Calcilytics inhibit the proliferation and migration of human prostate cancer PC-3 cells
The carcinogenesis and development of prostate cancer are mediated by enhanced Ca2+ signaling. In the present study, the pharmacological profile of the Ca2+-sensing receptor (CaSR) antagonists (calcilytics) was examined in human prostate cancer PC-3 cells. NPS2143 and Calhex 231 blocked extracellula...
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doaj-98b164a323c64cf39919b8dda4566a002020-11-25T00:44:51ZengElsevierJournal of Pharmacological Sciences1347-86132019-03-011393254257Calcilytics inhibit the proliferation and migration of human prostate cancer PC-3 cellsAya Yamamura0Md Junayed Nayeem1Motohiko Sato2Corresponding author. Fax: +81 561 63 9809.; Department of Physiology, Aichi Medical University, 1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, JapanDepartment of Physiology, Aichi Medical University, 1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, JapanDepartment of Physiology, Aichi Medical University, 1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, JapanThe carcinogenesis and development of prostate cancer are mediated by enhanced Ca2+ signaling. In the present study, the pharmacological profile of the Ca2+-sensing receptor (CaSR) antagonists (calcilytics) was examined in human prostate cancer PC-3 cells. NPS2143 and Calhex 231 blocked extracellular Ca2+-induced increases in cytosolic [Ca2+]. NPS2143 and Calhex 231 inhibited cell proliferation (IC50 = 7.4 and 10.3 μM, respectively) and migration. The exposure to NPS2143 or Calhex 231 down-regulated CaSR protein expression. These results demonstrated that calcilytics inhibited cell proliferation/migration and down-regulated CaSR expression in human prostate cancer cells, suggesting their potential as novel therapeutic drugs for prostate cancer. Keywords: Calcium-sensing receptor, Calcilytic, Prostate cancerhttp://www.sciencedirect.com/science/article/pii/S1347861319300131 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Aya Yamamura Md Junayed Nayeem Motohiko Sato |
spellingShingle |
Aya Yamamura Md Junayed Nayeem Motohiko Sato Calcilytics inhibit the proliferation and migration of human prostate cancer PC-3 cells Journal of Pharmacological Sciences |
author_facet |
Aya Yamamura Md Junayed Nayeem Motohiko Sato |
author_sort |
Aya Yamamura |
title |
Calcilytics inhibit the proliferation and migration of human prostate cancer PC-3 cells |
title_short |
Calcilytics inhibit the proliferation and migration of human prostate cancer PC-3 cells |
title_full |
Calcilytics inhibit the proliferation and migration of human prostate cancer PC-3 cells |
title_fullStr |
Calcilytics inhibit the proliferation and migration of human prostate cancer PC-3 cells |
title_full_unstemmed |
Calcilytics inhibit the proliferation and migration of human prostate cancer PC-3 cells |
title_sort |
calcilytics inhibit the proliferation and migration of human prostate cancer pc-3 cells |
publisher |
Elsevier |
series |
Journal of Pharmacological Sciences |
issn |
1347-8613 |
publishDate |
2019-03-01 |
description |
The carcinogenesis and development of prostate cancer are mediated by enhanced Ca2+ signaling. In the present study, the pharmacological profile of the Ca2+-sensing receptor (CaSR) antagonists (calcilytics) was examined in human prostate cancer PC-3 cells. NPS2143 and Calhex 231 blocked extracellular Ca2+-induced increases in cytosolic [Ca2+]. NPS2143 and Calhex 231 inhibited cell proliferation (IC50 = 7.4 and 10.3 μM, respectively) and migration. The exposure to NPS2143 or Calhex 231 down-regulated CaSR protein expression. These results demonstrated that calcilytics inhibited cell proliferation/migration and down-regulated CaSR expression in human prostate cancer cells, suggesting their potential as novel therapeutic drugs for prostate cancer. Keywords: Calcium-sensing receptor, Calcilytic, Prostate cancer |
url |
http://www.sciencedirect.com/science/article/pii/S1347861319300131 |
work_keys_str_mv |
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