Evidence map›Paper›PMID 24309015›Full record

ReviewAdvanced drug delivery reviews2014

In vitro models of tumor vessels and matrix: engineering approaches to investigate transport limitations and drug delivery in cancer.

Bo Ri Seo, Peter DelNero, Claudia Fischbach

Abstract readReview
In one paragraph

Review in Advanced drug delivery reviews, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

37 citing papers in PubMed, 73 citations in OpenAlex.

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  10. Patient-Derived In Vitro and In Vivo Models of Cancer.Advances in experimental medicine and biology · 2022
    Article
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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

3 authors at 1 institution in 1 country.

Bo Ri Seo *Department of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA.
Peter DelNero *Department of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA.
Claudia FischbachDepartment of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA.
Cornell University · US

Funding

Clinical and Translational Science CenterUL1TR000457 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI IMPERATO-MCGINLEY, JULIANNE L · 2012 to 2016
$46.0M
TRANS-NETWORK PROJECTSU54CA143876 · NCI · CORNELL UNIVERSITY · PI SHULER, MICHAEL L · 2009 to 2014
$12.6M
Breast microcalcifications and their role in breast cancer bone metastasisR01CA173083 · NCI · CORNELL UNIVERSITY · PI FISCHBACH, CLAUDIA · 2012 to 2016
$1.7M
Microfluidic tumor models to analyze the role of physicochemical cues in the angiRC1CA146065 · NCI · CORNELL UNIVERSITY · PI FISCHBACH, CLAUDIA, MITTAL, VIVEK · 2009 to 2010
$1.0M
Fibronectin and its role in tumor stiffness and vascularizationR21CA161532 · NCI · CORNELL UNIVERSITY · PI FISCHBACH, CLAUDIA, GOURDON, DELPHINE · 2011 to 2012
$363k
NCATS NIH HHS UL1 TR000457NCI NIH HHS R01 CA173083NCI NIH HHS R01CA173083NCI NIH HHS R21 CA161532NCI NIH HHS R21CA161532NCI NIH HHS RC1 CA146065NCI NIH HHS U54 CA143876NCI NIH HHS U54CA143876
6 · The paper itself

Abstract

Tumor-stroma interactions have emerged as critical determinants of drug efficacy. However, the underlying biological and physicochemical mechanisms by which the microenvironment regulates therapeutic response remain unclear, due in part to a lack of physiologically relevant in vitro platforms to accurately interrogate tissue-level phenomena. Tissue-engineered tumor models are beginning to address this shortcoming. By allowing selective incorporation of microenvironmental complexity, these platforms afford unique access to tumor-associated signaling and transport dynamics. This review will focus on engineering approaches to study drug delivery as a function of tumor-associated changes of the vasculature and extracellular matrix (ECM). First, we review current biological understanding of these components and discuss their impact on transport processes. Then, we evaluate existing microfluidic, tissue engineering, and materials science strategies to recapitulate vascular and ECM characteristics of tumors, and finish by outlining challenges and future directions of the field that may ultimately improve anti-cancer therapies.

Indexed as

AnimalsAntineoplastic AgentsBiological TransportDrug Delivery SystemsHumansNeoplasmsNeovascularization, PathologicTissue EngineeringAntineoplastic AgentsDrug transport in cancerEngineering models of tumorTumor angiogenesisTumor desmoplasiaTumor microenvironment

Identifiers

PMID24309015
PMCPMC4019703
OpenAlexW1989294445

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.