4.6 Article

Activating caspase-8/Bid/ROS signaling to promote apoptosis of breast cancer cells by folate-modified albumin baicalin-loaded nanoparticles

Journal

NANOTECHNOLOGY
Volume 33, Issue 43, Pages -

Publisher

IOP Publishing Ltd
DOI: 10.1088/1361-6528/ac197b

Keywords

baicalin; albumin nanoparticles; folate; apoptosis; breast cancer

Funding

  1. projects of International Cooperation and Exchanges of National Natural Science Foundation of China [82020108033]
  2. Natural Science Foundation of Guangdong Province [2019A1515011286]
  3. Foshan 'Summit Plan' of building high-level hospitals

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This study developed an active targeting delivery system using folate-conjugated albumin nanoparticles to improve the bioavailability and therapeutic efficacy of baicalin. It was found that the constructed carrier increased targeted uptake efficiency and cytotoxicity, and promoted apoptosis in breast cancer through the regulation of key proteins in the extrinsic apoptotic pathway.
Abnormal apoptosis can lead to uncontrolled cell growth, aberrant homeostasis or the accumulation of mutations. Therapeutic agents that re-establish the normal functions of apoptotic signaling pathways offer an attractive strategy for the treatment of breast cancer. Baicalin (BA) is one of the natural compounds with anti-proliferation and pro-apoptosis activities against numerous tumor cells. However, low bioavailability restricts the clinical application of BA. In order to improve its therapeutic efficacy and study the mechanism of actions, active targeting delivery systems were developed for targeting tumor environment and selective cell killing effects. It emphasized on the construction of folate-conjugated albumin nanoparticles loaded with baicalin (FA-BSANPs/BA) and mechanisms of which on the promotion of breast cancer apoptosis. The physicochemical properties and structural characteristics of FA-BSANPs/BA were investigated. Cell experiments were carried out to study the targeted anti-breast cancer effects of FA-BSANPs/BA and its mechanism. The results showed that FA-BSANPs/BA was successfully constructed with stable structural characteristics and sustained release effects. Cellular uptake and MTT showed that it increased targeted uptake efficiency and cytotoxicity. Flow cytometry and western blot confirmed that it promoted apoptosis by increasing the expression of caspase-8 and ROS, and decreasing the level of Bid. It is suggested that the pro-apoptotic mechanism of FA-BSANPs/BA is related to regulation of key proteins in extrinsic apoptotic pathway. In conclusion, FA-BSANPs/BA is a good delivery carrier and significantly inhibits the breast cancer growth compared with free BA. The mechanism of FA-BSANPs/BA promoting apoptosis of breast cancer may be due to its action on the caspase-8/Bid/ROS pathway.

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