Gu Yan, Chow Mathilda Jing, Kapoor Anil, Mei Wenjuan, Jiang Yanzhi, Yan Judy, De Melo Jason, Seliman Maryam, Yang Huixiang, Cutz Jean-Claude, Bonert Michael, Major Pierre, Tang Damu
Division of Nephrology, Department of Medicine, McMaster University, St. Joseph's Hospital, Hamilton, Ontario, Canada; the Research Institute of St Joe's Hamilton, St. Joseph's Hospital, Hamilton, Ontario, Canada; the Hamilton Center for Kidney Research, St. Joseph's Hospital, Hamilton, Ontario, Canada.
the Hamilton Center for Kidney Research, St. Joseph's Hospital, Hamilton, Ontario, Canada; Department of Surgery, McMaster University, Hamilton, Ontario, Canada.
Transl Oncol. 2018 Aug;11(4):1012-1022. doi: 10.1016/j.tranon.2018.06.003. Epub 2018 Jun 30.
Butyrylcholinesterase (BChE) is a plasma enzyme that hydrolyzes ghrelin and bioactive esters, suggesting a role in modulating metabolism. Serum BChE is reduced in cancer patients. In prostate cancer (PC), the down-regulation is associated with disease recurrence. Nonetheless, how BChE is expressed in PC and its impact on PC remain unclear. We report here the biphasic changes of BChE expression in PC. In vitro, BChE expression was decreased in more tumorigenic PC stem-like cells (PCSLCs), DU145, and PC3 cells compared to less tumorigenic non-stem PCs and LNCaP cells. On the other hand, BChE was expressed at a higher level in LNCaP cells than immortalized but non-tumorigenic prostate epithelial BPH-1 cells. In vivo, BChE expression was up-regulated in DU145 xenografts compared to LNCaP xenografts; DU145 cell-derived lung metastases displayed comparable levels of BChE as subcutaneous tumors. Furthermore, LNCaP xenografts produced in castrated mice exhibited a significant increase of BChE expression compared to xenografts generated in intact mice. In patients, BChE expression was down-regulated in PCs (n = 340) compared to prostate tissues (n = 86). In two independent PC populations MSKCC (n = 130) and TCGA Provisional (n = 490), BChE mRNA levels were reduced from World Health Organization grade group 1 (WHOGG 1) PCs to WHOGG 3 PCs, followed by a significant increase in WHOGG 5 PCs. The up-regulation was associated with a reduction in disease-free survival (P = .008). Collectively, we demonstrated for the first time a biphasic alteration of BChE, its down-regulation at early stage of PC and its up-regulation at advanced PC.
丁酰胆碱酯酶(BChE)是一种血浆酶,可水解胃饥饿素和生物活性酯,提示其在调节代谢中发挥作用。癌症患者的血清BChE水平降低。在前列腺癌(PC)中,BChE下调与疾病复发相关。然而,BChE在PC中的表达情况及其对PC的影响仍不清楚。我们在此报告了BChE在PC中的双相变化。在体外,与致瘤性较低的非干细胞性PC和LNCaP细胞相比,在致瘤性更强的PC干细胞样细胞(PCSLCs)、DU145和PC3细胞中,BChE表达降低。另一方面,BChE在LNCaP细胞中的表达水平高于永生化但无致瘤性的前列腺上皮BPH-1细胞。在体内,与LNCaP异种移植瘤相比,DU145异种移植瘤中BChE表达上调;DU145细胞来源的肺转移瘤中BChE水平与皮下肿瘤相当。此外,与完整小鼠体内产生的异种移植瘤相比,去势小鼠体内产生的LNCaP异种移植瘤中BChE表达显著增加。在患者中,与前列腺组织(n = 86)相比,PC(n = 340)中BChE表达下调。在两个独立的PC群体MSKCC(n = 130)和TCGA临时队列(n = 490)中,BChE mRNA水平从世界卫生组织1级(WHOGG 1)PC降至WHOGG 3级PC,随后在WHOGG 5级PC中显著升高。这种上调与无病生存期缩短相关(P = .008)。总体而言,我们首次证明了BChE的双相改变,即在PC早期下调,在晚期上调。