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Transcriptome Sequencing Explores the Mechanism of Baicalin on Bone Cancer Pain

INTRODUCTION: Bone cancer pain is characterized by persistent pain, usually requiring drugs to relieve pain. Baicalin, a flavonoid compound extracted from Scutellaria baicalensis, which has antioxidant and analgesic effects. But, the effect of baicalin on bone cancer pain is unclear. Thus, this stud...

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Autores principales: Wang, Aitao, Guo, Dongmei, Cheng, Hongyu, Jiang, Hui, Liu, Xiaojuan, Yun, Zhizhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8605882/
https://www.ncbi.nlm.nih.gov/pubmed/34815689
http://dx.doi.org/10.2147/JIR.S336028
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author Wang, Aitao
Guo, Dongmei
Cheng, Hongyu
Jiang, Hui
Liu, Xiaojuan
Yun, Zhizhong
author_facet Wang, Aitao
Guo, Dongmei
Cheng, Hongyu
Jiang, Hui
Liu, Xiaojuan
Yun, Zhizhong
author_sort Wang, Aitao
collection PubMed
description INTRODUCTION: Bone cancer pain is characterized by persistent pain, usually requiring drugs to relieve pain. Baicalin, a flavonoid compound extracted from Scutellaria baicalensis, 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 ALPP, DUSP1, CYR61, ALPPL2, SPP1 and TLR4. 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.
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spelling pubmed-86058822021-11-22 Transcriptome Sequencing Explores the Mechanism of Baicalin on Bone Cancer Pain Wang, Aitao Guo, Dongmei Cheng, Hongyu Jiang, Hui Liu, Xiaojuan Yun, Zhizhong J Inflamm Res Original Research INTRODUCTION: Bone cancer pain is characterized by persistent pain, usually requiring drugs to relieve pain. Baicalin, a flavonoid compound extracted from Scutellaria baicalensis, 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 ALPP, DUSP1, CYR61, ALPPL2, SPP1 and TLR4. 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. Dove 2021-11-16 /pmc/articles/PMC8605882/ /pubmed/34815689 http://dx.doi.org/10.2147/JIR.S336028 Text en © 2021 Wang et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Wang, Aitao
Guo, Dongmei
Cheng, Hongyu
Jiang, Hui
Liu, Xiaojuan
Yun, Zhizhong
Transcriptome Sequencing Explores the Mechanism of Baicalin on Bone Cancer Pain
title Transcriptome Sequencing Explores the Mechanism of Baicalin on Bone Cancer Pain
title_full Transcriptome Sequencing Explores the Mechanism of Baicalin on Bone Cancer Pain
title_fullStr Transcriptome Sequencing Explores the Mechanism of Baicalin on Bone Cancer Pain
title_full_unstemmed Transcriptome Sequencing Explores the Mechanism of Baicalin on Bone Cancer Pain
title_short Transcriptome Sequencing Explores the Mechanism of Baicalin on Bone Cancer Pain
title_sort transcriptome sequencing explores the mechanism of baicalin on bone cancer pain
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8605882/
https://www.ncbi.nlm.nih.gov/pubmed/34815689
http://dx.doi.org/10.2147/JIR.S336028
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