Evidence map›Paper›PMID 36384128›Full record

ArticleCell reports2022

Pan-cancer analysis of tissue and single-cell HIF-pathway activation using a conserved gene signature.

Olivia Lombardi, Ran Li, Silvia Halim, Hani Choudhry, Peter J Ratcliffe, David R Mole

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.6field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. HIF-1 and HIF-2 in cancer: structure, regulation, and therapeutic prospects.Cellular and molecular life sciences : CMLS · 2025
    Review
  19. Article
  20. Article
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

6 authors at 3 institutions in 2 countries.

Olivia LombardiNDM Research Building, University of Oxford, Old Road Campus, Headington, Oxford OX3 7FZ, UK.
Ran LiNDM Research Building, University of Oxford, Old Road Campus, Headington, Oxford OX3 7FZ, UK.
Silvia HalimNDM Research Building, University of Oxford, Old Road Campus, Headington, Oxford OX3 7FZ, UK.
Hani ChoudhryDepartment of Biochemistry, Faculty of Science, Center of Innovation in Personalized Medicine, King Fahd Center for Medical Research, King Abdulaziz University, Jeddah, Saudi Arabia.
Peter J RatcliffeLudwig Institute for Cancer Research, University of Oxford, Old Road Campus, Headington, Oxford OX3 7FZ, UK; The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
David R MoleNDM Research Building, University of Oxford, Old Road Campus, Headington, Oxford OX3 7FZ, UK. Electronic address: david.mole@ndm.ox.ac.uk.
University of Oxford · GBKing Abdulaziz University · SAThe Francis Crick Institute · GB

Funding

Cancer Research UK 16016Cancer Research UK FC001501Medical Research Council FC001501Wellcome Trust 106241/Z/14/ZWellcome Trust 203141/Z/16/ZWellcome Trust FC001501
6 · The paper itself

Abstract

Activation of cellular hypoxia pathways, orchestrated by HIF (hypoxia-inducible factor) transcription factors, is a common feature of multiple tumor types, resulting from microenvironment factors and oncogenic mutation. Although they help drive many of the "hallmarks" of cancer and are associated with poor outcome and resistance to therapy, the transcriptional targets of HIF vary considerably depending on the cell type. By integrating 72 genome-wide assays of HIF binding and transcriptional regulation from multiple cancer types, we define a consensus set of 48 HIF target genes that is highly conserved across cancer types and cell lineages. These genes provide an effective marker of HIF activation in bulk and single-cell transcriptomic analyses across a wide range of cancer types and in malignant and stromal cell types. This allows the tissue-orchestrated responses to the hypoxic tumor microenvironment and to oncogenic HIF activation to be deconvoluted at the tumor and single-cell level.

Indexed as

NeoplasmsCell HypoxiaHumansHypoxiaTranscription FactorsTumor MicroenvironmentTranscription FactorscancerCP: cancergene signatureHIFhypoxiaoxygen-sensingsingle-celltranscriptiontranscriptomicstumorigenesisVHL

Identifiers

PMID36384128
PMCPMC9869179
OpenAlexW4309107095

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.