Magmas expression in neoplastic human prostate

被引:26
作者
Jubinsky, PT [1 ]
Short, MK
Mutema, G
Morris, RE
Ciraolo, GM
Li, MM
机构
[1] Albert Einstein Coll Med, Div Pediat Hematol Oncol, Bronx, NY 10467 USA
[2] Univ Cincinnati, Sch Med, Dept Pathol, Cincinnati, OH USA
[3] Univ Cincinnati, Sch Med, Dept Cell Biol Neurobiol & Anat, Cincinnati, OH USA
[4] Montefiore Med Ctr, Dept Pathol, Bronx, NY 10467 USA
关键词
D O I
10.1007/s10735-004-3840-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Magmas, is a 13-kDa mitochondrial protein which is ubiquitously expressed in eukaryotic cells. It was identified as a granulocyte-macrophage-colony stimulating factor (GM-CSF) inducible gene in hematopoietic cells and has a key role in the transport of mitochondrial proteins in yeast. Because GM-CSF receptor levels are elevated in prostate cancer, Magmas expression was examined in normal and neoplastic tissue. Magmas protein levels were barely detectible in non-neoplastic prostate glands. Increased amounts were observed in some samples of intraepithelial neoplasia. Approximately one half of the adenocarcinoma samples examined had weak Magmas expression, while the remainder had intermediate to high levels. The increased Magmas observed in malignant tissue was a result of higher protein expression and not from changes in mitochondrial content. Interestingly, in some patients, the normal prostate tissue had more Magmas message than the malignant portion. The results indicated that Magmas expression in prostate cancer is heterogeneous and independent of clinical stage and Gleason score. Further studies are needed to determine if Magmas expression has prognostic significance in prostate cancer.
引用
收藏
页码:69 / 75
页数:7
相关论文
共 46 条
  • [1] The black-pearl gene of Drosophila defines a novel conserved protein family and is required for larval growth and survival
    Becker, S
    Gehrsitz, A
    Bork, P
    Buchner, S
    Buchner, E
    [J]. GENE, 2001, 262 (1-2) : 15 - 22
  • [2] Birckbichler PJ, 2000, CANCER-AM CANCER SOC, V89, P412, DOI 10.1002/1097-0142(20000715)89:2<412::AID-CNCR29>3.0.CO
  • [3] 2-O
  • [4] Bostwick DG, 1998, CANCER-AM CANCER SOC, V82, P2256, DOI 10.1002/(SICI)1097-0142(19980601)82:11<2256::AID-CNCR22>3.0.CO
  • [5] 2-S
  • [6] BRANDES D, 1964, LAB INVEST, V13, P1541
  • [7] Bussemakers MJG, 1999, CANCER RES, V59, P5975
  • [8] Chung TDK, 1999, PROSTATE, V38, P199
  • [9] Human glandular kallikrein 2 (hK2) expression in prostatic intraepithelial neoplasia and adenocarcinoma: A novel prostate cancer marker
    Darson, MF
    Pacelli, A
    Roche, P
    Rittenhouse, HG
    Wolfert, RL
    Young, CYF
    Klee, GG
    Tindall, DJ
    Bostwick, DG
    [J]. UROLOGY, 1997, 49 (06) : 857 - 862
  • [10] BINDING OF EPIDERMAL GROWTH-FACTOR BY HUMAN NORMAL, HYPERTROPHIC, AND CARCINOMATOUS PROSTATE
    DAVIES, P
    EATON, CL
    [J]. PROSTATE, 1989, 14 (02) : 123 - 132