Model systems of prostate cancer: Uses and limitations

被引:74
作者
Navone, NM
Logothetis, CJ
von Eschenbach, AC
Troncoso, P
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Urol, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
关键词
cell lines; xenografts; LNCaP; MDA PCa 2a; MDA PCa 2b; PC; 3;
D O I
10.1023/A:1006165017279
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A valid experimental model system reflects the system under study and is reproducible. Model systems of prostate cancer that accurately reflect the different disease stages are necessary to ensure a proper experimental design aimed at increasing our understanding of the biology of the disease and such models are essential tools to accelerate development of new therapies for prostate cancer. Until recently, a limited number of experimental systems were available and more suitable models derived from human specimens have only recently been developed and become available for use. In addition, transgenic techniques have also permitted the development of unique mouse models. The difficulty in establishing model systems may reflect the complex requirements necessary for cancer progression and should lead us to interpret results from model systems with caution. It is unlikely that a single model system that faithfully reflects the whole process of cancer development and progression will be developed. However, thoughtful use of the available model systems will permit the study of a significant portion of prostate cancer progression. In this review we summarize the properties of the prostate cancer model systems in use and defined their utility and limitations. This review will guide the investigator seeking models with which to test specific hypotheses pertaining to prostate cancer.
引用
收藏
页码:361 / 371
页数:11
相关论文
共 76 条
  • [1] [Anonymous], COMPREHENSIVE ORGANI
  • [2] FIBROBLAST-MEDIATED ACCELERATION OF HUMAN EPITHELIAL TUMOR-GROWTH INVIVO
    CAMPS, JL
    CHANG, SM
    HSU, TC
    FREEMAN, MR
    HONG, SJ
    ZHAU, HE
    VONESCHENBACH, AC
    CHUNG, LWK
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (01) : 75 - 79
  • [3] CATALONA WJ, 1994, NEW ENGL J MED, V331, P996
  • [4] INTERACTION BETWEEN PROSTATIC FIBROBLAST AND EPITHELIAL-CELLS IN CULTURE - ROLE OF ANDROGEN
    CHANG, SM
    CHUNG, LWK
    [J]. ENDOCRINOLOGY, 1989, 125 (05) : 2719 - 2727
  • [5] CHAPRONIERE DM, 1986, CANCER RES, V46, P819
  • [6] Isolation and characterization of PAGE-1 and GAGE-7 -: New genes expressed in the LNCaP prostate cancer progression model that share homology with melanoma-associated antigens
    Chen, ME
    Lin, SH
    Chung, LWK
    Sikes, RA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (28) : 17618 - 17625
  • [7] A 6-kb promoter fragment mimics in transgenic mice the prostate-specific and androgen-regulated expression of the endogenous prostate-specific antigen gene in humans
    Cleutjens, KBJM
    vanderKorput, HAGM
    EhrenvanEekelen, CC
    Sikes, RA
    Fasciana, C
    Chung, LW
    Trapman, J
    [J]. MOLECULAR ENDOCRINOLOGY, 1997, 11 (09) : 1256 - 1265
  • [8] STROMAL-EPITHELIAL INTERACTIONS .1. INDUCTION OF PROSTATIC PHENOTYPE IN UROTHELIUM OF TESTICULAR FEMINIZED (TFM/Y) MICE
    CUNHA, GR
    CHUNG, LWK
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1981, 14 (12) : 1317 - 1321
  • [9] DUNNING W. F., 1963, NATL CANCER INST MONOGR, V12, P351
  • [10] Eastham JA, 1995, CLIN CANCER RES, V1, P1111