Analysis of androgen regulated homeobox gene NKX3.1 during prostate carcinogenesis

被引:32
作者
Korkmaz, CG
Korkmaz, KS
Manola, J
Xi, ZJ
Risberg, B
Danielsen, H
Kung, J
Sellers, WR
Loda, M
Saatcioglu, F [1 ]
机构
[1] Univ Oslo, Dept Mol Biosci, Oslo, Norway
[2] Univ Oslo, Ctr Biotechnol, Oslo, Norway
[3] Norwegian Radium Hosp, Dept Pathol, Oslo, Norway
[4] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pathol, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[6] Univ Sheffield, Div Genom Med, Sheffield, S Yorkshire, England
基金
美国国家卫生研究院;
关键词
prostate; prostatic neoplasms; androgens; homeodomain proteins; gene expression;
D O I
10.1097/01.ju.0000136526.78535.b8
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
Purpose: NKX3.1 is an androgen regulated gene that is largely specific to the prostate for expression and it is predicted to encode a homeobox protein. Null alleles of NKX3.1 in mice results in impaired prostate development as well as hyperplasia and dysplasia of the prostate. In addition, the NKX3.1 gene maps to a region of high loss of heterozygosity in prostate cancer in humans, suggesting that NKX3.1 might have a direct role in prostate carcinogenesis, possibly functioning as a tumor suppressor protein. Previous studies of the levels of NKX3.1 mRNA or protein in prostate cancer specimens have resulted in conflicting findings. Materials and Methods: To resolve this issue we assessed NKX3.1 expression by mRNA in situ analysis and immunohistochemistry on the same prostate cancer tissue arrays. Results: Data showed that NKX3.1 mRNA and protein levels in prostate cancer specimens are correlated, suggesting that most regulation is at the transcriptional level. There was no correlation of NKX3.1 expression levels with tumor grade or clinical stage. In general there was a suggestion that worse clinical features at surgery were associated with lower IHC stain scores. In particular, extracapsular extension but not seminal vesicle invasion inversely correlated with NKX3.1 expression. Conclusions: Together these data suggest that NKX3.1 does not function as a typical tumor suppressor protein in prostate cancer but it may still have important regulatory roles during prostate cancer progression.
引用
收藏
页码:1134 / 1139
页数:6
相关论文
共 22 条
  • [1] Roles for Nkx3.1 in prostate development and cancer
    Bhatia-Gaur, R
    Donjacour, AA
    Sciavolino, PJ
    Kim, M
    Desai, N
    Young, P
    Norton, CR
    Gridley, T
    Cardiff, RD
    Cunha, GR
    Abate-Shen, C
    Shen, MM
    [J]. GENES & DEVELOPMENT, 1999, 13 (08) : 966 - 977
  • [2] Prostate-specific and androgen-dependent expression of a novel homeobox gene
    Bieberich, CJ
    Fujita, K
    He, WW
    Jay, G
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (50) : 31779 - 31782
  • [3] Bowen C, 2000, CANCER RES, V60, P6111
  • [4] Overview: Hormone refractory prostate cancer
    Crawford, ED
    Rosenblum, M
    Ziada, AM
    Lange, PH
    [J]. UROLOGY, 1999, 54 (6A) : 1 - 7
  • [5] Cancer statistics, 2001
    Greenlee, RT
    Hill-Harmon, MB
    Murray, T
    Thun, M
    [J]. CA-A CANCER JOURNAL FOR CLINICIANS, 2001, 51 (01) : 15 - 36
  • [6] A novel human prostate-specific, androgen-regulated homeobox gene (NKX3.1) that maps to 8p21, a region frequently deleted in prostate cancer
    He, WW
    Sciavolino, PJ
    Wing, J
    Augustus, M
    Hudson, P
    Meissner, PS
    Curtis, RT
    Shell, BK
    Bostwick, DG
    Tindall, DJ
    Gelmann, EP
    AbateShen, C
    Carter, KC
    [J]. GENOMICS, 1997, 43 (01) : 69 - 77
  • [7] Studies on prostate cancer II The effects of castration on advanced carcinoma of the prostate gland
    Huggins, C
    Stevens, RE
    Hodges, CV
    [J]. ARCHIVES OF SURGERY, 1941, 43 (02) : 209 - 223
  • [8] Cooperativity of Nkx3.1 and Pten loss of function in a mouse model of prostate carcinogenesis
    Kim, MJ
    Cardiff, RD
    Desai, N
    Banach-Petrosky, WA
    Parsons, R
    Shen, MM
    Abate-Shen, C
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (05) : 2884 - 2889
  • [9] Molecular cloning and characterization of STAMP1, a highly prostate-specific six transmembrane protein that is overexpressed in prostate cancer
    Korkmaz, KS
    Elbi, C
    Korkmaz, CG
    Loda, M
    Hager, GL
    Saatcioglu, F
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (39) : 36689 - 36696
  • [10] Full-length cDNA sequence and genomic organization of human NKX3A -: alternative forms and regulation by both androgens and estrogens
    Korkmaz, KS
    Korkmaz, CG
    Ragnhildstveit, E
    Kizildag, S
    Pretlow, TG
    Saatcioglu, F
    [J]. GENE, 2000, 260 (1-2) : 25 - 36