Evidence map›Paper›PMID 37328795›Full record

ArticleBMC cancer2023

MicroRNA-5195-3p mediated malignant biological behaviour of insulin-resistant liver cancer cells via SOX9 and TPM4.

Jing Yan, Bei Xie, Ye Tian, Wenqin An, Zhiheng Peng, Zhuan Liu, Jing Li, Linjing Li

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2023. 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
0.7field-weighted citation impact, top 24% 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, 3 citations in OpenAlex.

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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 3 institutions in 1 country.

Jing Yan *Department of Clinical Laboratory Center, The Second Hospital of Lanzhou University, Lanzhou, 730000, Gansu, China.
Bei Xie *Department of Medical Laboratory Animal Science, School of Basic Medical Sciences, Lanzhou University, Lanzhou, 730000, Gansu, China. xieb@lzu.edu.cn.
Ye Tian *Department of Clinical Laboratory Center, The Second Hospital of Lanzhou University, Lanzhou, 730000, Gansu, China.
Wenqin AnThe First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, Gansu, China.
Zhiheng PengDepartment of Clinical Laboratory Center, The Second Hospital of Lanzhou University, Lanzhou, 730000, Gansu, China.
Zhuan LiuDepartment of Clinical Laboratory Center, The Second Hospital of Lanzhou University, Lanzhou, 730000, Gansu, China.
Jing LiDepartment of Clinical Laboratory Center, The Second Hospital of Lanzhou University, Lanzhou, 730000, Gansu, China.
Linjing LiDepartment of Clinical Laboratory Center, The Second Hospital of Lanzhou University, Lanzhou, 730000, Gansu, China. lilinj@lzu.edu.cn.
Lanzhou University · CNLanzhou University Second Hospital · CNGansu Provincial Maternal and Child Health Hospital · CN

Funding

Internationally Technological Cooperation Project of Gansu Province 18YF1WA117National Natural Science Foundation of China 82060531
6 · The paper itself

Abstract

backgroundPrimary liver cancer is a malignant tumour of the digestive system, ranking second in cancer mortality in China. In different types of cancer, such as liver cancer, microRNAs (miRNAs) have been shown to be dysregulated. However, little is known about the role of miR-5195-3p in insulin-resistant liver cancer. METHODS AND

resultsIn this study, in vitro and in vivo experiments were conducted to identify the altered biological behaviour of insulin-resistant hepatoma cells (HepG2/IR), and we proved that HepG2/IR cells had stronger malignant biological behaviour. Functional experiments showed that enhanced expression of miR-5195-3p could inhibit the proliferation, migration, invasion, epithelial-mesenchymal transition (EMT) and chemoresistance of HepG2/IR cells, while impaired expression of miR-5195-3p in HepG2 cells resulted in the opposite effects. Bioinformatics prediction and dual luciferase reporter gene assays proved that SOX9 and TPM4 were the target genes of miR-5195-3p in hepatoma cells.

conclusionsIn conclusion, our study demonstrated that miR-5195-3p plays a critical role in insulin-resistant hepatoma cells and might be a potential therapeutic target for liver cancer.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsMicroRNAsCell Line, TumorCell MovementCell ProliferationEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansInsulinSOX9 Transcription FactorTropomyosinInsulinMicroRNAsMIRN5195 microRNA, humanSOX9 protein, humanSOX9 Transcription FactorTPM4 protein, humanTropomyosinInsulin resistanceLiver cancerMalignant biological behaviourmiR-5195-3pSOX9TPM4

Identifiers

PMID37328795
PMCPMC10273698
OpenAlexW4380987234

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.