Evidence map›Paper›PMID 31164632›Full record

ArticleCell death & disease2019

The roles and mechanism of IFIT5 in bladder cancer epithelial-mesenchymal transition and progression.

Jun Huang, U-Ging Lo, Shiqi Wu, Bin Wang, Rey-Chen Pong, Chih-Ho Lai, Ho Lin, Dalin He, Jer-Tsong Hsieh, Kaijie Wu

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

24 citing papers in PubMed, 42 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 3 countries.

Jun HuangDepartment of Urology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, P.R. China.
U-Ging LoDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Shiqi WuDepartment of Urology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, P.R. China.
Bin WangDepartment of Urology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, P.R. China.
Rey-Chen PongDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Chih-Ho LaiDepartment of Microbiology and Immunology, Graduate Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
Ho LinDepartment of Life Sciences, National Chung Hsing University, Taichung, Taiwan.ORCID http://orcid.org/0000-0001-7849-9137
Dalin HeDepartment of Urology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, P.R. China.
Jer-Tsong HsiehDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA. jt.hsieh@utsouthwestern.edu.
Kaijie WuDepartment of Urology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, P.R. China. kaijie_wu@163.com.
First Affiliated Hospital of Xi'an Jiaotong University · CNThe University of Texas Southwestern Medical Center · USCentral South University · CNChang Gung University · TWKaohsiung Medical University · TWNational Chung Hsing University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prognosis of bladder cancer (BCa) depends on several key factors including anatomical site, tumor grade, and stage. In general, muscle-invasive bladder cancer (MIBC) is associated with higher incidence of distant metastasis compared with Non-muscle-invasive bladder cancer (NMIBC). Treatment outcome of the patients with metastatic BCa has been very poor with ~15% of overall survival rate. Thus, it is apparently important to understand the underlying biology for metastatic progression of BCa. Although epithelial-mesenchymal transition (EMT) has long been implicated in BCa metastasis and treatment resistance, the underlying mechanism is not fully understood. In this study, we have identified that the expression of interferon induced protein with tetratricopeptide repeats 5 (IFIT5) is positively correlated with pathological characteristics, and predicts a poor prognosis of BCa patients. Since the function of IFIT5 in BCa has not yet been characterized, we demonstrate that IFIT5 can induce EMT, promote cell migration and invasion, and increase the expression of ICAM1 in BCa via down-regulation of mature miR-99a. Moreover, ICAM1 is shown as a direct target of miR-99a. Overall, we conclude that IFIT5 is a new oncogene in BCa.

Indexed as

AnimalsCell Line, TumorCell MovementCell ProliferationDisease ProgressionEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansIntercellular Adhesion Molecule-1MaleMiceMice, NudeMicroRNAsNeoplasm MetastasisNeoplasm ProteinsPrognosisICAM1 protein, humanIFIT5 protein, humanIntercellular Adhesion Molecule-1MicroRNAsMIRN99 microRNA, humanNeoplasm Proteins

Identifiers

PMID31164632
PMCPMC6547745
OpenAlexW2948670827

What OpenQuestion holds

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LicenceCC BY
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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.