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蟾毒灵通过抑制 STAT3 信号通路抑制肿瘤微环境介导的血管生成。

Bufalin suppresses tumour microenvironment-mediated angiogenesis by inhibiting the STAT3 signalling pathway.

机构信息

Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200062, China.

Institute of Translational Medicine, Shanghai University, Shanghai, 200444, China.

出版信息

J Transl Med. 2021 Sep 8;19(1):383. doi: 10.1186/s12967-021-03058-z.

DOI:10.1186/s12967-021-03058-z
PMID:34496870
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8424978/
Abstract

BACKGROUND

Antiangiogenic therapy has increasingly become an important strategy for the treatment of colorectal cancer. Recent studies have shown that the tumour microenvironment (TME) promotes tumour angiogenesis. Bufalin is an active antitumour compound whose efficacy has been indicated by previous studies. However, there are very few studies on the antiangiogenic effects of bufalin.

METHODS

Herein, human umbilical vein endothelial cell (HUVEC) tube formation, migration and adhesion tests were used to assess angiogenesis in vitro. Western blotting and quantitative PCR were used to detect relevant protein levels and mRNA expression levels. A subcutaneous xenograft tumour model and a hepatic metastasis model were established in mice to investigate the influence of bufalin on angiogenesis mediated by the TME in vivo.

RESULTS

We found that angiogenesis mediated by cells in the TME was significantly inhibited in the presence of bufalin. The results demonstrated that the proangiogenic genes in HUVECs, such as VEGF, PDGFA, E-selectin and P-selectin, were downregulated by bufalin and that this downregulation was mediated by inhibition of the STAT3 pathway. Overexpression of STAT3 reversed the inhibitory effects of bufalin on angiogenesis. Furthermore, there was little reduction in angiogenesis when bufalin directly acted on the cells in the tumour microenvironment.

CONCLUSION

Our findings demonstrate that bufalin suppresses tumour microenvironment-mediated angiogenesis by inhibiting the STAT3 signalling pathway in vascular endothelial cells, revealing that bufalin may be used as a new antiangiogenic adjuvant therapy medicine to treat colorectal cancer.

摘要

背景

抗血管生成治疗已逐渐成为治疗结直肠癌的重要策略。最近的研究表明,肿瘤微环境(TME)促进肿瘤血管生成。蟾毒灵是一种具有抗肿瘤活性的化合物,其功效已被之前的研究表明。然而,关于蟾毒灵的抗血管生成作用的研究很少。

方法

在此,通过人脐静脉内皮细胞(HUVEC)管形成、迁移和黏附试验评估体外血管生成。Western blot 和定量 PCR 用于检测相关蛋白水平和 mRNA 表达水平。在小鼠中建立皮下异种移植肿瘤模型和肝转移模型,以研究蟾毒灵对 TME 介导的血管生成的影响。

结果

我们发现,存在蟾毒灵时,TME 中的细胞介导的血管生成明显受到抑制。结果表明,HUVEC 中的促血管生成基因,如 VEGF、PDGFA、E-选择素和 P-选择素,被蟾毒灵下调,这种下调是通过抑制 STAT3 通路介导的。STAT3 的过表达逆转了蟾毒灵对血管生成的抑制作用。此外,当蟾毒灵直接作用于肿瘤微环境中的细胞时,对血管生成的抑制作用较小。

结论

我们的研究结果表明,蟾毒灵通过抑制血管内皮细胞中的 STAT3 信号通路来抑制肿瘤微环境介导的血管生成,表明蟾毒灵可能被用作治疗结直肠癌的新的抗血管生成辅助治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55c/8424978/4d332b1e1d65/12967_2021_3058_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55c/8424978/210e1c53d45d/12967_2021_3058_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55c/8424978/58f11498cf8a/12967_2021_3058_Fig2_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55c/8424978/0b13ef8686d5/12967_2021_3058_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55c/8424978/7cbd9b719cb7/12967_2021_3058_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55c/8424978/4d332b1e1d65/12967_2021_3058_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55c/8424978/210e1c53d45d/12967_2021_3058_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55c/8424978/58f11498cf8a/12967_2021_3058_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55c/8424978/04a88687000d/12967_2021_3058_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55c/8424978/0b742295ec7d/12967_2021_3058_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55c/8424978/0b13ef8686d5/12967_2021_3058_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55c/8424978/7cbd9b719cb7/12967_2021_3058_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55c/8424978/4d332b1e1d65/12967_2021_3058_Fig7_HTML.jpg

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本文引用的文献

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Silencing c-Myc Enhances the Antitumor Activity of Bufalin by Suppressing the HIF-1α/SDF-1/CXCR4 Pathway in Pancreatic Cancer Cells.沉默c-Myc通过抑制胰腺癌细胞中的HIF-1α/SDF-1/CXCR4通路增强蟾蜍灵的抗肿瘤活性。
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Bufalin reverses multidrug resistance by regulating stemness through the CD133/nuclear factor-κB/MDR1 pathway in colorectal cancer.
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