Zhang Chong-Yu, Zhu Yu, Rui Wen-Bin, Dai Jun, Shen Zhou-Jun
Department of Urology, Ruijin Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
Asian J Androl. 2015 Jan-Feb;17(1):106-10. doi: 10.4103/1008-682X.137613.
Recent evidence suggests that the human kallikrein 7 (KLK7) is differentially regulated in a variety of tumors. The aim of this study was to determine the expression of kallikrein-related peptidase 7 and KLK7 in our large collection of prostate samples. Between August 2000 and December 2012, 116 patients with histologically confirmed prostate cancer (PCa) and 92 with benign prostate hyperplasia (BPH) were recruited into the study. Using immunohistochemistry, quantitative reverse transcription polymerase chain reaction (RT-PCR) and western blot, kallikrein-related peptidase 7 expression in BPH and PCa tissues was determined at the mRNA and protein levels. The relationships between kallikrein-related peptidase 7 mRNA expression and clinicopathological features were analyzed. A total of 64 of 92 (69.57%) benign cases showed positive staining for KLK7 and 23 of 116 (19.83%) malignant cases showed positive, the difference of KLK7 expression between PCa and BPH was statistically significant (P < 0.001). The expression level of kallikrein-related peptidase 7 mRNA was significantly decreased in PCa tissues compared with that in BPH tissues and normal prostate tissue. Kallikrein-related peptidase 7 mRNA exhibited different expression patterns in terms of localization depending on pathological category of PCa. Similarly, our western immunoblot analyses demonstrated that the protein expression levels of KLK7 was lower in PCa than in BPH tissues and normal prostate tissue. Kallikrein-related peptidase 7 and KLK7 expression are down-regulated in PCa and lower expression of kallikrein-related peptidase 7 closely correlates with higher Gleason score and higher prostate-specific antigen level.
最近的证据表明,人组织激肽释放酶7(KLK7)在多种肿瘤中受到不同程度的调控。本研究的目的是确定激肽释放酶相关肽酶7和KLK7在我们大量前列腺样本中的表达情况。2000年8月至2012年12月期间,116例经组织学确诊的前列腺癌(PCa)患者和92例良性前列腺增生(BPH)患者被纳入本研究。采用免疫组织化学、定量逆转录聚合酶链反应(RT-PCR)和蛋白质印迹法,在mRNA和蛋白质水平上测定BPH和PCa组织中激肽释放酶相关肽酶7的表达。分析激肽释放酶相关肽酶7 mRNA表达与临床病理特征之间的关系。92例良性病例中有64例(69.57%)KLK7染色呈阳性,116例恶性病例中有23例(19.83%)呈阳性,PCa和BPH之间KLK7表达的差异具有统计学意义(P < 0.001)。与BPH组织和正常前列腺组织相比,PCa组织中激肽释放酶相关肽酶7 mRNA的表达水平显著降低。根据PCa的病理类型,激肽释放酶相关肽酶7 mRNA在定位方面表现出不同的表达模式。同样,我们的蛋白质免疫印迹分析表明,PCa中KLK7的蛋白质表达水平低于BPH组织和正常前列腺组织。激肽释放酶相关肽酶7和KLK7表达在PCa中下调,激肽释放酶相关肽酶7的低表达与更高的Gleason评分和更高的前列腺特异性抗原水平密切相关。