The Synergistic Inhibitory Effect of Combination Drug Treatment of Enteromorpha Prolifera Polysaccaharide and Doxorubicin Hydrochloride on A549 Cell.

IF 3.3 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Frontiers in bioscience (Landmark edition) Pub Date : 2024-08-21 DOI:10.31083/j.fbl2908300
Yanwei Li, Li Liu, Yueting Xing, Jiajia Wang, Wei Yin, Yingying Huang, Chun Guo, Nan Zhou
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Abstract

Background: As a common drug for tumor therapy, doxorubicin hydrochloride (DOX) is not yet widely used as a clinical solution. This is due to its toxicity and potential drug resistance.

Objective: This study investigated the inhibitory effect of enteromorpha prolifera polysaccaharide (EPP) combined with doxorubicin hydrochloride (DOX) on A549 cells, which fall into the cell line of human non-small cell lung cancer (NSCLC). It also explained the attenuated and synergistic effect of enteromorpha acid polysaccharide along with its synergistic effect on DOX.

Methods: To evaluate the proliferation inhibitory effect of EPP, DOX and both combined, we monitored cell growth curve and morphology using the real-time cell function analysis and imaging system-xCELLigence RTCA eSight system (eSight system). Flow cytometry was used to monitor cell apoptosis rate and cell cycle distribution. Mitochondrial function was tested by the energy metabolism analysis system.

Results: EPP could work with DOX to inhibit the proliferation of A549 cells. Growth curve showed that when 0.4 mg/mL of EPP was mixed with 0.2 µg/mL of DOX for 24 h, the mixure liquid had a significant inhibitory effect on the proliferation of A549 cells (p < 0.0001). The cells had lower cell adhesiveness, shrinking cell membrane, cytoplasmic aggregation, and hyperchromatic nuclei. According to the flow cytometry results, the combined drug of EPP and DOX could significantly increase the apoptosis rate of A549 cells (p < 0.0001), and block the cell cycle in the G1-S phase. Based on the results of the real-time energy metabolism, we found that the combined drug could significantly reduce A549 cells' ATP production rate and inhibit their mitochondrial respiratory function.

Conclusions: The combination of EPP and DOX can block cell cycle, inhibit cell mitochondrial function, promote cell apoptosis, and enhance the killing ability of DOX on tumor cells. This study supports the antitumor activity of enterococcus acid polysaccharide and provides insights on reducing doxorubicin toxicity and drug resistance. It holds great significance for applying traditional Chinese natural medicine in clinical disease treatment.

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Enteromorpha Prolifera Polysaccaharide 和盐酸多柔比星联合用药对 A549 细胞的协同抑制作用
背景:作为治疗肿瘤的常用药物,盐酸多柔比星(DOX)尚未广泛应用于临床。这主要是由于其毒性和潜在的耐药性:本研究探讨了肠藻多糖(EPP)联合盐酸多柔比星(DOX)对人类非小细胞肺癌(NSCLC)细胞系 A549 细胞的抑制作用。该研究还解释了肠藻酸多糖与 DOX 协同作用的减弱和协同效应:方法:为了评估 EPP、DOX 以及两者联合使用的增殖抑制效果,我们使用实时细胞功能分析和成像系统--xCELLigence RTCA eSight 系统(eSight 系统)监测细胞生长曲线和形态。流式细胞术用于监测细胞凋亡率和细胞周期分布。能量代谢分析系统检测线粒体功能:结果:EPP 可与 DOX 共同抑制 A549 细胞的增殖。生长曲线显示,当 0.4 毫克/毫升的 EPP 与 0.2 微克/毫升的 DOX 混合 24 小时后,混合液对 A549 细胞的增殖有显著的抑制作用(p < 0.0001)。细胞粘附性降低,细胞膜收缩,细胞质聚集,细胞核高色素化。流式细胞术结果显示,EPP 和 DOX 联合用药能显著提高 A549 细胞的凋亡率(p < 0.0001),并能阻滞 G1-S 期的细胞周期。根据实时能量代谢的结果,我们发现联合用药可明显降低A549细胞的ATP生成率,抑制其线粒体呼吸功能:结论:EPP 和 DOX 联合用药能阻断细胞周期,抑制细胞线粒体功能,促进细胞凋亡,增强 DOX 对肿瘤细胞的杀伤能力。本研究证实了肠球菌酸性多糖的抗肿瘤活性,并为降低多柔比星的毒性和耐药性提供了启示。这对将中国传统天然药物应用于临床疾病治疗具有重要意义。
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