Evidence map›Paper›PMID 31043779›Full record

ArticleInternational journal of nanomedicine2019

Targeting EZH2 for glioma therapy with a novel nanoparticle-siRNA complex.

Xiang Wang, Yuanqi Hua, Guangya Xu, Senyi Deng, Daoke Yang, Xiang Gao

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Review
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  6. Review
  7. Review
  8. Review
  9. Article
  10. Small Interfering RNA for Gliomas Treatment: Overcoming Hurdles in Delivery.Frontiers in cell and developmental biology · 2022
    Review
  11. Article
  12. Review
  13. In vivo gene delivery mediated by non-viral vectors for cancer therapy.Journal of controlled release : official journal of the Controlled Release Society · 2020
    Review
  14. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Xiang WangDepartment of Neurosurgery, Institute of Neurosurgery, State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, Collaborative Innovation Center for Biotherapy, Chengdu 610041, China, xianggao@scu.edu.cn.
Yuanqi HuaDepartment of Neurosurgery, Institute of Neurosurgery, State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, Collaborative Innovation Center for Biotherapy, Chengdu 610041, China, xianggao@scu.edu.cn.
Guangya XuDepartment of Neurosurgery, Institute of Neurosurgery, State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, Collaborative Innovation Center for Biotherapy, Chengdu 610041, China, xianggao@scu.edu.cn.
Senyi DengDepartment of Neurosurgery, Institute of Neurosurgery, State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, Collaborative Innovation Center for Biotherapy, Chengdu 610041, China, xianggao@scu.edu.cn.
Daoke YangTumor Hospital of First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Xiang GaoDepartment of Neurosurgery, Institute of Neurosurgery, State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, Collaborative Innovation Center for Biotherapy, Chengdu 610041, China, xianggao@scu.edu.cn.
Sichuan University · CNFirst Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFor the past few years, gene-therapy has recently shown considerable clinical benefit in cancer therapy, and the applications of gene therapies in cancer treatments continue to increase perennially. EZH2, an ideal candidate for tumor gene therapy, plays an important role in the tumorigenesis.

methodsIn this study, we developed a novel gene delivery system with a self-assembly method by Methoxy polyethylene glycol-polycaprolactone (MPEG-PCL) and DOTAP(DMC). And EZH2si-DMC was used to research anti-glioma both in vitro and in vivo.

resultsDMC with zeta-potential value of 36.7 mV and size of 35.6 nm showed good performance in the delivery siRNA to glioma cell in vitro with high 98% transfection efficiency. EZH2si-DMC showed good anti-glioma effect in vitro through inducing cell apoptosis and inhibiting cell growth. What's more, treatment of tumor-bearing mice with DMC-EZH2si complex had significantly inhibited tumor growth at the subcutaneous model in vivo by inhibiting EZH2 protein expression, promoting apoptosis and reducing proliferation.

conclusionThe EZH2 siRNA and DMC complex may be used to treat the glioma in clinical as a new drug.

Indexed as

Molecular Targeted TherapyAnimalsAntineoplastic AgentsApoptosisCell Line, TumorCell ProliferationDisease Models, AnimalEnhancer of Zeste Homolog 2 ProteinFatty Acids, MonounsaturatedFemaleGliomaHumansMice, Inbred BALB CMicellesMice, NudeNanoparticles1,2-dioleoyloxy-3-(trimethylammonium)propaneAntineoplastic AgentsEnhancer of Zeste Homolog 2 ProteinFatty Acids, MonounsaturatedMicellesmonomethoxypolyethylene glycolpolycaprolactonePolyestersPolyethylene GlycolsQuaternary Ammonium CompoundsRNA, Small InterferingDOTAPEZH2gene therapygliomaMPEG-PCLtumorigenesis

Identifiers

PMID31043779
PMCPMC6472285
OpenAlexW2939928460

What OpenQuestion holds

Textmetadata
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.