4.7 Article

Ferroptosis-induced anticancer effect of resveratrol with a biomimetic nano-delivery system in colorectal cancer treatment

期刊

ASIAN JOURNAL OF PHARMACEUTICAL SCIENCES
卷 17, 期 5, 页码 751-766

出版社

SHENYANG PHARMACEUTICAL UNIV
DOI: 10.1016/j.ajps.2022.07.006

关键词

Resveratrol; Red-blood-cell membrane; Colorectal cancer; Ferroptosis; IRGD

资金

  1. National Natural Science Foundation of China
  2. High-level startup fund of Nanjing Medical University
  3. Natural Science Foundation of Jiangsu Province
  4. [81773211]
  5. [81871942]
  6. [82073308]
  7. [KY109RC2019010]
  8. [BK20201086]

向作者/读者索取更多资源

This study demonstrated for the first time that Resveratrol could inhibit the growth of colon cancer cells through the ROS-dependent ferroptosis pathway and promote ferroptosis by downregulating specific proteins. Biomimetic nanocarriers were developed to improve the delivery efficiency of Resveratrol for colorectal cancer treatment.
Ferroptosis is a novel form of programmed cell death impelled by iron-dependent lipid peroxidation, which may be a potential strategy for cancer therapy. Here we demonstrated for the first time that Resveratrol (RSV), a traditional Chinese medicine (TCM) chemical monomer, could effectually inhibit the growth of colon cancer cells through the ROS-dependent ferroptosis pathway. Mechanistically, RSV evoked the increase of reactive oxygen species and lipid peroxidation in colorectal cancer cells, and eventually lead to ferroptosis. Furthermore, RSV could promote ferroptosis by downregulating the expression of the channel protein solute carrier family 7 member 11 (SLC7A11) and glutathione peroxidase 4 (GPX4). To improve the delivery efficiency of RSV, a biomimetic nanocarrier was developed by coating RSV-loaded poly(epsilon-caprolactone)-poly(ethylene glycol) (PCL-PEG) nanoparticles with erythrocyte membrane (RSV-NPs@RBCm). The RSV-NPs@RBCm provide the possibility to escape macrophage phagocytosis and have a long circulation effect. In addition, when coupled with a tumor-penetrating peptide iRGD, which could trigger enhanced tissue penetration tumor-specifically, the delivery of RSV-NPs@RBCm into tumors would be significantly improved results from the in vivo study demonstrated an excellent treatment efficacy for CRC. Altogether, our study highlighted the therapeutic potential of RSV as a ferroptosis-inducing anticancer agent and when loaded into a biomimetic nanoplatform, it might pave the way for the application of RSV loaded nanosystems for colorectal cancer treatment.(c) 2022 Shenyang Pharmaceutical University. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )

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