A combination of sorafenib and nilotinib reduces the growth of castrate-resistant prostate cancer

Monica Archibald,1 Tara Pritchard,1 Hayley Nehoff,1 Rhonda J Rosengren,1 Khaled Greish,1,2 Sebastien Taurin1 1Department of Pharmacology and Toxicology, University of Otago, Dunedin, New Zealand; 2Aljawhara Centre for Molecular Medicine, Arabian Gulf University, Manama, Kingdom of Bahrain Abstract...

Full description

Bibliographic Details
Main Authors: Archibald M, Pritchard T, Nehoff H, Rosengren RJ, Greish K, Taurin S
Format: Article
Language:English
Published: Dove Medical Press 2016-01-01
Series:International Journal of Nanomedicine
Subjects:
Online Access:https://www.dovepress.com/a-combination-of-sorafenib-and-nilotinib-reduces-the-growth-of-castrat-peer-reviewed-article-IJN
_version_ 1818845499933851648
author Archibald M
Pritchard T
Nehoff H
Rosengren RJ
Greish K
Taurin S
author_facet Archibald M
Pritchard T
Nehoff H
Rosengren RJ
Greish K
Taurin S
author_sort Archibald M
collection DOAJ
description Monica Archibald,1 Tara Pritchard,1 Hayley Nehoff,1 Rhonda J Rosengren,1 Khaled Greish,1,2 Sebastien Taurin1 1Department of Pharmacology and Toxicology, University of Otago, Dunedin, New Zealand; 2Aljawhara Centre for Molecular Medicine, Arabian Gulf University, Manama, Kingdom of Bahrain Abstract: Castrate-resistant prostate cancer (CRPC) remains incurable due to the lack of effective therapies. Several tyrosine kinases have been implicated in the development and growth of CRPC, as such targeting these kinases may offer an alternative therapeutic strategy. We established the combination of two tyrosine kinase inhibitors (TKIs), sorafenib and nilotinib, as the most cytotoxic. In addtion, to improve their bioavailability and reduce their metabolism, we encapsulated sorafenib and nilotinib into styrene-co-maleic acid micelles. The micelles’ charge, size, and release rate were characterized. We assessed the effect of the combination on the cytotoxicity, cell cycle, apoptosis, protein expression, tumor spheroid integrity, migration, and invasion. The micelles exhibited a mean diameter of 100 nm, a neutral charge, and appeared highly stable. The micellar TKIs promoted greater cytotoxicity, decreased cell proliferation, and increased apoptosis relative to the free TKIs. In addition, the combination reduced the expression and activity of several tyrosine kinases and reduced tumor spheroid integrity and metastatic potential of CRPC cell lines more efficiently than the single treatments. The combination increased the therapeutic potential and demonstrated the relevance of a targeted combination therapy for the treatment of CRPC. In addition, the efficacy of the encapsulated drugs provides the basis for an in vivo preclinical testing. Keywords: sorafenib, nilotinib, castrate-resistant prostate cancer, tyrosine kinase inhibitors, nanomedicine
first_indexed 2024-12-19T05:30:38Z
format Article
id doaj.art-59e61614d14143069f88a7a245383ea5
institution Directory Open Access Journal
issn 1178-2013
language English
last_indexed 2024-12-19T05:30:38Z
publishDate 2016-01-01
publisher Dove Medical Press
record_format Article
series International Journal of Nanomedicine
spelling doaj.art-59e61614d14143069f88a7a245383ea52022-12-21T20:34:15ZengDove Medical PressInternational Journal of Nanomedicine1178-20132016-01-012016Issue 117920125170A combination of sorafenib and nilotinib reduces the growth of castrate-resistant prostate cancerArchibald MPritchard TNehoff HRosengren RJGreish KTaurin SMonica Archibald,1 Tara Pritchard,1 Hayley Nehoff,1 Rhonda J Rosengren,1 Khaled Greish,1,2 Sebastien Taurin1 1Department of Pharmacology and Toxicology, University of Otago, Dunedin, New Zealand; 2Aljawhara Centre for Molecular Medicine, Arabian Gulf University, Manama, Kingdom of Bahrain Abstract: Castrate-resistant prostate cancer (CRPC) remains incurable due to the lack of effective therapies. Several tyrosine kinases have been implicated in the development