整合转录组学及网络药理学研究仙连解毒方干预结直肠“炎-癌转化”的机制

Mechanistic Analysis of Xianlian Jiedu Decoction in Inflammation-Associated Colorectal Carcinogenesis Based on Transcriptomics and Network Pharmacology

  • 摘要:
    目的 探讨仙连解毒方对结肠炎相关性结直肠癌的干预作用及可能的作用机制。
    方法 采用AOM/DSS联合诱导的CAC小鼠模型,利用超高效液相色谱-四极杆飞行时间质谱技术鉴定给药后结肠组织中的原形成分,并进一步通过网络药理学、分子对接、转录组测序及关键通路相关基因的验证,系统探讨仙连解毒方对结肠炎相关性结直肠癌的干预作用及其潜在机制。
    结果 在AOM/DSS诱导的CAC小鼠模型中,仙连解毒方给药显著改善了肿瘤相关病理特征,具体表现为肿瘤数量减少和结肠长度恢复,同时缓解了疾病活动指数。利用UPLC-Q-TOF/MS在结肠组织中分析鉴定出22种来源于仙连解毒方的成分。此外仙连解毒方可明显下调结肠组织中多种炎症因子的表达,并上调紧密连接蛋白的表达水平。仙连解毒方干预后PPAR信号通路被激活,而Wnt信号通路活性被抑制。PPAR通路相关基因Pparα、Cpt1a和Ehhadh表达上调(P<0.05,P<0.01),而Wnt通路相关基因Axin2和Lef1表达下调(P<0.05,P<0.01)。
    结论 仙连解毒方可通过上调PPAR信号通路和抑制Wnt信号通路干预结直肠的炎-癌转化。

     

    Abstract:
    OBJECTIVE To investigate the therapeutic effects of Xianlian Jiedu Decoction (XLJDD) on colitis-associated colorectal cancer (CAC) and to explore its potential underlying mechanisms.
    METHODS An azoxymethane/dextran sulfate sodium (AOM/DSS)-induced CAC mouse model was established. UPLC-Q-TOF/MS was employed to identify prototype compounds present in colonic tissue after XLJDD administration. Network pharmacology analysis, molecular docking, transcriptomic sequencing, and validation of key pathway-related genes were further conducted to systematically elucidate the intervention effects and potential mechanisms of XLJDD against CAC.
    RESULTS In the AOM/DSS-induced CAC mouse model, XLJDD treatment markedly improved tumor-associated pathological features, as evidenced by reduced tumor burden, restored colon length, and alleviated disease activity index (DAI). UPLC-Q-TOF/MS analysis identified 22 exogenous compounds derived from XLJDD in colonic tissue. In addition, XLJDD significantly downregulated the expression of multiple inflammatory cytokines while upregulating tight junction-related genes in the colon. Transcriptomic analysis revealed that XLJDD treatment enhanced overall PPAR signaling pathway activity while suppressing the Wnt signaling pathway. Consistently, the expression levels of PPAR pathway-related genes Pparα, Cpt1a, and Ehhadh were upregulated following XLJDD intervention (P<0.05, P<0.01), whereas the Wnt pathway-related genes Axin2 and Lef1 were significantly downregulated (P<0.05, P<0.01).
    CONCLUSION XLJDD may intervene in inflammation-associated colorectal carcinogenesis by activating the PPAR signaling pathway and suppressing the Wnt signaling pathway.

     

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