Evidence map›Paper›PMID 35682900›Full record

ArticleInternational journal of molecular sciences2022

Molecular Mechanisms Underlying the Elevated Expression of a Potentially Type 2 Diabetes Mellitus Associated SCD1 Variant.

Kinga Tibori, Gabriella Orosz, Veronika Zámbó, Péter Szelényi, Farkas Sarnyai, Viola Tamási, Zsolt Rónai, Judit Mátyási, Blanka Tóth, Miklós Csala and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  11. Sweet pepper extract reduces fat storage inFood science & nutrition · 2024
    Article
  12. Article
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  15. New Advances in Diabetes Genetics.International journal of molecular sciences · 2023
    Article
  16. Review
  17. 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

11 authors at 2 institutions in 1 country.

Kinga TiboriDepartment of Molecular Biology, Semmelweis University, H-1085 Budapest, Hungary.ORCID 0000-0002-6808-4015
Gabriella OroszDepartment of Molecular Biology, Semmelweis University, H-1085 Budapest, Hungary.
Veronika ZámbóDepartment of Molecular Biology, Semmelweis University, H-1085 Budapest, Hungary.
Péter SzelényiDepartment of Molecular Biology, Semmelweis University, H-1085 Budapest, Hungary.ORCID 0000-0002-7966-9801
Farkas SarnyaiDepartment of Molecular Biology, Semmelweis University, H-1085 Budapest, Hungary.ORCID 0000-0002-5525-5508
Viola TamásiDepartment of Molecular Biology, Semmelweis University, H-1085 Budapest, Hungary.
Zsolt RónaiDepartment of Molecular Biology, Semmelweis University, H-1085 Budapest, Hungary.ORCID 0000-0002-0909-7932
Judit MátyásiDepartment of Inorganic and Analytical Chemistry, Budapest University of Technology and Economics, H-1111 Budapest, Hungary.
Blanka TóthDepartment of Inorganic and Analytical Chemistry, Budapest University of Technology and Economics, H-1111 Budapest, Hungary.
Miklós CsalaDepartment of Molecular Biology, Semmelweis University, H-1085 Budapest, Hungary.ORCID 0000-0002-3829-4361
Éva KereszturiDepartment of Molecular Biology, Semmelweis University, H-1085 Budapest, Hungary.ORCID 0000-0003-4778-3332
Semmelweis University · HUBudapest University of Technology and Economics · HU

Funding

Hungarian Scientific Research Fund FK138115, K125201, K131680Ministry of Innovation and Technology of Hungary from the National Research, Development and Innovation Fund TKP2021-EGA-24, TKP2021-EGA-02
6 · The paper itself

Abstract

Disturbances in lipid metabolism related to excessive food intake and sedentary lifestyle are among major risk of various metabolic disorders. Stearoyl-CoA desaturase-1 (SCD1) has an essential role in these diseases, as it catalyzes the synthesis of unsaturated fatty acids, both supplying for fat storage and contributing to cellular defense against saturated fatty acid toxicity. Recent studies show that increased activity or over-expression of SCD1 is one of the contributing factors for type 2 diabetes mellitus (T2DM). We aimed to investigate the impact of the common missense rs2234970 (M224L) polymorphism on SCD1 function in transfected cells. We found a higher expression of the minor Leu224 variant, which can be attributed to a combination of mRNA and protein stabilization. The latter was further enhanced by various fatty acids. The increased level of Leu224 variant resulted in an elevated unsaturated: saturated fatty acid ratio, due to higher oleate and palmitoleate contents. Accumulation of Leu224 variant was found in a T2DM patient group, however, the difference was statistically not significant. In conclusion, the minor variant of rs2234970 polymorphism might contribute to the development of obesity-related metabolic disorders, including T2DM, through an increased intracellular level of SCD1.

Indexed as

Diabetes Mellitus, Type 2Metabolic DiseasesFatty AcidsHumansLipid MetabolismStearoyl-CoA DesaturaseFatty AcidsSCD1 protein, humanStearoyl-CoA Desaturasefatty acidsgenetic variationlipotoxicitymetabolic disordersobesityoleatesingle nucleotide polymorphismstearoyl-CoA desaturase-1type 2 diabetes mellitus

Identifiers

PMID35682900
PMCPMC9181825
OpenAlexW4281655157

What Socratic holds

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Registered trials

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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 Socratic graph.