Evidence map›Paper›PMID 33502104›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2021

Rapid 3D Bioprinting of Glioblastoma Model Mimicking Native Biophysical Heterogeneity.

Min Tang, Shashi Kant Tiwari, Kriti Agrawal, Matthew Tan, Jason Dang, Trevor Tam, Jing Tian, Xueyi Wan, Jacob Schimelman, Shangting You and 3 more

Abstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing 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

67 citing papers in PubMed.

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7 more citing papers are in PubMed but not listed here.

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

13 authors.

Min TangDepartment of NanoEngineering, University of California San Diego, La Jolla, CA, 92093, USA.
Shashi Kant TiwariDivision of Genetics, Department of Pediatrics, Institute for Genomic Medicine, Program in Immunology, University of California San Diego, La Jolla, CA, 92093, USA.
Kriti AgrawalDivision of Genetics, Department of Pediatrics, Institute for Genomic Medicine, Program in Immunology, University of California San Diego, La Jolla, CA, 92093, USA.
Matthew TanDivision of Genetics, Department of Pediatrics, Institute for Genomic Medicine, Program in Immunology, University of California San Diego, La Jolla, CA, 92093, USA.
Jason DangDivision of Genetics, Department of Pediatrics, Institute for Genomic Medicine, Program in Immunology, University of California San Diego, La Jolla, CA, 92093, USA.
Trevor TamDepartment of Bioengineering, University of California San Diego, La Jolla, CA, 92093, USA.
Jing TianDepartment of Bioengineering, University of California San Diego, La Jolla, CA, 92093, USA.
Xueyi WanDepartment of Bioengineering, University of California San Diego, La Jolla, CA, 92093, USA.
Jacob SchimelmanDepartment of NanoEngineering, University of California San Diego, La Jolla, CA, 92093, USA.
Shangting YouDepartment of NanoEngineering, University of California San Diego, La Jolla, CA, 92093, USA.
Qinghui XiaDepartment of NanoEngineering, University of California San Diego, La Jolla, CA, 92093, USA.
Tariq M RanaDivision of Genetics, Department of Pediatrics, Institute for Genomic Medicine, Program in Immunology, University of California San Diego, La Jolla, CA, 92093, USA.
Shaochen ChenDepartment of NanoEngineering, University of California San Diego, La Jolla, CA, 92093, USA.ORCID 0000-0001-6876-497X

Funding

U of Calif, San Diego Neuroscience Microscopy ImagingP30NS047101 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GLEESON, JOSEPH G, ZHENG, BINHAI · 2003 to 2022
$9.0M
Virology CoreP01CA177322 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHANDA, SUMIT K · 2014 to 2018
$8.7M
Investigating the molecular mechanisms of HIV/AIDS associated neurological disorders using microglia and cerebral organoids derived from induced pluripotent stem cellsR01DA049524 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RANA, TARIQ M · 2019 to 2023
$3.9M
Modeling HIV/AIDS Associated Neurological Disorders with Human Pluripotent CellsDP1DA039562 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RANA, TARIQ M · 2015 to 2020
$3.9M
Identification and Regulation of RNA Modification by HIV infection and MethamphetamineR01DA046171 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RANA, TARIQ M · 2018 to 2022
$3.1M
Bioprinting Plant Virus Nanoparticles for Immunotherapy and Relapse Prevention of Ovarian CancerR01CA253615 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHEN, SHAOCHEN, FIERING, STEVEN · 2020 to 2024
$3.1M
Rapid 3D bioprinting of biomimetic vascularized tissue constructsR01EB021857 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHEN, SHAOCHEN, DOKMECI, MEHMET REMZI · 2016 to 2019
$2.1M
Illumina NovaSeq 6000 Sequencing SystemS10OD026929 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JEPSEN, KRISTEN LYNN · 2019 to 2019
$600k
m6A-RNA demethylase ALKBH5 inhibitors for the treatment of glioblastomaR21NS118250 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RANA, TARIQ M · 2020 to 2020
$434k
NCI NIH HHS P01 CA177322NCI NIH HHS R01 CA253615NIBIB NIH HHS R01 EB021857NIDA NIH HHS DP1 DA039562NIDA NIH HHS R01 DA046171NIDA NIH HHS R01 DA049524NIH HHS S10 OD026929NINDS NIH HHS P30 NS047101NINDS NIH HHS R21 NS118250
6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is the most lethal primary brain tumor characterized by high cellular and molecular heterogeneity, hypervascularization, and innate drug resistance. Cellular components and extracellular matrix (ECM) are the two primary sources of heterogeneity in GBM. Here, biomimetic tri-regional GBM models with tumor regions, acellular ECM regions, and an endothelial region with regional stiffnesses patterned corresponding to the GBM stroma, pathological or normal brain parenchyma, and brain capillaries, are developed. Patient-derived GBM cells, human endothelial cells, and hyaluronic acid derivatives are used to generate a species-matched and biochemically relevant microenvironment. This in vitro study demonstrates that biophysical cues are involved in various tumor cell behaviors and angiogenic potentials and promote different molecular subtypes of GBM. The stiff models are enriched in the mesenchymal subtype, exhibit diffuse invasion of tumor cells, and induce protruding angiogenesis and higher drug resistance to temozolomide. Meanwhile, the soft models demonstrate enrichment in the classical subtype and support expansive cell growth. The three-dimensional bioprinting technology utilized in this study enables rapid, flexible, and reproducible patient-specific GBM modeling with biophysical heterogeneity that can be employed by future studies as a tunable system to interrogate GBM disease mechanisms and screen drug compounds.

Indexed as

BioprintingBrain NeoplasmsGlioblastomaCell Line, TumorEndothelial CellsHumansTumor Microenvironment3D printingangiogenesisbiophysical regulationglioblastomastiffness

Identifiers

PMID33502104
PMCPMC8049977

What OpenQuestion holds

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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.