| Literature DB >> 31298024 |
Han Young Kim1, Mikyung Kang2, Yeon Woong Choo1, Seok-Hyeong Go2, Sung Pil Kwon1, Seuk Young Song1, Hee Su Sohn1, Jihye Hong2, Byung-Soo Kim1,2,3.
Abstract
Liposomes are clinically used as drug carriers for cancer therapy; however, unwanted leakage of the encapsulated anticancer drug and poor tumor-targeting efficiency of liposomes may generate toxic side effects on healthy cells and lead to failure of tumor eradication. To overcome these limitations, we functionalized liposomes with a photosensitizer (KillerRed, KR)-embedded cancer cell membrane (CCM). A lipid adjuvant was also embedded in the lipocomplex to promote the anticancer immune response. KR proteins were expressed on CCM and did not leak from the lipocomplex. Owing to the homotypic affinity of the CCM for the source cancer cells, the lipocomplex exhibited a 3.3-fold higher cancer-targeting efficiency in vivo than a control liposome. The liposome functionalized with KR-embedded CCM and lipid adjuvant generated cytotoxic reactive oxygen species in photodynamic therapy and effectively induced anticancer immune responses, inhibiting primary tumor growth and lung metastasis in homotypic tumor-bearing mice. Taken together, the lipocomplex technology may improve liposome-based cancer therapy.Entities:
Keywords: Adjuvant; cancer cell membrane; cancer immunotherapy; homotypic targeting; liposome; photodynamic therapy
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Year: 2019 PMID: 31298024 DOI: 10.1021/acs.nanolett.9b01571
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189