Evidence map›Paper›PMID 30317248›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2018

Long Non-Coding RNA DUXAP8 Enhances Renal Cell Carcinoma Progression via Downregulating miR-126.

Tao Huang, Xiao Wang, Xiaokun Yang, Jianlei Ji, Qinghai Wang, Xuan Yue, Zheng Dong

Open access · bronzeAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
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  4. A novel prognostic NScientific reports · 2023
    Article
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  10. Review
  11. LncRNAFrontiers in genetics · 2022
    Article
  12. LncRNA-DUXAP8 Regulation of the Wnt/β-Catenin Signaling Pathway to Inhibit Glycolysis and Induced Apoptosis in Acute Myeloid LeukemiaTurkish journal of haematology : official journal of Turkish Society of Haematology · 2021
    Article
  13. Review
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  19. 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

7 authors at 2 institutions in 1 country.

Tao HuangDepartment of Kidney Transplantation, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China (mainland).
Xiao WangDepartment of Kidney Transplantation, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China (mainland).
Xiaokun YangDepartment of Urology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China (mainland).
Jianlei JiDepartment of Kidney Transplantation, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China (mainland).
Qinghai WangDepartment of Kidney Transplantation, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China (mainland).
Xuan YueDepartment of Kidney Transplantation, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China (mainland).
Zheng DongDepartment of Kidney Transplantation, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China (mainland).
Affiliated Hospital of Qingdao University · CNQingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Renal cell carcinoma (RCC) is one of the common malignant tumors in the urinary system, which endangers human health for a long time. The past decade, the molecular biology of renal cell carcinoma has made considerable progress, so that we have a more profound understanding of renal cell carcinoma. Molecular biological mechanism of renal cell carcinoma remains to be explored. Evidence indicates that long non-coding RNAs (lncRNAs) may be important players in human cancer progression, including RCC. In this study, we found that a newly discovered pseudogene-derived lncRNA named DUXAP8, a 2107-bp RNA, was remarkably upregulated in RCC. MATERIAL AND METHODS Expression of lncRNA DUXAP8 was determined by a qRT-PCR assay in RCC tissues. The proliferation and invasion of RCC cell were measured by a cell proliferation assay and a Transwell invasion assay. Expression of miR-126 was detected by real-time PCR. Interactions between lncRNA DUXAP8 and miR-126 were measured by a luciferase reporter assay and an RNA-pull down assay. In vivo experiments were used to detect tumor formation. RESULTS Together, our study not only identifies lncRNA DUXAP8 as a negative regulator of renal cancer with potential clinical value, but also reveals a regulatory mechanism by long non-coding RNAs to control tumor development. CONCLUSIONS Results from this study provide evidence that lncRNA DUXAP8 enhances renal cell carcinoma progression via downregulating of miR-126, which offers a new approach for the treatment of RCC.

Indexed as

ApoptosisCarcinoma, Renal CellCell Line, TumorCell MovementCell ProliferationDisease ProgressionDown-RegulationGene Expression Regulation, NeoplasticHumansKidney NeoplasmsMicroRNAsRNA, Long NoncodingMicroRNAsMIRN126 microRNA, humanRNA, Long Noncoding

Identifiers

PMID30317248
PMCPMC6198709
OpenAlexW2896411726

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.