Wang Xiaodong, Chen Wei, Zhuang Dongfang, Deng Wenbin
School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.
Key Laboratory of State Administration of Traditional Chinese Medicine, Dongguan HEC Cordyceps R&D Co., Ltd., Dongguan 523850, China.
ACS Omega. 2025 Aug 5;10(32):35488-35496. doi: 10.1021/acsomega.4c11098. eCollection 2025 Aug 19.
Although cisplatin (DDP) is commonly used in the clinical treatment of lung cancer, the associated side effects remained serious. Chinese medicine can be used to increase the sensitivity of the body to antitumor drugs while reducing their adverse effects. polysaccharide (CSP), which is derived from , has already been demonstrated to regulate immune function, but the effects of CSP in combination with DDP have not yet been reported. In this study, we explore the synergistic and attenuated toxicity effects of CSP combined with DDP. Our results revealed that DDP and DDP + CSP combination treatment both induced cytotoxicity in LLC1 lung cancer cells and SK-MEL-28 melanoma cancer cells, and that CSP significantly increased tumor cell death. Moreover, cell toxicity in DDP-treated RAW 264.7 cells was suppressed by CSP. In a mouse model generated on LLC1 tumor-bearing mice, CSP and DDP combination treatment significantly increased DDP-induced tumor cell death. Western analysis revealed that this was achieved via CSP regulation of the expression levels of proteins involved in pyroptosiscaspase-1 and gasdermin D (GSDMD). In addition, CSP reduced oxidative stress levels to help alleviate the acute renal toxicity caused by DDP. In summary, our study provides further evidence of the efficacy of CSP and it lays a foundation for the clinical use of CSP as an adjuvant chemotherapy drug.
尽管顺铂(DDP)常用于肺癌的临床治疗,但其相关副作用仍然严重。中药可用于提高机体对抗肿瘤药物的敏感性,同时降低其不良反应。从[具体来源未给出]提取的多糖(CSP)已被证明可调节免疫功能,但CSP与DDP联合使用的效果尚未见报道。在本研究中,我们探究了CSP与DDP联合使用的协同作用和减毒作用。我们的结果显示,DDP及DDP + CSP联合治疗均能诱导LLC1肺癌细胞和SK-MEL-28黑色素瘤癌细胞产生细胞毒性,且CSP显著增加肿瘤细胞死亡。此外,CSP抑制了DDP处理的RAW 264.7细胞的细胞毒性。在LLC1荷瘤小鼠建立的模型中,CSP与DDP联合治疗显著增加了DDP诱导的肿瘤细胞死亡。蛋白质免疫印迹分析显示,这是通过CSP调节与细胞焦亡相关的蛋白质——半胱天冬酶-1和gasdermin D(GSDMD)的表达水平来实现的。此外,CSP降低了氧化应激水平,有助于减轻DDP引起的急性肾毒性。总之,我们的研究进一步证明了CSP的疗效,并为CSP作为辅助化疗药物的临床应用奠定了基础。