QUANTITATION OF NM23 EXPRESSION IN HUMAN PROSTATE TISSUES

被引:27
作者
FISHMAN, JR
GUMERLOCK, PH
MEYERS, FJ
WHITE, RWD
机构
[1] UNIV CALIF DAVIS, CTR CANC, SCH MED, DEPT INT MED, DIV HEMATOL ONCOL, SACRAMENTO, CA 95817 USA
[2] SCH MED, DEPT UROL, CANC & MOLEC RES LAB, SACRAMENTO, CA USA
关键词
PROSTATIC HYPERTROPHY; PROSTATIC NEOPLASMS; NEOPLASM METASTASIS; POLYMERASE CHAIN REACTION;
D O I
10.1016/S0022-5347(17)32862-8
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The NM23 gene family (nm23-H1 and nm23-H2) has been reported as a measure of metastatic potential. The goal of this study was to discriminate nm23-H1 and nm23-H2 gene expression in benign and malignant human prostate tissue and to determine the relationship of their expression to tumor stages. Specimens included 5 benign prostatic hyperplasias (BPH), 11 primary prostate adenocarcinomas (CaP) (5 stage B, 5 stage C and 1 stage D1), 2 pelvic lymph nodes with metastases and 3 prostate cancer cell lines derived from metastatic lesions. Polymerase chain reaction analysis of mRNA (RNA/PCR) was used to amplify transcripts of both NM23 genes and a normalizing gene (c-N-ras) to determine the relative levels of expression. A significant difference was shown between the BPH specimens and the cell lines from metastatic prostate cancer for nm23-H2 expression (p = 0.037) and the nm23-H1/nm23-H2 gene expression ratio (p = 0.037). The nm23-H1/nm23-H2 ratio increased significantly (p = 0.026, tau-b = 0.377) from BPH, through the CaP stages, to the cell lines. The expression of nm23-H2 decreased significantly (p = 0.002, tau-b = -0.517) from BPH, through the CaP stages, to the cell lines. Thus, while nm23-H2 appears to be significant for characterizing stages of CaP, an understanding of the metastatic phenotype will require further analysis of both NM23 genes.
引用
收藏
页码:202 / 207
页数:6
相关论文
共 43 条
  • [1] BACKER JM, 1993, ONCOGENE, V8, P497
  • [2] BARNES R, 1991, AM J PATHOL, V139, P245
  • [3] BEVILACQUA G, 1989, CANCER RES, V49, P5185
  • [4] A DROSOPHILA GENE THAT IS HOMOLOGOUS TO A MAMMALIAN GENE ASSOCIATED WITH TUMOR-METASTASIS CODES FOR A NUCLEOSIDE DIPHOSPHATE KINASE
    BIGGS, J
    HERSPERGER, E
    STEEG, PS
    LIOTTA, LA
    SHEARN, A
    [J]. CELL, 1990, 63 (05) : 933 - 940
  • [5] BOS JL, 1989, CANCER RES, V49, P4683
  • [6] ASSOCIATION OF NM23-H1 ALLELIC DELETIONS WITH DISTANT METASTASES IN COLORECTAL-CARCINOMA
    COHN, KH
    WANG, FS
    DESOTOLAPAIX, F
    SOLOMON, WB
    PATTERSON, LG
    ARNOLD, MR
    WEIMAR, J
    FELDMAN, JG
    LEVY, AT
    LEONE, A
    STEEG, PS
    [J]. LANCET, 1991, 338 (8769) : 722 - 724
  • [7] Ferre F, 1992, PCR Methods Appl, V2, P1
  • [8] GILLES AM, 1991, J BIOL CHEM, V266, P8784
  • [9] GOLDEN A, 1993, ONCOGENES TUMOR SUPP, P353
  • [10] GUMERLOCK PH, 1991, CANCER RES, V51, P1632