Evidence map›Paper›PMID 29163771›Full record

ArticleOncotarget2017

Inhibition of HOX/PBX dimer formation leads to necroptosis in acute myeloid leukemia cells.

Raed A Alharbi, Hardev S Pandha, Guy R Simpson, Ruth Pettengell, Krzysztof Poterlowicz, Alexander Thompson, Kevin Harrington, Mohamed El-Tanani, Richard Morgan

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

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  9. Regulated cell death in cisplatin-induced AKI: relevance ofAmerican journal of physiology. Renal physiology · 2021
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  13. The Role of theGenes · 2019
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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

9 authors at 6 institutions in 2 countries.

Raed A AlharbiDepartment of Laboratory Medicine, Faculty of Applied Medical Sciences, Albaha University, Albaha, Saudi Arabia.
Hardev S PandhaFaculty of Health and Medical Sciences, University of Surrey, Guildford, UK.
Guy R SimpsonFaculty of Health and Medical Sciences, University of Surrey, Guildford, UK.
Ruth PettengellSt. George's, University of London, London, UK.
Krzysztof PoterlowiczInstitute of Cancer Therapeutics, University of Bradford, Bradford, UK.
Alexander ThompsonDivision of Cancer and Stem Cells, Centre for Biomolecular Sciences, University of Nottingham, Nottingham, UK.
Kevin HarringtonTargeted Therapy Team, Chester Beatty Laboratories, Institute of Cancer Research, London, UK.
Mohamed El-TananiInstitute of Cancer Therapeutics, University of Bradford, Bradford, UK.
Richard MorganInstitute of Cancer Therapeutics, University of Bradford, Bradford, UK.
University of Bradford · GBUniversity of Surrey · GBAl Baha University · SAInstitute of Cancer Research · GBSt George's, University of London · GBUniversity of Nottingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The HOX genes encode a family of transcription factors that have key roles in both development and malignancy. Disrupting the interaction between HOX proteins and their binding partner, PBX, has been shown to cause apoptotic cell death in a range of solid tumors. However, despite HOX proteins playing a particularly significant role in acute myeloid leukemia (AML), the relationship between HOX gene expression and patient survival has not been evaluated (with the exception of

Indexed as

acute myeloid leukemiaHOXHXR9necroptosisprotein kinase C

Identifiers

PMID29163771
PMCPMC5685692
OpenAlexW2744694395

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.