tanner M, Stokke T, Chen L, Smith HS, et al (1994) Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization. Proc Natl Acad Sci USA 91: 2156-2160
21. Kitao S, Shimamoto A, Goto M, Miller RW, Smithson WA, Lindor NM, Furuichi Y (1999) Mutations in RECQL4 cause a subset of cases with Rothmund-Thomson syndrome. Nat Genet 22:82-84
22. Kong A, Cox NJ (1997) Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet 61:1179-1188
23. Kosary CL, Ries LAG, Miller BA, Hankey BF, Harras A, Edwards BK (eds) (1995) SEER cancer statistics review, 1973-1991: tables and graphs. NIH Publ. No. 96-2789. National Cancer Institute, Bethesda, MD
24. Lange E, Chen H, Brierley K, Perrone E, Bock C, Gillanders E, Ray M, et al (1999) Linkage analysis of 153 prostate cancer families over a 30-cM region containing the putative susceptibility locus HPCX. Clin Cancer Res 5:4013-4020
25. McIndoe RA, Stanford JL, Gibbs M, Jarvik GP, Brandzel S, Neal CL, Li S, et al (1997) Linkage analysis of 49 high-risk families does not support a common familial prostate cancer-susceptibility gene at 1q24-25. Am J Hum Genet 61: 347-353
26. Meikle AW, Stanish WM (1982) Familial prostatic cancer risk and low testosterone. J Clin Endocrinol Metab 54: 1104-1108
27. Mohapatra G, Kim DH, Feuerstein BG (1995) Detection of multiple gains and losses of genetic material in ten glioma cell lines by comparative genomic hybridization. Genes Chromosomes Cancer 13:86-93
28. Monroe KR, Yu MC, Kolonel LN, Coetzee GA, Wilkens LR, Ross RK, Henderson BE (1995) Evidence of an X-linked or recessive genetic component to prosate cancer risk. Nat Med 1:827-829
29. Neuhausen S, Farnham J, Kort E, Tavtigian S, Skolnick M, Cannon-Albright L (1999) Prostate cancer susceptibility locus HPC1 in Utah high-risk pedigrees. Hum Mol Genet 8: 2437-2442
30. Ott J (1996) Complex traits on the map. Nature 379:772-773
31. Peters J, Wroe SF, Wells CA, Miller HJ, Bodle D, Beechey CV, Williamson CM, et al (1999) A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromsoame 2. Proc Natl Acad Sci USA 96:3830-3835
32. Risch N, Giuiffra L (1992) Model misspecification and multipoint linkage analysis. Hum Hered 42:77-92
33. Savitsky K, Bar-Shira A, Gilad S, Rotmen G, Ziv Y, Vanagaite L, Tale DA, et al (1995) A single ataxia telangiectasia gene with a product similar to PI-3 kinase. Science 268: 1749-1753
34. Schaid DJ, McDonnell SK, Blute ML, Thibodeau SN (1998) Evidence for autosomal dominant inheritance of prostate cancer. Am J Hum Genet 62:1425-1438
35. Schlegel J, Stumm G, Scherthan H, Bocker T, Zirngibl H, Ruschoff J, Hofstadter F (1995) Comparative genomic in situ hybridization of colon carcinomas with replication error. Cancer Res 55:6002-6005
36. Searle AG, Peters J, Lyon MF, Hall JG, Evans EP, Edwards JH, Buckles VJ (1989) Chromosome maps of man and mouse. IV. Ann Hum Genet 53:89-140
37. Smith JR, Freije D, Carpten JD, Grönberg H, Xu J, Isaacs SD, Brownstein MJ, et al (1996) Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search. Science 274:1371-1374
38. Solinas-Toldo S, Wallrapp C, Muller-Pillasch F, Bentz M, Gress T, Lichter P (1996) Mapping of chromosomal imbalances in pancreatic carcinoma by comparative genomic hybridization. Cancer Res 56:3803-3807
39. Spitz MR, Currier RD, Fueger JJ, Babaian RJ, Newell GR (1991) Familial patterns of prostate cancer: a case-control analysis. J Urol 146:1305-1307
40. Steinberg GD, Carter BS, Beaty TH, Childs B, Wals, PC (1990) Family history and the risk of prostate cancer. Prostate 17: 337-347
41. Suarez BK, Lin J, Burmester JK, Broman KW, Weber JL, Banerjee TK, Goddard KAB, et al (2000) A genome screen of multiplex sibships with prostate cancer. Am J Hum Genet 66:933-944
42. Whittemore AS, Wu AH, Kolonel LN, John EM, Gallagher RP, Howe GR, West DW, et al (1995) Family history and prostate cancer risk in black, white and Asian men in the United States and Canada. Am J Epidemiol 141:732-740
43. Whittemore AS, Lin IG, Oakley-Girvan I, Gallagher RP, Halper J, Kolonel LN, Wu AH, et al (1999) No evidence of linkage for chromosome 1q42.2-43 in prostate cancer. Am J Hum Genet 65:254-256
44. Weinstein LS, Wu S (1999) The role of genomic imprinting of Galpha in the pathogenesis of Albright hereditary osteodystrophy. Trends Endocrinol Metab 10:81-85
45. Woolf CM (1960) An investigation of the familial aspects of carcinoma of the prostate. Cancer 13:739-744
46. Xu J, Meyers D, Freije D, Isaacs S, Wiley K, Nusskern D, Ewing C, et al (1998) Evidence for a prostate cancer susceptibility locus on the X chromosome. Nat Genet 20: 175-179
47. Xu J, International Consortium for Prostate Cancer Genetics (2000). Combined analysis of hereditary prostate cancer linkage to 1q24-25: results from 772 hereditary prostate cancer families from the International Consortium for Prostate Cancer Genetics. Am J Hum Genet 66:945-957