Evidence map›Paper›PMID 27073718›Full record

ArticleAmerican journal of cancer research2016

MicroRNA-373 promotes migration and invasion in human esophageal squamous cell carcinoma by inhibiting TIMP3 expression.

Wenzhi Liu, Mengkao Li, Xiangming Chen, Dakai Zhang, Lin Wei, Zicheng Zhang, Shuang Wang, Li Meng, Shan Zhu, Baosheng Li

Erratum issuedOpen 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. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

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  12. TIMP-3 as a therapeutic target for cancer.Therapeutic advances in medical oncology · 2019
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Wenzhi LiuDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong UniversityJinan, Shandong Province, P. R. China; Department of Clinical Oncology, Taian Central HospitalTaian, Shandong Province, P. R. China.
Mengkao LiDepartment of Neurosurgery, Taian Central Hospital Taian, Shandong Province, P. R. China.
Xiangming ChenDepartment of Clinical Oncology, Taian Central Hospital Taian, Shandong Province, P. R. China.
Dakai ZhangDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong UniversityJinan, Shandong Province, P. R. China; University of Jinan, School of Medicine and Life Sciences, Shandong Academy of Medical SciencesJinan, Shandong Province, P. R. China.
Lin WeiDepartment of Clinical Oncology, Taian Central Hospital Taian, Shandong Province, P. R. China.
Zicheng ZhangDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong University Jinan, Shandong Province, P. R. China.
Shuang WangDepartment of Clinical Oncology, Taian Central Hospital Taian, Shandong Province, P. R. China.
Li MengDepartment of Clinical Oncology, Taian Central Hospital Taian, Shandong Province, P. R. China.
Shan ZhuDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong UniversityJinan, Shandong Province, P. R. China; University of Jinan, School of Medicine and Life Sciences, Shandong Academy of Medical SciencesJinan, Shandong Province, P. R. China.
Baosheng LiDepartment of Clinical Oncology, Taian Central Hospital Taian, Shandong Province, P. R. China.
Taian City Central Hospital · CNShandong First Medical University · CNShandong Tumor Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Esophageal squamous cell carcinoma (ESCC) is the predominant pathological type of esophageal carcinoma in Asia. MicroRNAs (miRNAs) are a class of 19-22-nucleotide non-coding RNAs acting on target mRNAs that function as either oncogenes or anti-oncogenes. It has been confirmed that miR-373 expression varies among different tumor types. However, its mechanism is still unclear in ESCC. In our current study, we found that miR-373 expression was upregulated in ESCC tissues compared with matched adjacent normal tissues, as well as in the plasma of ESCC patients compared with that of healthy volunteers. Overexpression of miR-373 in ECA109 cells enhanced proliferation, G1-phase cell proportion, migration, and invasion. On the other hand, suppression of miR-373 in KYSE410 cells decreased proliferation, G1-phase cell proportion, migration, and invasion and also improved cell apoptosis. Moreover, we found that TIMP3, which was reported to suppress invasion and metastasis of ESCC, was a direct target of miR-373. Overexpression of miR-373 in ECA109 caused a reduction of TIMP3 mRNA and protein, whereas suppression of miR-373 in KYSE410 led to an increase of TIMP3 mRNA and protein. Introducing TIMP3 in miR-373 over-expressed cells or knocking down TIMP3 in miR-373 suppressed cells could partially abrogate the effect of miR-373 on migration and invasion. Therefore, these results prove that as an oncogene, miRNA-373 would be an important and reliable biomarker for ESCC diagnosis and treatment by targeting TIMP3.

Indexed as

Esophageal cancermicroRNA-373oncogeneTIMP3

Identifiers

PMID27073718
PMCPMC4759392
OpenAlexW2340788614

What OpenQuestion holds

Textmetadata
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Registered trials

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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.