Yousef George M, Scorilas Andreas, Chang Albert, Rendl Laura, Diamandis Maria, Jung Klaus, Diamandis Eleftherios P
Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, 600 University Avenue, Toronto, Ontario M5G 1X5, Canada.
Prostate. 2002 May 1;51(2):126-32. doi: 10.1002/pros.10067.
Kallikreins are a subgroup of serine proteases with diverse physiological functions. Many kallikrein genes are differentially expressed in various malignancies and prostate specific antigen (PSA; encoded by the KLK3 gene) is the best tumor marker for prostate cancer. Human glandular kallikrein (hK2; encoded by the KLK2 gene) is an emerging tumor marker for prostate cancer. KLK5 is a newly discovered human kallikrein gene which shares a high degree of homology and is located adjacent to KLK2 and KLK3 genes on chromosome 19q13.4. Like KLK2 and KLK3, the KLK5 gene is regulated by steroid hormones in the BT-474 breast cancer cell line. We have previously shown that KLK5 is differentially expressed in ovarian and breast cancer.
We compared the expression of KLK5 in 29 pairs of histologically confirmed normal and prostate cancer tissues by quantitative RT-PCR using the LightCycler technology.
KLK5 expression was significantly lower in cancer tissues compared to their normal counterparts. Lowest levels of expression were found in T3 stage tumors compared with T1 and T2. Also, a significant negative correlation was found between Gleason score and KLK5 expression.
KLK5 should be further studied as a potential new prognostic marker in prostate cancer, whose expression is negatively correlated with cancer aggressiveness.
激肽释放酶是丝氨酸蛋白酶的一个亚群,具有多种生理功能。许多激肽释放酶基因在各种恶性肿瘤中差异表达,前列腺特异性抗原(PSA;由KLK3基因编码)是前列腺癌的最佳肿瘤标志物。人腺激肽释放酶(hK2;由KLK2基因编码)是一种新兴的前列腺癌肿瘤标志物。KLK5是一个新发现的人激肽释放酶基因,与KLK2和KLK3基因具有高度同源性,位于19号染色体q13.4上,与KLK2和KLK3基因相邻。与KLK2和KLK3一样,KLK5基因在BT - 474乳腺癌细胞系中受类固醇激素调控。我们之前已经表明KLK5在卵巢癌和乳腺癌中差异表达。
我们使用LightCycler技术通过定量逆转录聚合酶链反应(RT - PCR)比较了29对经组织学证实的正常前列腺组织和前列腺癌组织中KLK5的表达。
与正常组织相比,癌组织中KLK5的表达显著降低。与T1和T2期肿瘤相比,T3期肿瘤中KLK5的表达水平最低。此外,Gleason评分与KLK5表达之间存在显著的负相关。
KLK5作为前列腺癌潜在的新预后标志物应进一步研究,其表达与癌症侵袭性呈负相关。