4.7 Article

Combined effects of avasimibe immunotherapy, doxorubicin chemotherapy, and metal-organic frameworks nanoparticles on breast cancer

Journal

JOURNAL OF CELLULAR PHYSIOLOGY
Volume 235, Issue 5, Pages 4814-4823

Publisher

WILEY
DOI: 10.1002/jcp.29358

Keywords

avasimibe; breast cancer; chemotherapy; doxorubicin; EPR effect; immunotherapy

Funding

  1. National Natural Science Foundation of China [31470738, 31870728]
  2. National Basic Research Program of China [2014CB910103]
  3. Science Foundation of Wuhan University [2042016kf0169]

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CD8(+) T cells play a vital role in cancer immunotherapy and can be shaped by metabolism. Avasimibe is an acyl coenzyme A-cholesterol acyltransferase (ACAT) inhibitor, which has been clinically verified safe in other phase III clinical trials. It can potentiate the killing function of CD8(+) T cells by modulating cholesterol metabolism. Doxorubicin (DOX) is an anticancer drug widely used in many cancers to induce tumor cell apoptosis. Unfortunately, DOX also can induce toxic and side effects in many organs, compromising its usage and efficacy. Herein, we report the combinational usage of avasimibe and a safe pH sensitive nano-drug delivery system composing of DOX and metal-organic frameworks nanoparticles (MNPs). Our findings demonstrated that DOX-MNPs treatment inhibited tumor growth with good safety profile and avasimibe treatment combined DOX-MNPs treatment exhibited a better efficacy than monotherapies in 4T1 breast cancer therapy.

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