Evidence map›Paper›PMID 30456884›Full record

ReviewAging cell2019

LncRNAs regulating stemness in aging.

António Sousa-Franco, Kenny Rebelo, Simão Teixeira da Rocha, Bruno Bernardes de Jesus

Open access · goldAbstract readReview
In one paragraph

Review in Aging cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

28 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Liuwei Dihuang Prevents Human Umbilical Vein Endothelial Cells SenescenceCombinatorial chemistry & high throughput screening · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Role of exosome-derived miRNAs in diabetic wound angiogenesis.Molecular and cellular biochemistry · 2024
    Review
  9. Article
  10. Article
  11. Review
  12. Expression ofMolecular therapy. Nucleic acids · 2023
    Article
  13. Article
  14. A TNature aging · 2023
    Article
  15. Review
  16. Involvement of lncRNA TUG1 in HIV-1 Tat-Induced Astrocyte Senescence.International journal of molecular sciences · 2023
    Article
  17. Article
  18. Article
  19. Review
  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

4 authors at 1 institution in 1 country.

António Sousa-FrancoInstituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisboa, Portugal.
Kenny RebeloInstituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisboa, Portugal.
Simão Teixeira da RochaInstituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisboa, Portugal.
Bruno Bernardes de JesusInstituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisboa, Portugal.ORCID 0000-0002-6407-3466
University of Lisbon · PT

Funding

Fundação para a Ciência e a Tecnologia IF/00166/2014Fundação para a Ciência e a Tecnologia IF/00242/2014Fundo Europeu de Desenvolvimento Regional (FEDER) LISBOA-01-0145-FEDER-007391Fundo Europeu de Desenvolvimento Regional (FEDER) LISBOA-01-0145-FEDER-016394Fundo Europeu de Desenvolvimento Regional (FEDER) LISBOA-01-0145-FEDER-028534Fundo Europeu de Desenvolvimento Regional (FEDER) PTDC/BEX-BCM/2612/2014Fundo Europeu de Desenvolvimento Regional (FEDER) PTDC/BIM-MED/0032/2014
6 · The paper itself

Abstract

One of the most outstanding observations from next-generation sequencing approaches was that only 1.5% of our genes code for proteins. The biggest part is transcribed but give rise to different families of RNAs without coding potential. The functional relevance of these abundant transcripts remains far from elucidated. Among them are the long non-coding RNAs (lncRNAs), a relatively large and heterogeneous group of RNAs shown to be highly tissue-specific, indicating a prominent role in processes controlling cellular identity. In particular, lncRNAs have been linked to both stemness properties and detrimental pathways regulating the aging process, being novel players in the intricate network guiding tissue homeostasis. Here, we summarize the up-to-date information on the role of lncRNAs that affect stemness and hence impact upon aging, highlighting the likelihood that lncRNAs may represent an unexploited reservoir of potential therapeutic targets for reprogramming applications and aging-related diseases.

Indexed as

Cellular ReprogrammingCellular SenescenceEpigenesis, GeneticHumansRNA, Long NoncodingStem CellsRNA, Long Noncodingagingepigeneticslong non-coding RNAs (lncRNAs)stem cells

Identifiers

PMID30456884
PMCPMC6351848
OpenAlexW2900459963

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.