4.7 Article

Engineering Exosome-Like Nanovesicles Derived from Asparagus cochinchinensis Can Inhibit the Proliferation of Hepatocellular Carcinoma Cells with Better Safety Profile

期刊

INTERNATIONAL JOURNAL OF NANOMEDICINE
卷 16, 期 -, 页码 1575-1586

出版社

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IJN.S293067

关键词

exosome; exosome-like nanovesicles; Asparagus cochinchinensis; engineering exosome; antitumor

资金

  1. National Natural Science Foundation of China [81803456]
  2. Young Elite Scientists Sponsorship Program by CAST [2017QNRC001]
  3. Key project at the central government level: The ability establishment of sustainable use for valuable Chinese medicine resources [2060302-1907-04]
  4. Natural Science Research of Jiangsu Higher Education Institutions of China [20KJA360004]
  5. Jiangsu Postgraduate Research & Practice Innovation Program [KYCX20_1497, KYCX20_1498]
  6. Six Talent Peaks Project of Jiangsu Province [SWYY-057]
  7. QingLan Project of Jiangsu Province of China

向作者/读者索取更多资源

This study presents a promising functional nano platform derived from edible Asparagus cochinchinensis that can be utilized in anti-tumor therapy with minimal side effects.
Background: Exosomes are a type of membrane vesicles secreted by living cells. Recent studies suggest exosome-like nanovesicles (ELNVs) from fruits and vegetables are involved in tissue renewal process and functional regulation against inflammatory diseases or cancers. However, there are few reports on ELNVs derived from medicinal plants. Methods: ELNVs derived from Asparagus cochinchinensis (Low.) Men. (ACNVs) were isolated and characterized. Cytotoxicity, antiproliferative and apoptosis-inducing capacity of ACNVs against hepatoma carcinoma cell were assessed. The endocytosis mechanism of ACNVs was evaluated on Hep G2 cells in the presence of different endocytosis inhibitors. In vivo distribution of ACNVs was detected in healthy and tumor-bearing mice after scavenger receptors (SRs) blockade. PEG engineering of ACNVs was achieved through optimizing the pharmacokinetic profiles. In vivo antitumor activity and toxicity were evaluated in Hep G2 cell xenograft model. Results: ACNVs were isolated and purified using a differential centrifugation method accompanied by sucrose gradient ultracentrifugation. The optimized ACNVs had an average size of about 119 nm and showed a typical cup-shaped nanostructure containing lipids, proteins, and RNAs. ACNVs were found to possess specific antitumor cell proliferation activity associated with an apoptosis-inducing pathway. ACNVs could be internalized into tumor cells mainly via phagocytosis, but they were quickly cleared once entering the blood. Blocking the SRs or PEGylation decoration prolonged the blood circulation time and increased the accumulation of ACNVs in tumor sites. In vivo antitumor results showed that PEGylated ACNVs could significantly inhibit tumor growth without side effects. Conclusion: This study provides a promising functional nano platform derived from edible Asparagus cochinchinensis that can be used in antitumor therapy with negligible side effects.

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