Evidence map›Paper›PMID 33692661›Full record

ArticleAdvanced functional materials2020

Endothelial Regulation of Drug Transport in a 3D Vascularized Tumor Model.

Kristina Haase, Giovanni S Offeddu, Mark R Gillrie, Roger D Kamm

Open access · bronzeAbstract read
In one paragraph

Article in Advanced functional materials, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
2.7field-weighted citation impact, top 7% 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

71 citing papers in PubMed, 129 citations in OpenAlex.

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  14. Advances and challenges in human 3D solid tumor models.Advanced functional materials · 2025
    Article
  15. A Biomimetic Human Multi-Cellular In Vitro Model of the Blood-Brain Barrier.International journal of molecular sciences · 2025
    Article
  16. Article
  17. Review
  18. Article
  19. Bioengineering vascularization.Development (Cambridge, England) · 2024
    Review
  20. Article

11 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

4 authors at 2 institutions in 2 countries.

Kristina HaaseMassachusetts Institute of Technology, Massachusetts, 02139, USA.
Giovanni S OffedduMassachusetts Institute of Technology, Massachusetts, 02139, USA.
Mark R GillrieMassachusetts Institute of Technology, Massachusetts, 02139, USA; University of Calgary, Calgary, T2N 1N4, Canada.
Roger D KammMassachusetts Institute of Technology, Massachusetts, 02139, USA.
Massachusetts Institute of Technology · USUniversity of Calgary · CA

Funding

Development of Physiologic Tissue Models to Assess Tumor Explant Response to Immune Checkpoint BlockadeU01CA214381 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BARBIE, DAVID A, KAMM, ROGER D · 2017 to 2021
$3.5M
Development of 3D vascularized model of Blood Brain Barrier and its application to Alzheimer disease researchR21NS105027 · NINDS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI KAMM, ROGER D · 2019 to 2020
$457k
NCI NIH HHS U01 CA214381NINDS NIH HHS R21 NS105027
6 · The paper itself

Abstract

Drug discovery and efficacy in cancer treatments are limited by the inability of pre-clinical models to predict successful outcomes in humans. Limitations remain partly due to their lack of a physiologic tumor microenvironment (TME), which plays a considerable role in drug delivery and tumor response to therapy. Chemotherapeutics and immunotherapies rely on transport through the vasculature, via the smallest capillaries and stroma to the tumor, where passive and active transport processes are at play. Here, a 3D vascularized tumor on-chip is used to examine drug delivery in a relevant TME within a large bed of perfusable vasculature. This system demonstrates highly localized pathophysiological effects of two tumor spheroids (Skov3 and A549) which cause significant changes in vessel density and barrier function. Paclitaxel (Taxol) uptake is examined through diffusivity measurements, functional efflux assays and accumulation of the fluorescent-conjugated drug within the TME. Due to vascular and stromal contributions, differences in the response of vascularized tumors to Taxol (shrinkage and CD44 expression) are apparent compared with simpler models. This model specifically allows for examination of spatially resolved tumor-associated endothelial dysfunction, likely improving the representation of

Indexed as

drug transportengineered vesselsmulti-drug resistanceP-gpvascularized tumor

Identifiers

PMID33692661
PMCPMC7939067
OpenAlexW3035648717

What OpenQuestion holds

Textmetadata
LicenceTDM
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.