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Biphasic Alteration of Butyrylcholinesterase (BChE) During Prostate Cancer Development
Authors:Yan Gu  Mathilda Jing Chow  Anil Kapoor  Wenjuan Mei  Yanzhi Jiang  Judy Yan  Jason De Melo  Maryam Seliman  Huixiang Yang  Jean-Claude Cutz  Michael Bonert  Pierre Major  Damu Tang
Affiliation:2. the Research Institute of St Joe''s Hamilton, St. Joseph''s Hospital, Hamilton, Ontario, Canada;3. the Hamilton Center for Kidney Research, St. Joseph''s Hospital, Hamilton, Ontario, Canada;4. Department of Surgery, McMaster University, Hamilton, Ontario, Canada;11. Division of Anatomical Pathology, Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada;12. Division of Medical Oncology, Department of Oncology, McMaster University, Hamilton, Ontario, Canada
Abstract: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.
Keywords:Address all correspondence to: Damu Tang   T3310   St. Joseph's Hospital   50 Charlton Ave East   Hamilton   Ontario   Canada   L8N 4A6. or Pierre Major   699 Concession Street   Hamilton   Ontario   Canada   L8V 5C2.
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