Evidence map›Paper›PMID 36759348›Full record

ArticleDiabetologia2023

Tcf7l2 in hepatocytes regulates de novo lipogenesis in diet-induced non-alcoholic fatty liver disease in mice.

Da Som Lee, Tae Hyeon An, Hyunmi Kim, Eunsun Jung, Gyeonghun Kim, Seung Yeon Oh, Jun Seok Kim, Hye Jin Chun, Jaeeun Jung, Eun-Woo Lee and 15 more

Open access · hybridFull text read
In one paragraph

Article in Diabetologia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Lipid Droplet Dynamics in Alcoholic Steatohepatitis.The American journal of pathology · 2026
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Relationship between Abnormal Lipid Metabolism and Gallstone Formation.The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi · 2025
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Cellular heterogeneity and plasticity during NAFLD progression.Frontiers in molecular biosciences · 2023
    Review
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

25 authors at 7 institutions in 1 country.

Da Som LeeGraduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0002-6535-7583
Tae Hyeon AnMetabolic Regulation Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0001-8339-767X
Hyunmi KimMetabolic Regulation Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0002-5596-4320
Eunsun JungBiotherapeutics Translational Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0002-5900-6138
Gyeonghun KimCollege of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-1990-3002
Seung Yeon OhKorea Mouse Phenotyping Center (KMPC), Seoul National University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-9673-9587
Jun Seok KimDivision of Life Sciences, Korea University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-5667-6793
Hye Jin ChunDepartment of Systems Biology, Glycosylation Network Research Center, Yonsei University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-8129-7077
Jaeeun JungEnvironmental Diseases Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0001-5179-4603
Eun-Woo LeeMetabolic Regulation Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0002-5156-0003
Baek-Soo HanDepartment of Functional Genomics, KRIBB School of Bioscience, University of Science and Technology (UST), Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0003-3610-7216
Dai Hoon HanDepartment of Surgery, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0003-2787-7876
Yong-Ho LeeDepartment of Systems Biology, Glycosylation Network Research Center, Yonsei University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-6219-4942
Tae-Su HanDepartment of Functional Genomics, KRIBB School of Bioscience, University of Science and Technology (UST), Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0002-9280-5898
Keun HurDepartment of Biochemistry and Cell Biology, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.ORCID https://orcid.org/0000-0002-6944-2718
Chul-Ho LeeDepartment of Functional Genomics, KRIBB School of Bioscience, University of Science and Technology (UST), Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0002-6996-5746
Dae-Soo KimEnvironmental Diseases Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0002-4999-1613
Won Kon KimMetabolic Regulation Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0002-1289-0333
Jun Won ParkDivision of Biomedical Convergence, College of Biomedical Science, Kangwon National University, ChunCheon-si, Gangwon-do, Republic of Korea.ORCID https://orcid.org/0000-0003-4677-1786
Seung-Hoi KooDivision of Life Sciences, Korea University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-8769-2879
Je Kyung SeongCollege of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0003-1177-6958
Sang Chul LeeMetabolic Regulation Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0002-1507-3267
Hail KimGraduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea. hailkim@kaist.edu.ORCID https://orcid.org/0000-0002-6652-1349
Kwang-Hee BaeMetabolic Regulation Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea. khbae@kribb.re.kr.ORCID https://orcid.org/0000-0002-5868-2556
Kyoung-Jin OhMetabolic Regulation Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, Republic of Korea. kjoh80@kribb.re.kr.ORCID http://orcid.org/0000-0002-2224-7202
Korea Research Institute of Bioscience and Biotechnology · KRKorea Advanced Institute of Science and Technology · KRSeoul National University · KRYonsei University · KRKorea University · KRKangwon National University · KRKyungpook National University · KR

Funding

Korea Research Institute of Bioscience and Biotechnology KGM5392212National Research Foundation of Korea 2020R1A2C2102308
6 · The paper itself

Abstract

aims/hypothesisNon-alcoholic fatty liver disease (NAFLD) associated with type 2 diabetes may more easily progress towards severe forms of non-alcoholic steatohepatitis (NASH) and cirrhosis. Although the Wnt effector transcription factor 7-like 2 (TCF7L2) is closely associated with type 2 diabetes risk, the role of TCF7L2 in NAFLD development remains unclear. Here, we investigated how changes in TCF7L2 expression in the liver affects hepatic lipid metabolism based on the major risk factors of NAFLD development.

methodsTcf7l2 was selectively ablated in the liver of C57BL/6N mice by inducing the albumin (Alb) promoter to recombine Tcf7l2 alleles floxed at exon 5 (liver-specific Tcf7l2-knockout [KO] mice: Alb-Cre;Tcf7l2

resultsAlb-Cre;Tcf7l2 CONCLUSIONS/

interpretationIn mice, loss of hepatic Tcf7l2 contributes to liver steatosis by inducing preferential metabolism of carbohydrates via DNL activation. Therefore, TCF7L2 could be a promising regulator of the NAFLD associated with high-carbohydrate diets and diabetes since TCF7L2 deficiency may lead to development of NAFLD by promoting utilisation of excess glucose pools through activating DNL. DATA AVAILABILITY: RNA-sequencing data have been deposited into the NCBI GEO under the accession number GSE162449 ( www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE162449 ).

Indexed as

Diabetes Mellitus, Type 2Non-alcoholic Fatty Liver DiseaseAnimalsDiet, High-FatGlucoseHepatocytesLipogenesisLiverMiceMice, Inbred C57BLTranscription Factor 7-Like 2 ProteinTriglyceridesGlucoseTcf7l2 protein, mouseTranscription Factor 7-Like 2 ProteinTriglyceridesCarbohydrateDe novo lipogenesisFatty acidGlucoseInsulinLipogenesisNAFLDTCF7L2TG accumulationType 2 diabetes

Identifiers

PMID36759348
PMCPMC10036287
OpenAlexW4319827634

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LicenceCC BY
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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 OpenQuestion graph.