Evidence map›Paper›PMID 29453454›Full record

ArticleScientific reports2018

A Microvascularized Tumor-mimetic Platform for Assessing Anti-cancer Drug Efficacy.

Shantanu Pradhan, Ashley M Smith, Charles J Garson, Iman Hassani, Wen J Seeto, Kapil Pant, Robert D Arnold, Balabhaskar Prabhakarpandian, Elizabeth A Lipke

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 6% 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

55 citing papers in PubMed, 1 synthesis or guideline pooled it, 88 citations in OpenAlex.

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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 2 institutions in 1 country.

Shantanu PradhanDepartment of Chemical Engineering, Auburn University, Auburn, AL, 36849, USA.
Ashley M SmithBiomedical Technology, CFD Research Corporation, Huntsville, AL, 35806, USA.
Charles J GarsonBiomedical Technology, CFD Research Corporation, Huntsville, AL, 35806, USA.
Iman HassaniDepartment of Chemical Engineering, Auburn University, Auburn, AL, 36849, USA.
Wen J SeetoDepartment of Chemical Engineering, Auburn University, Auburn, AL, 36849, USA.
Kapil PantBiomedical Technology, CFD Research Corporation, Huntsville, AL, 35806, USA.
Robert D ArnoldDepartment of Drug Discovery and Development, Auburn University, Auburn, AL, 36849, USA.ORCID 0000-0001-6143-3991
Balabhaskar PrabhakarpandianBiomedical Technology, CFD Research Corporation, Huntsville, AL, 35806, USA.
Elizabeth A LipkeDepartment of Chemical Engineering, Auburn University, Auburn, AL, 36849, USA. elipke@auburn.edu.ORCID 0000-0002-3465-5609
Auburn University · USCFD Research Corporation (United States) · US

Funding

Secretory Phospholipases sPLA2 and their Receptors for Delivering NanoparticlesR01EB016100 · NIBIB · AUBURN UNIVERSITY AT AUBURN · PI ARNOLD, ROBERT D · 2013 to 2016
$1.3M
NCI NIH HHS HHSN261201400037CNIBIB NIH HHS R01 EB016100
6 · The paper itself

Abstract

Assessment of anti-cancer drug efficacy in in vitro three-dimensional (3D) bioengineered cancer models provides important contextual and relevant information towards pre-clinical translation of potential drug candidates. However, currently established models fail to sufficiently recapitulate complex tumor heterogeneity. Here we present a chip-based tumor-mimetic platform incorporating a 3D in vitro breast cancer model with a tumor-mimetic microvascular network, replicating the pathophysiological architecture of native vascularized breast tumors. The microfluidic platform facilitated formation of mature, lumenized and flow-aligned endothelium under physiological flow recapitulating both high and low perfused tumor regions. Metastatic and non-metastatic breast cancer cells were maintained in long-term 3D co-culture with stromal fibroblasts in a poly(ethylene glycol)-fibrinogen hydrogel matrix within adjoining tissue chambers. The interstitial space between the chambers and endothelium contained pores to mimic the "leaky" vasculature found in vivo and facilitate cancer cell-endothelial cell communication. Microvascular pattern-dependent flow variations induced concentration gradients within the 3D tumor mass, leading to morphological tumor heterogeneity. Anti-cancer drugs displayed cell type- and flow pattern-dependent effects on cancer cell viability, viable tumor area and associated endothelial cytotoxicity. Overall, the developed microfluidic tumor-mimetic platform facilitates investigation of cancer-stromal-endothelial interactions and highlights the role of a fluidic, tumor-mimetic vascular network on anti-cancer drug delivery and efficacy for improved translation towards pre-clinical studies.

Indexed as

Antineoplastic AgentsBiomimeticsDrug Screening Assays, AntitumorEquipment DesignHumansLab-On-A-Chip DevicesMCF-7 CellsMicrovesselsTumor MicroenvironmentAntineoplastic Agents

Identifiers

PMID29453454
PMCPMC5816595
OpenAlexW2803451575

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.