Evidence map›Paper›PMID 27446528›Full record

ArticleMedChemComm2016

Fatty Acid Transport Proteins: Targeting FATP2 as a Gatekeeper Involved in the Transport of Exogenous Fatty Acids.

Paul N Black, Constance Ahowesso, David Montefusco, Nipun Saini, Concetta C DiRusso

Open access · greenAbstract read
In one paragraph

Article in MedChemComm, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

46 citing papers in PubMed, 67 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

5 authors at 1 institution in 1 country.

Paul N BlackDepartment of Biochemistry, University of Nebraska, Lincoln, NE.
Constance AhowessoDepartment of Biochemistry, University of Nebraska, Lincoln, NE.
David MontefuscoDepartment of Biochemistry, University of Nebraska, Lincoln, NE.
Nipun SainiDepartment of Biochemistry, University of Nebraska, Lincoln, NE.
Concetta C DiRussoDepartment of Biochemistry, University of Nebraska, Lincoln, NE.
University of Nebraska–Lincoln · US

Funding

High throughput screens for fatty acid uptake inhibitorsR01DK071076 · NIDDK · UNIVERSITY OF NEBRASKA LINCOLN · PI BLACK, PAUL N., DIRUSSO, CONCETTA C. · 2006 to 2013
$2.4M
MOLECULAR ANALYSIS OF FATTY ACID TRANSPORT IN EUKARYOTESR01GM056840 · NIGMS · UNIVERSITY OF NEBRASKA LINCOLN · PI BLACK, PAUL N., DIRUSSO, CONCETTA C. · 1998 to 2010
$2.3M
NIDDK NIH HHS R01 DK071076NIGMS NIH HHS R01 GM056840
6 · The paper itself

Abstract

The fatty acid transport proteins (FATP) are classified as members of the Solute Carrier 27 (Slc27) family of proteins based on their ability to function in the transport of exogenous fatty acids. These proteins, when localized to the plasma membrane or at intracellular membrane junctions with the endoplasmic reticulum, function as a gate in the regulated transport of fatty acids and thus represent a therapeutic target to delimit the acquisition of fatty acids that contribute to disease as in the case of fatty acid overload. To date, FATP1, FATP2, and FATP4 have been used as targets in the selection of small molecule inhibitors with the goal of treating insulin resistance and attenuating dietary absorption of fatty acids. Several studies targeting FATP1 and FATP4 were based on the intrinsic acyl CoA synthetase activity of these proteins and not on transport directly. While several classes of compounds were identified as potential inhibitors of fatty acid transport,

Identifiers

PMID27446528
PMCPMC4948302
OpenAlexW2283724211

What OpenQuestion holds

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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.