Evidence map›Paper›PMID 29149101›Full record

ReviewCell death and differentiation2018

How does p53 induce apoptosis and how does this relate to p53-mediated tumour suppression?

Brandon J Aubrey, Gemma L Kelly, Ana Janic, Marco J Herold, Andreas Strasser

Open access · bronzeAbstract readReview
In one paragraph

Review in Cell death and differentiation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 773 papers.

0numbers the graph read from it
0cells of the map it votes in
773citing papers in PubMed
31.0field-weighted citation impact, top 1% 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

773 citing papers in PubMed, 1,347 citations in OpenAlex.

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  12. On the Edge of Benefit and Harm: Reactive Oxygen Species in Cancer.International journal of molecular sciences · 2026
    Review
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713 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

5 authors at 2 institutions in 1 country.

Brandon J AubreyThe Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Gemma L KellyThe Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Ana JanicThe Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Marco J HeroldThe Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
Andreas StrasserThe Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
University of Melbourne · AUWalter and Eliza Hall Institute of Medical Research · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumour suppressor gene TP53 is mutated in ~50% of human cancers. In addition to its function in tumour suppression, p53 also plays a major role in the response of malignant as well as nontransformed cells to many anticancer therapeutics, particularly those that cause DNA damage. P53 forms a homotetrameric transcription factor that is reported to directly regulate ~500 target genes, thereby controlling a broad range of cellular processes, including cell cycle arrest, cell senescence, DNA repair, metabolic adaptation and cell death. For a long time, induction of apoptotic death in nascent neoplastic cells was regarded as the principal mechanism by which p53 prevents tumour development. This concept has, however, recently been challenged by the findings that in striking contrast to Trp53-deficient mice, gene-targeted mice that lack the critical effectors of p53-induced apoptosis do not develop tumours spontaneously. Remarkably, even mice lacking all mediators critical for p53-induced apoptosis, G1/S boundary cell cycle arrest and cell senescence do not develop any tumours spontaneously. In this review we discuss current understanding of the mechanisms by which p53 induces cell death and how this affects p53-mediated tumour suppression and the response of malignant cells to anticancer therapy.

Indexed as

ApoptosisAnimalsHumansMiceMutationNeoplasmsProto-Oncogene Proteins c-bcl-2Signal TransductionTranscription FactorsTumor Suppressor Protein p53Proto-Oncogene Proteins c-bcl-2TP53 protein, humanTranscription FactorsTumor Suppressor Protein p53

Identifiers

PMID29149101
PMCPMC5729529
OpenAlexW2768768130

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.