A Multiparametric Serum Kallikrein Panel for Diagnosis of Non–Small Cell Lung Carcinoma

• Published in: Clinical cancer research 2008-03, Vol.14 (5), p.1355-1362
• Main Authors: PLANQUE, Chris, LIN LI, YINGYE ZHENG, SOOSAIPILLAI, Antoninus, RECKAMP, Karen, CHIA, David, DIAMANDIS, Eleftherios P, GOODGLICK, Lee
• Format: Article
• Language: English
• Subjects: Adenocarcinoma - blood; Adenocarcinoma - pathology; Adenocarcinoma, Bronchiolo-Alveolar - blood; Adenocarcinoma, Bronchiolo-Alveolar - pathology; Adult; Antineoplastic agents; Biological and medical sciences; Biomarkers, Tumor - blood; Carcinoma, Large Cell - blood; Carcinoma, Large Cell - pathology; Carcinoma, Non-Small-Cell Lung - blood; Carcinoma, Non-Small-Cell Lung - pathology; Case-Control Studies; Enzyme-Linked Immunosorbent Assay; Female; Gene Expression Regulation, Neoplastic; Human tissue kallikreins; Humans; Lung Neoplasms - blood; Lung Neoplasms - pathology; Male; Medical sciences; Middle Aged; multiparametric analysis; Neoplasm Recurrence, Local - blood; Neoplasm Recurrence, Local - pathology; non–small cell lung cancer; Pharmacology. Drug treatments; Pneumology; ROC Curve; serine proteases; serologic markers; Tissue Kallikreins - blood; Tumors of the respiratory system and mediastinum
• ISSN: 1078-0432; 1557-3265
• DOI: 10.1158/1078-0432.CCR-07-4117

Purpose: Human tissue kallikreins are a family of 15 secreted serine proteases. We have previously shown that the expression of several tissue kallikreins is significantly altered at the transcriptional level in lung cancer. Here, we examined the clinical value of 11 members of the tissue kallikrein family as potential biomarkers for lung cancer diagnosis. Experimental Design: Serum specimens from 51 patients with non–small cell lung cancer (NSCLC) and from 50 healthy volunteers were collected. Samples were analyzed for 11 kallikreins (KLK1, KLK4-8, and KLK10-14) by specific ELISA. Data were statistically compared and receiver operating characteristic curves were constructed for each kallikrein and for various combinations. Results: Compared with sera from normal subjects, sera of patients with NSCLC had lower levels of KLK5, KLK7, KLK8, KLK10, and KLK12, and higher levels of KLK11, KLK13, and KLK14. Expression of KLK11 and KLK12 was positively correlated with stage. With the exception of KLK5, expression of kallikreins was independent of smoking status and gender. KLK11, KLK12, KLK13, and KLK14 were associated with higher risk of NSCLC as determined by univariate analysis and confirmed by multivariate analysis. The receiver operating characteristic curve of KLK4, KLK8, KLK10, KLK11, KLK12, KLK13, and KLK14 combined exhibited an area under the curve of 0.90 (95% confidence interval, 0.87-0.97). Conclusions: We propose a multiparametric panel of kallikrein markers for lung cancer diagnosis with relatively good accuracy. This model requires validation with a larger series and may be further improved by addition of other biomarkers.