Evidence map›Paper›PMID 28074546›Full record

ReviewThe Journal of physiology2017

Hypoxia and cellular metabolism in tumour pathophysiology.

Scott K Parks, Yann Cormerais, Jacques Pouysségur

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 3% 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

80 citing papers in PubMed, 1 synthesis or guideline pooled it, 146 citations in OpenAlex.

  1. Pooled it
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  12. Hypoxia-driven angiogenesis and metabolic reprogramming in vascular tumors.Frontiers in cell and developmental biology · 2025
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20 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 2 countries.

Scott K ParksMedical Biology Department, Centre Scientifique de Monaco, 8 Quai Antoine 1er, MC-98000, Monaco, Principality of Monaco.ORCID 0000-0002-6558-7856
Yann CormeraisMedical Biology Department, Centre Scientifique de Monaco, 8 Quai Antoine 1er, MC-98000, Monaco, Principality of Monaco.
Jacques PouysségurMedical Biology Department, Centre Scientifique de Monaco, 8 Quai Antoine 1er, MC-98000, Monaco, Principality of Monaco.
Scientific Centre of Monaco · MCCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer cells are optimised for growth and survival via an ability to outcompete normal cells in their microenvironment. Many of these advantageous cellular adaptations are promoted by the pathophysiological hypoxia that arises in solid tumours due to incomplete vascularisation. Tumour cells are thus faced with the challenge of an increased need for nutrients to support the drive for proliferation in the face of a diminished extracellular supply. Among the many modifications occurring in tumour cells, hypoxia inducible factors (HIFs) act as essential drivers of key pro-survival pathways via the promotion of numerous membrane and cytosolic proteins. Here we focus our attention on two areas: the role of amino acid uptake and the handling of metabolic acid (CO

Indexed as

Amino Acid Transport SystemsAnimalsCarbonic AnhydrasesCell HypoxiaHumansHypoxiaHypoxia-Inducible Factor 1, alpha SubunitNeoplasmsTumor MicroenvironmentAmino Acid Transport SystemsCarbonic AnhydrasesHypoxia-Inducible Factor 1, alpha Subunitamino-acid transportcell proliferationpH regulationtumour hypoxia

Identifiers

PMID28074546
PMCPMC5390873
OpenAlexW2568192015

What OpenQuestion holds

Textmetadata
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.