Evidence map›Paper›PMID 31894478›Full record

ArticleHuman cell2020

MiR-490-5p functions as tumor suppressor in childhood neuroblastoma by targeting MYEOV.

Jinfeng Wang, Xin Zhang, Hongyue Yao, Yuan Le, Wei Zhou, Jing Li, Lingling Lu, Meixue Chen, Xiang Li

Abstract read
PubMed Publisher
In one paragraph

Article in Human cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 15% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. 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

9 authors at 1 institution in 1 country.

Jinfeng WangDepartment of Pediatrics, Jinzhou Medical University First Affiliated Hospital, Jinzhou, 121000, Liaoning, China.
Xin ZhangDepartment of Oncology, Jinzhou Medical University First Affiliated Hospital, No. 2, Section 5, Renmin Street, Guta District, Jinzhou, 121000, Liaoning, China. zhang_xin0203@outlook.com.
Hongyue YaoDepartment of Pediatrics, Jinzhou Medical University First Affiliated Hospital, Jinzhou, 121000, Liaoning, China.
Yuan LeDepartment of Pediatrics, Jinzhou Medical University First Affiliated Hospital, Jinzhou, 121000, Liaoning, China.
Wei ZhouDepartment of Pediatrics, Jinzhou Medical University First Affiliated Hospital, Jinzhou, 121000, Liaoning, China.
Jing LiDepartment of Pediatrics, Jinzhou Medical University First Affiliated Hospital, Jinzhou, 121000, Liaoning, China.
Lingling LuDepartment of Pediatrics, Jinzhou Medical University First Affiliated Hospital, Jinzhou, 121000, Liaoning, China.
Meixue ChenDepartment of Pediatrics, Jinzhou Medical University First Affiliated Hospital, Jinzhou, 121000, Liaoning, China.
Xiang LiDepartment of Pediatrics, Jinzhou Medical University First Affiliated Hospital, Jinzhou, 121000, Liaoning, China.
Jinzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuroblastoma (NB) is the most common extracranial solid tumor derived from neural crest in children. Recently, the role of miRNA has been studied extensively in the development of NB. Here, we investigated the clinical significance of microRNA-490-5p (miR-490-5p) in NB. A total of 72 pairs of NB tumor tissues and matched adjacent normal nerve tissues were collected from NB patients. The expression of miR-490-5p was significantly down-regulated in NB tissues and cell lines using quantitative real-time PCR. Using Pearson Chi-square test and Kaplan-Meier analysis, we found that significantly decreased miR-490-5p levels were correlated with INSS stage, lymph-node metastasis, and poor survival prognosis in NB patients. MiR-490-5p overexpression significantly suppressed cell proliferation migration, invasion, and induced cell cycle G0/G1 arrest and cell apoptosis in NB cell lines (SH-SY5Y and SK-N-SH) using CCK-8, flow cytometry, and transwell assays. Mechanistically, MYEOV was confirmed as a target gene of miR-490-5p by luciferase reporter assay. Furthermore, MYEOV knockdown imitated, while overexpression rescued the changes in the biological features of miR-490-5p on NB cells. Our results demonstrated for the first time that miR-490-5p functions as a tumor suppressor in NB by targeting MYEOV, which might provide novel approaches for the treatment of NB.

Indexed as

Molecular Targeted TherapyChildHumansMicroRNAsNeuroblastomaProto-Oncogene ProteinsMicroRNAsMIRN490 microRNA, humanMYEOV protein, humanProto-Oncogene ProteinsmiR-490-5pMYEOVNeuroblastomaPrognosisTumor suppressor

Identifiers

PMID31894478
OpenAlexW2997358476

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.