Evidence map›Paper›PMID 27524492›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

hsa-miR-135a-1 inhibits prostate cancer cell growth and migration by targeting EGFR.

Bin Xu, Tao Tao, Yiduo Wang, Fang Fang, Yeqing Huang, Shuqiu Chen, Weidong Zhu, Ming Chen

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

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  15. Potential Five-MicroRNA Signature Model for the Prediction of Prognosis in Patients with Wilms Tumor.Medical science monitor : international medical journal of experimental and clinical research · 2019
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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.

Bin XuDepartment of Urology, Zhongda Hospital, School of Medicine, Southeast University, 87 Dingjia Bridge Hunan Road, Nanjing, 210009, China.
Tao TaoDepartment of Urology, Zhongda Hospital, School of Medicine, Southeast University, 87 Dingjia Bridge Hunan Road, Nanjing, 210009, China.
Yiduo WangDepartment of Urology, Zhongda Hospital, School of Medicine, Southeast University, 87 Dingjia Bridge Hunan Road, Nanjing, 210009, China.
Fang FangDepartment of Immunology, Bengbu Medical College, Bengbu, China.
Yeqing HuangDepartment of Urology, Zhongda Hospital, School of Medicine, Southeast University, 87 Dingjia Bridge Hunan Road, Nanjing, 210009, China.
Shuqiu ChenDepartment of Urology, Zhongda Hospital, School of Medicine, Southeast University, 87 Dingjia Bridge Hunan Road, Nanjing, 210009, China.
Weidong ZhuDepartment of Urology, Zhongda Hospital, School of Medicine, Southeast University, 87 Dingjia Bridge Hunan Road, Nanjing, 210009, China.
Ming ChenDepartment of Urology, Zhongda Hospital, School of Medicine, Southeast University, 87 Dingjia Bridge Hunan Road, Nanjing, 210009, China. mingchenseu@126.com.
Zhongda Hospital Southeast University · CNBengbu Medical College · CNSoutheast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate cancer is one of the leading causes of death in men worldwide. Differentially expressed microRNAs (miRNAs) are associated with metastatic prostate cancer. However, their potential roles for affecting prostate cancer initiation and progression remain largely unknown. Here, we examined the aberrant expression profiles of miRNAs in human metastatic prostate cancer tissues. We further validated our miRNA expression data using two large, independent clinical prostate cancer datasets from the Memorial Sloan Kettering Cancer Center (MSKCC) and The Cancer Genome Atlas (TCGA). Our data support a model in which hsa-miR-135-1 acts as a potential tumor suppressor in metastatic prostate cancer. First, its downregulation was positively correlated with late TNM stage, high Gleason score, and adverse prognosis. Second, cell growth, cell cycle progression, cell migration and invasion, and xenograft tumor formation were dramatically inhibited by miR-135a overexpression. Third, in the microarray gene expression data analysis using Gene Set Enrichment Analysis (GSEA), Database for Annotation, Visualization and Integrated Discovery (DAVID) analysis, Ingenuity Pathway Analysis (IPA), and Oncomine concept analysis, we showed that miR-135a targets multiple oncogenic pathways including epidermal growth factor receptor (EGFR), which we verified using functional experimental assays. These results help advance our understanding of the function of miRNAs in metastatic prostate cancer and provide a basis for further clinical investigation.

Indexed as

Cell MovementCell ProliferationGene Expression Regulation, NeoplasticAdenocarcinomaAnimalsApoptosisBlotting, WesternCase-Control StudiesCell CycleDisease ProgressionErbB ReceptorsHumansMaleMiceMice, NudeMicroRNAsEGFR protein, humanErbB ReceptorsMicroRNAsMIRN135 microRNA, humanRNA, MessengerEGFRMetastasismiRNAProstate cancer

Identifiers

PMID27524492
OpenAlexW2517869136

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.