Evidence map›Paper›PMID 29115525›Full record

ArticleMolecular medicine reports2018

MicroRNA‑103 regulates tumorigenesis in colorectal cancer by targeting ZO‑1.

Jin Ke, Weiwei Shao, Yasu Jiang, Junfei Xu, Feng Li, Jun Qin

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. MiR-103a-3p promotes tumour glycolysis in colorectal cancer via hippo/YAP1/HIF1A axis.Journal of experimental & clinical cancer research : CR · 2020
    Article
  8. Article
  9. MiR-769 Inhibits Colorectal Cancer Cell Proliferation and Invasion by Targeting HEY1.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  10. MicroRNA-103 regulates the progression in endometrial carcinoma through ZO-1.International journal of immunopathology and pharmacology
    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

6 authors at 3 institutions in 1 country.

Jin KeDepartment of General Surgery, The Affiliated Hospital of Nantong University, Nantong University, Nantong, Jiangsu 226001, P.R. China.
Weiwei ShaoDepartment of General Surgery, The Fourth Affiliated Hospital of Nantong University, Nantong University, Yancheng, Jiangsu 224000, P.R. China.
Yasu JiangDepartment of General Surgery, The Second Affiliated Hospital of Nantong University, Nantong University, Nantong, Jiangsu 226001, P.R. China.
Junfei XuDepartment of General Surgery, The Affiliated Hospital of Nantong University, Nantong University, Nantong, Jiangsu 226001, P.R. China.
Feng LiDepartment of Gastroenterology, The Affiliated Hospital of Nantong University, Nantong University, Nantong, Jiangsu 226001, P.R. China.
Jun QinDepartment of General Surgery, The Affiliated Hospital of Nantong University, Nantong University, Nantong, Jiangsu 226001, P.R. China.
Nantong University · CNAffiliated Hospital of Nantong University · CNSecond Affiliated Hospital of Nantong University

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Given the emerging role of microRNAs (miRs) in cancer progression, the present study investigated the role and underlying mechanism of miR‑103 in colorectal cancer (CRC). Reverse transcription‑quantitative polymerase chain reaction was conducted to quantify the expression levels of miR‑103 in clinical specimens and cell lines. The role of miR‑103 in CRC was examined using MTT, colony formation and transwell assays. In addition, a luciferase reporter assay was used to confirm an associated between the 3' untranslated region of zonula occuldens‑1 (ZO‑1) and miR‑103. The results demonstrated that miR‑103 was upregulated in CRC. Overexpression of miR‑103 promoted CRC cell proliferation and migration in vitro, whereas downregulation of miR‑103 inhibited cell proliferation and migration. ZO‑1 was identified as a direct target of miR‑103, revealing its expression to be inversely correlated with miR‑103 expression in CRC samples. In conclusion, the present study revealed that miR‑103 has strong tumor‑promoting effects via of targeting ZO‑1 in CRC and has potential development of miRNA‑based targeted approaches for the treatment of CRC.

Indexed as

RNA Interference3' Untranslated RegionsCell MovementCell ProliferationCell SurvivalCell Transformation, NeoplasticColorectal NeoplasmsComputational BiologyGene Expression Regulation, NeoplasticGenes, ReporterHumansMicroRNAsZonula Occludens-1 Protein3' Untranslated RegionsMicroRNAsMIRN103 microRNA, humanZonula Occludens-1 Protein

Identifiers

PMID29115525
PMCPMC5780155
OpenAlexW2767305692

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.