Yu Bin, Yan Xida, Zhu Yuanying, Luo Ting, Sohail Muhammad, Ning Hong, Xu Hui
NHC Key Laboratory of Nuclear Technology Medical Transformation, Department of Pharmacy, Mianyang Central Hospital, Mianyang, China.
Key Laboratory of Molecular Pharmacology and Drug Evaluation, School of Pharmacy, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong, Yantai University, Yantai, China.
Front Pharmacol. 2023 Aug 15;14:1227528. doi: 10.3389/fphar.2023.1227528. eCollection 2023.
To analyze the clinical characteristics of adverse reactions/events based on chemotherapy in cancer patients, and then explore the potential mechanism of Danggui Buxue Decoction (DBD) against chemotherapy-induced bone marrow suppression (BMS). Retrospectively collected and evaluated were the clinical data of patients in a hospital who experienced adverse reactions/events brought on by chemotherapeutic medications between 2015 and 2022. We explored the potential mechanism of DBD against BMS using network pharmacology based on the findings of the adverse reactions/events analysis. 151 instances (72.25%) experienced adverse reactions/events from a single chemotherapy medication. Besides, platinum-based medications produced the most unfavorable effects. The study also found that chemotherapy caused the highest number of cases of BMS, including platinum drugs. Consequently, BMS is the most prevalent adverse reaction disease caused by chemotherapy found in this part. According to network pharmacology findings, DBD can prevent BMS primarily involving 1,510 primary targets and 19 key active ingredients. Based on the enrichment analysis, PI3K-AKT, TNF, MAPK, and IL-17 signaling pathways made up the majority of the DBD-resisting BMS pathways. Molecular docking displayed that kaempferol, the major active ingredient of DBD, had the highest binding energy (-10.08 kJ mol) with PTGS2 (a key target of BMS). Cancer patients who received chemotherapy had a risk to develop BMS. Regular blood tests should be performed while taking medicine; early discovery and treatment can reduce a patient's risk of experiencing adverse reactions/events. Additionally, this study demonstrated that DBD, through a variety of targets and pathways, may be crucial in avoiding BMS.
分析癌症患者化疗不良反应/事件的临床特征,进而探讨当归补血汤(DBD)防治化疗所致骨髓抑制(BMS)的潜在机制。回顾性收集并评估了某医院2015年至2022年期间经历化疗药物所致不良反应/事件患者的临床资料。基于不良反应/事件分析结果,运用网络药理学方法探讨DBD防治BMS的潜在机制。151例(72.25%)患者出现单一化疗药物的不良反应/事件。此外,铂类药物产生的不良反应最为严重。研究还发现,化疗导致的BMS病例数最多,包括铂类药物。因此,BMS是该研究中发现的化疗最常见的不良反应疾病。根据网络药理学研究结果,DBD可预防BMS,主要涉及1510个主要靶点和19种关键活性成分。基于富集分析,PI3K-AKT、TNF、MAPK和IL-17信号通路是DBD抵抗BMS的主要通路。分子对接显示,DBD的主要活性成分山奈酚与PTGS2(BMS的关键靶点)具有最高的结合能(-10.08 kJ/mol)。接受化疗的癌症患者有发生BMS的风险。服药期间应定期进行血液检查;早期发现和治疗可降低患者发生不良反应/事件的风险。此外,本研究表明,DBD可能通过多种靶点和通路在预防BMS方面发挥关键作用。