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转录组测序探索黄芩苷治疗骨癌疼痛的机制。

Transcriptome Sequencing Explores the Mechanism of Baicalin on Bone Cancer Pain.

作者信息

Wang Aitao, Guo Dongmei, Cheng Hongyu, Jiang Hui, Liu Xiaojuan, Yun Zhizhong

机构信息

Department of Anesthesiology, Inner Mongolia People's Hospital, Hohhot, Inner Mongolia, 010017, People's Republic of China.

Department of Anesthesiology, Inner Mongolia Medical University, Hohhot, Inner Mongolia, 010110, People's Republic of China.

出版信息

J Inflamm Res. 2021 Nov 16;14:5999-6010. doi: 10.2147/JIR.S336028. eCollection 2021.

Abstract

INTRODUCTION

Bone cancer pain is characterized by persistent pain, usually requiring drugs to relieve pain. Baicalin, a flavonoid compound extracted from , which has antioxidant and analgesic effects. But, the effect of baicalin on bone cancer pain is unclear. Thus, this study aimed to explore the mechanism of baicalin on SD rats with bone cancer pain.

MATERIALS AND METHODS

The MADB-106 breast cancer cells-induced bone pain model was constructed and carried out baicalin treatment. The therapeutic effect of baicalin on bone cancer pain model was observed by hematoxylin-eosin staining and immunofluorescence staining. We also performed transcriptome sequencing analysis of baicalin in the treatment of bone metastases. Also, RT-qPCR and ELISA were used to detect the expression levels of inflammation factors.

RESULTS

After baicalin treatment, osteoclast activation was inhibited and the number of bone trabeculae was increased. Baicalin inhibited the protein expression level of inflammatory factors (IL-1β, IL-6, TNF-α and PGE2) in the bone metastases group. Based on the transcriptome sequencing of the bone metastases group and the baicalin treatment group, baicalin inhibited the expression of and . RT-qPCR was also used to validate the expression levels of these cytokine genes.

CONCLUSION

Baicalin had a certain inhibitory effect on the SD rat model of bone metastasis cancer. These insights can guide future research on the molecular mechanism of bone cancer pain and provide a theoretical basis for baicalin in the treatment of bone pain caused by breast cancer in the future.

摘要

引言

骨癌疼痛的特点是持续性疼痛,通常需要药物来缓解疼痛。黄芩苷是从[未提及具体植物]中提取的一种黄酮类化合物,具有抗氧化和镇痛作用。但是,黄芩苷对骨癌疼痛的影响尚不清楚。因此,本研究旨在探讨黄芩苷对骨癌疼痛的SD大鼠的作用机制。

材料与方法

构建MADB - 106乳腺癌细胞诱导的骨痛模型并进行黄芩苷治疗。通过苏木精 - 伊红染色和免疫荧光染色观察黄芩苷对骨癌疼痛模型的治疗效果。我们还对黄芩苷治疗骨转移进行了转录组测序分析。此外,采用RT - qPCR和ELISA检测炎症因子的表达水平。

结果

黄芩苷治疗后,破骨细胞活化受到抑制,骨小梁数量增加。黄芩苷抑制了骨转移组中炎症因子(IL - 1β、IL - 6、TNF - α和PGE2)的蛋白表达水平。基于骨转移组和黄芩苷治疗组的转录组测序,黄芩苷抑制了[未提及具体基因]和[未提及具体基因]的表达。RT - qPCR也用于验证这些细胞因子基因的表达水平。

结论

黄芩苷对骨转移癌的SD大鼠模型有一定的抑制作用。这些见解可为未来骨癌疼痛分子机制的研究提供指导,并为黄芩苷未来治疗乳腺癌引起的骨痛提供理论依据。

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