Anti-cancer effects of green synthesized gold nanoparticles using leaf extract of Annona muricata. L against squamous cell carcinoma cell line 15 through apoptotic pathway

Q2 Dentistry
S. Jeslin, Veeran Veeravarmal, Prasanth Thankappan, Paramasivam Arumugam, Percy Ida Augustine, R. Franklin, Dr. S. Jeslin Mary
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引用次数: 0

Abstract

Background: Oral cancer remains one of the most dreadful diseases in developing nations. Currently, there has been a rise in the prevalence of tongue squamous cell carcinoma (SCC), with a poor prognosis. The use of standard treatment approaches against oral cancer patients brings about several side effects. In recent years, nanomedicine has provided a versatile platform for developing new targeted therapeutic modalities. However, safety remains a concern in the synthesis of nanoparticles (NPs). Therefore, the present study aims to synthesize safer phytoconstituent-mediated gold NPs (AuNPs) utilizing leaf extracts of Annona muricata, where the biochemical components of the plant leaf act as the reducing and capping agents in the synthesis of NPs, and to evaluate its anti-cancer activity against SCC. Materials and Methods: In this in vitro experimental study, AuNPs were synthesized through an effective, simple, and ecologically sound green synthesis method. After characterization of these synthesized AuNPs, in vitro assays such as 3-(4, 5-dimethylthiazole2-yl)-2, 5-biphenyl tetrazolium bromide, wound healing, and clonogenic assays were carried out to investigate the anti-cancer potential of green synthesized AuNPs in the human tongue SCC cell line (SCC-15), and the possible mechanism of action was evaluated through gene and protein expression analysis of Bax, Bcl-2, and p53 genes. The results were expressed as mean ± standard deviation using Statistical Package for Social Sciences (SPSS) 20.0 software and Student's t-test was performed for experimental data. P ≤0.05 were considered statistically significant. Results: The in vitro assays demonstrated that the synthesized AuNPs are exhibiting anti-cancer activity by apoptosis of SCC-15 cells in a dose-dependent manner. Further, it also revealed a highly significant decrease in anti-apoptotic Bcl-2 gene expression, whereas pro-apoptotic genes p53 and Bax revealed a highly significant increase, which is statistically significant compared to the control (P < 0.05). Conclusion: Our findings demonstrated that the AuNPs synthesized from A. muricata leaf extract could act as a novel anticancer agent, particularly against SCC, after further scrutiny.
利用鼠尾草叶提取物合成的绿色金纳米粒子通过凋亡途径对鳞癌细胞株15的抗癌作用。L 通过凋亡途径对鳞状细胞癌细胞系 15 的抗癌作用
背景:口腔癌仍然是发展中国家最可怕的疾病之一。目前,舌鳞状细胞癌(SCC)的发病率有所上升,且预后不良。对口腔癌患者采用标准治疗方法会带来一些副作用。近年来,纳米医学为开发新的靶向治疗模式提供了一个多功能平台。然而,在合成纳米粒子(NPs)的过程中,安全性仍然是一个令人担忧的问题。因此,本研究旨在利用鼠尾草叶提取物合成更安全的植物成分介导的金 NPs(AuNPs),其中植物叶片的生化成分在合成 NPs 的过程中充当还原剂和封端剂,并评估其对 SCC 的抗癌活性。材料与方法:在这项体外实验研究中,我们采用了一种有效、简单且无害生态的绿色合成方法合成了 AuNPs。在对这些合成的 AuNPs 进行表征后,进行了 3-(4,5-二甲基噻唑-2-基)-2,5-联苯四唑溴化物、伤口愈合和克隆生成试验等体外试验,以研究绿色合成 AuNPs 在人舌 SCC 细胞系(SCC-15)中的抗癌潜力,并通过 Bax、Bcl-2 和 p53 基因的基因和蛋白表达分析评估其可能的作用机制。实验结果采用社会科学统计软件包(SPSS)20.0软件以均数±标准差表示,并对实验数据进行学生t检验。P≤0.05为差异有统计学意义。结果体外实验表明,合成的 AuNPs 具有抗癌活性,能以剂量依赖的方式使 SCC-15 细胞凋亡。此外,研究还发现,抗凋亡基因 Bcl-2 的表达量显著减少,而促凋亡基因 p53 和 Bax 的表达量显著增加,与对照组相比,差异有统计学意义(P < 0.05)。结论我们的研究结果表明,由 A. muricata 叶提取物合成的 AuNPs 经进一步研究后可作为一种新型抗癌剂,尤其是针对 SCC。
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来源期刊
Dental Research Journal
Dental Research Journal Dentistry-Dentistry (all)
CiteScore
1.70
自引率
0.00%
发文量
70
审稿时长
52 weeks
期刊介绍: Dental Research Journal, a publication of Isfahan University of Medical Sciences, is a peer-reviewed online journal with Bimonthly print on demand compilation of issues published. The journal’s full text is available online at http://www.drjjournal.net. The journal allows free access (Open Access) to its contents and permits authors to self-archive final accepted version of the articles on any OAI-compliant institutional / subject-based repository. The journal will cover technical and clinical studies related to health, ethical and social issues in field of Dentistry. Articles with clinical interest and implications will be given preference.
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