Department of Biochemistry and Molecular Biology, University of Athens, Athens GR-15701, Greece.
Second Department of Internal Medicine, Propaedeutic, University of Athens, University General Hospital "Attikon", Athens GR-12462, Greece.
Clin Biochem. 2015 Sep;48(13-14):849-54. doi: 10.1016/j.clinbiochem.2015.04.007. Epub 2015 Apr 17.
Plasma kallikrein, also known as Fletcher factor or kallikrein B1 (KLKB1), is a serine endopeptidase, like its homologs tissue kallikrein and kallikrein-related peptidases (KLKs). Its physiological role is to catalyze the release of kinins and other vasoactive peptides. Several KLKs have been proposed as putative tumor biomarkers with significant diagnostic and/or prognostic value in human malignancies arising from solid tumors; the most prominent example is the worldwide use of KLK3 (prostate-specific antigen, PSA) in prostate cancer diagnostics. The aim of this study was to analyze KLKB1 mRNA expression in B-cell chronic lymphocytic leukemia (CLL) patients and to examine its diagnostic value as a novel molecular biomarker in CLL.
Total RNA was isolated from peripheral blood mononuclear cells of sixty-nine patients previously diagnosed with CLL and thirty-one healthy blood donors. After cDNA preparation, a sensitive and cost-effective quantitative real-time PCR (qRT-PCR) methodology was developed and applied for KLKB1 mRNA quantification. Last, we carried out a biostatistical analysis to assess the clinical significance of KLKB1 mRNA expression.
According to our findings, KLKB1 mRNA expression is significantly higher in CLL patients than in healthy blood donors. Furthermore, KLKB1 mRNA levels are negatively correlated with CD38 expression, an established prognostic biomarker in CLL. Most importantly, KLKB1 mRNA expression possesses important diagnostic value, distinguishing very efficiently CLL patients from non-leukemic population.
KLKB1 mRNA expression is a putative molecular biomarker in CLL, meriting investigation in large cohorts of CLL patients and non-leukemic controls.
血浆激肽释放酶,又称 Fletcher 因子或激肽释放酶 B1(KLKB1),是一种丝氨酸内肽酶,与其同源物组织激肽释放酶和激肽释放酶相关肽(KLKs)相似。其生理作用是催化激肽和其他血管活性肽的释放。几种 KLKs 已被提议作为潜在的肿瘤生物标志物,在源于实体瘤的人类恶性肿瘤中具有重要的诊断和/或预后价值;最突出的例子是 KLK3(前列腺特异性抗原,PSA)在前列腺癌诊断中的全球应用。本研究旨在分析 B 细胞慢性淋巴细胞白血病(CLL)患者中 KLKB1 mRNA 的表达,并研究其作为 CLL 新型分子生物标志物的诊断价值。
从先前诊断为 CLL 的 69 例患者和 31 例健康献血者的外周血单核细胞中分离总 RNA。在 cDNA 制备后,开发并应用了一种灵敏且具有成本效益的实时定量 PCR(qRT-PCR)方法来定量 KLKB1 mRNA。最后,我们进行了生物统计学分析,以评估 KLKB1 mRNA 表达的临床意义。
根据我们的发现,CLL 患者的 KLKB1 mRNA 表达明显高于健康献血者。此外,KLKB1 mRNA 水平与 CD38 表达呈负相关,CD38 是 CLL 中已建立的预后生物标志物。最重要的是,KLKB1 mRNA 表达具有重要的诊断价值,能够非常有效地将 CLL 患者与非白血病人群区分开来。
KLKB1 mRNA 表达是 CLL 的潜在分子生物标志物,值得在大量 CLL 患者和非白血病对照中进行研究。