Evidence map›Paper›PMID 38001392›Full record

ArticleBiochemical genetics2024

FTO Knockdown-Mediated Maturation of miR-383-5p Inhibits Malignant Advancement of Pancreatic Cancer by Targeting ITGA3.

Wei Zhang, Shilong Han, Yifeng Yuan, Minjie Xu, Anle Ding, Maoquan Li

Abstract read
PubMed Publisher
In one paragraph

Article in Biochemical genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
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  6. 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

6 authors at 4 institutions in 1 country.

Wei ZhangDepartment of Radiology, Children's Hospital of Nanjing Medical University, No. 72, Guangzhou Road, Gulou District, Nanjing, 210008, China.
Shilong HanDepartment of Interventional and Vascular Surgery, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301, Yanchang Road, Jing'an District, Shanghai, 200072, China.
Yifeng YuanDepartment of Interventional and Vascular Surgery, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301, Yanchang Road, Jing'an District, Shanghai, 200072, China.
Minjie XuDepartment of Interventional and Vascular Surgery, Shanghai Tenth People's Hospital, Tongji University School of Medicine, No. 301, Yanchang Road, Jing'an District, Shanghai, 200072, China.
Anle DingAnHui University of Science and Technology, No. 168, Taifeng Road, Huainan, 232001, Anhui, China.
Maoquan LiDepartment of Interventional and Vascular Surgery, Shanghai Tenth People's Hospital, School of Clinical Medicine of Nanjing Medical University, No. 301, Yanchang Road, Jing'an District, Shanghai, 200072, China. drlimaoquan@hotmail.com.
Tongji University · CNAnhui University of Science and Technology · CNNanjing Medical University · CNShanghai Tenth People's Hospital · CN

Funding

Research Project of Shanghai Municipal Health Commission (Youth) 20204Y0169
6 · The paper itself

Abstract

m6A demethylase FTO is confirmed to be involved in pancreatic cancer progression. FTO regulates miRNA processing. To investigate the regulatory effect of FTO on miR-383-5p and its role in pancreatic cancer. The expression of miR-383-5p, ITGA3, and FTO was predicted using bioinformatic analysis in tissues and was measured using qPCR in cells. Cell biological functions were investigated using MTT assay, Transwell assay, sphere formation assay, and qPCR. The targeting relationship between miR-383-5p and ITGA3 was evaluated using the dual-luciferase reporter assay. The effect of FTO on miR-383-5p processing was evaluated using RIP and MeRIP assay. FTO expression was upregulated in pancreatic cancer and silencing of FTO promoted the processing of miR-383-5p in an m6A-dependent manner. m6A-modified miRNA processing was recognized by IGF2BP1. Downregulation of miR-383-5p reversed FTO knockdown-induced inhibition of cellular processes. The FTO/miR-383-5p/ITGA3 axis facilitated cell viability, metastasis, and stemness in pancreatic cancer.

Indexed as

Alpha-Ketoglutarate-Dependent Dioxygenase FTOIntegrin alpha3MicroRNAsPancreatic NeoplasmsCell Line, TumorGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansRNA-Binding ProteinsAlpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, humanIGF2BP1 protein, humanIntegrin alpha3ITGA3 protein, humanMicroRNAsMIRN383 microRNA, humanRNA-Binding ProteinsFTOInvasionITGA3MigrationmiR-383-5pPancreatic cancerStemness

Identifiers

PMID38001392
OpenAlexW4388967056

What OpenQuestion holds

Textmetadata
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.