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Biphasic Alteration of Butyrylcholinesterase (BChE) During Prostate Cancer Development

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 i...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031255/
https://www.ncbi.nlm.nih.gov/pubmed/29966864
http://dx.doi.org/10.1016/j.tranon.2018.06.003
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author 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
author_facet 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
author_sort Gu, Yan
collection PubMed
description 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.
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spelling pubmed-60312552018-07-10 Biphasic Alteration of Butyrylcholinesterase (BChE) During Prostate Cancer Development 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 Transl Oncol Original article 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. Neoplasia Press 2018-06-30 /pmc/articles/PMC6031255/ /pubmed/29966864 http://dx.doi.org/10.1016/j.tranon.2018.06.003 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original article
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
Biphasic Alteration of Butyrylcholinesterase (BChE) During Prostate Cancer Development
title Biphasic Alteration of Butyrylcholinesterase (BChE) During Prostate Cancer Development
title_full Biphasic Alteration of Butyrylcholinesterase (BChE) During Prostate Cancer Development
title_fullStr Biphasic Alteration of Butyrylcholinesterase (BChE) During Prostate Cancer Development
title_full_unstemmed Biphasic Alteration of Butyrylcholinesterase (BChE) During Prostate Cancer Development
title_short Biphasic Alteration of Butyrylcholinesterase (BChE) During Prostate Cancer Development
title_sort biphasic alteration of butyrylcholinesterase (bche) during prostate cancer development
topic Original article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031255/
https://www.ncbi.nlm.nih.gov/pubmed/29966864
http://dx.doi.org/10.1016/j.tranon.2018.06.003
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