Evidence map›Paper›PMID 29266795›Full record

ArticleJournal of cellular and molecular medicine2018

LncRNA-DANCR contributes to lung adenocarcinoma progression by sponging miR-496 to modulate mTOR expression.

Qing-Chun Lu, Zhuang-Hua Rui, Zhong-Liang Guo, Wang Xie, Shan Shan, Tao Ren

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 3% 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

52 citing papers in PubMed, 1 synthesis or guideline pooled it, 86 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Competing endogenous RNAs in lung cancer.Cancer biology & medicine · 2021
    Review
  19. Review
  20. Long Non-coding RNA DANCR in Cancer: Roles, Mechanisms, and Implications.Frontiers in cell and developmental biology · 2021
    Review
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

6 authors at 2 institutions in 1 country.

Qing-Chun LuDepartment of Respiratory Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China.
Zhuang-Hua RuiDepartment of Respiratory Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China.
Zhong-Liang GuoDepartment of Respiratory Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China.
Wang XieDepartment of Respiratory Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China.
Shan ShanDepartment of Respiratory Medicine, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, China.
Tao RenDepartment of Respiratory Medicine, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, China.ORCID 0000-0003-0845-3058
Shanghai East Hospital · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs) have emerged as new and important regulators of pathological processes including tumour development. In this study, we demonstrated that differentiation antagonizing non-protein coding RNA (DANCR) was up-regulated in lung adenocarcinoma (ADC) and that the knockdown of DANCR inhibited tumour cell proliferation, migration and invasion and restored cell apoptosis rescued; cotransfection with a miR-496 inhibitor reversed these effects. Luciferase reporter assays showed that miR-496 directly modulated DANCR; additionally, we used RNA-binding protein immunoprecipitation (RIP) and RNA pull-down assays to further confirm that the suppression of DANCR by miR-496 was RISC-dependent. Our study also indicated that mTOR was a target of miR-496 and that DANCR could modulate the expression levels of mTOR by working as a competing endogenous RNA (ceRNA). Furthermore, the knockdown of DANCR reduced tumour volumes in vivo compared with those of the control group. In conclusion, this study showed that DANCR might be an oncogenic lncRNA that regulates mTOR expression through directly binding to miR-496. DANCR may be regarded as a biomarker or therapeutic target for ADC.

Indexed as

Gene Expression Regulation, NeoplasticAdenocarcinoma of LungAnimalsAntagomirsApoptosisBase SequenceBinding SitesCell Line, TumorCell MovementCell ProliferationDisease ProgressionHEK293 CellsHumansLung NeoplasmsMaleMiceAntagomirsDANCR long noncoding RNA, humanMicroRNAsMIRN496 microRNA, humanMTOR protein, humanRNA-Induced Silencing ComplexRNA, Long NoncodingTOR Serine-Threonine KinasesceRNADANCRlung adenocarcinomamiR-496mTORsponge

Identifiers

PMID29266795
PMCPMC5824415
OpenAlexW2779372229

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.