Evidence map›Paper›PMID 30988628›Full record

ArticleOncoTargets and therapy2019

TRIB3 suppresses proliferation and invasion and promotes apoptosis of endometrial cancer cells by regulating the AKT signaling pathway.

Junjie Qu, Binya Liu, Bilan Li, Guiqiang Du, Yiran Li, Jingyun Wang, Laman He, Xiaoping Wan

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

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  17. TRIB3 promotes hepatocellular carcinoma growth and predicts poor prognosis.Cancer biomarkers : section A of Disease markers · 2020
    Observational
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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 1 institution in 1 country.

Junjie QuDepartment of Gynaecology, Shanghai First Maternity and Infant Hospital, Tongji University, Shanghai 201204, China, wanxiaoping22@163.com.
Binya LiuDepartment of Gynaecology, Shanghai First Maternity and Infant Hospital, Tongji University, Shanghai 201204, China, wanxiaoping22@163.com.
Bilan LiDepartment of Gynaecology, Shanghai First Maternity and Infant Hospital, Tongji University, Shanghai 201204, China, wanxiaoping22@163.com.
Guiqiang DuDepartment of Gynaecology, Shanghai First Maternity and Infant Hospital, Tongji University, Shanghai 201204, China, wanxiaoping22@163.com.
Yiran LiDepartment of Gynaecology, Shanghai First Maternity and Infant Hospital, Tongji University, Shanghai 201204, China, wanxiaoping22@163.com.
Jingyun WangDepartment of Gynaecology, Shanghai First Maternity and Infant Hospital, Tongji University, Shanghai 201204, China, wanxiaoping22@163.com.
Laman HeDepartment of Gynaecology, Shanghai First Maternity and Infant Hospital, Tongji University, Shanghai 201204, China, wanxiaoping22@163.com.
Xiaoping WanDepartment of Gynaecology, Shanghai First Maternity and Infant Hospital, Tongji University, Shanghai 201204, China, wanxiaoping22@163.com.
Shanghai First Maternity and Infant Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aim of this study was to examine the effect of

methodsImmunohistochemical analysis was performed to measure the expression level of TRIB3 in normal endometrium tissues and EC tissues. Overexpression and shRNA knockdown techniques were applied by transfecting EC cells (ISK and AN3CA), and the effect of TRIB3 on EC cell biological behaviors was evaluated. Cell Counting Kit-8 and colony formation assays were utilized to investigate EC cell proliferation ability, and flow cytometry was performed to assess the apoptosis of EC cells. Moreover, the migration and invasion of EC cells were detected by transwell assay, and the levels of MMP-2 and MMP-9 were measured by ELISA. Additionally, Western blot analysis was carried out to determine the levels of AKT and p-AKT.

resultsThe expression level of TRIB3 was higher in EC than normal endometrium tissues, and its overexpression promoted apoptosis and suppressed proliferation of EC cells. Furthermore, TRIB3 retarded the migration and invasion of EC cells and decreased the levels of MMP-2 and MMP-9. Conversely, TRIB3 inhibition enhanced the expression levels of MMP-2 and MMP-9, and proliferation and migration of EC cells but suppressed their apoptosis. Similarly, TRIB3 overexpression reduced while its knockdown increased the level of p-AKT.

conclusion

Indexed as

Drosophila tribbles homolog 3endometrial carcinomasendometriumoverexpressionshRNA knockdown

Identifiers

PMID30988628
PMCPMC6441550
OpenAlexW2924909238

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.