Evidence map›Paper›PMID 31952262›Full record

ArticleInternational journal of molecular sciences2020

Beneficial Effects of SREBP Decoy Oligodeoxynucleotide in an Animal Model of Hyperlipidemia.

Hyun-Jin An, Jung-Yeon Kim, Mi-Gyeong Gwon, Hyemin Gu, Hyun-Ju Kim, Jaechan Leem, Sung Won Youn, Kwan-Kyu Park

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. 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
3.5field-weighted citation impact, top 7% 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, 24 citations in OpenAlex.

  1. Article
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  6. Review
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  8. Article
  9. Article
  10. Review
  11. Article
  12. Anti-Obesity and Anti-Hyperglycemic Effects ofInternational journal of molecular sciences · 2022
    Article
  13. Article
  14. Therapeutic mechanism ofFrontiers in pharmacology · 2022
    Article
  15. Decoy Technology as a Promising Therapeutic Tool for Atherosclerosis.International journal of molecular sciences · 2021
    Review
  16. RNA-PROTACs: Degraders of RNA-Binding Proteins.Angewandte Chemie (International ed. in English) · 2021
    Article
  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

8 authors at 1 institution in 1 country.

Hyun-Jin AnDepartment of Pathology, College of Medicine, Catholic University of Daegu, Daegu 42472, Korea.
Jung-Yeon KimDepartment of Immunology, College of Medicine, Catholic University of Daegu, Daegu 42472, Korea.
Mi-Gyeong GwonDepartment of Pathology, College of Medicine, Catholic University of Daegu, Daegu 42472, Korea.
Hyemin GuDepartment of Pathology, College of Medicine, Catholic University of Daegu, Daegu 42472, Korea.
Hyun-Ju KimDepartment of Pathology, College of Medicine, Catholic University of Daegu, Daegu 42472, Korea.
Jaechan LeemDepartment of Immunology, College of Medicine, Catholic University of Daegu, Daegu 42472, Korea.ORCID 0000-0003-2329-4374
Sung Won YounDepartment of Radiology, College of Medicine, Catholic University of Daegu, Daegu 42472, Korea.ORCID 0000-0001-9491-1347
Kwan-Kyu ParkDepartment of Pathology, College of Medicine, Catholic University of Daegu, Daegu 42472, Korea.
Daegu Catholic University · KR

Funding

National Research Foundation of Korea NRF-2017R1D1A1B03030700National Research Foundation of Korea NRF-2018R1A6A3A11047996
6 · The paper itself

Abstract

Hyperlipidemia is a chronic disorder that plays an important role in the development of cardiovascular diseases, type II diabetes, atherosclerosis, hypertension, and non-alcoholic fatty liver disease. Hyperlipidemias have created a worldwide health crisis and impose a substantial burden not only on personal health but also on societies and economies. Transcription factors in the sterol regulatory element binding protein (SREBP) family are key regulators of the lipogenic genes in the liver. SREBPs regulate lipid homeostasis by controlling the expression of a range of enzymes required for the synthesis of endogenous cholesterol, fatty acids, triacylglycerol, and phospholipids. Thereby, SREBPs have been considered as targets for the treatment of metabolic diseases. The aim of this study was to investigate the beneficial functions and the possible underlying molecular mechanisms of SREBP decoy ODN, which is a novel inhibitor of SREBPs, in high-fat diet (HFD)-fed hyperlipidemic mice. Our studies using HFD-induced hyperlipidemia animal model revealed that SREBB decoy ODN inhibited the increased expression of fatty acid synthetic pathway, such as SREBP-1c, FAS, SCD-1, ACC1, and HMGCR. In addition, SREBP decoy ODN decreased pro-inflammatory cytokines, including TNF-α, IL-1β, IL-8, and IL-6 expression. These results suggest that SREBP decoy ODN exerts its anti-hyperlipidemia effects in HFD-induced hyperlipidemia mice by regulating their lipid metabolism and inhibiting lipogenesis through inactivation of the SREPB pathway.

Indexed as

Disease Models, AnimalAnimalsBiosynthetic PathwaysCytokinesDiet, High-FatFatty AcidsGene Expression RegulationHyperlipidemiasInflammation MediatorsLipid MetabolismLipogenesisMaleMice, Inbred C57BLOligodeoxyribonucleotidesSterol Regulatory Element Binding Protein 1CytokinesFatty AcidsInflammation MediatorsOligodeoxyribonucleotidesSterol Regulatory Element Binding Protein 1Decoy oligodeoxynucleotideHyperlipidemia 3keyword 1SREBP 2

Identifiers

PMID31952262
PMCPMC7014099
OpenAlexW2999786740

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.