4.7 Article

Green Synthesis of Silver Nanoparticles Using Annona muricata Extract as an Inducer of Apoptosis in Cancer Cells and Inhibitor for NLRP3 Inflammasome via Enhanced Autophagy

期刊

NANOMATERIALS
卷 11, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/nano11020384

关键词

Annona muricata; silver nanoparticle; anticancer; apoptosis; autophagy; IL-1 beta; NLRP3

资金

  1. Deputyship for Research and innovation Ministry of Education in Saudi Arabia [IFKSURG-33]

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This study demonstrates that silver nanoparticles prepared using Annona muricata peel extract exhibit anti-proliferative activity against leukemia cell lines, while also significantly increasing autophagy and reducing levels of IL-1 beta and NLRP3. This suggests that AgNPs could be a potent therapy for various types of cancer and an alternative treatment for preventing inflammation by enhancing autophagy.
Annona muricata is one of the most important traditional medicinal plants which contains numerous chemicals that exhibit various pharmacological properties. In this study, silver nanoparticies were prepared using A. muricata peel extract as a reducing agent and the effect was enhanced through A. muricata like pharmaceutical activity. AgNPs formation was confirmed by color changes, UV-visible spectroscopy, SEM, DLS, and XRD. The anti-proliferative activity of AgNPs against THP-1, AMJ-13, and HBL cell lines was studied. Apoptotic markers were tested using AO/EtBr staining assay, cell cycle phases using flowcytometry, and the expression of P53. Autophagy takes an essential part in controlling inflammasome activation by primary bone marrow-derived macrophages (BMDMs). We report novel functions for AgNPs-affected autophagy, represented by the control of the release of IL-1 beta, caspase-1, adaptor protein apoptosis-associated speck-like protein containing a CARD (ASC), and NLRP3 in BMDMs following treatment with LPS+ATP. The current study revealed that the AgNPs inhibited THP-1 and AMJ-13 cell proliferation. Meanwhile, the AgNPs significantly increased autophagy and reduced IL-1b and NLRP3 levels in both in vivo and in vitro models. The secretion of IL-1 beta was reduced whereas the degradation of NLRP3 inflammasome was enhanced. These findings propose that AgNPs apply an anti-proliferative activity against THP-1 and AMJ-13 cells through the stimulation of apoptosis via mitochondrial damage and induction of p53 protein pathway. In addition, AgNP-induced autophagy reduced the levels of IL-1 beta and NLRP3 inflammasome activation. This indicated that the AgNPs augment autophagy controlled by the IL-1 beta pathway via two different novel mechanisms. The first one is regulating activation of the IL-1 beta, caspase-1, and ASC, while the second is NLRP3 targeting for lysosomal degradation. Overall, this study suggests that AgNPs could be a potent therapy for various types of cancer and an alternative treatment for preventing inflammation via enhancing autophagy.

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