Evidence map›Paper›PMID 33463324›Full record

ReviewACS biomaterials science & engineering2020

Polymeric Biomaterial Scaffolds for Tumoricidal Stem Cell Glioblastoma Therapy.

Kathryn M Moore, Ananya B Murthy, Elizabeth G Graham-Gurysh, Shawn D Hingtgen, Eric M Bachelder, Kristy M Ainslie

Open access · greenAbstract readReview
In one paragraph

Review in ACS biomaterials science & engineering, 2020. 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
1.2field-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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Biomaterial-basedCancer pathogenesis and therapy · 2023
    Review
  9. Review
  10. 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

6 authors at 1 institution in 1 country.

Kathryn M MooreJoint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Chapel Hill, North Carolina 27599, United States.ORCID 0000-0002-1820-8382
Ananya B MurthyDivision of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.
Elizabeth G Graham-GuryshDivision of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.ORCID 0000-0002-2130-5706
Shawn D HingtgenDivision of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.
Eric M BachelderDivision of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.ORCID 0000-0002-8572-888X
Kristy M AinslieJoint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Chapel Hill, North Carolina 27599, United States.
University of North Carolina at Chapel Hill · US

Funding

Nanofiber matrices to improve neural stem cell-mediated cancer therapyR01NS097507 · NINDS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HINGTGEN, SHAWN · 2016 to 2020
$1.6M
Combination Therapy of Stem Cells and Drug Eluting Scaffolds to Treat GlioblastomaF32CA225199 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GURYSH, ELIZABETH GRACE · 2019 to 2020
$133k
NCI NIH HHS F32 CA225199NINDS NIH HHS R01 NS097507
6 · The paper itself

Abstract

Glioblastoma (GBM) is the most common primary brain tumor and has a poor prognosis; as such, there is an urgent need to develop innovative new therapies. Tumoricidal stem cells are an emerging therapy that has the potential to combat limitations of traditional local and systemic chemotherapeutic strategies for GBM by providing a source for high, sustained concentrations of tumoricidal agents locally to the tumor. One major roadblock for tumoricidal stem cell therapy is that the persistence of tumoricidal stem cells injected as a cell suspension into the GBM surgical resection cavity is limited. Polymeric biomaterial scaffolds have been utilized to enhance the delivery of tumoricidal stem cells in the surgical resection cavity and extend their persistence in the brain, ultimately increasing their therapeutic efficacy against GBM. In this review, we examine three main scaffold categories explored for tumoricidal stem cell therapy: microcapsules, hydrogels, and electrospun scaffolds. Furthermore, considering the significant impact of surgery on the brain and recurrent GBM, we survey a brief history of orthotopic models of GBM surgical resection.

Indexed as

Brain NeoplasmsGlioblastomaBiocompatible MaterialsHumansNeoplasm Recurrence, LocalStem CellsBiocompatible MaterialselectrospinningHydrogelslocal drug deliverymicrocapsulessurgical resection

Identifiers

PMID33463324
PMCPMC10373914
OpenAlexW3034770143

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.