Evidence map›Paper›PMID 31391772›Full record

ArticleWorld journal of gastroenterology2019

MiR-205 mediated APC regulation contributes to pancreatic cancer cell proliferation.

Rui-Feng Qin, Jia Zhang, Hao-Ran Huo, Zeng-Jiang Yuan, Jia-Dong Xue

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 24% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Antioxidants (Basel, Switzerland) · 2024
    Article
  3. Review
  4. Article
  5. Article
  6. microRNA-205 in prostate cancer: Overview to clinical translation.Biochimica et biophysica acta. Reviews on cancer · 2022
    Review
  7. Review
  8. Review
  9. Computational and Bioinformatics Methods for MicroRNA Gene Prediction.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
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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

5 authors at 1 institution in 1 country.

Rui-Feng QinThird Department of General Surgery, Handan Central Hospital, Handan 056000, Hebei Province, China. ruifengqin89@163.com.
Jia ZhangThird Department of General Surgery, Handan Central Hospital, Handan 056000, Hebei Province, China.
Hao-Ran HuoThird Department of General Surgery, Handan Central Hospital, Handan 056000, Hebei Province, China.
Zeng-Jiang YuanThird Department of General Surgery, Handan Central Hospital, Handan 056000, Hebei Province, China.
Jia-Dong XueThird Department of General Surgery, Handan Central Hospital, Handan 056000, Hebei Province, China.
Handan College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPancreatic cancer is a deadly malignancy with aggressive properties. MicroRNAs (miRNAs) participate in the pathogenesis of a variety of diseases and molecular processes by targeting functional mRNAs. Nevertheless, the regulatory role of miRNAs in signaling pathways involved in pancreatic cancer remains largely unknown.

aimTo explore the molecular regulation involved in pancreatic cancer and potential mechanisms of miR-205.

methodsMicroarray analysis was performed to investigate the expression profile of miRNAs in pancreatic cancer. Expression of miR-205 was validated by qRT-PCR. Target prediction and functional enrichment analysis were employed to seek potential target genes of miR-205 and potential functions of these genes. The target binding of miR-205 and adenomatous polyposis coli (APC) was validated by luciferase reporter assay. APC protein expression in pancreatic cancer was validated by qRT-PCR and Western blot. Proliferation was evaluated by MTT and colony formation assays.

resultsA large number of miRNAs with altered expression were identified in pancreatic cancer. MiR-205 was significantly up-regulated. APC was found to be a validated target of miR-205 and down-regulated in pancreatic cancer. Proliferation experiments showed that miR-205 could promote cell proliferation in pancreatic cancer by targeting APC.

conclusionThe above findings suggested that miR-205 mediated APC regulation contributes to pancreatic cancer development, which could be considered as a novel prognostic biomarker for clinical care.

Indexed as

Gene Expression Regulation, NeoplasticAdenomatous Polyposis Coli ProteinAgedAged, 80 and overBiomarkers, TumorCell ProliferationDown-RegulationFemaleGene Expression ProfilingHumansMaleMicroRNAsMiddle AgedOligonucleotide Array Sequence AnalysisPancreasPancreatic NeoplasmsAdenomatous Polyposis Coli ProteinAPC protein, humanBiomarkers, TumorMicroRNAsMIR205, humanAdenomatous polyposis coliMicroarrayMiR-205Pancreatic cancerProliferation

Identifiers

PMID31391772
PMCPMC6676546
OpenAlexW2964657369

What OpenQuestion holds

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LicenceCC BY-NC
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.