Li Bihui, Deng Yanyan, Lin Xuqiang, Wan Xiaowei, Liu Jiaqi
Department of Oncology The Second Affiliated Hospital of Guilin Medical University Guilin China.
Department of Gynecology, Guigang City People's Hospital The Eighth Affiliated Hospital of Guangxi Medical University Guigang China.
Food Sci Nutr. 2023 Jun 29;11(10):5999-6009. doi: 10.1002/fsn3.3534. eCollection 2023 Oct.
Ferroptosis has gained extreme purpose in targeting cancer treatment. , a traditional Chinese herb, has potential anticancer properties, but the action and mechanism against ovarian cancer remain undetailed. Pachyman ( polysaccharides) refers to the pharmacologically bioactive ingredients rich in . This study aimed to identify the potent actions and the network mechanisms of pachyman against ovarian cancer through preclinical analysis. Online-accessible database or platform was employed to predict candidate genes and core targets associated with ferroptosis in pachyman against ovarian cancer. Enrichment analyses were used to characterize the functional action and signaling mechanism in pachyman to treat ovarian cancer. Molecular docking imitation was conducted for verification of core target proteins. Network analysis uncovered that there were 30 mutual and 13 core genes targeting ferroptosis in pachyman and/against ovarian cancer, and additional enrichment analysis characterized that these core genes may act synergistically through multiple biological processes and molecular pathways associated with ferroptosis, including anti-inflammatory action, immunoregulation, and microenvironment modulation. The strongest affinities in core target proteins between pachyman and sarcoma (SRC), signal transducer, and activator of transcription 3 (STAT3) were further validated using molecular docking method. In conclusion, pachyman may induce antiovarian cancer potentials via regulating ferroptosis-associated biological functions and pharmacological mechanisms based on current bioinformatics findings. We reason that pachyman, the beneficial nutraceuticals, may be used clinically for future application in ovarian cancer treatment.
铁死亡在靶向癌症治疗中具有重要意义。茯苓,一种传统中药,具有潜在的抗癌特性,但其对卵巢癌的作用和机制仍不明确。茯苓多糖是富含于茯苓中的具有药理活性的成分。本研究旨在通过临床前分析确定茯苓多糖对卵巢癌的有效作用及网络机制。利用在线数据库或平台预测与茯苓多糖抗卵巢癌铁死亡相关的候选基因和核心靶点。采用富集分析来表征茯苓多糖治疗卵巢癌的功能作用和信号传导机制。进行分子对接模拟以验证核心靶蛋白。网络分析发现,茯苓多糖中存在30个相互作用的基因和13个靶向铁死亡的核心基因,这些基因与卵巢癌相关,进一步的富集分析表明,这些核心基因可能通过与铁死亡相关的多个生物学过程和分子途径协同发挥作用,包括抗炎作用、免疫调节和微环境调节。利用分子对接方法进一步验证了茯苓多糖与肉瘤(SRC)、信号转导和转录激活因子3(STAT3)之间在核心靶蛋白中的最强亲和力。总之,根据目前的生物信息学研究结果,茯苓多糖可能通过调节与铁死亡相关的生物学功能和药理机制来诱导抗卵巢癌的潜力。我们认为,茯苓这种有益的营养保健品,未来可能在卵巢癌治疗中得到临床应用。