Institute of Energy Metabolism and Health, Shanghai 10th People's Hospital, Tongji University School of Medicine, Shanghai 200072, P. R. China.
Department of Respiratory Medicine, Shanghai 10th People's Hospital, Tongji University School of Medicine, Shanghai 200072, P. R. China.
Am J Chin Med. 2022;50(5):1361-1386. doi: 10.1142/S0192415X22500586. Epub 2022 Jun 8.
Lung cancer is the most commonly diagnosed cancer and the leading cause of cancer death worldwide. Amygdalin, a natural compound commonly distributed in plants of the Rosaceae species, owns anticancer activity, less side effects, wide source, and relatively low price. Although the apoptosis is a central process activated by amygdalin in cancer cells, the underlying molecular mechanisms through which amygdalin induces the apoptosis of lung cancer cells remain poorly understood. In this research work, amygdalin could suppress the proliferation of lung cancer A549 and PC9 cells by CCK8 assay. Amygdalin significantly promoted the apoptosis of lung cancer A549 and PC9 cells stained with Annexin V-FITC/PI by flow cytometry assay. Furthermore, amygdalin dose-dependently decreased the mitochondrial membrane potential (MMP) with JC-1 dye by flow cytometry. To investigate the underlying molecular mechanisms through which amygdalin induced mitochondria-mediated apoptosis of cancer cells, the differentially-expressed genes with a fold change >2.0 and < 0.05 were acquired from the cDNA microarray analysis. The results of qRT-PCR further confirmed that the differentially-expressed level of the NF[Formula: see text]B-1 gene was most obviously enhanced in lung cancer cells treated with amygdalin. The results of immunofluorescence staining, Western blotting and siRNA knockdown indicated that amygdalin induced mitochondria-mediated apoptosis of lung cancer cells via enhancing the expression of NF[Formula: see text]B-1 and inactivating NF[Formula: see text]B signaling cascade and further changing the expressions of proteins (Bax, Bcl-2, cytochrome C, caspase 9, caspase 3 and PARP) related to apoptosis, which were further checked by study of the lung cancer cell xenograft mice model accompanying with immunohistochemical staining and TUNEL staining. Our results indicated that amygdalin might be a potential activator of NF[Formula: see text]B-1, which sheds more light on the molecular mechanism of anticancer effects of amygdalin. These results highlighted amygdalin as a potential therapeutic anticancer agent, which warrants its development as a therapy for lung cancer.
肺癌是世界上最常见的癌症诊断和癌症死亡的主要原因。苦杏仁苷是一种天然化合物,广泛存在于蔷薇科植物中,具有抗癌活性、副作用小、来源广泛、价格相对较低等特点。虽然细胞凋亡是苦杏仁苷在癌细胞中激活的中心过程,但苦杏仁苷诱导肺癌细胞凋亡的潜在分子机制仍知之甚少。在这项研究工作中,通过 CCK8 检测,苦杏仁苷可以抑制肺癌 A549 和 PC9 细胞的增殖。通过流式细胞术检测,苦杏仁苷显著促进肺癌 A549 和 PC9 细胞的凋亡,经 Annexin V-FITC/PI 染色。此外,苦杏仁苷剂量依赖性地降低了 JC-1 染料标记的线粒体膜电位 (MMP) 通过流式细胞术。为了研究苦杏仁苷诱导癌细胞线粒体介导凋亡的潜在分子机制,从 cDNA 微阵列分析中获得了差异表达基因,其倍数变化 >2.0 和 <0.05。qRT-PCR 的结果进一步证实,用苦杏仁苷处理后,NF[Formula: see text]B-1 基因的差异表达水平在肺癌细胞中最为明显增强。免疫荧光染色、Western blot 和 siRNA 敲低的结果表明,苦杏仁苷通过增强 NF[Formula: see text]B-1 的表达和失活 NF[Formula: see text]B 信号级联,进一步改变与凋亡相关的蛋白 (Bax、Bcl-2、细胞色素 C、caspase 9、caspase 3 和 PARP) 的表达,从而诱导肺癌细胞的线粒体介导凋亡,这在肺癌细胞异种移植小鼠模型中进一步通过免疫组织化学染色和 TUNEL 染色进行了研究。我们的结果表明,苦杏仁苷可能是 NF[Formula: see text]B-1 的潜在激活剂,这为苦杏仁苷的抗癌作用的分子机制提供了更多的线索。这些结果强调了苦杏仁苷作为一种潜在的治疗性抗癌药物的作用,值得进一步开发用于治疗肺癌。