Evaluation of the prognostic significance of MSMB and CRISP3 in prostate cancer using automated image analysis

被引:30
作者
Dahlman, Anna [1 ,2 ]
Rexhepaj, Elton [3 ]
Brennan, Donal J. [3 ]
Gallagher, William M. [3 ]
Gaber, Alexander [2 ]
Lindgren, Anna [4 ]
Jirstrom, Karin [2 ]
Bjartell, Anders [1 ,2 ]
机构
[1] Lund Univ, Skane Univ Hosp, Div Urol Canc, Dept Clin Sci, Malmo, Sweden
[2] Lund Univ, Skane Univ Hosp, Ctr Mol Pathol, Dept Lab Med, Malmo, Sweden
[3] Univ Coll Dublin, UCD Conway Inst, UCD Sch Biomol & Biomed Sci, Dublin 2, Ireland
[4] Lund Univ, Dept Math Stat, Ctr Math Sci, Lund, Sweden
基金
瑞典研究理事会;
关键词
outcome prediction; PSP94; tissue biomarker; RICH SECRETORY PROTEIN-3; 94; AMINO-ACIDS; BETA-MICROSEMINOPROTEIN; RADICAL PROSTATECTOMY; FUNCTIONAL-ANALYSIS; BINDING-PROTEIN; MESSENGER-RNA; TUMOR-GROWTH; EXPRESSION; TISSUE;
D O I
10.1038/modpathol.2010.238
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Despite prostate cancer being the most frequent cancer in men in the Western world, tissue biomarkers for predicting disease recurrence after surgery have not been incorporated into clinical practice. Our group has previously identified beta-microseminoprotein (MSMB) and cysteine-rich secretory protein-3 (CRISP3) as independent predictors of biochemical recurrence after radical prostatectomy. The purpose of the present study was to use automated image analysis, enabling quantitative determination of MSMB and CRISP3 expressions in a large cohort and to validate the previous findings. MSMB and CRISP3 protein expressions were assessed on tissue microarrays constructed from 3268 radical prostatectomy specimens. Whole-slide digital images were captured, and a novel cytoplasmic algorithm was used to develop a quantitative scoring model for cytoplasmic staining. Classification regression tree analysis was used to group patients, with different risk for biochemical recurrence, depending on level of protein expression. Patients with tumors expressing high levels of MSMB had a significantly reduced risk for biochemical recurrence after radical prostatectomy (HR = 0.468; 95% CI 0.394-0.556; P<0.001). Multivariate analysis adjusted for clinicopathological parameters revealed that MSMB expression was an independent predictor of decreased risk of recurrence (HR = 0.710; 95% CI 0.578-0.872; P<0.001). We found no correlation between CRISP3 expression and biochemical recurrence. In this current study, we applied a novel image analysis on a large independent cohort and successfully verified that MSMB is a strong independent factor, predicting favorable outcome after radical prostatectomy for localized prostate cancer. Modern Pathology (2011) 24, 708-719; doi:10.1038/modpathol.2010.238; published online 14 January 2011
引用
收藏
页码:708 / 719
页数:12
相关论文
共 48 条
  • [1] IMMUNOHISTOCHEMICAL DISTRIBUTION OF THE 3 PREDOMINANT SECRETORY PROTEINS IN THE PARENCHYMA OF HYPERPLASTIC AND NEOPLASTIC PROSTATE-GLANDS
    ABRAHAMSSON, PA
    LILJA, H
    FALKMER, S
    WADSTROM, LB
    [J]. PROSTATE, 1988, 12 (01) : 39 - 46
  • [2] ABRAHAMSSON PA, 1989, CLIN CHEM, V35, P1497
  • [3] A PSP94-derived peptide PCK3145 inhibits MMP-9 secretion and triggers CD44 cell surface shedding:: Implication in tumor metastasis
    Annabi, B
    Bouzeghrane, M
    Currie, JC
    Hawkins, R
    Dulude, H
    Daigneault, L
    Ruiz, M
    Wisniewski, J
    Garde, S
    Rabbani, SA
    Panchal, C
    Wu, JZJ
    Béliveau, R
    [J]. CLINICAL & EXPERIMENTAL METASTASIS, 2005, 22 (05) : 429 - 439
  • [4] Contribution of the 37-kDa laminin receptor precursor in the anti-metastatic PSP94-derived peptide PCK3145 cell surface binding
    Annabi, Borhane
    Currie, Jean-Christophe
    Bouzeghrane, Mounia
    Dulude, Helene
    Daigneault, Luc
    Garde, Seema
    Rabbani, Shafaat A.
    Panchal, Chandra
    Wu, Jinzi J.
    Beliveau, Richard
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 346 (01) : 358 - 366
  • [5] Asmann YW, 2002, CANCER RES, V62, P3308
  • [6] The gene encoding the prostatic tumor suppressor PSP94 is a target for repression by the Polycomb group protein EZH2
    Beke, L.
    Nuytten, M.
    Van Eynde, A.
    Beullens, M.
    Bollen, M.
    [J]. ONCOGENE, 2007, 26 (31) : 4590 - 4595
  • [7] Gene expression profiling of human prostate cancer stem cells reveals a pro-inflammatory phenotype and the importance of extracellular matrix interactions
    Birnie, Richard
    Bryce, Steven D.
    Roome, Claire
    Dussupt, Vincent
    Droop, Alastair
    Lang, Shona H.
    Berry, Paul A.
    Hyde, Catherine F.
    Lewis, John L.
    Stower, Michael J.
    Maitland, Norman J.
    Collins, Anne T.
    [J]. GENOME BIOLOGY, 2008, 9 (05)
  • [8] Immunohistochemical detection of cysteine-rich secretory protein 3 in tissue and in serum from men with cancer or benign enlargement of the prostate gland
    Bjartell, A
    Johansson, R
    Björk, T
    Gadaleanu, V
    Lundwall, Å
    Lilja, H
    Kjeldsen, L
    Udby, L
    [J]. PROSTATE, 2006, 66 (06) : 591 - 603
  • [9] Association of cysteine-rich secretory protein 3 and β-microseminoprotein with outcome after radical prostatectomy
    Bjartell, Anders S.
    Al-Ahmadie, Hikmat
    Serio, Angel M.
    Eastham, James A.
    Eggener, Scott E.
    Fine, Samson W.
    Udby, Lene
    Gerald, William L.
    Vickers, Andrew J.
    Lilja, Hans
    Reuter, Victor E.
    Scardino, Peter T.
    [J]. CLINICAL CANCER RESEARCH, 2007, 13 (14) : 4130 - 4138
  • [10] Altered cytoplasmic-to-nuclear ratio of survivin is a prognostic indicator in breast cancer
    Brennan, Donal J.
    Rexhepaj, Elton
    O'Brien, Sallyann L.
    McSherry, Elaine
    O'Connor, Darran P.
    Fagan, Ailis
    Culhane, Aedin C.
    Higgins, Desmond G.
    Jirstrom, Karin
    Millikan, Robert C.
    Landberg, Goran
    Duffy, Michael J.
    Hewitt, Stephen M.
    Gallaghe, William M.
    [J]. CLINICAL CANCER RESEARCH, 2008, 14 (09) : 2681 - 2689