Evidence map›Paper›PMID 21297665›Full record

ReviewOncogene2011

Bax inhibitor 1 in apoptosis and disease.

K S Robinson, A Clements, A C Williams, C N Berger, G Frankel

Abstract readReview
PubMed Publisher
In one paragraph

Review in Oncogene, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

41 citing papers in PubMed, 98 citations in OpenAlex.

  1. Article
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  4. Characterization of theInternational journal of molecular sciences · 2024
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  5. Unravelling the Transcriptional Response ofInternational journal of molecular sciences · 2024
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  8. International journal of molecular sciences · 2023
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  11. Review
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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.

K S RobinsonCentre for Molecular Microbiology and Infection, Division of Cell and Molecular Biology, Imperial College London, London, UK.
A Clements
A C Williams
C N Berger
G Frankel
Imperial College London · GBUniversity of Bristol · GB

Funding

Cancer Research UK 11975Wellcome Trust
6 · The paper itself

Abstract

Bax inhibitor 1 (BI-1) was originally discovered as an inhibitor of Bax-induced apoptosis; this review highlights the fundamental importance of BI-1 in a wider context, including in tissue homeostasis and as a regulator of cellular stress. BI-1 has been shown to interact with a broad range of partners to inhibit many facets of apoptosis, such as reactive oxygen species production, cytosolic acidification and calcium levels as well as endoplasmic reticulum stress signalling pathways. BI-1's anti-apoptotic action initially enables the cell to adapt to stress, although if the stress is prolonged or severe the actions of BI-1 may promote apoptosis. This almost universal anti-apoptotic capacity has been shown to be manipulated during infection with enteropathogenic and enterohaemorrhagic Escherichia coli inhibiting host cell death through direct interaction between their effector NleH and BI-1. In addition, BI-1 activity is important in a large number of cancers, promoting metastasis by modulating actin dynamics, a process dependent upon the BI-1 C-terminus and BI-1:actin interaction. Manipulation of BI-1 therefore has the potential for significant therapeutic benefit in a wide range of human diseases.

Indexed as

ApoptosisAmino Acid SequenceApoptosis Regulatory ProteinsCalciumHumansMembrane ProteinsModels, BiologicalMolecular Sequence DataNeoplasmsReactive Oxygen SpeciesSequence Homology, Amino AcidApoptosis Regulatory ProteinsCalciumMembrane ProteinsReactive Oxygen SpeciesTMBIM6 protein, human

Identifiers

PMID21297665
OpenAlexW1967683520

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.