蜜炙黄芪与醋莪术药对通过MAPK/NF-κB信号通路治疗结肠炎相关性结直肠癌的机制:体内外研究

Mechanism of hedysari radix praeparata cum melle and curcumae rhizoma herb pair in colitis-associated colorectal cancer through the MAPK/NF-κB signaling pathway: an investigation in vivo and in vitro.

作者信息Ting Liu, Yugui Zhang, Feiyun Gao, Zhuanhong Zhang, Maomao Wang, Cui Ma, Yanjun Wang, Dingcai Ma, Zhe Wang, Xingke Yan, Yuefeng Li
PMID40405896
发布时间2025-05-08
DOI10.3389/fchem.2025.1551722

实验完整度

包含体外细胞模型(SW620)和体内小鼠模型(AOM/DSS诱导的CAC),并进行了功能验证(增殖、凋亡、迁移、侵袭)和机制验证(Western blot检测MAPK/NF-κB通路蛋白)。

主要模型

SW620人结肠癌细胞系 AOM/DSS诱导的CAC小鼠模型

重点核对

HRCR-MIAS对SW620细胞的IC50值(24h: 9.42%, 48h: 5.74%, 72h: 4.01%) 5-Fu阳性对照浓度(50 μM) HRCR低、中、高剂量(3.413, 6.825, 13.650 g/kg) CAC小鼠造模时间(112天)

摘要

Introduction: Astragali Radix (AR) - Curcumae Rhizoma (vinegar processed, CR) herb pair was recorded in 'YIXUE ZHONGZHONG CANXILU' to treat colitis-associated colorectal cancer (CAC). Hedysari Radix (HR) was categorized under the AR entry in 'SHENNONG BENCAO JING'. HR is still an alternative to AR paired with CR clinically in northwest China. Hedysari Radix Praeparata Cum Melle (HRPCM) is a product that HR fries with honey to enhance the therapeutic effect. However, the mechanism of HRPCM paired with CR (HRCR) in CAC needs to be further elucidated.Methods: HRCR-MIAS were prepared using the eversion intestinal sac method. UHPLC Q-Exactive-MS investigated the compositions in HRCR-MIAS. Then, the mechanism of HRCR in CAC mice was predicted based on network pharmacology analysis in combination with the compositions in HRCR-MIAS. The pharmacodynamic effects of HRCR-MIAS for SW620 colon cancer cells were invested in vitro. The efficacies of HRCR low-, middle-, and high-dose groups (HRCR-L, 3.413 g/kg; HRCR-M, 6.825 g/kg; HRCR-H, 13.650 g/kg) in CAC mice were explored. Enzyme-linked immunosorbent assay (ELISA) kits were employed to assay The inflammatory factors levels, like IL-1β, IL-6, IL-10, and TNF-α in serum. The expressions of the intestinal permeability proteins, such as Claudin-1, Occludin, and ZO-1, were detected via immunohistochemical (IHC) analysis. Finally, the predicted signalling was verified by Western blot (WB).Results: 855 common components were identified in HRCR and HRCR-MIAS, and 25 specific components in HRCR-MIAS were pointed out. Based on network pharmacology analysis, the inflammatory response and the cross-linked MAPK signalling and NF-kB signalling were predicted to be the main reasons for HRCR in CAC. HRCR-MIAS inhibited the proliferation, induced apoptosis, regulated the cell cycle progression, and restrained the SW620 cells' ability to migrate and invade in vitro. The outcomes of the WB experiment exhibited that HRCR-MIAS inhibited the expression of key proteins such as MEKK1, RAS, ERK, IKB and NF-kB in the MAPK/NF-kB signalling pathway of SW620 cells. The study in vivo found that the different doses of HRCR recovered the loss of body weight, the shortened colon length, the increased tumour counts, the abnormal changes in spleen and thymus indices, the colonic lesions, the unbalanced inflammatory factors levels like IL-10, IL-6, IL-1β, and TNF-α in serum, and the down-regulated intestinal permeability proteins such as Claudin-1, Occludin, and ZO-1. Experimental validation by WB confirmed that HRCR inhibited the expression of the key proteins, including MEKK1 RAS, ERK, IKB, and NF-kB, in the MAPK/NF-kB signalling in CAC mice.Discussion: HRCR not only suppresses the process of colonic inflammation and improves intestinal permeability but also relieves CAC by inhibiting the activated MAPK/NF-kB signalling cascade to alleviate CAC.

