Evidence map›Paper›PMID 29270737›Full record

ReviewJournal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban2017

Long non-coding RNA ANRIL in gene regulation and its duality in atherosclerosis.

Jie-Shan Chi, Jian-Zhou Li, Jing-Jing Jia, Ting Zhang, Xiao-Ma Liu, Li Yi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

39 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Review
  3. Metamorphosis and lncRNAs: A Close Relationship.Genesis (New York, N.Y. : 2000) · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. Regulatory RNAs in immunosenescence.Immunity, inflammation and disease · 2024
    Review
  8. Article
  9. Journal of clinical medicine · 2023
    Article
  10. Association of Common Variants ofInternational journal of molecular sciences · 2023
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Long Non-Coding RNA Epigenetics.International journal of molecular sciences · 2021
    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

6 authors at 2 institutions in 1 country.

Jie-Shan ChiDepartment of Neurology, Peking University Shenzhen Hospital, Shenzhen, 518000, China.
Jian-Zhou LiDepartment of Neurology, Peking University Shenzhen Hospital, Shenzhen, 518000, China.
Jing-Jing JiaDepartment of Neurology, Peking University Shenzhen Hospital, Shenzhen, 518000, China.
Ting ZhangDepartment of Neurology, Peking University Shenzhen Hospital, Shenzhen, 518000, China.
Xiao-Ma LiuDepartment of Neurology, Peking University Shenzhen Hospital, Shenzhen, 518000, China.
Li YiDepartment of Neurology, Peking University Shenzhen Hospital, Shenzhen, 518000, China. yilitj@hotmail.com.
Peking University Shenzhen Hospital · CNShantou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The antisense transcript long non-coding RNA (lncRNA) (antisense non-coding RNA in the INK4 locus, ANRIL) is an antisense of the cyclin-dependent kinase inhibitor 2B (CDKN2B) gene on chromosome 9p21 that contains an overlapping 299-bp region and shares a bidirectional promoter with alternate open reading frame (ARF). In the context of gene regulation, ANRIL is responsible for directly recruiting polycomb group (PcG) proteins, including polycomb repressive complex-1 (PRC-1) and polycomb repressive complex-2 (PRC-2), to modify the epigenetic chromatin state and subsequently inhibit gene expression in cis-regulation. On the other hand, previous reports have indicated that ANRIL is capable of binding to a specific site or sequence, including the Alu element, E2F transcription factor 1 (E2F1), and CCCTC-binding factor (CTCF), to achieve trans-regulation functions. In addition to its function in cell proliferation, adhesion and apoptosis, ANRIL is very closely associated with atherosclerosis- related diseases. The different transcripts and the SNPs that are related to atherosclerotic vascular diseases (ASVD-SNPs) are inextricably linked to the development and progression of atherosclerosis. Linear transcripts have been shown to be a risk factor for atherosclerosis, whereas circular transcripts are protective against atherosclerosis. Furthermore, ANRIL also acts as a component of the inflammatory pathway involved in the regulation of inflammation, which is considered to be one of the causes of atherosclerosis. Collectively, ANRIL plays an important role in the formation of atherosclerosis, and the artificial modification of ANRIL transcripts should be considered following the development of this disease.

Indexed as

Epigenesis, GeneticGenetic Predisposition to DiseaseAlternative SplicingAlu ElementsAtherosclerosisCCCTC-Binding FactorChromosomes, Human, Pair 9Cyclin-Dependent Kinase Inhibitor p15E2F1 Transcription FactorHumansPolycomb Repressive Complex 1Polycomb Repressive Complex 2Promoter Regions, GeneticRNA, Long NoncodingRNA, MessengerSignal TransductionCCCTC-Binding FactorCDKN2B antisense RNA, humanCDKN2B protein, humanCTCF protein, humanCyclin-Dependent Kinase Inhibitor p15E2F1 protein, humanE2F1 Transcription FactorPolycomb Repressive Complex 1Polycomb Repressive Complex 2RNA, Long NoncodingRNA, MessengerANRILatherosclerosisdualitygene regulation

Identifiers

PMID29270737
OpenAlexW2781587278

What OpenQuestion holds

Textmetadata
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.