Evidence map›Paper›PMID 27137869›Full record

ArticleJournal of cellular biochemistry2016

N(ϵ) -Carboxymethyllysine Increases the Expression of miR-103/143 and Enhances Lipid Accumulation in 3T3-L1 Cells.

Ann-Katrin Holik, Barbara Lieder, Nicole Kretschy, Mark M Somoza, Sandra Held, Veronika Somoza

Open access · hybridAbstract read
In one paragraph

Article in Journal of cellular biochemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

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  10. The AlkamideFrontiers in pharmacology · 2017
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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

6 authors at 2 institutions in 2 countries.

Ann-Katrin HolikFaculty of Chemistry, Department of Nutritional and Physiological Chemistry, University of Vienna, Althanstraße 14, Vienna 1090, Austria.
Barbara LiederFaculty of Chemistry, Christian Doppler Laboratory for Bioactive Aroma Compounds, University of Vienna, Althanstraße 14, Vienna 1090, Austria.
Nicole KretschyFaculty of Chemistry, Department of Inorganic Chemistry, University of Vienna, Althanstraße 14, Vienna 1090, Austria.
Mark M SomozaFaculty of Chemistry, Department of Inorganic Chemistry, University of Vienna, Althanstraße 14, Vienna 1090, Austria.
Sandra HeldDepartment of Food Science, University of Wisconsin, Madison, Wisconsin.
Veronika SomozaFaculty of Chemistry, Department of Nutritional and Physiological Chemistry, University of Vienna, Althanstraße 14, Vienna 1090, Austria.
University of Vienna · ATUniversity of Wisconsin System · US

Funding

Austrian Science Fund FWF P 23797
6 · The paper itself

Abstract

Advanced glycation endproducts, formed in vivo, but also by the Maillard reaction upon thermal treatment of foods, have been associated with the progression of pathological conditions such as diabetes mellitus. In addition to the accumulation with age, exogenous AGEs are introduced into the circulation from dietary sources. In this study, we investigated the effects of addition of free N(ϵ) -carboxymethyllysine (CML), a well-characterized product of the Maillard reaction, on adipogenesis in 3T3-L1 preadipocytes. Treatment with 5, 50, or 500 μM CML resulted in increased lipid accumulation to similar extents, by 11.5 ± 12.6%, 12.9 ± 8.6%, and 12.8 ± 8.5%, respectively. Long-term treatment with 500 μM CML during adipogenesis resulted in increases in miR-103 and miR-143 levels, two miRNAs described to be involved in impaired glucose homeostasis and increased lipid accumulation. Furthermore, the expression of genes associated with these miRNAs, consisting of Akt1, PI3k, and Cav1 was regulated by CML. Short-term treatment of mature 3T3-L1 adipocytes with CML resulted in decreased basal glucose uptake. These results, indicate that the addition of protein-free CML to 3T3-L1 cells influence parameters associated with adipogenesis and glucose homeostasis at transcriptional, and functional level; this indicates that free CML derived from exogenous sources, in addition to protein-bound CML may be relevant in this context. J. Cell. Biochem. 117: 2413-2422, 2016. © 2016 The Authors. Journal of Cellular Biochemistry Published by Wiley Periodicals, Inc.

Indexed as

3T3-L1 CellsAdipocytesAdipogenesisAnimalsApoptosisBlotting, WesternCell ProliferationFatty AcidsGlucoseHumansLipid MetabolismLysineMiceMicroRNAsReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionFatty AcidsGlucoseLysineMicroRNAsMIRN103 microRNA, mouseMIRN143 microRNA, mouseN(6)-carboxymethyllysineRNA, Messenger3T3-L1ADIPOGENESISmicroRNAN-epsilon-carboxymethyllysine

Identifiers

PMID27137869
PMCPMC4982050
OpenAlexW2346616655

What OpenQuestion holds

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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.