Evidence map›Paper›PMID 29744393›Full record

ReviewBioactive materials2016

Development of bioactive materials for glioblastoma therapy.

Jun Yang, Yan Li, Tianlu Zhang, Xin Zhang

Abstract readReview
In one paragraph

Review in Bioactive materials, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Synthesis, Characterization, andFrontiers in pharmacology · 2020
    Article
  8. The Extracellular Matrix and Biocompatible Materials in Glioblastoma Treatment.Frontiers in bioengineering and biotechnology · 2019
    Review
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

4 authors.

Jun YangNational Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, China.
Yan LiNational Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, China.
Tianlu ZhangNational Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, China.
Xin ZhangNational Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma is the most common and deadly human brain cancers. Unique barriers hinder the drug delivering pathway due to the individual position of glioblastoma, including blood-brain barrier and blood-brain tumor barrier. Numerous bioactive materials have been exploited and applied as the transvascular delivery carriers of therapeutic drugs. They promote site-specific accumulation and long term release of the encapsulated drugs at the tumor sites and reduce side effects with systemic delivery. And the delivery systems exhibit a certain extent of anti-glioblastoma effect and extend the median survival time. However, few of them step into the clinical trials. In this review, we will investigate the recent studies of bioactive materials for glioblastoma chemotherapy, including the inorganic materials, lipids and polymers. These bioactive materials construct diverse delivery vehicles to trigger tumor sites in brain intravenously. Herein, we exploit their functionality in drug delivery and discuss the deficiency for the featured tumors, to provide guidance for establishing optimized therapeutic drug formulation for anti-glioblastoma therapy and pave the way for clinical application.

Indexed as

ALA, α-lipoic acidBAG3, Bcl-2 associated athanogene 3BBB, blood-brain barrierBioactive materialBlood-brain barrierBlood-brain tumor barrierBTB, blood-brain tumor barrierChemotherapyCNS, central nervous systemCPT, camptothecincRGD, cyclic Arg-Gly-AspDACHPt, dichloro-(1,2-diaminocyclohexane)platinum (II)DCs, dendritic cellsDHA, dehydroascorbic acidDOX, doxorubicinDPPC, 1,2-dihexadecanoyl-rac-glycero-3-phosphocholineFA, folateGCV, ganciclovirGlioblastomaGLUT1, glucose transporter isoform 1IL, interleukinMMPs, matrix metalloproteinasesPTX, paclitaxelROS, reactive oxygen speciesSN38, 7-ethyl-10-hydroxy-camptothecinTAT, transactivator of transcriptionTEG, tetra(ethylene glycol)TfR, transferrin receptorTMZ, temozolomideTNF, tumor necrosis factor

Identifiers

PMID29744393
PMCPMC5883963

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.