Evidence map›Paper›PMID 25123665›Full record

ArticleNucleic acids research2014

7SL RNA represses p53 translation by competing with HuR.

Kotb Abdelmohsen, Amaresh C Panda, Min-Ju Kang, Rong Guo, Jiyoung Kim, Ioannis Grammatikakis, Je-Hyun Yoon, Dawood B Dudekula, Ji Heon Noh, Xiaoling Yang and 2 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed
–field-weighted citation impact
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

101 citing papers in PubMed.

  1. Review
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  16. Regulatory RNAs in immunosenescence.Immunity, inflammation and disease · 2024
    Review
  17. Article
  18. Review
  19. Article
  20. Review

41 more citing papers are in PubMed but not listed here.

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

12 authors.

Kotb AbdelmohsenLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA abdelmohsenk@mail.nih.gov.
Amaresh C PandaLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Min-Ju KangLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Rong GuoLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Jiyoung KimLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Ioannis GrammatikakisLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Je-Hyun YoonLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Dawood B DudekulaLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Ji Heon NohLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Xiaoling YangLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Jennifer L MartindaleLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Myriam GorospeLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA abdelmohsenk@mail.nih.gov.

Funding

Post-transcriptional Regulation Of Proliferative and Stress Response GenesZIAAG000511 · NIA · NATIONAL INSTITUTE ON AGING · PI GOROSPE, MYRIAM · 2009 to 2025
$25.4M
Influence of Post-transcriptional Gene Regulation on Cell Senescence and AgingZIAAG000393 · NIA · NATIONAL INSTITUTE ON AGING · PI GOROSPE, MYRIAM · 2009 to 2025
$24.1M
Intramural NIH HHS
6 · The paper itself

Abstract

Noncoding RNAs (ncRNAs) and RNA-binding proteins are potent post-transcriptional regulators of gene expression. The ncRNA 7SL is upregulated in cancer cells, but its impact upon the phenotype of cancer cells is unknown. Here, we present evidence that 7SL forms a partial hybrid with the 3'-untranslated region (UTR) of TP53 mRNA, which encodes the tumor suppressor p53. The interaction of 7SL with TP53 mRNA reduced p53 translation, as determined by analyzing p53 expression levels, nascent p53 translation and TP53 mRNA association with polysomes. Silencing 7SL led to increased binding of HuR to TP53 mRNA, an interaction that led to the promotion of p53 translation and increased p53 abundance. We propose that the competition between 7SL and HuR for binding to TP53 3'UTR contributes to determining the magnitude of p53 translation, in turn affecting p53 levels and the growth-suppressive function of p53. Our findings suggest that targeting 7SL may be effective in the treatment of cancers with reduced p53 levels.

Indexed as

Gene Expression Regulation, NeoplasticProtein Biosynthesis3' Untranslated RegionsAutophagyBinding, CompetitiveCell Cycle CheckpointsCell Line, TumorCell ProliferationCellular SenescenceELAV ProteinsHeLa CellsHumansNeoplasmsRNA, MessengerRNA, Small CytoplasmicSignal Recognition Particle3' Untranslated Regions7SL RNAELAV ProteinsRNA, MessengerRNA, Small CytoplasmicSignal Recognition ParticleTumor Suppressor Protein p53

Identifiers

PMID25123665
PMCPMC4150789

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.