Diagnostic and prognostic role of the insulin growth factor pathway members insulin-like growth factor-II and insulin-like growth factor binding protein-3 in serous effusions

被引:17
作者
Slipicevic, Ana [1 ]
Oy, Geir Frode [2 ]
Askildt, Inger Cecilie [1 ]
Holth, Arild [1 ]
Hellesylt, Ellen [1 ]
Florenes, Vivi Ann [1 ]
Davidson, Ben [1 ,3 ]
机构
[1] Natl Hosp Norway, Norwegian Radium Hosp, Med Ctr, Div Pathol, N-0310 Oslo, Norway
[2] Natl Hosp Norway, Norwegian Radium Hosp, Med Ctr, Dept Tumor Biol, N-0310 Oslo, Norway
[3] Univ Oslo, Fac Med, Fac Div Radiumhosp, N-0316 Oslo, Norway
关键词
Insulin-like growth factor; Effusions; Carcinoma; Mesothelioma; Survival; OVARIAN-CARCINOMA; MESOTHELIAL ORIGIN; GENE-EXPRESSION; POOR SURVIVAL; CELLS; INSULIN-LIKE-GROWTH-FACTOR-BINDING-PROTEIN-3; METHYLATION; PERITONEAL; CYTOLOGY; CANCERS;
D O I
10.1016/j.humpath.2008.10.003
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We recently reported on higher expression of the insulin-like growth factor path-way genes IGF-II and IGFBP3 in serous ovarian/peritoneal carcinoma compared to malignant peritoneal mesothelioma. The present study analyzed the diagnostic and clinical role of these proteins in serous effusions. Effusions (n = 327), including 294 carcinomas (205 ovarian, 48 breast, 17 cervical/endometrial, 12 lung, 12 g gastrointestinal/genitourinary) and 33 malignant mesotheliomas, were immunostained for insulin-like growth factor-II and insulin-like growth factor binding protein-3. Surgical ovarian carcinoma (n = 124) and peritoneal mesothelioma (n = 18) specimens were additionally studied. Insulin-like growth factor binding protein-3 levels were measured in 148 effusion supernatants (114 ovarian carcinomas, 18 breast carcinomas, 16 mesotheliomas) using enzyme-linked immunosorbent assay. Insulin-like growth factor binding protein-3 promoter methylation was analyzed in 11 ovarian carcinoma effusions. Insulin-like growth factor binding protein-3 (P = .002) and insulin-like growth factor-II (P < .001) expression by immunohistochemistry was significantly higher in carcinomas compared to mesotheliomas, with diagnostic sensitivity of 77% and 70% and specificity of 55% and 70%, respectively. In surgical specimens, insulin-like growth factor binding protein-3 expression was higher in ovarian carcinomas compared to peritoneal mesotheliomas (P = 007), whereas insulin-like growth factor-II expression was comparable (P = .505). Insulin-like growth factor binding protein-3 levels by enzyme-linked immunosorbent assay were comparable in the 3 analyzed cancer types. Insulinlike growth factor binding protein-3 promoter methylation was found in 6 of I I effusions. High insulin-like growth factor binding protein-3 expression in prechemotherapy and high insulin-like growth factor-II expression in postchemotherapy ovarian carcinoma effusions correlated with poor overall survival (P = .031 and P = .024, respectively). Insulin-like growth factor-II expression in postchemotherapy effusions was an independent prognostic factor in Cox multivariate analysis (P = .04). In conclusion, insulin-like growth factor-II and insulin-like growth factor binding protein-3 are more frequently expressed in metastatic carcinomas compared to mesothelioma in effusions but are less specific than currently used markers. Insulin-like growth factor-II and insulin-like growth factor binding protein-3 may be novel prognostic markers in metastatic ovarian carcinoma. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:527 / 537
页数:11
相关论文
共 29 条
[1]   IGF-binding proteins - the pieces are failing into place [J].
Bach, LA ;
Headey, SJ ;
Norton, RS .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2005, 16 (05) :228-234
[2]  
Banerjee A K, 1994, Eur J Surg Oncol, V20, P33
[3]   D2-40 is not a specific marker for cells of mesothelial origin in serous effusions [J].
Bassarova, Assia V. ;
Nesland, Jahn M. ;
Davidson, Ben .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2006, 30 (07) :878-882
[4]  
Bedrossian CWM., 1994, Malignant Effusions A Multimodal Approach to Cytologic Diagnosis
[5]   Natural history of stage IV epithelial ovarian cancer [J].
Bonnefoi, H ;
A'Hern, RP ;
Fisher, C ;
Macfarlane, V ;
Barton, D ;
Blake, P ;
Shepherd, JH ;
Gore, ME .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (03) :767-775
[6]   Malignant effusions: From diagnosis to biology [J].
Davidson, B .
DIAGNOSTIC CYTOPATHOLOGY, 2004, 31 (04) :246-254
[7]   Detection of cancer cells in effusions from patients diagnosed with gynaecological malignancies -: Evaluation of five epithelial markers [J].
Davidson, B ;
Risberg, B ;
Kristensen, G ;
Kvalheim, G ;
Emilsen, E ;
Bjåmer, A ;
Berner, A .
VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY, 1999, 435 (01) :43-49
[8]   The role of desmin and N-cadherin in effusion cytology - A comparative study using established markers of mesothelial and epithelial cells [J].
Davidson, B ;
Nielsen, S ;
Christensen, J ;
Asschenfeldt, P ;
Berner, A ;
Risberg, B ;
Johansen, P .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2001, 25 (11) :1405-1412
[9]  
Davidson Ben, 2007, Critical Reviews in Oncogenesis, V13, P189
[10]   MUC4 is Upregulated in ovarian carcinoma effusions and differentiates carcinoma cells from mesothelial cell [J].
Davidson, Ben ;
Baekelandt, Mark ;
Shih, Le-Ming .
DIAGNOSTIC CYTOPATHOLOGY, 2007, 35 (12) :756-760