Interleukin-8 serum levels in patients with benign prostatic hyperplasia and prostate cancer

被引:138
作者
Veltri, RW
Miller, MC
Zhao, G
Ng, A
Marley, GM
Wright, GL
Vessella, RL
Ralph, D
机构
[1] Urocor Inc, Urosci Grp, Oklahoma City, OK 73104 USA
[2] Eastern Virginia Med Sch, Dept Immunol Microbiol, Norfolk, VA 23501 USA
[3] Eastern Virginia Med Sch, Dept Urol, Norfolk, VA 23501 USA
[4] Univ Washington, Dept Urol, Seattle, WA 98195 USA
[5] Virginia Prostate Ctr, Norfolk, VA USA
关键词
D O I
10.1016/S0090-4295(98)00455-5
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
Objectives, Using arbitrarily primed polymerase chain reaction (AP-PCR) ribonucleic acid (RNA) fingerprinting, we discovered a messenger RNA (mRNA) that encoded the cytokine interleukin-8 (IL-8) that was up-regulated in the peripheral blood leukocytes (PBLs) of patients with metastatic prostate cancer (CaP) compared with similar cells from healthy individuals. We compared the total prostate-specific antigen (PSA) levels, the free/total (f/t) PSA ratios, and the immunoreactive IL-8 serum concentrations in patients with either biopsy-confirmed benign prostatic hyperplasia (BPH) or CaP. Methods. The sera from 35 apparently healthy normal volunteers and 146 patients with biopsy-confirmed BPH and CaP obtained from two academic centers were retrospectively examined to determine the serum levels of IL-8, total PSA (tPSA), and the f/t PSA ratio, Logistic regression and trend analysis statistical methods were used to assess the results. Results. Normals (n = 35), BPH patients (n = 53), patients with clinical Stages A to C CaP (n = 81), and patients with metastatic CaP (n = 12) had mean levels of IL-8 of 6.8, 6.5, 15.6, and 27.8 pg/mL, respectively. The IL-8 serum concentrations correlated with increasing CaP stage and also differentiated BPH from clinical Stages A, B, C, or D CaP better than tPSA and performed similarly to the f/t PSA ratio. The combination of the IL-8 levels and f/t PSA ratios using multivariate logistic regression analysis distinguished BPH from Stages A, B, C, or D CaP or only Stages A and B with a receiver operating characteristic area under the curve of 89.8% and 87.5%, respectively (P < 0.0001). Conclusions. The IL-8 serum concentration in our clinically well-defined patient sample was independent of the f/t PSA ratio as a predictor of CaP. When test samples are controlled for extraneous clinical origin of inflammation or infection, the combination of the IL-8 and f/t PSA assay results may offer an improved approach for distinguishing BPH from CaP. UROLOGY 53: 139-147, 1999. (C) 1999, Elsevier Science Inc. All rights reserved.
引用
收藏
页码:139 / 147
页数:9
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