Evidence map›Paper›PMID 33214683›Full record

ArticleBritish journal of cancer2021

HOX genes promote cell proliferation and are potential therapeutic targets in adrenocortical tumours.

Jeffrey C Francis, Jennifer R Gardiner, Yoan Renaud, Ritika Chauhan, Yacob Weinstein, Celso Gomez-Sanchez, Anne-Marie Lefrançois-Martinez, Jérôme Bertherat, Pierre Val, Amanda Swain

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
3.1field-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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. A Systematic Review onInternational journal of molecular sciences · 2021
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  8. Comprehensive summary: the role of PBX1 in development and cancers.Frontiers in cell and developmental biology · 2024
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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

10 authors at 4 institutions in 4 countries.

Jeffrey C FrancisDivision of Cancer Biology, The Institute of Cancer Research, 237 Fulham Road, London, UK.ORCID http://orcid.org/0000-0001-6646-5749
Jennifer R GardinerDivision of Cancer Biology, The Institute of Cancer Research, 237 Fulham Road, London, UK.
Yoan RenaudGenétique Reproduction & Développement, CNRS UMR 6293, Inserm U1103, Université Clermont Auvergne, 63001, Clermont-Ferrand, France.
Ritika ChauhanTumour Profiling Unit, The Institute of Cancer Research, 237 Fulham Road, London, UK.
Yacob WeinsteinThe Shraga Segal Dept. of Microbiology, Immunology and Genetics, Faculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheva, 84105, Israel.
Celso Gomez-SanchezDivision of Endocrinology, Medical Service, G.V. (Sonny) Montgomery VA Medical Center, 1500 E. Woodrow Wilson Dr, Jackson, MS, 39216, USA.
Anne-Marie Lefrançois-MartinezGenétique Reproduction & Développement, CNRS UMR 6293, Inserm U1103, Université Clermont Auvergne, 63001, Clermont-Ferrand, France.
Jérôme BertheratInstitut Cochin, Inserm U1016, CNRS UMR 8104, Université Paris Descartes, UMR-S1016, 75014, Paris, France.
Pierre ValGenétique Reproduction & Développement, CNRS UMR 6293, Inserm U1103, Université Clermont Auvergne, 63001, Clermont-Ferrand, France.
Amanda SwainDivision of Cancer Biology, The Institute of Cancer Research, 237 Fulham Road, London, UK. amanda.swain@icr.ac.uk.ORCID http://orcid.org/0000-0001-8666-1608
Centre National de la Recherche Scientifique · FRInstitute of Cancer Research · GBBen-Gurion University of the Negev · ILG.V. (Sonny) Montgomery VA Medical Center · US

Funding

Tracking and Evaluation CoreU54GM115428 · NIGMS · UNIVERSITY OF MISSISSIPPI MED CTR · PI COMPRETTA, CAROLINE E. · 2016 to 2025
$38.2M
Adrenal cell ATP1A1 mutations and mechanisms of aldosterone biosynthesisR01HL144847 · NHLBI · UNIVERSITY OF MISSISSIPPI MED CTR · PI GOMEZ-SANCHEZ, CELSO ENRIQUE · 2019 to 2022
$1.3M
Regulation of Mineralocorticoid Receptor ActionI01BX004681 · VA · G V SONNY MONTGOMERY VA MEDCIAL CENTER · PI GOMEZ-SANCHEZ, CELSO ENRIQUE · 2021 to 2023
–
BLRD VA I01 BX004681NHLBI NIH HHS R01 HL144847NIGMS NIH HHS U54 GM115428RCUK | Medical Research Council (MRC) G0901645/1RCUK | Medical Research Council (MRC) MR/N009916/1
6 · The paper itself

Abstract

backgroundUnderstanding the pathways that drive adrenocortical carcinoma (ACC) is essential to the development of more effective therapies. This study investigates the role of the transcription factor HOXB9 and other HOX factors in ACC and its treatment.

methodsWe used transgenic mouse models to determine the role of Hoxb9 in adrenal tumour development. Patient transcriptomic data was analysed for the expression of HOX genes and their association with disease. Drug response studies on various adrenocortical models were done to establish novel therapeutic options.

resultsOur human ACC dataset analyses showed high expression of HOXB9, and other HOX factors, are associated with poorer prognosis. Transgenic overexpression of Hoxb9 in the adrenal cortex of mice with activated Ctnnb1 led to larger adrenal tumours. This phenotype was preferentially observed in male mice and was characterised by more proliferating cells and an increase in the expression of cell cycle genes, including Ccne1. Adrenal tumour cells were found to be dependent on HOX function for survival and were sensitive to a specific peptide inhibitor.

conclusionsThese studies show Hoxb9 can promote adrenal tumour progression in a sex-dependent manner and have identified HOX factors as potential drug targets, leading to novel therapeutic approaches in ACC.

Indexed as

Adrenal Cortex NeoplasmsAdrenocortical CarcinomaAnimalsCell ProliferationFemaleGene ExpressionHomeodomain ProteinsHumansMaleMiceMice, TransgenicMolecular Targeted TherapyPeptidesHomeodomain ProteinsHOXB9 protein, humanHoxb9 protein, mousePeptides

Identifiers

PMID33214683
PMCPMC7884796
OpenAlexW3105900724

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.