Kabir Syed Rashel, Alam Mohammad Taufiq, Uddin Md Belal
Department of Biochemistry and Molecular Biology, Faculty of Science, University of Rajshahi, Rajshahi, 6205, Bangladesh.
Department of Applied Chemistry and Chemical Engineering, University of Rajshahi, Rajshahi, 6205, Bangladesh.
Biochem Biophys Rep. 2024 Sep 5;40:101818. doi: 10.1016/j.bbrep.2024.101818. eCollection 2024 Dec.
Recently, we have reported that biogenic silver/silver chloride nanoparticles from (-AgCl-NPs) and (-Ag/AgCl-NPs) inhibited different cancer cells by inducing apoptosis and several genes alteration. Here for the first time, we assessed the effects of these two nanoparticles on human lung (A549) and hepatocellular (SMMC-7721) carcinoma cell lines. AgCl-NPs and -Ag/AgCl-NPs inhibited A549 cell growth with IC values of 22.7 and 59.7 μg/ml and the calculated IC values for SMMC-7721 cell were 89.3 and 126.3 μg/ml, respectively. -AgCl-NPs exerted higher cytotoxicity against HEK293T cells than doxorubicin and -Ag/AgCl-NPs. Both the nanoparticles induced apoptosis in A549 and SMMC-7721 cell lines. A significant rise of early apoptotic cells and late apoptotic cells was found for A549 cells after treatment with -AgCl-NPs and stained with FITC-annexin V/PI. Apoptosis in A549 cells was further confirmed by monitoring the alteration of the expression level of several genes using real-time PCR and cell cycle arrest by flowcytometry after treatment with -AgCl-NPs. The expression of STAT-3, TNFα, and EGFR genes was decreased with the increase of caspase-8, FAS, and FADD gene expression. G/M cell cycle phase was arrested after treatment of A549 cells with -AgCl-NPs.
最近,我们报道了源自(-AgCl-NPs)和(-Ag/AgCl-NPs)的生物源银/氯化银纳米颗粒通过诱导细胞凋亡和若干基因改变来抑制不同的癌细胞。在此,我们首次评估了这两种纳米颗粒对人肺癌(A549)和肝癌(SMMC-7721)细胞系的影响。AgCl-NPs和-Ag/AgCl-NPs抑制A549细胞生长,其IC值分别为22.7和59.7μg/ml,而计算得出的SMMC-7721细胞的IC值分别为89.3和126.3μg/ml。-AgCl-NPs对HEK293T细胞的细胞毒性比阿霉素和-Ag/AgCl-NPs更高。这两种纳米颗粒均在A549和SMMC-7721细胞系中诱导细胞凋亡。在用-AgCl-NPs处理并用FITC-膜联蛋白V/PI染色后,发现A549细胞中早期凋亡细胞和晚期凋亡细胞显著增加。在用-AgCl-NPs处理后,通过实时PCR监测若干基因表达水平的变化以及通过流式细胞术检测细胞周期停滞,进一步证实了A549细胞中的细胞凋亡。随着半胱天冬酶-8、FAS和FADD基因表达的增加,STAT-3、TNFα和EGFR基因的表达降低。在用-AgCl-NPs处理A549细胞后,G/M细胞周期阶段被阻滞。