Evidence map›Paper›PMID 27186421›Full record

ArticleAmerican journal of cancer research2016

MiR-654-5p attenuates breast cancer progression by targeting EPSTI1.

Yu-Yan Tan, Xiao-Yun Xu, Jin-Feng Wang, Cheng-Wu Zhang, Sheng-Chu Zhang

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.3field-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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

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  5. Comprehensive Analysis of hsa-miR-654-5p's Tumor-Suppressing Functions.International journal of molecular sciences · 2022
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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

5 authors at 1 institution in 1 country.

Yu-Yan TanDepartment of General Surgery, The First College of Clinical Medical Science, China Three Gorges UniversityYichang 443003, Hubei, China; Department of General Surgery, Zhongda Hospital, School of Medicine, Southeast UniversityNanjing 210009, Jiangsu, China.
Xiao-Yun XuDepartment of Intensive Care Unit, The First College of Clinical Medical Science, China Three Gorges University Yichang 443003, Hubei, China.
Jin-Feng WangDepartment of General Surgery, The First College of Clinical Medical Science, China Three Gorges University Yichang 443003, Hubei, China.
Cheng-Wu ZhangDepartment of General Surgery, The First College of Clinical Medical Science, China Three Gorges University Yichang 443003, Hubei, China.
Sheng-Chu ZhangDepartment of General Surgery, The First College of Clinical Medical Science, China Three Gorges University Yichang 443003, Hubei, China.
China Three Gorges University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) dysregulation is a common event in a variety of human diseases including breast cancer. However, clinical relevance and biological role of miR-654-5p in the progression of breast cancer remain greatly elusive. Herein, the expression levels of miR-654-5p were aberrantly downregulated in human breast cancer specimens and four breast cancer cell lines. Low expression of miR-654-5p was strongly associated with advanced TNM stage and lymph node metastasis as well as a poor survival. Functional analysis showed that miR-654-5p overexpression inhibited cell growth and invasion, and induced cell apoptosis in two aggressive breast cancer cells. Further studies demonstrated that Epithelial stromal interaction 1 (EPSTI1) was a direct target gene of miR-654-5p and showed an inverse correlation with miR-654-5p expression. Forced expression of EPSTI1 could abrogate the inhibitory effect of miR-654-5p on the growth and invasion of breast cancer cells as well as apoptosis-induced ability. In conclusion, the present study highlights that miR-654-5p acts as a tumor suppressor in breast cancer through directly targeting EPSTI1, and their functional regulation may open a novel avenue with regard to the therapeutic target for breast cancer.

Indexed as

breast cancerEPSTI1miR-654-5pmiRNAsurvival

Identifiers

PMID27186421
PMCPMC4859678
OpenAlexW2403965880

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.