Evaluation of some tissue and serum biomarkers in prostatic carcinoma among Egyptian males

Citation
Mi. Ahmed et al., Evaluation of some tissue and serum biomarkers in prostatic carcinoma among Egyptian males, CLIN BIOCH, 32(6), 1999, pp. 439-445
Citations number
49
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
CLINICAL BIOCHEMISTRY
ISSN journal
00099120 → ACNP
Volume
32
Issue
6
Year of publication
1999
Pages
439 - 445
Database
ISI
SICI code
0009-9120(199908)32:6<439:EOSTAS>2.0.ZU;2-Q
Abstract
Objectives: The purpose of this study is to evaluate the role of soluble E- cadherin as a serum marker and bcl-2 and DNA content as tissue markers in c haracterization and management of prostatic adenocarcinoma (PC) among Egypt ian males. Design and Methods: The study group included 71 patients with prostatic ade nocarcinoma, 30 patients with benign prostatic hyperplasia (BPH), and 20 no rmal male subjects. Serum soluble E-cadherin (sE-cadherin) and PSA were qua ntified by ELISA and MEIA (microparticle enzyme immunoassay) techniques, re spectively. Tissue samples were investigated for bcl-2 chromosomal transloc ation t(14;18) by polymerase chain reaction (PGR) together with detection o f bcl-2 protein expression by immunohistochemistry. The results were correl ated with DNA content las defined by flow cytometric analysis) and also wit h traditional clinicopathologic parameters. Results: Our data revealed that, serum PSA was superior to sE-cadherin as a marker for PC with a sensitivity of 83% compared to 59% in case of E-cadhe rin at the same specificity (96.6%). Combination of both markers raised the sensitivity to 90%. E-cadherin correlated with Gleason score. Ploidy statu s, synthetic phase fraction (SPF), and proliferation index (PI) correlated significantly with tumor Gleason score. PI was also correlated to clinical stage. bcl-2 protein was overexpressed in 14% of PC and it showed a trend f or correlation with tumor Gleason score (p = 0.06). We failed to detect chr omosomal t(14;18) in the bcl-2 gene in all the studied tumors. Conclusions: E-Cadherin is a clinically useful biomarker in PC specially in combination with PSA. DNA content changes and bcl-2 oncogene may account f or tumorogenesis and may assist in prognostication of PC. Copyright (C) 199 9 The Canadian Society of Clinical Chemists.