Evidence map›Paper›PMID 31737900›Full record

ArticleBioscience reports2020

Long non-coding RNA DSCAM-AS1 contributes to the tumorigenesis of cervical cancer by targeting miR-877-5p/ATXN7L3 axis.

Jie Liang, Shujuan Zhang, Wei Wang, Yan Xu, Atikan Kawuli, Jiaqi Lu, Xuemei Xiu

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

7 authors at 2 institutions in 1 country.

Jie LiangDepartment of Gynaecology, Second People's Hospital in Kashgar, Xinjiang Uyhur Autonomous Region, No.1, Health Road, Kashgar 844000, Xinjiang, China.
Shujuan ZhangDepartment of Medical Oncology, Second People's Hospital in Kashgar, Xinjiang Uyhur Autonomous Region, No.1, Health Road, Kashgar 844000, Xinjiang, China.
Wei WangDepartment of Medical Oncology, The First People's Hospital in Kashgar, Xinjiang Uyhur Autonomous Region, No.120, Yingbin Road, Kashgar 844000, Xinjiang, China.
Yan XuDepartment of Gynaecology, Second People's Hospital in Kashgar, Xinjiang Uyhur Autonomous Region, No.1, Health Road, Kashgar 844000, Xinjiang, China.
Atikan KawuliDepartment of Medical Oncology, Second People's Hospital in Kashgar, Xinjiang Uyhur Autonomous Region, No.1, Health Road, Kashgar 844000, Xinjiang, China.
Jiaqi LuDepartment of Gynaecology, Second People's Hospital in Kashgar, Xinjiang Uyhur Autonomous Region, No.1, Health Road, Kashgar 844000, Xinjiang, China.
Xuemei XiuDepartment of Medical Oncology, Second People's Hospital in Kashgar, Xinjiang Uyhur Autonomous Region, No.1, Health Road, Kashgar 844000, Xinjiang, China.
People's Hospital of Xinjiang Uygur Autonomous Region · CNXian Yang Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer (CC) is ranked as the fourth most common cancer that occurs in women universally, which normally causes pain in the lower belly. Plenty of studies have stated that the expression of long non-coding RNAs (lncRNAs) is linked to the cellular development of many kinds of cancers. DSCAM-AS1 has been reported to act as an oncogene in other cancer types and the aim of our study was to uncover the function and regulatory mechanism of DSCAM-AS1 in CC. In this research, our findings presented that DSCAM-AS1 expression was up-regulated in CC cells. DSCAM-AS1 led to the development of CC by enhancing cell proliferation, migration and invasion ability. DSCAM-AS1 was verified to combine with miR-877-5p and down-regulate the expression of miR-877-5p. Results also showed that ATXN7L3 was a downstream target gene of miR-877-5p and it was unfavorably modulated by miR-877-5p. Enhanced expression of ATXN7L3 counterbalanced the DSCAM-AS1 knockdown effect on the progression of CC. This was the first time to analyze the underlying regulatory mechanism of the oncogenic DSCAM-AS1. Our findings clarified that DSCAM-AS1 played as an oncogenic lncRNA by targeting miR-877-5p/ATXN7L3 axis to promote CC progression, which may provide insights into the prevention of CC.

Indexed as

CarcinogenesisCell Adhesion MoleculesCell LineCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHeLa CellsHumansMicroRNAsTranscription FactorsUp-RegulationUterine Cervical NeoplasmsATXN7L3 protein, humanCell Adhesion MoleculesDSCAM protein, humanMicroRNAsMIRN877 microRNA, humanTranscription FactorsATXN7L3cervical cancerDSCAM-AS1miR-877-5p

Identifiers

PMID31737900
PMCPMC6944662
OpenAlexW2984255859

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.