Preparation and antitumor activity of selenium nanocomposite stabilized by AAGL from Agerocybe aegerita

化学 立体化学 有机化学
作者
Ying Chen,Yanxia Jin,Weidong Wang,Yueyang Zhang,Hui Sun,Aobo Wu,Haibo Zhu,Yongsheng Gong,Xiaoyu Wang,Lei Tian,Jicheng Pan
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:: 137002-137002
标识
DOI:10.1016/j.ijbiomac.2024.137002
摘要

Selenium nanoparticles (SeNPs) have limited bioavailability because of their poor stability in aqueous solutions. AAGL, a naturally active protein, extracted from Agrocybe aegerita has strong antitumor activity. However, AAGL has been used to stabilize SeNPs, and whether it exerts anti-lung cancer effects remains unknown. In this study, a novel nanocomposite, AAGL-SeNPs, was prepared using AAGL-encapsulated SeNPs. The particle size of the AAGL-SeNPs was approximately 206.1 nm, which was uniform and well dispersed in aqueous solution and showed satisfactory stability. AAGL-SeNPs was non-toxic and reduced the hepatotoxicity of AAGL in mice. Importantly, AAGL-SeNPs inhibited the proliferation of lung cancer cells and suppressed tumor growth in tumor-bearing mice. AAGL-SeNPs enhanced the cytotoxic effects on lung cancer cells by stimulating immune cells. In addition, the combination of AAGL-SeNPs and osimertinib inhibited lung cancer, and AAGL-SeNPs reversed osimertinib resistance in H1975 cells. Mechanistically, Krüppel-like transcriptional factor 4 (KLF4) was identified by data-independent acquisition mass spectrometry (DIA-MS), and its expression levels in lung cancer increased after AAGL-SeNPs treatment. This study demonstrated that nanocomposite AAGL-SeNPs is stable, safe, and has excellent antitumor efficacy, which will be a potential therapeutic drug for lung cancer treatment.
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