Evidence map›Paper›PMID 25813153›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2015

Tumor suppressive microRNA-200a inhibits renal cell carcinoma development by directly targeting TGFB2.

Ruijing Lu, Ziliang Ji, Xiaoqing Li, Jie Qin, Guanghui Cui, Jing Chen, Qingna Zhai, Chunjuan Zhao, Wei Zhang, Zhendong Yu

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
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

21 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
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  7. Observational
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  11. Kelch-like protein 14 promotes proliferation and migration of ovarian cancer cells.International journal of clinical and experimental pathology · 2020
    Article
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  13. Review
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  19. Long non-coding RNA ATB promotes glioma malignancy by negatively regulating miR-200a.Journal of experimental & clinical cancer research : CR · 2016
    Article
  20. Downregulation of lncRNA-ATB correlates with clinical progression and unfavorable prognosis in pancreatic cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
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

10 authors at 4 institutions in 2 countries.

Ruijing LuCentral Laboratory, Peking University Shenzhen Hospital, Shenzhen, 518036, China.
Ziliang JiDepartment of Urology, Longgang District People's Hospital of Shenzhen, Shenzhen, 518172, China.
Xiaoqing LiCentral Laboratory, Peking University Shenzhen Hospital, Shenzhen, 518036, China.
Jie QinCentral Laboratory, Peking University Shenzhen Hospital, Shenzhen, 518036, China.
Guanghui CuiCentral Laboratory, Peking University Shenzhen Hospital, Shenzhen, 518036, China.
Jing ChenCentral Laboratory, Peking University Shenzhen Hospital, Shenzhen, 518036, China.
Qingna ZhaiCentral Laboratory, Peking University Shenzhen Hospital, Shenzhen, 518036, China.
Chunjuan ZhaoCentral Laboratory, Peking University Shenzhen Hospital, Shenzhen, 518036, China.
Wei ZhangBiomedical Research Institute, Shenzhen Peking University - the Hong Kong University of Science and Technology Medical Center, Shenzhen, 518036, China. zhangweispace@163.com.
Zhendong YuCentral Laboratory, Peking University Shenzhen Hospital, Shenzhen, 518036, China. dongboyaa@163.com.
Peking University Shenzhen Hospital · CNShenzhen Maternity and Child Healthcare Hospital · CNHong Kong University of Science and Technology · HKLonggang Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A large body of evidence indicates that microRNAs play a critical role in tumor initiation and progression by negatively regulating oncogenes or tumor suppressor genes. Here, we report that the expression of miR-200a was notably downregulated in 45 renal cell carcinoma (RCC) samples. Restoration of miR-200a suppressed cell proliferation, migration, and invasion in two RCC cell lines. Furthermore, we used an epithelial-to-mesenchymal transition PCR array to explore the putative target genes of miR-200a. By performing quantitative real-time PCR, ELISA, and luciferase reporter assays, transforming growth factor beta2 (TGFB2) was validated as a direct target gene of miR-200a. Moreover, siRNA-mediated knockdown of TGFB2 partially phenocopied the effect of miR-200a overexpression. These results suggest that miR-200a suppresses RCC development via directly targeting TGFB2, indicating that miR-200a may present a novel target for diagnostic and therapeutic strategies in RCC.

Indexed as

Carcinoma, Renal CellCell Line, TumorCell MovementCell ProliferationEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticGene Knockout TechniquesHumansMicroRNAsNeoplasm InvasivenessRNA, Small InterferingTransforming Growth Factor beta2MicroRNAsMIRN200 microRNA, humanRNA, Small InterferingTGFB2 protein, humanTransforming Growth Factor beta2miR-200aRenal cell carcinomaTGFB2Tumor suppressor

Identifiers

PMID25813153
OpenAlexW1981828355

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.