Evidence map›Paper›PMID 28203087›Full record

ArticleOncoTargets and therapy2017

miR-17 as a diagnostic biomarker regulates cell proliferation in breast cancer.

Fangliang Yang, Yuan Li, Lingyun Xu, Yulan Zhu, Haiyan Gao, Lin Zhen, Lin Fang

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

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  17. miR-17-5p promotes migration and invasion in breast cancer cells by repressing netrin 4.International journal of clinical and experimental pathology · 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

7 authors at 2 institutions in 2 countries.

Fangliang YangDepartment of Thyroid and Breast Surgery, Changzhou No 2 People's Hospital Affiliated to Nanjing Medical University, Changzhou; Department of Thyroid and Breast Surgery, Shanghai No 10 People's Hospital, Clinical College of Nanjing Medical University, Shanghai, People's Republic of China.
Yuan LiDepartment of Thyroid and Breast Surgery, Changzhou No 2 People's Hospital Affiliated to Nanjing Medical University, Changzhou.
Lingyun XuDepartment of Thyroid and Breast Surgery, Changzhou No 2 People's Hospital Affiliated to Nanjing Medical University, Changzhou.
Yulan ZhuDepartment of Thyroid and Breast Surgery, Changzhou No 2 People's Hospital Affiliated to Nanjing Medical University, Changzhou.
Haiyan GaoDepartment of Thyroid and Breast Surgery, Changzhou No 2 People's Hospital Affiliated to Nanjing Medical University, Changzhou.
Lin ZhenDepartment of Thyroid and Breast Surgery, Changzhou No 2 People's Hospital Affiliated to Nanjing Medical University, Changzhou.
Lin FangDepartment of Thyroid and Breast Surgery, Shanghai No 10 People's Hospital, Clinical College of Nanjing Medical University, Shanghai, People's Republic of China.
Breast Center · CHShanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicroRNAs (miRNAs) have been shown to be involved in the initiation and progression of cancers in the literature. In this study, we aimed to evaluate the clinicopathological role of miR-17 in breast cancer. MATERIALS AND

methodsThe expression of miR-17 was measured in 132 breast cancer tissues and paired adjacent normal tissues by using real-time quantitative polymerase chain reaction. The association between miR-17 expression levels and clinicopathological parameters was also analyzed. 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and flow cytometry assays were used to investigate the role of miR-17 in the regulation of breast cancer cells.

resultsThe expression of miR-17 was remarkably increased in breast cancer tissues and cell lines. Clinical association analysis revealed that a high expression of miR-17 was prominently associated with poor survival time in breast cancer. Overexpression of miR-17 promoted cell proliferation and induced tumor growth.

conclusionOur findings clarified that the upregulation of miR-17 played a vital role in breast cancer progression and suggested that miR-17 could be used as a prognostic biomarker for breast cancer.

Indexed as

biomarkerbreast cancercell proliferationmiR-17

Identifiers

PMID28203087
PMCPMC5293507
OpenAlexW2582081012

What OpenQuestion holds

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LicenceCC BY-NC
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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.