Evidence map›Paper›PMID 34638823›Full record

ArticleInternational journal of molecular sciences2021

Survivin' Acute Myeloid Leukaemia-A Personalised Target for inv(16) Patients.

Jochen Greiner, Elliott Brown, Lars Bullinger, Robert K Hills, Vanessa Morris, Hartmut Döhner, Ken I Mills, Barbara-Ann Guinn

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Molecular Mechanisms and Therapies of Myeloid Leukaemia.International journal of molecular sciences · 2022
    Article
  8. Increasing Role of Targeted Immunotherapies in the Treatment of AML.International journal of molecular sciences · 2022
    Review
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

8 authors.

Jochen GreinerDepartment of Internal Medicine, Diakonie Hospital Stuttgart, 70176 Stuttgart, Germany.ORCID 0000-0003-1256-173X
Elliott BrownDepartment of Biomedical Sciences, University of Hull, Hull HU6 7RX, UK.
Lars BullingerDepartment of Hematology, Oncology and Tumor Immunology, Charité-Universitätsmedizin Berlin, 13353 Berlin, Germany.
Robert K HillsNuffield Department of Population Health, Richard Doll Building, University of Oxford, Oxford OX3 7LF, UK.
Vanessa MorrisDepartment of Biomedical Sciences, University of Hull, Hull HU6 7RX, UK.
Hartmut DöhnerDepartment of Internal Medicine III, University of Ulm, Helmholtzstr. 10, 89081 Ulm, Germany.
Ken I MillsPatrick G. Johnson Centre for Cancer Research, Queen's University Belfast, Lisburn Road, Belfast BT9 7AE, UK.ORCID 0000-0002-6362-4481
Barbara-Ann GuinnDepartment of Biomedical Sciences, University of Hull, Hull HU6 7RX, UK.ORCID 0000-0003-0639-4541

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite recent advances in therapies including immunotherapy, patients with acute myeloid leukaemia (AML) still experience relatively poor survival rates. The Inhibition of Apoptosis (IAP) family member, survivin, also known by its gene and protein name, Baculoviral IAP Repeat Containing 5 (BIRC5), remains one of the most frequently expressed antigens across AML subtypes. To better understand its potential to act as a target for immunotherapy and a biomarker for AML survival, we examined the protein and pathways that BIRC5 interacts with using the Kyoto Encyclopedia of Genes and Genomes (KEGG), search tool for recurring instances of neighbouring genes (STRING), WEB-based Gene Set Analysis Toolkit, Bloodspot and performed a comprehensive literature review. We then analysed data from gene expression studies. These included 312 AML samples in the Microarray Innovations In Leukemia (MILE) dataset. We found a trend between above median levels of BIRC5 being associated with improved overall survival (OS) but this did not reach statistical significance (

Indexed as

Databases, Nucleic AcidGene Expression Regulation, LeukemicDisease-Free SurvivalFemaleGene Expression ProfilingHumansLeukemia, Myeloid, AcuteMaleNeoplasm ProteinsOligonucleotide Array Sequence AnalysisSurvival RateSurvivinBIRC5 protein, humanNeoplasm ProteinsSurvivinacute myeloid leukaemiaBIRC5Core Binding Factor (CBF)inv(16)overall survivalsurvivin

Identifiers

PMID34638823
PMCPMC8508831

What OpenQuestion holds

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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.