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题名

The long intergenic non-protein coding RNA 472 (LINC00472) aggravates neuropathic pain through the microRNA-300/high mobility group box protein 1 axis: a study using the chronic constrictive injury rat model

作者
通讯作者Wang, Zheyin
发表日期
2021-10-01
DOI
发表期刊
ISSN
2224-5820
EISSN
2224-5839
卷号10期号:11
摘要
["Background: This study investigated the role and molecular mechanisms of the long intergenic nonprotein coding RNA 472 (LINC00472) in neuropathic pain using a chronic constrictive injury (CCI) rat model.","Methods: CCI rat model was established and PC12 cells were induced by LPS to simulate neuropathological injury in vivo and in vitro. The levels of LINC00472, miR-300, and high mobility group box protein 1 (HMGB1) in the spinal cord tissue of CCI rats and PC12 pheochromocytoma cells were assessed by qRT-PCR and western blot. The effects of LINC00472 on neuropathic pain in the CCI rats were observed by their pain behavior. ELISA was used to detect the levels of inflammatory cytokines in rat tissues and cells. The molecular mechanisms of LINC00472 were verified by luciferase experiments, RNA immunoprecipitation, and RNA pull down assays.","Results: The expression of LINC00472 and HMGB1 were upregulated, and the expression of miR-300 was downregulated in the spinal cord tissues of CCI rats and in PC12 cells. The upregulation of LINC00472 in CCI rats significantly induced the occurrence of neuropathic pain. In addition, downregulation of LINC00472 inhibited the inflammatory response of CCI rats and PC12 cells. This study identified miR-300 as a target gene of LINC00472, and HMGB1 as the target gene of miR-300. Further experiments confirmed that the expression of anti-miR-300 could partially reverse the anti-inflammatory effects and the reduction of neuropathic pain induced by low expression of LINC00472.","Conclusions: LINC00472 promotes the progression of neuropathic pain by reducing miR-300 expression and increasing HMGB1 expression. The LINC00472/miR-300/HMGB1 axis may be a novel therapeutic target for neuropathic pain."]
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语种
英语
学校署名
第一 ; 通讯
WOS研究方向
Health Care Sciences & Services
WOS类目
Health Care Sciences & Services
WOS记录号
WOS:000720323100001
出版者
来源库
Web of Science
引用统计
被引频次[WOS]:2
成果类型期刊论文
条目标识符http://sustech.caswiz.com/handle/2SGJ60CL/256826
专题南方科技大学第一附属医院
作者单位
1.Southern Univ Sci & Technol, Affiliated Hosp 1, Shenzhen Peoples Hosp, Dept Pain Med, Shenzhen 518020, Peoples R China
2.Nanjing Med Univ, Affiliated Wuxi Peoples Hosp 2, Dept Anesthesiol, Wuxi, Jiangsu, Peoples R China
第一作者单位南方科技大学第一附属医院
通讯作者单位南方科技大学第一附属医院
第一作者的第一单位南方科技大学第一附属医院
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GB/T 7714
Zhang, Juan,Liu, Jiao,Ling, Diyang,et al. The long intergenic non-protein coding RNA 472 (LINC00472) aggravates neuropathic pain through the microRNA-300/high mobility group box protein 1 axis: a study using the chronic constrictive injury rat model[J]. Annals of Palliative Medicine,2021,10(11).
APA
Zhang, Juan,Liu, Jiao,Ling, Diyang,Zhao, Yan,&Wang, Zheyin.(2021).The long intergenic non-protein coding RNA 472 (LINC00472) aggravates neuropathic pain through the microRNA-300/high mobility group box protein 1 axis: a study using the chronic constrictive injury rat model.Annals of Palliative Medicine,10(11).
MLA
Zhang, Juan,et al."The long intergenic non-protein coding RNA 472 (LINC00472) aggravates neuropathic pain through the microRNA-300/high mobility group box protein 1 axis: a study using the chronic constrictive injury rat model".Annals of Palliative Medicine 10.11(2021).
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