实验结论

提炼研究问题、关键发现与证据,快速把握文章的核心贡献。

研究问题
蜜炙黄芪与醋莪术药对(HRCR)在结肠炎相关性结直肠癌(CAC)中的作用及其分子机制尚不清楚,需要进一步阐明。
核心机制
HRCR通过抑制MAPK/NF-κB信号级联通路,抑制结肠炎症并改善肠道通透性,从而缓解CAC。
主要证据
体外实验中,HRCR-MIAS抑制SW620细胞增殖、诱导凋亡、调节周期、抑制迁移和侵袭,并降低MEKK1、RAS、ERK、IKB、NF-kB表达;体内实验中,HRCR改善CAC小鼠体重下降、结肠缩短、肿瘤数目增加等症状,降低促炎因子(IL-1β、IL-6、TNF-α)水平,升高抗炎因子(IL-10),增强肠道通透性蛋白(Claudin-1、Occludin、ZO-1)表达,并抑制MAPK/NF-κB通路蛋白表达。
研究意义
该研究为HRCR治疗CAC提供了潜在机制,并为临床应用提供参考。

研究路径

按研究推进顺序梳理实验设计、验证步骤与关键观察。

1

制备HRCR提取物和含药肠吸收液

获取HRCR的体内吸收成分,用于体外实验

采用外翻肠囊法制备HRCR-MIAS,并通过UHPLC Q-Exactive-MS分析其成分。

2

网络药理学预测靶点和通路

预测HRCR治疗CAC的潜在靶点和信号通路

基于HRCR-MIAS成分和网络药理学分析,预测炎症反应和MAPK/NF-κB信号通路是HRCR治疗CAC的主要机制。

3

体外药效评估

评估HRCR-MIAS对结肠癌细胞SW620的抑制作用

用不同浓度HRCR-MIAS处理SW620细胞,检测增殖、凋亡、周期、迁移和侵袭。

4

体外机制验证

验证HRCR-MIAS对MAPK/NF-κB通路蛋白表达的影响

通过Western blot检测SW620细胞中RAS、MEKK1、ERK、IKB、NF-κB的表达。

5

体内药效评估

评估HRCR对CAC小鼠模型的治疗效果

建立AOM/DSS诱导的CAC小鼠模型,给予不同剂量HRCR干预,观察一般状态、结肠长度、肿瘤数目、脏器指数、结肠病理和炎症因子水平。

6

体内机制验证

验证HRCR对CAC小鼠MAPK/NF-κB通路蛋白表达的影响

通过Western blot检测结肠组织中RAS、MEKK1、ERK、IKB、NF-κB的表达。

研究方法

按研究目的归类文中使用的方法,便于定位所需技术。

产品清单

实验环节名称品牌货号
L-15培养基HyCloneAJ30725631
胎牛血清----
青霉素-链霉素Solarbio20221012
5-氟尿嘧啶--FA211108
CCK-8试剂盒New Cell & Molecular BiotechC6005
膜联蛋白V-FITC----
碘化丙啶----
DNA染色和透化溶液----
基质胶----
RIPA裂解液SolarbioR0010
BCA蛋白浓度测定试剂盒SolarbioR0020
RAS抗体Abcamab52939
ERK抗体Abcamab201015
p-ERK抗体Cell Signaling Technology#4695
MEKK1抗体Santa Cruz BiotechnologyI1710
IkB抗体Abcamab32518
NF-kB抗体Abcamab32536
GAPDH抗体ImmunowayYM3092
β-actin抗体Affinity#AF7018
台罗德溶液Procell Life Science& TechnologyWH2923Z031
TNF-α ELISA试剂盒Shanghai Enzyme-linked Biotechnology20230629-20852A
IL-6 ELISA试剂盒Shanghai Enzyme-linked Biotechnology20230629-20188A
IL-10 ELISA试剂盒Shanghai Enzyme-linked Biotechnology20230629-20162A
IL-1β ELISA试剂盒Shanghai Enzyme-linked Biotechnology20230629-20506A
Claudin-1抗体Affinity64f7244
Occludin抗体AbcamGR3243495-28
ZO-1抗体Affinity44h7470

关键环节

汇总复现实验时建议重点确认的条件及原文阅读提示。

环节核对要点
细胞培养
SW620细胞系来源(中国科学院细胞库),培养基(L-15,10%FBS,1%青霉素-链霉素),培养条件(37°C,5% CO2)
阅读提示:Methods 2.4.1
细胞增殖检测
细胞接种密度(6×10^3 cells/well),药物浓度梯度(HRCR-MIAS 4%-14%,5-Fu 25-6400 μM),干预时间(24,48,72h),CCK-8孵育时间(2h)
阅读提示:Methods 2.4.2, Figure 5
细胞凋亡和周期检测
Annexin V-FITC/PI染色,DNA染色溶液,流式细胞仪检测
阅读提示:Methods 2.4.3
细胞迁移和侵袭检测
划痕实验(细胞密度80-90%,无血清培养基),Transwell实验(1×10^5 cells/well,8 μm孔径,Matrigel 1:8稀释,48h)
阅读提示:Methods 2.4.4, 2.4.5
体内动物模型
C57/6J小鼠,AOM/DSS诱导,HRCR剂量(3.413, 6.825, 13.650 g/kg),SASP阳性对照(0.455 g/kg),干预周期112天
阅读提示:Methods 2.5.1, Figure 8