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解毒散结合 PD-L1 抑制剂抑制结直肠癌细胞上皮间质转化及转移潜能。

Inhibition to Epithelial-Mesenchymal Transition and Metastatic Potential In Colorectal Cancer Cell By Combination of Traditional Chinese Medicine Formulation Jiedu Sangen Decoction and PD-L1 Inhibitor.

机构信息

The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.

The First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.

出版信息

Integr Cancer Ther. 2020 Jan-Dec;19:1534735420972486. doi: 10.1177/1534735420972486.

Abstract

BACKGROUND

Jiedu Sangen Decoction (JSD), a traditional Chinese medicine formula, has been widely applied in the treatment of gastrointestinal cancer, especially in colorectal cancer. Our study mainly aimed to assess the combined efficacy of Jiedu Sangen aqueous extract (JSAE) and a PD-L1 inhibitor (PI) in colon cancer cells migration and invasion, along with epithelial-mesenchymal transition, and then provide deep insights into the potential mechanism.

METHODS

We explored the inhibitory effects on invasion and metastasis and the reverse effect on EMT process in CT-26 colon cancer cell via Transwell migration assay, Matrigel invasion assay and confocal laser scanning microscopy. Furthermore, regulation in expression of EMT-related proteins and molecular biomarkers and underlying signal pathway proteins were detected through Western blotting and IHC.

RESULTS

The combination of JSD and PD-L1 inhibitor could inhibit migration, invasive ability and EMT of CT-26 cells in a concentration-dependent manner. Meanwhile, JSD combined with PD-L1 inhibitor could also remarkably reverse EMT and metastasis in vivo. In addition, the protein expression of N-cadherin, Slug, Snail, Vimentin was down-regulated along with E-cadherin s up-regulation with the combination of JSD and PD-L1 inhibitor, while that of PI3K/AKT was notably down-regulated.

CONCLUSIONS

These findings indicated that JSAE and a PD-L1 inhibitor could drastically inhibit the migration and invasion of colorectal cancer by reversing EMT through the PI3K/AKT signaling pathway.

摘要

背景

解毒散根汤(JSD)是一种中药方剂,已广泛应用于胃肠道癌的治疗,尤其是结直肠癌。我们的研究主要旨在评估 JSD 水提物(JSAE)与 PD-L1 抑制剂(PI)联合对结肠癌细胞迁移和侵袭的协同作用,以及上皮-间充质转化(EMT),并深入探讨其潜在机制。

方法

我们通过 Transwell 迁移实验、Matrigel 侵袭实验和共聚焦激光扫描显微镜研究 JSAE 与 PD-L1 抑制剂联合对 CT-26 结肠癌细胞侵袭和转移的抑制作用及 EMT 过程的逆转作用。进一步通过 Western blot 和免疫组化检测 EMT 相关蛋白和分子标志物及相关信号通路蛋白的表达水平。

结果

JSD 与 PD-L1 抑制剂联合呈浓度依赖性抑制 CT-26 细胞的迁移、侵袭能力和 EMT。此外,JSD 联合 PD-L1 抑制剂还能显著逆转 EMT 和体内转移。同时,JSD 联合 PD-L1 抑制剂还能下调 N-钙黏蛋白、Slug、Snail 和波形蛋白的蛋白表达,上调 E-钙黏蛋白的表达,而 PI3K/AKT 表达明显下调。

结论

这些发现表明,JSAE 与 PD-L1 抑制剂通过 PI3K/AKT 信号通路逆转 EMT,可显著抑制结直肠癌细胞的迁移和侵袭。

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