Liposomal delivery of dexamethasone attenuates prostate cancer bone metastatic tumor growth In Vivo. Issue 8 (8th February 2015)
- Record Type:
- Journal Article
- Title:
- Liposomal delivery of dexamethasone attenuates prostate cancer bone metastatic tumor growth In Vivo. Issue 8 (8th February 2015)
- Main Title:
- Liposomal delivery of dexamethasone attenuates prostate cancer bone metastatic tumor growth In Vivo
- Authors:
- Kroon, Jan
Buijs, Jeroen T.
van der Horst, Geertje
Cheung, Henry
van der Mark, Maaike
van Bloois, Louis
Rizzo, Larissa Y.
Lammers, Twan
Pelger, Rob C.
Storm, Gert
van der Pluijm, Gabri
Metselaar, Josbert M. - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pros22963-sec-0001" sec-type="section"> <title>Background</title> <p>The inflammatory tumor microenvironment, and more specifically the tumor‐associated macrophages, plays an essential role in the development and progression of prostate cancer towards metastatic bone disease. Tumors are often characterized by a leaky vasculature, which ‐ combined with the prolonged circulation kinetics of liposomes ‐ leads to efficient tumor localization of these drug carriers, via the so‐called enhanced permeability and retention (EPR) ‐effect. In this study, we evaluated the utility of targeted, liposomal drug delivery of the glucocorticoid dexamethasone in a model of prostate cancer bone metastases.</p> </sec> <sec id="pros22963-sec-0002" sec-type="section"> <title>Methods</title> <p>Tumor‐bearing Balb‐c nu/nu mice were treated intravenously with 0.2–1.0–5.0 mg/kg/week free‐ and liposomal DEX for 3–4 weeks and tumor growth was monitored by bioluminescent imaging.</p> </sec> <sec id="pros22963-sec-0003" sec-type="section"> <title>Results</title> <p>Intravenously administered liposomes localize efficiently to bone metastases in vivo and treatment of established bone metastases with (liposomal) dexamethasone resulted in a significant inhibition of tumor growth up to 26 days after initiation of treatment. Furthermore, 1.0 mg/kg liposomal dexamethasone significantly outperformed<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pros22963-sec-0001" sec-type="section"> <title>Background</title> <p>The inflammatory tumor microenvironment, and more specifically the tumor‐associated macrophages, plays an essential role in the development and progression of prostate cancer towards metastatic bone disease. Tumors are often characterized by a leaky vasculature, which ‐ combined with the prolonged circulation kinetics of liposomes ‐ leads to efficient tumor localization of these drug carriers, via the so‐called enhanced permeability and retention (EPR) ‐effect. In this study, we evaluated the utility of targeted, liposomal drug delivery of the glucocorticoid dexamethasone in a model of prostate cancer bone metastases.</p> </sec> <sec id="pros22963-sec-0002" sec-type="section"> <title>Methods</title> <p>Tumor‐bearing Balb‐c nu/nu mice were treated intravenously with 0.2–1.0–5.0 mg/kg/week free‐ and liposomal DEX for 3–4 weeks and tumor growth was monitored by bioluminescent imaging.</p> </sec> <sec id="pros22963-sec-0003" sec-type="section"> <title>Results</title> <p>Intravenously administered liposomes localize efficiently to bone metastases in vivo and treatment of established bone metastases with (liposomal) dexamethasone resulted in a significant inhibition of tumor growth up to 26 days after initiation of treatment. Furthermore, 1.0 mg/kg liposomal dexamethasone significantly outperformed 1.0 mg/kg free dexamethasone, and was found to be well‐tolerated at clinically‐relevant dosages that display potent anti‐tumor efficacy.</p> </sec> <sec id="pros22963-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Liposomal delivery of the glucocorticoid dexamethasone inhibits the growth of malignant bone lesions. We believe that liposomal encapsulation of dexamethasone offers a promising new treatment option for advanced, metastatic prostate cancer which supports further clinical evaluation. Prostate 75: 815–824, 2015. © 2015 The Authors. <italic>The Prostate</italic>, published by Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Prostate. Volume 75:Issue 8(2015)
- Journal:
- Prostate
- Issue:
- Volume 75:Issue 8(2015)
- Issue Display:
- Volume 75, Issue 8 (2015)
- Year:
- 2015
- Volume:
- 75
- Issue:
- 8
- Issue Sort Value:
- 2015-0075-0008-0000
- Page Start:
- 815
- Page End:
- 824
- Publication Date:
- 2015-02-08
- Subjects:
- Prostate -- Diseases -- Periodicals
616 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-0045 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pros.22963 ↗
- Languages:
- English
- ISSNs:
- 0270-4137
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6935.194000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3733.xml