Evidence map›Paper›PMID 31828133›Full record

ArticleBioMed research international2019

Palmitic Acid Induces MicroRNA-221 Expression to Decrease Glucose Uptake in HepG2 Cells via the PI3K/AKT/GLUT4 Pathway.

Fang Huang, Jie Chen, Jingwen Wang, Pingping Zhu, Wenting Lin

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

26 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
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  15. Cardiometabolic Risk Factors Associated With Type 2 Diabetes Mellitus: A Mechanistic Insight.Clinical medicine insights. Endocrinology and diabetes · 2023
    Review
  16. Review
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  19. Article
  20. 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

5 authors at 1 institution in 1 country.

Fang HuangSchool of Public Health, Fujian Medical University, Xueyuan Road 1, Minghou District, Fuzhou City, Fujian Province, China.ORCID https://orcid.org/0000-0001-6298-4779
Jie ChenSchool of Public Health, Fujian Medical University, Xueyuan Road 1, Minghou District, Fuzhou City, Fujian Province, China.
Jingwen WangSchool of Public Health, Fujian Medical University, Xueyuan Road 1, Minghou District, Fuzhou City, Fujian Province, China.
Pingping ZhuSchool of Public Health, Fujian Medical University, Xueyuan Road 1, Minghou District, Fuzhou City, Fujian Province, China.
Wenting LinSchool of Public Health, Fujian Medical University, Xueyuan Road 1, Minghou District, Fuzhou City, Fujian Province, China.
Fujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity-related insulin resistance and high fatty acid concentrations occur during the development of type 2 diabetes mellitus. The role of high concentrations of plasma-free fatty acids is not fully understood. In this study, palmitic acid (PA, 0.8 mM for 24 h) induced the expression of miR-221 that bound to phosphoinositide 3-kinases (PI3K) mRNA to inhibit glucose uptake by HepG2 cells. Compared with controls, PA significantly decreased glucose uptake, increased insulin receptor substrate-2 (IRS-2) and miR-221 expression, and decreased phosphoinositide 3-kinase (PI3K), protein kinase B (AKT), and glucose transporter type 4 (GLUT4) mRNA expression. Luciferase reporter assay revealed that miR-221 binding inhibited PI3K expression. Transfection of HepG2 cells with an miR-221 mimic induced miR-221 expression and inhibited the PI3K/AKT pathway. PA decreased glucose uptake in HepG2 cells by inducing the expression of miR-221, which bound to PI3K mRNA and suppressed PI3K/AKT signaling. miR-221 may be a novel target for preventing and treating obesity-induced insulin resistance.

Indexed as

Diabetes Mellitus, Type 2Fatty AcidsGene Expression RegulationGlucoseGlucose Transporter Type 4Hep G2 CellsHumansInsulinInsulin Receptor Substrate ProteinsInsulin ResistanceMicroRNAsObesityOncogene Protein v-aktPalmitic AcidPhosphatidylinositol 3-KinasesRNA, MessengerFatty AcidsGlucoseGlucose Transporter Type 4InsulinInsulin Receptor Substrate ProteinsIRS2 protein, humanMicroRNAsMIR221, humanOncogene Protein v-aktPalmitic AcidPhosphatidylinositol 3-KinasesRNA, MessengerSLC2A4 protein, human

Identifiers

PMID31828133
PMCPMC6885153
OpenAlexW2989117384

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.