Xiaohu Ouyang, Wang Jingbo, Qiu Xiaoyuan, Song Shuxin, Li Junyi, Luo Shanshan, Chen Qianyun, Hu Desheng
Department of Integrated Traditional Chinese and Western Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Heliyon. 2024 Oct 19;10(20):e39564. doi: 10.1016/j.heliyon.2024.e39564. eCollection 2024 Oct 30.
The Sophora alopecuroide - Taraxacum Decoction (STD) is a traditional Chinese herbal formulation that has demonstrated significant potential in combating tumors. Despite its apparent effectiveness, the specific mechanisms through which STD exerts its anti-tumor properties remain largely unexplored and are yet to be fully understood. In our study, we provided evidence that STD effectively inhibits cellular growth and movement, as well as halting the cell cycle at the G2/M checkpoint. Furthermore, our pharmacological network analysis indicated that STD might induce cell death through a process known as ferroptosis. This hypothesis was substantiated by observing important biochemical changes associated with ferroptosis, including a decrease in glutathione (GSH) levels, an increase in iron accumulation, and elevated levels of reactive oxygen species (ROS) and lipid peroxidation. Additionally, we noted a significant rise in the expression of pro-ferroptosis genes such as Keap1, Nrf2, and HO-1, further supporting our findings. Significantly, and in line with the results, STD also showed a strong ability to inhibit tumor growth by inducing ferroptosis in a subcutaneous tumor model. Additionally, STD treatment changed the tumor immune microenvironment (TIME), as seen by an increase in CD107a CD8 and NK cells within the tumor. These findings demonstrate that STD induces ferroptosis and alters TIME to combat tumors, suggesting that STD may be a viable alternative treatment for patients with NSCLC.
苦参 - 蒲公英汤(STD)是一种传统的中药配方,已显示出在对抗肿瘤方面具有显著潜力。尽管其效果明显,但STD发挥抗肿瘤特性的具体机制在很大程度上仍未被探索,尚未完全了解。在我们的研究中,我们提供了证据表明STD能有效抑制细胞生长和移动,并在G2/M检查点使细胞周期停滞。此外,我们的药理网络分析表明,STD可能通过一种称为铁死亡的过程诱导细胞死亡。通过观察与铁死亡相关的重要生化变化,包括谷胱甘肽(GSH)水平降低、铁积累增加以及活性氧(ROS)和脂质过氧化水平升高,这一假设得到了证实。此外,我们注意到促铁死亡基因如Keap1、Nrf2和HO-1的表达显著增加,进一步支持了我们的发现。重要的是,与结果一致,STD在皮下肿瘤模型中也显示出通过诱导铁死亡来强烈抑制肿瘤生长的能力。此外,STD治疗改变了肿瘤免疫微环境(TIME),表现为肿瘤内CD107a CD8和NK细胞增加。这些发现表明,STD通过诱导铁死亡和改变TIME来对抗肿瘤,提示STD可能是NSCLC患者一种可行的替代治疗方法。