Evidence map›Paper›PMID 27186275›Full record

ArticleAmerican journal of translational research2016

miR-132 targeting E2F5 suppresses cell proliferation, invasion, migration in ovarian cancer cells.

Hang Tian, Lei Hou, Yu-Mei Xiong, Jun-Xiang Huang, Wen-Hua Zhang, Yong-Ying Pan, Xing-Rong Song

RetractedOpen access · greenAbstract readRetracted Publication
In one paragraph

Article in American journal of translational research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 40 citations in OpenAlex.

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  18. Frontiers in oncology · 2019
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Hang TianDepartment of Anesthesiology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University Guangzhou 510623, China.
Lei HouDepartment of Anesthesiology, Shanxi Cancer Hospital Taiyuan 030013, China.
Yu-Mei XiongDepartment of Pediatric Emergency, Guangzhou Women and Children's Medical Center, Guangzhou Medical University Guangzhou 510623, China.
Jun-Xiang HuangDepartment of Anesthesiology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University Guangzhou 510623, China.
Wen-Hua ZhangDepartment of Anesthesiology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University Guangzhou 510623, China.
Yong-Ying PanDepartment of Anesthesiology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University Guangzhou 510623, China.
Xing-Rong SongDepartment of Anesthesiology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University Guangzhou 510623, China.
Guangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulating evidence showed that microRNA-132 (miR-132) are involved in development and progression of several types of cancers, however, the function and underlying molecular mechanism of miR-132 in ovarian cancer remains unclear. In this study we investigated the biological roles and molecular mechanism of miR-132 in ovarian cancer. Here, we found that that the expression levels of miR-132 were dramatically decreased in ovarian cancer cell lines and clinical ovarian cancer tissue samples. Then, we found that introduction of miR-132 significantly suppressed the proliferation, colony formation, migration and invasion of ovarian cancer cells. Mechanism investigation revealed that miR-132 inhibited the expression of transcription factor E2F5 by specifically targeting its mRNA 3'UTR. Moreover, the expression level of E2F5 was significantly increased in ovarian cancer tissues than in the adjacent normal tissues, and its expression was inversely correlated with miR-132 expression in clinical ovarian cancer tissues. Additionally, silencing E2F5 was able to inhibit the proliferation, colony formation, migration and invasion of ovarian cancer cells, parallel to the effect of miR-132 overexpression on the ovarian cancer cells. Meanwhile, overexpression of E2F5 reversed the inhibition effect mediated by miR-132 overexpression. These results indicate that miR-132 suppresses the cell proliferation, invasion, migration in ovarian cancer cells by targeting E2F5.

Indexed as

E2F5invasionmigrationOvarian cancerproliferation

Identifiers

PMID27186275
PMCPMC4859634
OpenAlexW2408443094

What OpenQuestion holds

Textmetadata
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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.