Evidence map›Paper›PMID 34658364›Full record

ArticleEndocrine-related cancer2021

Developmental role of PHD2 in the pathogenesis of pseudohypoxic pheochromocytoma.

Luise Eckardt, Maria Prange-Barczynska, Emma J Hodson, James W Fielding, Xiaotong Cheng, Joanna D C C Lima, Samvid Kurlekar, Gillian Douglas, Peter J Ratcliffe, Tammie Bishop

Open access · hybridAbstract read
In one paragraph

Article in Endocrine-related cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. PHD1-3 oxygen sensors in vivo-lessons learned from gene deletions.Pflugers Archiv : European journal of physiology · 2024
    Review
  3. Hif-2α programs oxygen chemosensitivity in chromaffin cells.The Journal of clinical investigation · 2024
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. 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

10 authors at 5 institutions in 2 countries.

Luise EckardtTarget Discovery Institute, University of Oxford, Oxford, UK.
Maria Prange-BarczynskaTarget Discovery Institute, University of Oxford, Oxford, UK.
Emma J HodsonThe Francis Crick Institute, London, UK.
James W FieldingTarget Discovery Institute, University of Oxford, Oxford, UK.
Xiaotong ChengTarget Discovery Institute, University of Oxford, Oxford, UK.
Joanna D C C LimaTarget Discovery Institute, University of Oxford, Oxford, UK.
Samvid KurlekarTarget Discovery Institute, University of Oxford, Oxford, UK.
Gillian DouglasBHF Centre of Research Excellence, Division of Cardiovascular Medicine, Radcliffe Department of Medicine, John Radcliffe Hospital, University of Oxford, Oxford, UK.
Peter J RatcliffeTarget Discovery Institute, University of Oxford, Oxford, UK.
Tammie BishopTarget Discovery Institute, University of Oxford, Oxford, UK.ORCID 0000-0003-3308-9139
University of Oxford · GBHeidelberg University · DEJohn Radcliffe Hospital · GBThe Francis Crick Institute · GBUniversity of Cambridge · GB

Funding

Cancer Research UK FC001501Medical Research Council FC001501Wellcome Trust 106241/Z/14/ZWellcome Trust FC001501
6 · The paper itself

Abstract

Despite a general role for the HIF hydroxylase system in cellular oxygen sensing and tumour hypoxia, cancer-associated mutations of genes in this pathway, including PHD2, PHD1, EPAS1 (encoding HIF-2α) are highly tissue-restricted, being observed in pseudohypoxic pheochromocytoma and paraganglioma (PPGL) but rarely, if ever, in other tumours. In an effort to understand that paradox and gain insights into the pathogenesis of pseudohypoxic PPGL, we constructed mice in which the principal HIF prolyl hydroxylase, Phd2, is inactivated in the adrenal medulla using TH-restricted Cre recombinase. Investigation of these animals revealed a gene expression pattern closely mimicking that of pseudohypoxic PPGL. Spatially resolved analyses demonstrated a binary distribution of two contrasting patterns of gene expression among adrenal medullary cells. Phd2 inactivation resulted in a marked shift in this distribution towards a Pnmt-/Hif-2α+/Rgs5+ population. This was associated with morphological abnormalities of adrenal development, including ectopic TH+ cells within the adrenal cortex and external to the adrenal gland. These changes were ablated by combined inactivation of Phd2 with Hif-2α, but not Hif-1α. However, they could not be reproduced by inactivation of Phd2 in adult life, suggesting that they arise from dysregulation of this pathway during adrenal development. Together with the clinical observation that pseudohypoxic PPGL manifests remarkably high heritability, our findings suggest that this type of tumour likely arises from dysregulation of a tissue-restricted action of the PHD2/HIF-2α pathway affecting adrenal development in early life and provides a model for the study of the relevant processes.

Indexed as

Adrenal Gland NeoplasmsParagangliomaPheochromocytomaAnimalsBasic Helix-Loop-Helix ProteinsHumansHypoxia-Inducible Factor 1, alpha SubunitHypoxia-Inducible Factor-Proline DioxygenasesMiceBasic Helix-Loop-Helix ProteinsEgln1 protein, mouseHypoxia-Inducible Factor 1, alpha SubunitHypoxia-Inducible Factor-Proline Dioxygenasesadrenal medullaHIFhypoxiaPHDpheochromocytoma

Identifiers

PMID34658364
PMCPMC8558849
OpenAlexW3201848506

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.