Evidence map›Paper›PMID 30887657›Full record

ArticleJournal of cellular and molecular medicine2019

FER1L4/miR-372/E2F1 works as a ceRNA system to regulate the proliferation and cell cycle of glioma cells.

Liang Xia, Dekang Nie, Guangtao Wang, Caixing Sun, Gao Chen

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.7field-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

35 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Co-upregulation ofJournal of dental sciences · 2022
    Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. LncRNAFrontiers in cell and developmental biology · 2022
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 3 institutions in 1 country.

Liang XiaDepartment of Neurosurgery, The second Affiliated Hospital of Medical College of Zhejiang University, Hangzhou, Zhejiang Province, China.
Dekang NieDepartment of Neurosurgery, Yancheng First Peoples' Hospital, Yancheng, Jiangsu Province, PR China.
Guangtao WangDepartment of Neurosurgery, The second Affiliated Hospital of Medical College of Zhejiang University, Hangzhou, Zhejiang Province, China.
Caixing SunDepartment of Neurosurgery, Zhejiang Cancer Hospital, Hangzhou, Zhejiang Province, China.ORCID 0000-0001-9857-5416
Gao ChenDepartment of Neurosurgery, The second Affiliated Hospital of Medical College of Zhejiang University, Hangzhou, Zhejiang Province, China.
Second Affiliated Hospital of Zhejiang University · CNZhejiang Cancer Hospital · CNNantong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non-coding RNAs have recently become a key regulatory factor for cancers, whereas FER1L4, a newly discovered long non-coding RNA, has been mostly studied in gastric carcinoma and colon cancer cases. The functions and molecular mechanism of FER1L4 have been rarely reported in glioma malignant phenotypes. In this study, it was found that the expression of LncRNA FER1L4 is upregulated in high-grade gliomas than in low-grade cases and that a high expression of LncRNA FER1L4 predicts poor prognosis of gliomas. Meanwhile, in vitro study suggests that expression of FER1L4 with SiRNA knockdown obviously suppresses cell cycle and proliferation. It is further demonstrated by experiments that the FER1L4 knockdown suppresses growth of in vivo glioma. Besides, it is found in our study that LncRNA FER1L4 expression is positively correlated with E2F1 mRNA expression. After knockdown of FER1L4 expression, E2F1 expression is significantly down-regulated, whereas the expression of miR-372 is significantly up-regulated; the up-regulation of miR-372 leads to significant down-regulation of FER1L4 and E2F1 expression. In addition, it is also found that FER1L4 can be used as competitive endogenous RNA to interact or bind with miR-371 and thereby up-regulate E2F1, thus promoting the cycle and proliferation of glioma cells. It may be one of the molecular mechanisms in which FER1L4 plays its oncogene-like role in gliomas.

Indexed as

ApoptosisCell CycleCell Line, TumorCell MovementCell ProliferationE2F1 Transcription FactorGene Expression Regulation, NeoplasticGene Knockdown TechniquesGliomaHumansMicroRNAsRNA, Long NoncodingE2F1 protein, humanE2F1 Transcription FactorMicroRNAsMIRN372 microRNA, humanRNA, Long NoncodingceRNAE2F1FER1L4gliomaproliferation

Identifiers

PMID30887657
PMCPMC6484322
OpenAlexW2924014465

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.