Evidence map›Paper›PMID 31910062›Full record

ArticleRNA biology2020

The p53 family reaches the final frontier: the variegated regulation of the dark matter of the genome by the p53 family in cancer.

Marco Napoli, Elsa R Flores

Abstract read
In one paragraph

Article in RNA biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. [Research Advances of EGFR-TP53 Co-mutation in Advanced Non-small Cell Lung Cancer].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2022
    Review
  3. Article
  4. Review
  5. Article
  6. 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

2 authors.

Marco NapoliDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center and Research Institute , Tampa, FL, USA.ORCID 0000-0001-7192-5252
Elsa R FloresDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center and Research Institute , Tampa, FL, USA.ORCID 0000-0002-6173-2403

Funding

Identification of non-coding RNAs to therapeutically target undruggable pathways in metastatic lung adenocarcinoma and squamous cell carcinomaR35CA197452 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI FLORES, ELSA R · 2016 to 2022
$6.4M
NCI NIH HHS R35 CA197452
6 · The paper itself

Abstract

The tumour suppressor p53 and its paralogues, p63 and p73, are essential to maintain cellular homoeostasis and the integrity of the cell's genetic material, thus meriting the title of 'guardians of the genome'. The p53 family members are transcription factors and fulfill their activities by controlling the expression of protein-coding and non-coding genes. Here, we review how the latter group transcended from the 'dark matter' of the transcriptome, providing unexpected and intriguing anti-cancer therapeutic strategies.

Indexed as

Biomarkers, TumorGene Expression Regulation, NeoplasticMultigene FamilyCell NucleusGene Regulatory NetworksHumansMicroRNAsNeoplasmsRibosomesRNA, CircularRNA, Long NoncodingRNA StabilityRNA, TransferSignal TransductionStress, PhysiologicalTumor Suppressor Protein p53Biomarkers, TumorMicroRNAsRNA, CircularRNA, Long NoncodingRNA, TransferTumor Suppressor Protein p53cancercircRNAslncRNAsmiRNAsp53p63p73

Identifiers

PMID31910062
PMCPMC7567494

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.