Racial differences in prostate cancer related to loss of heterozygosity on chromosome 8p12-23

被引:8
作者
Kalapurakal, JA
Jacob, ANK
Kim, PY
Najjar, DD
Hsieh, YC
Ginsberg, P
Daskal, I
Asbell, SO
Kandpal, RP
机构
[1] Temple Univ, Sch Med, Fels Inst Canc Res & Mol Biol, Philadelphia, PA 19140 USA
[2] Northwestern Mem Hosp, Dept Radiat Oncol, Chicago, IL USA
[3] Albert Einstein Med Ctr, Dept Radiat Oncol, Philadelphia, PA USA
[4] Northwestern Univ, Dept Prevent Med, Chicago, IL USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 1999年 / 45卷 / 04期
关键词
prostate cancer; race; loss of heterozygosity; tumor suppressor gene; chromosome; 8p;
D O I
10.1016/S0360-3016(99)00283-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine if there is a racial difference in prostate cancer related to loss of heterozygosity (LOH) on chromosome 8p12-23, the region most frequently altered in prostate cancer. Methods and Materials: A total of 51 prostate cancer patients, consisting of 23 African Americans and 28 Caucasians, were included in this study. All patients underwent radical prostatectomy, and patients in the two racial subgroups were matched for median serum PSA, Gleason score, and pathological stage of cancer. Paired normal prostate and cancer tissue DNA was isolated and amplified with 13 polymorphic markers mapped to 8p12-23 by radiolabeled polymerase chain reaction. The amplified products were resolved by polyacrylamide gel electrophoresis, autoradiographed, and analyzed for allelic losses. Results: The overall incidence of LOH at 8p12-23 was 53%, and 16% showed homozygous deletions. The incidence of LOH in Caucasians was 68% compared to 35% in African Americans. On univariate (p = 0.02) and multivariate logistic regression analysis (p = 0.02), only Caucasian race was a significant predictor for LOH. The other clinicopathologic parameters did not have any significant effect on incidence of LOH. Conclusion: These results highlight the independent influence of Caucasian race on incidence of LOH at 8p12-23, and suggest that genetic differences at specific tumor suppressor loci may be a factor responsible for racial variations observed in prostate cancer. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:835 / 840
页数:6
相关论文
共 30 条
  • [1] YEAST ARTIFICIAL CHROMOSOME AND RADIATION HYBRID MAP OF LOCI IN CHROMOSOME BAND 8P22, A COMMON REGION OF ALLELIC LOSS IN MULTIPLE HUMAN CANCERS
    BOOKSTEIN, R
    LEVY, A
    MACGROGAN, D
    LEWIS, TB
    WEISSENBACH, J
    OCONNELL, P
    LEACH, RJ
    [J]. GENOMICS, 1994, 24 (02) : 317 - 323
  • [2] Physical mapping of chromosome 8p22 markers and their homozygous deletion in a metastatic prostate cancer
    Bova, GS
    MacGrogan, D
    Levy, A
    Pin, SS
    Bookstein, R
    Isaacs, WB
    [J]. GENOMICS, 1996, 35 (01) : 46 - 54
  • [3] BOVA GS, 1993, CANCER RES, V53, P3869
  • [4] ALLELIC LOSS OF CHROMOSOME-16Q AND CHROMOSOME-10Q IN HUMAN PROSTATE-CANCER
    CARTER, BS
    EWING, CM
    WARD, WS
    TREIGER, BF
    AALDERS, TW
    SCHALKEN, JA
    EPSTEIN, JI
    ISAACS, WB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (22) : 8751 - 8755
  • [5] Cher ML, 1998, CLIN CANCER RES, V4, P1273
  • [6] Cher ML, 1996, CANCER RES, V56, P3091
  • [7] Devgan SA, 1997, PROSTATE, V33, P9, DOI 10.1002/(SICI)1097-0045(19970915)33:1<9::AID-PROS2>3.0.CO
  • [8] 2-H
  • [9] EMMERTBUCK MR, 1995, CANCER RES, V55, P2959
  • [10] Godley PA, 1996, CANCER EPIDEM BIOMAR, V5, P115