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芍药软肝合剂对肝癌小鼠肠道菌群的调节作用。

Regulation of Shaoyao Ruangan Mixture on Intestinal Flora in Mice With Primary Liver Cancer.

机构信息

1 Second Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, People's Republic of China.

2 Zhejiang Cancer Hospital, Hangzhou, People's Republic of China.

出版信息

Integr Cancer Ther. 2019 Jan-Dec;18:1534735419843178. doi: 10.1177/1534735419843178.

Abstract

BACKGROUND

Shaoyao Ruangan mixture (SRM) has been applied clinically for more than 20 years in Zhejiang Cancer Hospital to treat patients with primary liver cancer (PLC). Intestinal microecology plays an important role in the emergence of liver diseases. This study aimed to reveal connections among SRM, intestinal microbiota and PLC, and the potential targets of SRM for liver cancer.

METHODS

We established a control group, a PLC model group, and a treatment group of mice to analyze the inhibitory effect of SRM on PLC and its intestinal flora target. We also evaluated drug efficacy of SRM and analyzed specific changes in intestinal flora by 16S rDNA sequencing of stools. As the serum interleukin (IL)-10 level could be an independent prognostic factor for unresectable liver cancer, we detected IL-10 levels and analyzed their association with the abundance of specific bacteria.

RESULTS

Liver tumors in the treatment group were smaller and fewer than those in the model group ( P = .046). The abundance of Bacteroides was significantly higher in the model group than that in the control group, while SRM significantly reduced the increasing abundance of Bacteroides in mice with PLC. We found that the IL-10 level was positively correlated with the abundance of Bacteroides.

CONCLUSION

SRM can effectively inhibit the progression of PLC and increase Bacteroides abundance. In view of the association between Bacteroides and liver cancer and the significant positive correlation between Bacteroides and IL-10 levels, Bacteroides may be the target intestinal flora of SRM to inhibit PLC.

摘要

背景

芍药软肝合剂(SRM)在浙江肿瘤医院临床应用 20 余年,用于治疗原发性肝癌(PLC)患者。肠道微生态在肝病的发生中起着重要作用。本研究旨在揭示 SRM 与肠道微生物群和 PLC 之间的联系,以及 SRM 治疗肝癌的潜在靶点。

方法

我们建立了对照组、PLC 模型组和 SRM 治疗组的小鼠,以分析 SRM 对 PLC 及其肠道菌群靶标的抑制作用。我们还评估了 SRM 的药效,并通过粪便 16S rDNA 测序分析肠道菌群的特定变化。由于血清白细胞介素(IL)-10 水平可能是不可切除肝癌的独立预后因素,我们检测了 IL-10 水平,并分析了其与特定细菌丰度的关系。

结果

治疗组的肝肿瘤比模型组小且少(P=0.046)。模型组中拟杆菌的丰度明显高于对照组,而 SRM 可显著降低 PLC 小鼠中拟杆菌丰度的增加。我们发现 IL-10 水平与拟杆菌的丰度呈正相关。

结论

SRM 能有效抑制 PLC 的进展,增加拟杆菌的丰度。鉴于拟杆菌与肝癌之间的关联以及拟杆菌与 IL-10 水平之间的显著正相关,拟杆菌可能是 SRM 抑制 PLC 的目标肠道菌群。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99a4/6477757/b9db8b1dfefa/10.1177_1534735419843178-fig1.jpg

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