Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22

被引:26
|
作者
Rahman, N
Teare, MD
Seal, S
Renard, H
Mangion, J
Cour, C
Thompson, D
Shugart, Y
Eccles, D
Devilee, P
Meijers, H
Nathanson, KL
Neuhausen, SL
Weber, B
Chang-Claude, J
Easton, DF
Goldgar, D
Stratton, MR
机构
[1] Inst Canc Res, Sect Canc Genet, Sutton SM2 5NG, Surrey, England
[2] Strangeways Res Lab, CRC, Genet Epidemiol Unit, Cambridge, England
[3] IARC, Lyon, France
[4] Princess Anne Hosp, Wessex Clin Genet Serv, Southampton, Hants, England
[5] Leiden Univ, Dept Human Genet, NL-2300 RA Leiden, Netherlands
[6] Erasmus Univ, Dept Clin Genet, NL-3000 DR Rotterdam, Netherlands
[7] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[8] Univ Penn, Dept Genet, Philadelphia, PA 19104 USA
[9] Univ Utah, Sch Med, Div Genet Epidemiol, Salt Lake City, UT USA
[10] Deutsch Krebsforschungszentrum, Div Genet Epidemiol, D-6900 Heidelberg, Germany
基金
英国医学研究理事会;
关键词
boast cancer; BRCA1; BRCA2; familial; chromosome; 8p;
D O I
10.1038/sj.onc.1203735
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several recent studies indicate that the majority of families with five or fen er cases of breast cancer and no cases of ovarian cancer are not due to BRCA1 or BRCA2. It has been proposed that a further breast cancer susceptibility gene that may account for some of these families is located on chromosome 8p12-p22, We have identified 31 site-specific breast cancer families that have a greater than 80% posterior probability of being due to genes other than BRCA1 or BRCA2. These families have been examined for linkage to 8p12-p22 using markers flanking the putative location of the gene. The overall multi-point LOD score is strongly negative across the whole 44 cM. The individual multi-point LOD score is negative in 23 families and only exceeds 0.5 in a single family (with a multi-point LOD score of 1.22). The maximum heterogeneity LOD score was 0.03 at marker D8S136 with estimated proportion linked (alpha) of 3% (95% CI 0-30%), These data do not lend support to the hypothesis that chromosome 8p12-p22 harbours a familial breast cancer susceptibility gene.
引用
收藏
页码:4170 / 4173
页数:4
相关论文
共 50 条
  • [1] Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22
    Nazneen Rahman
    M Dawn Teare
    Sheila Seal
    Helene Renard
    Jon Mangion
    Chantal Cour
    Deborah Thompson
    Yin Shugart
    Diana Eccles
    Peter Devilee
    Hanne Meijers
    Katherine L Nathanson
    Susan L Neuhausen
    Barbara Weber
    Jenny Chang-Claude
    Douglas F Easton
    David Goldgar
    Michael R Stratton
    Oncogene, 2000, 19 : 4170 - 4173
  • [2] Absence of evidence for a familiar breast cancer susceptibility gene at chromosome 8p12-p22.
    Rahman, N
    Teare, D
    Chang-Claude, J
    Easton, D
    Eccles, D
    Goldgar, D
    Mangion, J
    Meijers, H
    Seal, S
    Shugart, Y
    Stratton, M
    Thompson, D
    Weber, B
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A317 - A317
  • [3] Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families
    Susanne Seitz
    Klaus Rohde
    Erhard Bender
    Anita Nothnagel
    Konrad Kölble
    Peter M Schlag
    Siegfried Scherneck
    Oncogene, 1997, 14 : 741 - 743
  • [4] Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: Linkage analysis in German breast cancer families
    Seitz, S
    Rohde, K
    Bender, E
    Nothnagel, A
    Kolble, K
    Schlag, PM
    Scherneck, S
    ONCOGENE, 1997, 14 (06) : 741 - 743
  • [5] Indication for a possible third breast cancer predisposing gene, BRCA3, in the chromosome 8p12-p22 region
    Sobol, H
    Kerangueven, F
    Eisinger, F
    Essioux, L
    Noguchi, T
    Gesta, P
    Jacquemier, J
    Pebusque, MJ
    BonaitiPellie, C
    Birnbaum, D
    HEREDITARY CANCER, 1996, : 19 - 26
  • [6] Deletion mapping and linkage analysis provide strong indication for the involvement of the human chromosome region 8p12-p22 in breast carcinogenesis
    S Seitz
    K Rohde
    E Bender
    A Nothnagel
    H Pidde
    O-M Ullrich
    A El-Zehairy
    W Haensch
    B Jandrig
    K Kölble
    PM Schlag
    S Scherneck
    British Journal of Cancer, 1997, 76 : 983 - 991
  • [7] Deletion mapping and linkage analysis provide strong indication for the involvement of the human chromosome region 8p12-p22 in breast carcinogenesis
    Seitz, S
    Rohde, K
    Bender, E
    Nothnagel, A
    Pidde, H
    Ullrich, OM
    ElZehairy, A
    Haensch, W
    Jandrig, B
    Kolble, K
    Schlag, PM
    Scherneck, S
    BRITISH JOURNAL OF CANCER, 1997, 76 (08) : 983 - 991
  • [8] Localization of a novel susceptibility gene for familial ovarian cancer to chromosome 3p22-p25
    Sekine, M
    Nagata, H
    Tsuji, S
    Hirai, Y
    Fujimoto, S
    Hatae, M
    Kobayashi, I
    Fujii, T
    Nagata, I
    Ushijima, K
    Obata, K
    Suzuki, M
    Yoshinaga, M
    Umesaki, N
    Satoh, S
    Enomoto, T
    Motoyama, S
    Tanaka, K
    HUMAN MOLECULAR GENETICS, 2001, 10 (13) : 1421 - 1429
  • [9] Chromosome translocations in breast cancer with breakpoints at 8p12
    Courtay-Cahen, C
    Morris, JS
    Edwards, PAW
    GENOMICS, 2000, 66 (01) : 15 - 25
  • [10] Evidence for a familial esophageal cancer susceptibility gene on chromosome 13
    Hu, N
    Goldstein, AM
    Albert, PS
    Giffen, C
    Tang, ZZ
    Ding, T
    Taylor, PR
    Emmert-Buck, MR
    CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2003, 12 (10) : 1112 - 1115