Evidence map›Paper›PMID 33510836›Full record

ArticleOxidative medicine and cellular longevity2021

Fas-Associated Factor 1 Promotes Hepatic Insulin Resistance via JNK Signaling Pathway.

Bao Sun, Jiecan Zhou, Yongchao Gao, Fazhong He, Heng Xu, Xiaoping Chen, Wei Zhang, Ling Chen

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Melatonin Alleviates PMOxidative medicine and cellular longevity · 2022
    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 4 institutions in 1 country.

Bao SunDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.ORCID https://orcid.org/0000-0001-8305-5872
Jiecan ZhouInstitute of Clinical Medicine, The First Affiliated Hospital, University of South China, Hengyang 421001, China.ORCID https://orcid.org/0000-0002-3037-3997
Yongchao GaoDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.ORCID https://orcid.org/0000-0002-1631-7390
Fazhong HeZhuhai People's Hospital (Zhuhai Hospital Affiliated with Jinan University), Zhuhai 519000, China.ORCID https://orcid.org/0000-0001-5750-0135
Heng XuDepartment of Laboratory Medicine, National Key Laboratory of Biotherapy/Collaborative Innovation Center of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Chengdu 610041, China.ORCID https://orcid.org/0000-0002-7748-2621
Xiaoping ChenDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.ORCID https://orcid.org/0000-0002-2910-9152
Wei ZhangDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410078, China.ORCID https://orcid.org/0000-0002-6190-3129
Ling ChenDepartment of Gastrointestinal Surgery, Xiangya Hospital, Central South University, Changsha, Hunan 410078, China.ORCID https://orcid.org/0000-0002-9172-8720
Central South University · CNFirst Affiliated Hospital of University of South China · CNJinan University · CNSichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fas-associated factor 1 (FAF1), a member of the Fas death-inducing signaling complex, is reported to interact potentially with diverse proteins and function in diverse cellular possesses. It remains unclear, however, whether FAF1 is involved in hepatic metabolic disorder and insulin resistance. This study is aimed at elucidating the role and the molecular mechanism of FAF1 in hepatic insulin resistance. Rats treated with high-fat diets are used as hepatic insulin resistance animal models. Quantitative real-time PCR, immunohistochemistry, and immunofluorescence assay are utilized to detect the FAF1 expression. The expression of relevant proteins is detected by Western blotting. We determine ROS production, lipid accumulation, and glucose uptake by using flow cytometry. Immunoprecipitation is employed to investigate protein-protein interaction. We find that increased expression of FAF1 occurred in the livers of insulin-resistant rats. Using gain-of-function and loss-of-function approaches, we observe dramatic exacerbation of insulin resistance, upregulated gluconeogenesis genes, downregulated glucose transport genes, and enhanced ROS production by FAF1 overexpression, whereas downregulation of FAF1 leads to a completely opposite phenotype. Mechanistically, FAF1 interacts directly with c-Jun N-terminal kinase (JNK) and activates its phosphorylation, thereby blocking the downstream insulin signaling pathway and leading to insulin resistance. Our data indicate that FAF1 is a potent regulator in hepatic metabolic disorder and insulin resistance.

Indexed as

Insulin ResistanceMAP Kinase Signaling SystemAnimalsApoptosis Regulatory ProteinsInsulinLiverMaleMAP Kinase Kinase 4RatsApoptosis Regulatory ProteinsInsulinMAP Kinase Kinase 4

Identifiers

PMID33510836
PMCPMC7826235
OpenAlexW3126073578

What OpenQuestion holds

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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.