Immunomodulatory Lipocomplex Functionalized with Photosensitizer-Embedded Cancer Cell Membrane Inhibits Tumor Growth and Metastasis.
Han Young KimMikyung KangYeon Woong ChooSeok-Hyeong GoSung Pil KwonSeuk Young SongHee Su SohnJihye HongByung-Seok KimPublished in: Nano letters (2019)
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.
Keyphrases
- cancer therapy
- photodynamic therapy
- drug delivery
- immune response
- papillary thyroid
- squamous cell
- reactive oxygen species
- early stage
- quantum dots
- induced apoptosis
- emergency department
- signaling pathway
- toll like receptor
- type diabetes
- dendritic cells
- childhood cancer
- lymph node metastasis
- molecularly imprinted
- inflammatory response
- cell cycle arrest
- oxidative stress
- young adults
- metabolic syndrome
- endoplasmic reticulum stress
- diabetic rats