and growth of CRPC, as such targeting these kinases may offer an alternative therapeutic strategy. We established the combination of two tyrosine kinase inhibitors (TKIs), sorafenib and nilotinib, as the most cytotoxic. In addtion, to improve their bioavailability and reduce their metabolism, we encapsulated sorafenib and nilotinib into styrene-co-maleic acid micelles. The micelles’ charge, size, and release rate were characterized. We assessed the effect of the combination on the cytotoxicity, cell cycle, apoptosis, protein expression, tumor spheroid integrity, migration, and invasion. The micelles exhibited a mean diameter of 100 nm, a neutral charge, and appeared highly stable. The micellar TKIs promoted greater cytotoxicity, decreased cell proliferation, and increased apoptosis relative to the free TKIs. In addition, the combination reduced the expression and activity of several tyrosine kinases and reduced tumor spheroid integrity and metastatic potential of CRPC cell lines more efficiently than the single treatments. The combination increased the therapeutic potential and demonstrated the relevance of a targeted combination therapy for the treatment of CRPC. In addition, the efficacy of the encapsulated drugs provides the basis for an in vivo preclinical testing. Keywords: sorafenib, nilotinib, castrate-resistant prostate cancer, tyrosine kinase inhibitors, nanomedicinehttps://www.dovepress.com/a-combination-of-sorafenib-and-nilotinib-reduces-the-growth-of-castrat-peer-reviewed-article-IJNsorafenibnilotinibcastrate-resistant prostate cancertyrosine kinase inhibitorsnanomedicine
spellingShingle Archibald M
Pritchard T
Nehoff H
Rosengren RJ
Greish K
Taurin S
A combination of sorafenib and nilotinib reduces the growth of castrate-resistant prostate cancer
International Journal of Nanomedicine
sorafenib
nilotinib
castrate-resistant prostate cancer
tyrosine kinase inhibitors
nanomedicine
title A combination of sorafenib and nilotinib reduces the growth of castrate-resistant prostate cancer
title_full A combination of sorafenib and nilotinib reduces the growth of castrate-resistant prostate cancer
title_fullStr A combination of sorafenib and nilotinib reduces the growth of castrate-resistant prostate cancer
title_full_unstemmed A combination of sorafenib and nilotinib reduces the growth of castrate-resistant prostate cancer
title_short A combination of sorafenib and nilotinib reduces the growth of castrate-resistant prostate cancer
title_sort combination of sorafenib and nilotinib reduces the growth of castrate resistant prostate cancer
topic sorafenib
nilotinib
castrate-resistant prostate cancer
tyrosine kinase inhibitors
nanomedicine
url https://www.dovepress.com/a-combination-of-sorafenib-and-nilotinib-reduces-the-growth-of-castrat-peer-reviewed-article-IJN
work_keys_str_mv AT archibaldm acombinationofsorafenibandnilotinibreducesthegrowthofcastrateresistantprostatecancer
AT pritchardt acombinationofsorafenibandnilotinibreducesthegrowthofcastrateresistantprostatecancer
AT nehoffh acombinationofsorafenibandnilotinibreducesthegrowthofcastrateresistantprostatecancer
AT rosengrenrj acombinationofsorafenibandnilotinibreducesthegrowthofcastrateresistantprostatecancer
AT greishk acombinationofsorafenibandnilotinibreducesthegrowthofcastrateresistantprostatecancer
AT taurins acombinationofsorafenibandnilotinibreducesthegrowthofcastrateresistantprostatecancer
AT archibaldm combinationofsorafenibandnilotinibreducesthegrowthofcastrateresistantprostatecancer
AT pritchardt combinationofsorafenibandnilotinibreducesthegrowthofcastrateresistantprostatecancer
AT nehoffh combinationofsorafenibandnilotinibreducesthegrowthofcastrateresistantprostatecancer
AT rosengrenrj combinationofsorafenibandnilotinibreducesthegrowthofcastrateresistantprostatecancer
AT greishk combinationofsorafenibandnilotinibreducesthegrowthofcastrateresistantprostatecancer
AT taurins combinationofsorafenibandnilotinibreducesthegrowthofcastrateresistantprostatecancer