Laboratory of Molecular Pathology, Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University Olomouc 77515, Czech Republic.
Neoplasma. 2011;58(4):298-303.
Kallikrein-related peptidases 7 and 11 (KLK7/KLK11) share a high degree of structural similarity with PSA (KLK3) and other KLKs. The aim of this study was to evaluate differences in KLK7/ KLK11 expression in paired cancer/benign prostate foci and to determine possible associations with clinicopathological parameters. Seventy archived paraffin-embedded tissue samples obtained from radical prostatectomy were stained for KLK7, KLK11, PSA and PSMA and expression was evaluated semiquantitatively. The results showed statistically significant differences for all studied proteins between BPH and CaP foci. Both KLK7 (P=0.026) and KLK11 (P<0.001) expressions were decreased in prostate cancer cells compared to normal/benign prostate cells. Positive correlations were found for both KLK7 (Rs=0.74, P<0.001) and KLK11 (Rs=0.35, P=0.003) between CaP and BPH. We found a statistically significant upregulation of KLK11 in advanced cases compared to localized ones (P=0.026). For the first time, we report lower expression of KLK11 in CaP compared to BPH and slight upregulation of KLK11 in advanced tumors compared to localized ones. Our observations support the diagnostic potential of KLK7/KLK11 for early prostate cancers but further studies on larger cohorts are needed in order to validate the clinical value of these biomarkers and clarify their biological role in prostate development and tumorigenesis.
激肽释放酶相关肽酶 7 和 11(KLK7/KLK11)与 PSA(KLK3)和其他 KLKs 具有高度的结构相似性。本研究旨在评估配对的前列腺癌/良性前列腺灶中 KLK7/KLK11 的表达差异,并确定其与临床病理参数的可能关联。对 70 例来自根治性前列腺切除术的存档石蜡包埋组织样本进行 KLK7、KLK11、PSA 和 PSMA 染色,并进行半定量评估。结果表明,在 BPH 和 CaP 病灶中,所有研究的蛋白均存在统计学差异。与正常/良性前列腺细胞相比,前列腺癌细胞中 KLK7(P=0.026)和 KLK11(P<0.001)的表达均降低。KLK7(Rs=0.74,P<0.001)和 KLK11(Rs=0.35,P=0.003)在 CaP 和 BPH 之间均存在正相关。与局限性肿瘤相比,我们发现晚期肿瘤中 KLK11 的表达存在统计学显著上调(P=0.026)。我们首次报道 KLK11 在 CaP 中的表达低于 BPH,并且在晚期肿瘤中 KLK11 有轻微上调。我们的观察结果支持 KLK7/KLK11 对早期前列腺癌的诊断潜力,但需要进一步在更大的队列中进行研究,以验证这些生物标志物的临床价值,并阐明它们在前列腺发育和肿瘤发生中的生物学作用。