Evidence map›Paper›PMID 31167620›Full record

ArticleStroke2019

Silencing of Long Noncoding RNA Nespas Aggravates Microglial Cell Death and Neuroinflammation in Ischemic Stroke.

Yiming Deng, Duanduan Chen, Luyao Wang, Feng Gao, Bo Jin, Hong Lv, Guojun Zhang, Xuan Sun, Lian Liu, Dapeng Mo and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Stroke, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. The Role of Long Non-Coding RNA in Anxiety Disorders: A Literature Review.International journal of molecular sciences · 2025
    Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. LncRNAActa pharmaceutica Sinica. B · 2022
    Article
  16. Article
  17. Review
  18. Long Non-coding RNAs (lncRNAs), A New Target in Stroke.Cellular and molecular neurobiology · 2022
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 5 institutions in 2 countries.

Yiming DengDepartment of Interventional Neuroradiology, Beijing Tiantan Hospital, Capital Medical University, China (Y.D., F.G., X.S., L.L., D.M., N.M., L.S., X.H., Z.M.).
Duanduan ChenFrom the School of Life Science (D.C., T.Y.), Beijing Institute of Technology, China.
Luyao WangIntelligent Robotics Institute, School of Mechatronical Engineering (L.W.), Beijing Institute of Technology, China.
Feng GaoDepartment of Interventional Neuroradiology, Beijing Tiantan Hospital, Capital Medical University, China (Y.D., F.G., X.S., L.L., D.M., N.M., L.S., X.H., Z.M.).
Bo JinDepartment of Clinical Laboratory, Peking University First Hospital, Beijing, China (B.J., H.L., G.Z.).
Hong LvDepartment of Clinical Laboratory, Peking University First Hospital, Beijing, China (B.J., H.L., G.Z.).
Guojun ZhangDepartment of Clinical Laboratory, Peking University First Hospital, Beijing, China (B.J., H.L., G.Z.).
Xuan SunDepartment of Interventional Neuroradiology, Beijing Tiantan Hospital, Capital Medical University, China (Y.D., F.G., X.S., L.L., D.M., N.M., L.S., X.H., Z.M.).
Lian LiuDepartment of Interventional Neuroradiology, Beijing Tiantan Hospital, Capital Medical University, China (Y.D., F.G., X.S., L.L., D.M., N.M., L.S., X.H., Z.M.).
Dapeng MoDepartment of Interventional Neuroradiology, Beijing Tiantan Hospital, Capital Medical University, China (Y.D., F.G., X.S., L.L., D.M., N.M., L.S., X.H., Z.M.).
Ning MaDepartment of Interventional Neuroradiology, Beijing Tiantan Hospital, Capital Medical University, China (Y.D., F.G., X.S., L.L., D.M., N.M., L.S., X.H., Z.M.).
Ligang SongDepartment of Interventional Neuroradiology, Beijing Tiantan Hospital, Capital Medical University, China (Y.D., F.G., X.S., L.L., D.M., N.M., L.S., X.H., Z.M.).
Xiaochuan HuoDepartment of Interventional Neuroradiology, Beijing Tiantan Hospital, Capital Medical University, China (Y.D., F.G., X.S., L.L., D.M., N.M., L.S., X.H., Z.M.).
Tianyi YanFrom the School of Life Science (D.C., T.Y.), Beijing Institute of Technology, China.
Zhongrong MiaoDepartment of Interventional Neuroradiology, Beijing Tiantan Hospital, Capital Medical University, China (Y.D., F.G., X.S., L.L., D.M., N.M., L.S., X.H., Z.M.).
Capital Medical University · CNBeijing Tian Tan Hospital · CNBeijing Institute of Technology · CNChinese Institute for Brain Research · CNMinistry of Industry and Information Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Purpose- Ischemic stroke is one of the leading causes of morbidity and mortality worldwide and a major cause of long-term disability. Recently, long noncoding RNAs have been revealed, which are tightly associated with several human diseases. However, the functions of long noncoding RNAs in ischemic stroke still remain largely unknown. In the current study, for the first time, we investigated the role of long noncoding RNA Nespas in ischemic stroke. Methods- We used in vivo models of middle cerebral artery occlusion and in vitro models of oxygen-glucose deprivation to illustrate the effect of long noncoding RNA Nespas on ischemic stroke. Results- We found expression of Nespas was significantly increased in ischemic cerebral tissues and oxygen-glucose deprivation-treated BV2 cells in a time-dependent manner. Silencing of Nespas aggravated middle cerebral artery occlusion operation-induced IR injury and cell death. In addition, proinflammatory cytokine production and NF-κB (nuclear factor-κB) signaling activation were inhibited by Nespas overexpression. TAK1 (transforming growth factor-β-activated kinase 1) was found to directly interact with Nespas, and TAK1 activation was significantly suppressed by Nespas. At last, we found Nespas-inhibited TRIM8 (tripartite motif 8)-induced K63-linked polyubiquitination of TAK1. Conclusions- We showed that Nespas played anti-inflammatory and antiapoptotic roles in cultured microglial cells after oxygen-glucose deprivation stimulation and in mice after ischemic stroke by inhibiting TRIM8-related K63-linked polyubiquitination of TAK1.

Indexed as

Cell DeathGene SilencingAnimalsBrain IschemiaCells, CulturedCytokinesHumansInfarction, Middle Cerebral ArteryInflammationMAP Kinase Kinase Kinase 7MAP Kinase Kinase KinasesMiceMicrogliaNerve Tissue ProteinsRNA, Long NoncodingStrokeCytokinesMAP Kinase Kinase Kinase 7MAP Kinase Kinase KinasesNerve Tissue ProteinsRNA, Long NoncodingTrim8 protein, mouseUbiquitin-Protein Ligasescell deathlncRNAneuroinflammationstrokeTAK1

Identifiers

PMID31167620
PMCPMC6594728
OpenAlexW2954757680

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.