Cationic lipid-based nanoparticles mediate functional delivery of acetate to tumor cells in vivo leading to significant anticancer effects.

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ICR Authors

Authors

Brody, LP
Sahuri-Arisoylu, M
Parkinson, JR
Parkes, HG
So, PW
Hajji, N
Thomas, EL
Frost, GS
Miller, AD
Bell, JD

Document Type

Journal Article

Date

2017-01-01

Date Accepted

Abstract

Metabolic reengineering using nanoparticle delivery represents an innovative therapeutic approach to normalizing the deregulation of cellular metabolism underlying many diseases, including cancer. Here, we demonstrated a unique and novel application to the treatment of malignancy using a short-chain fatty acid (SCFA)-encapsulated lipid-based delivery system - liposome-encapsulated acetate nanoparticles for cancer applications (LITA-CAN). We assessed chronic in vivo administration of our nanoparticle in three separate murine models of colorectal cancer. We demonstrated a substantial reduction in tumor growth in the xenograft model of colorectal cancer cell lines HT-29, HCT-116 p53+/+ and HCT-116 p53-/-. Nanoparticle-induced reductions in histone deacetylase gene expression indicated a potential mechanism for these anti-proliferative effects. Together, these results indicated that LITA-CAN could be used as an effective direct or adjunct therapy to treat malignant transformation in vivo.

Citation

International journal of nanomedicine, 2017, 12 pp. 6677 - 6685

Source Title

Publisher

DOVE MEDICAL PRESS LTD

ISSN

1176-9114

eISSN

1178-2013

Research Team

Magnetic Resonance

Notes