Liao Ruomin, Zhang Yi, Mao Wenwei
Department of Respiratory, Shanghai Gerneral Hospital, Shanghai, 201620, China.
Department of Thoracic Surgery, Shanghai Gerneral Hospital, Shanghai, 201620, China.
Heliyon. 2024 May 14;10(11):e31212. doi: 10.1016/j.heliyon.2024.e31212. eCollection 2024 Jun 15.
Functionalized graphene oxide nanoparticles (NPs) have emerged as promising nanocarriers for drug delivery in lung cancer therapy. Quercetin and lurbinectedin encapsulated in graphene oxide (GO) NPs are tested for treating A549 lung cancer cells. Spectroscopic analyses show that graphene oxide functionalization creates a transparent, smooth surface for drug loading. Treatment with quercetin/lurbinectedin-loaded GO NPs induces notable cytotoxic effects in lung cancer cells, as evidenced by distinct morphological alterations and confirmed apoptotic cellular death observed through fluorescence microscopy. Additionally, our study highlights the impact of this approach on lung cancer metastasis, supported by qRT-PCR analysis of relative gene expression levels, including p53, Bax, Caspase-3, and Bcl 2, revealing robust molecular mechanisms underlying therapeutic efficacy against A549 and PC9 cell lines. Flow cytometric analyses further confirm the induction of cellular death in lung cancer cells following administration of the nanoformulation. Our findings show that quercetin/lurbinectedin-loaded GO NPs may be a promising lung cancer treatment, opening new avenues for targeted and effective therapies.
功能化氧化石墨烯纳米颗粒(NPs)已成为肺癌治疗中颇具前景的药物递送纳米载体。对包裹在氧化石墨烯(GO)纳米颗粒中的槲皮素和鲁比卡丁进行了治疗A549肺癌细胞的测试。光谱分析表明,氧化石墨烯功能化可为药物负载创造一个透明、光滑的表面。用负载槲皮素/鲁比卡丁的GO纳米颗粒进行治疗可在肺癌细胞中诱导显著的细胞毒性作用,通过荧光显微镜观察到的明显形态改变和确认的凋亡细胞死亡证明了这一点。此外,我们的研究强调了这种方法对肺癌转移的影响,对包括p53、Bax、Caspase - 3和Bcl 2在内的相关基因表达水平进行的qRT - PCR分析支持了这一点,揭示了针对A549和PC9细胞系的治疗效果背后强大的分子机制。流式细胞术分析进一步证实了纳米制剂给药后肺癌细胞中细胞死亡的诱导。我们的研究结果表明,负载槲皮素/鲁比卡丁的GO纳米颗粒可能是一种有前景的肺癌治疗方法,为靶向和有效的治疗开辟了新途径。