金黄色葡萄球菌细胞质提取物对肺癌细胞的细胞毒性和凋亡诱导特性:MTT 试验和 bax/bcl-2 基因表达分析的启示

IF 1 Q4 GENETICS & HEREDITY
Mehrshad Ahmadi , Bahareh Hajikhani , Atefeh Shamosi , Somayeh Yaslianifard , Fatemeh Sameni , Mostafa Qorbani , Mohammad Mohammadzadeh , Masoud Dadashi
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引用次数: 0

摘要

背景肺癌在男性和女性癌症发病率中均位居第二,是全球发病率和致死率最高的恶性肿瘤之一。近几十年来,细菌的治疗潜力在制药和治疗研究中得到了认可。虽然细菌历来与癌症致病有关,但最近的研究揭示了它们作为癌症靶向治疗有效制剂的潜力。然而,关于金黄色葡萄球菌(S. aureus)提取物的特征及其对肺癌细胞系的影响的数据十分有限。因此,本研究旨在通过评估 bax 和 bcl-2 基因的表达水平,研究金黄色葡萄球菌提取物对诱导肺癌细胞株 A549 和肺正常细胞株 MRC-5 细胞凋亡的影响。首先,利用超声技术制备了金黄色葡萄球菌的细胞质提取物,通过布拉德福德测定法确定了蛋白质的浓度,并利用 SDS-PAGE 确认了蛋白质的存在。将代表肺癌细胞株的 A549 和代表肺部正常细胞株的 MRC-5 暴露于不同浓度的细菌提取物中,用 MTT 法评估细胞活力。结果从金黄色葡萄球菌中提取的细胞质提取物能够调节细胞凋亡基因的表达水平。与对照组相比,bax 基因的表达量增加了五倍,而 bcl-2 基因的表达量则减少了一半以上。此外,MTT 试验结果表明,细菌细胞质提取物对癌细胞具有浓度依赖性细胞毒性,随着浓度的升高,细胞死亡显著增加。这些发现为创新癌症治疗和改善患者预后提供了令人兴奋的可能性,强调了金黄色葡萄球菌提取物在抗击肺癌方面的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytotoxic and apoptosis-inducing properties of Staphylococcus aureus cytoplasmic extract on lung cancer cells: Insights from MTT assay and bax/bcl-2 gene expression analysis

Background

Lung cancer ranks as the second most prevalent cancer in both men and women and stands as one of the most prevalent and lethal malignancies globally. In recent decades, the therapeutic potential of bacteria has gained recognition in pharmaceutical and therapeutic research. While bacteria have historically been associated with cancer causation, recent studies have unveiled their potential as efficacious agents for targeted cancer therapy. However, limited data exist on the characterization and impact of Staphylococcus aureus (S. aureus) extract on lung cancer cell lines. Consequently, this study aims to investigate the effect of S. aureus extract on inducing apoptosis in A549, a lung cancer cell line, and MRC-5, a lung normal cell line, by evaluating the expression levels of the bax and bcl-2 genes.

Methods

Initially, cytoplasmic extract of S. aureus was prepared using the sonication technique. The protein concentration was determined via the Bradford assay, and the presence of proteins was confirmed using SDS-PAGE. A549, representing a lung cancer cell line, and MRC-5, representing a lung normal cell line, were exposed to varying concentrations of bacterial extract, and cell viability was assessed using the MTT assay. Subsequently, the expression levels of the bax and bcl-2 genes were quantified utilizing the Real-Time PCR method.

Results

Cytoplasmic extract derived from S. aureus demonstrated the ability to modulate the expression levels of apoptotic genes. Relative to the control group, the bax gene exhibited a fivefold overexpression, while the expression of the bcl-2 gene decreased by more than half compared to the control. Furthermore, the results of the MTT assay indicated that the bacterial cytoplasmic extract exhibited concentration-dependent cytotoxicity on cancer cells, highlighting a significant increase in cell death with escalating concentrations.

Conclusions

This research highlights the potential of S. aureus extract for targeted lung cancer therapy by promoting cancer cell apoptosis while sparing normal cells. These findings open up exciting possibilities for innovative cancer treatments and improved patient outcomes, emphasizing the promise of S. aureus extract in the fight against lung cancer.

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来源期刊
Gene Reports
Gene Reports Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍: Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.
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