Evidence map›Paper›PMID 25483038›Full record

ArticleRNA biology2014

Comprehensive silencing of target-sharing microRNAs is a mechanism for SIRT1 overexpression in cancer.

Kotaro Kiga, Yoko Fukuda-Yuzawa, Masanobu Tanabe, Shoji Tsuji, Chihiro Sasakawa, Taro Fukao

Open access · hybridAbstract read
In one paragraph

Article in RNA biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Trending topics of SIRT1 in tumorigenicity.Biochimica et biophysica acta. General subjects · 2021
    Review
  3. Article
  4. SIRT5 downregulation is associated with poor prognosis in glioblastoma.Cancer biomarkers : section A of Disease markers · 2019
    Article
  5. Article
  6. Review
  7. Article
  8. 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 3 institutions in 2 countries.

Kotaro Kigaa Max-Planck-Institute of Immunobiology and Epigenetics ; Freiburg , Germany.
Yoko Fukuda-Yuzawa
Masanobu Tanabe
Shoji Tsuji
Chihiro Sasakawa
Taro Fukao
Max Planck Institute of Immunobiology and Epigenetics · DEThe University of Tokyo · JPKeio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of SIRT1 is frequently observed in various types of cancers, suggesting its potential role in malignancies. However, the molecular basis of how SIRT1 is elevated in cancer is less understood. Here we show that cancer-related SIRT1 overexpression is due to evasion of Sirt1 mRNA from repression by a group of Sirt1-targeting microRNAs (miRNAs) that might be robustly silenced in cancer. Our comprehensive library-based screening and subsequent miRNA gene profiling revealed a housekeeping gene-like broad expression pattern and strong CpG island-association of the Sirt1-targeting miRNA genes. This suggests aberrant CpG DNA methylation as the mechanistic background for malignant SIRT1 elevation. Our work also provides an example where epigenetic mechanisms cause the group-wide regulation of miRNAs sharing a common key target.

Indexed as

Gene Expression ProfilingGene Expression Regulation, Neoplastic3' Untranslated RegionsAnimalsAntineoplastic Agents, PhytogenicApoptosisBlotting, WesternCell Line, TumorCpG IslandsDNA MethylationEtoposideHeLa CellsHumansMiceMicroRNAsNeoplasms3' Untranslated RegionsAntineoplastic Agents, PhytogenicEtoposideMicroRNAsMIRN132 microRNA, humanMIRN212 microRNA, humanSIRT1 protein, humanSirtuin 1Tumor Suppressor Protein p533′UTR, 3′ untranslated region5-Aza-dC, 5-aza-2’-deoxycytidinecancerCGIs, CpG islandsDNA methylationE2F1, E2F transcription factor 1epigeneticsFOXO, forkhead box OHIC1, hypermethylated in cancer 1LXR, liver X receptorMicroRNAMyoD, myogenic differentiation 1NAD, nicotinamide adenine dinucleotideNF-κB, nuclear factor kappa-BOVCA1, ovarian cancer-associated gene 1 proteinOVCA2, ovarian cancer-associated gene 2 proteinp53, protein 53PARP, poly(ADP-ribose) polymerase-1PGC-1α, peroxisome proliferative activated receptor, gamma, coactivator 1 alphapri-miRNA, primary miRNAPUMA, p53-upregulated modulator of apoptosisSir2, Silent information regulator 2SIRT1SIRT1, sirtuin (silent mating type information regulation 2 homolog) 1 (S. cerevisiae)SMG6, smg-6 homolog, nonsense mediated mRNA decay factor (C. elegans)

Identifiers

PMID25483038
PMCPMC4615778
OpenAlexW1964845558

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.