Cargando…

Inhibition of Phospholipase D1 mRNA Expression Slows Down the Proliferation Rate of Prostate Cancer Cells That Have Transited to Androgen Independence

To explore the role of phospholipase D1 (PLD1) mRNA in transition of prostate cancer (PCa) cells to androgen independence, we used Arraystar Human LncRNA Microarray V3.0 to detect and compare the differential expression of PLD1 and its signaling pathway-related gene in standard androgen dependence p...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhou, Wu, Shi, Keqing, Ji, Lili, Wu, Ruihao, Chen, Yuehui, Tu, Hongxiang, Zhou, Beibei, Wang, Zhongyong, Zhang, Meijuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171019/
https://www.ncbi.nlm.nih.gov/pubmed/30310520
http://dx.doi.org/10.7150/jca.26689
_version_ 1783360719742304256
author Zhou, Wu
Shi, Keqing
Ji, Lili
Wu, Ruihao
Chen, Yuehui
Tu, Hongxiang
Zhou, Beibei
Wang, Zhongyong
Zhang, Meijuan
author_facet Zhou, Wu
Shi, Keqing
Ji, Lili
Wu, Ruihao
Chen, Yuehui
Tu, Hongxiang
Zhou, Beibei
Wang, Zhongyong
Zhang, Meijuan
author_sort Zhou, Wu
collection PubMed
description To explore the role of phospholipase D1 (PLD1) mRNA in transition of prostate cancer (PCa) cells to androgen independence, we used Arraystar Human LncRNA Microarray V3.0 to detect and compare the differential expression of PLD1 and its signaling pathway-related gene in standard androgen dependence prostate cancer (ADPC) cell line LNCaP before and after the occurrence of androgen independence prostate cancer (AIPC) transition. In addition, we used the shRNA lentiviral vector to inhibit the PLD1 mRNA expression and observed its effect on LNCaP cell proliferation after AIPC transition by using MTS method. The results showed that the expression level of PLD1 mRNA was increased by 373-fold after AIPC transition (P<0.05); the PI3K/AKT signaling pathway-related gene expression was also elevated (P<0.05); the growth rate of LNCaP cells that had transited to androgen independence was reduced by about 30% when the PLD1 mRNA expression was inhibited by the shRNA lentivirus as compared with the negative control group (P<0.05). All these results suggest that PLD1 mRNA and the related PI3K/AKT signaling pathway may play an important role in AIPC. Down-regulating the expression of PLD1 mRNA could to some extent inhibit the proliferation rate of PCa cells after AIPC transition.
format Online
Article
Text
id pubmed-6171019
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Ivyspring International Publisher
record_format MEDLINE/PubMed
spelling pubmed-61710192018-10-11 Inhibition of Phospholipase D1 mRNA Expression Slows Down the Proliferation Rate of Prostate Cancer Cells That Have Transited to Androgen Independence Zhou, Wu Shi, Keqing Ji, Lili Wu, Ruihao Chen, Yuehui Tu, Hongxiang Zhou, Beibei Wang, Zhongyong Zhang, Meijuan J Cancer Research Paper To explore the role of phospholipase D1 (PLD1) mRNA in transition of prostate cancer (PCa) cells to androgen independence, we used Arraystar Human LncRNA Microarray V3.0 to detect and compare the differential expression of PLD1 and its signaling pathway-related gene in standard androgen dependence prostate cancer (ADPC) cell line LNCaP before and after the occurrence of androgen independence prostate cancer (AIPC) transition. In addition, we used the shRNA lentiviral vector to inhibit the PLD1 mRNA expression and observed its effect on LNCaP cell proliferation after AIPC transition by using MTS method. The results showed that the expression level of PLD1 mRNA was increased by 373-fold after AIPC transition (P<0.05); the PI3K/AKT signaling pathway-related gene expression was also elevated (P<0.05); the growth rate of LNCaP cells that had transited to androgen independence was reduced by about 30% when the PLD1 mRNA expression was inhibited by the shRNA lentivirus as compared with the negative control group (P<0.05). All these results suggest that PLD1 mRNA and the related PI3K/AKT signaling pathway may play an important role in AIPC. Down-regulating the expression of PLD1 mRNA could to some extent inhibit the proliferation rate of PCa cells after AIPC transition. Ivyspring International Publisher 2018-09-08 /pmc/articles/PMC6171019/ /pubmed/30310520 http://dx.doi.org/10.7150/jca.26689 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Zhou, Wu
Shi, Keqing
Ji, Lili
Wu, Ruihao
Chen, Yuehui
Tu, Hongxiang
Zhou, Beibei
Wang, Zhongyong
Zhang, Meijuan
Inhibition of Phospholipase D1 mRNA Expression Slows Down the Proliferation Rate of Prostate Cancer Cells That Have Transited to Androgen Independence
title Inhibition of Phospholipase D1 mRNA Expression Slows Down the Proliferation Rate of Prostate Cancer Cells That Have Transited to Androgen Independence
title_full Inhibition of Phospholipase D1 mRNA Expression Slows Down the Proliferation Rate of Prostate Cancer Cells That Have Transited to Androgen Independence
title_fullStr Inhibition of Phospholipase D1 mRNA Expression Slows Down the Proliferation Rate of Prostate Cancer Cells That Have Transited to Androgen Independence
title_full_unstemmed Inhibition of Phospholipase D1 mRNA Expression Slows Down the Proliferation Rate of Prostate Cancer Cells That Have Transited to Androgen Independence
title_short Inhibition of Phospholipase D1 mRNA Expression Slows Down the Proliferation Rate of Prostate Cancer Cells That Have Transited to Androgen Independence
title_sort inhibition of phospholipase d1 mrna expression slows down the proliferation rate of prostate cancer cells that have transited to androgen independence
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6171019/
https://www.ncbi.nlm.nih.gov/pubmed/30310520
http://dx.doi.org/10.7150/jca.26689
work_keys_str_mv AT zhouwu inhibitionofphospholipased1mrnaexpressionslowsdowntheproliferationrateofprostatecancercellsthathavetransitedtoandrogenindependence
AT shikeqing inhibitionofphospholipased1mrnaexpressionslowsdowntheproliferationrateofprostatecancercellsthathavetransitedtoandrogenindependence
AT jilili inhibitionofphospholipased1mrnaexpressionslowsdowntheproliferationrateofprostatecancercellsthathavetransitedtoandrogenindependence
AT wuruihao inhibitionofphospholipased1mrnaexpressionslowsdowntheproliferationrateofprostatecancercellsthathavetransitedtoandrogenindependence
AT chenyuehui inhibitionofphospholipased1mrnaexpressionslowsdowntheproliferationrateofprostatecancercellsthathavetransitedtoandrogenindependence
AT tuhongxiang inhibitionofphospholipased1mrnaexpressionslowsdowntheproliferationrateofprostatecancercellsthathavetransitedtoandrogenindependence
AT zhoubeibei inhibitionofphospholipased1mrnaexpressionslowsdowntheproliferationrateofprostatecancercellsthathavetransitedtoandrogenindependence
AT wangzhongyong inhibitionofphospholipased1mrnaexpressionslowsdowntheproliferationrateofprostatecancercellsthathavetransitedtoandrogenindependence
AT zhangmeijuan inhibitionofphospholipased1mrnaexpressionslowsdowntheproliferationrateofprostatecancercellsthathavetransitedtoandrogenindependence