Evidence map›Paper›PMID 32159360›Full record

ArticleAmerican journal of physiology. Cell physiology2020

Hydrostatic pressure regulates CYP1A2 expression in human hepatocytes via a mechanosensitive aryl hydrocarbon receptor-dependent pathway.

Lewis Burton, Paula Scaife, Stuart W Paine, Howard R Mellor, Lynn Abernethy, Peter Littlewood, Cyril Rauch

Open access · hybridAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Lewis BurtonSchool of Veterinary Medicine and Science, University of Nottingham, Sutton Bonington, United Kingdom.ORCID 0000-0003-2170-9628
Paula ScaifeDivision of Medical Sciences and Graduate Entry Medicine, School of Medicine, University of Nottingham, Royal Derby Hospital Centre, Derby, United Kingdom.
Stuart W PaineSchool of Veterinary Medicine and Science, University of Nottingham, Sutton Bonington, United Kingdom.
Howard R MellorVertex Pharmaceuticals Europe Ltd., Abingdon Oxfordshire, United Kingdom.
Lynn AbernethyVertex Pharmaceuticals Europe Ltd., Abingdon Oxfordshire, United Kingdom.
Peter LittlewoodVertex Pharmaceuticals Europe Ltd., Abingdon Oxfordshire, United Kingdom.
Cyril RauchSchool of Veterinary Medicine and Science, University of Nottingham, Sutton Bonington, United Kingdom.
University of Nottingham · GBVertex Pharmaceuticals (United Kingdom) · GB

Funding

Biotechnology and Biological Sciences Research Council
6 · The paper itself

Abstract

Approximately 75% of xenobiotics are primarily eliminated through metabolism; thus the accurate scaling of metabolic clearance is vital to successful drug development. Yet, when data is scaled from in vitro to in vivo, hepatic metabolic clearance, the primary source of metabolism, is still commonly underpredicted. Over the past decades, with biophysics used as a key component to restore aspects of the in vivo environment, several new cell culture settings have been investigated to improve hepatocyte functionalities. Most of these studies have focused on shear stress, i.e., flow mediated by a pressure gradient. One potential conclusion of these studies is that hepatocytes are naturally "mechanosensitive," i.e., they respond to a change in their biophysical environment. We demonstrate that hepatocytes also respond to an increase in hydrostatic pressure that, we suggest, is directly linked to the lobule geometry and vessel density. Furthermore, we demonstrate that hydrostatic pressure improves albumin production and increases cytochrome

Indexed as

Basic Helix-Loop-Helix ProteinsCell Culture TechniquesCytochrome P-450 CYP1A2Gene Expression RegulationHepatocytesHep G2 CellsHumansHydrostatic PressureInactivation, MetabolicLiverMechanotransduction, CellularReceptors, Aryl HydrocarbonSignal TransductionAHR protein, humanBasic Helix-Loop-Helix ProteinsCYP1A2 protein, humanCytochrome P-450 CYP1A2Receptors, Aryl Hydrocarbondrug metabolismhepatocytesmechanosensitivity

Identifiers

PMID32159360
PMCPMC7294326
OpenAlexW3011613750

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.