Evidence map›Paper›PMID 30066895›Full record

ArticleOncology reports2018

MicroRNA‑320a suppresses tumour cell proliferation and invasion of renal cancer cells by targeting FoxM1.

Shiyue Zhao, Yangwei Wang, Yan Lou, Yonggang Wang, Jing Sun, Manyu Luo, Wen Li, Lining Miao

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in Oncology reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. A Review of Recent Research on the Role of MicroRNAs in Renal Cancer.Medical science monitor : international medical journal of experimental and clinical research · 2021
    Review
  6. Article
  7. Article
  8. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Shiyue ZhaoDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, Jilin 130041, P.R. China.
Yangwei WangDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, Jilin 130041, P.R. China.
Yan LouDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, Jilin 130041, P.R. China.
Yonggang WangDepartment of Cardiology, The First Hospital of Jilin University, Changchun, Jilin 130041, P.R. China.
Jing SunDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, Jilin 130041, P.R. China.
Manyu LuoDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, Jilin 130041, P.R. China.
Wen LiDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, Jilin 130041, P.R. China.
Lining MiaoDepartment of Nephrology, The Second Hospital of Jilin University, Changchun, Jilin 130041, P.R. China.
Second Affiliated Hospital of Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An increasing body of evidence has indicated that microRNAs (miRNAs/miRs) may play an important role in tumourigenesis and tumour progression. Recent studies have demonstrated that miR‑320a is aberrantly expressed in a variety of different types of human cancer. The results of the present study confirmed that the expression of miR‑320a was decreased in clinical specimens and cell lines. Expression of miR‑320a inhibited the growth and invasive ability of ACHN and Caki‑1 cells. Bioinformatics analysis and a luciferase reporter assay demonstrated that forkhead box protein M1 (FoxM1) was directly regulated by miR‑320a. Rescue experiments in vitro revealed that the upregulation of FoxM1 antagonized the miR‑320a‑mediated malignant phenotype in renal cancer. Furthermore, experiments employing a xenograft mouse model revealed that the upregulation of miR‑320a inhibited the proliferation of renal cancer cells in nude mice when FoxM1 protein expression was reduced. Collectively, the present study demonstrated a novel molecular interaction regulated by miR‑320a, which may provide a novel insight into the treatments for renal cancer.

Indexed as

Cell MovementCell ProliferationGene Expression Regulation, NeoplasticAdultAgedAnimalsApoptosisBiomarkers, TumorCarcinoma, Renal CellCase-Control StudiesFemaleFollow-Up StudiesForkhead Box Protein M1HumansKidney NeoplasmsMaleBiomarkers, TumorForkhead Box Protein M1FOXM1 protein, humanMicroRNAsMIRN320 microRNA, human

Identifiers

PMID30066895
PMCPMC6111456
OpenAlexW2884336609

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.