Evidence map›Paper›PMID 19190790›Full record

ArticleLab on a chip2009

A multipurpose microfluidic device designed to mimic microenvironment gradients and develop targeted cancer therapeutics.

Colin L Walsh, Brett M Babin, Rachel W Kasinskas, Jean A Foster, Marissa J McGarry, Neil S Forbes

Open access · greenAbstract read
In one paragraph

Article in Lab on a chip, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.7field-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

53 citing papers in PubMed, 124 citations in OpenAlex.

  1. Article
  2. Advanced Microfluidics for Single Cell-Based Cancer Research.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Progress and application of lung-on-a-chip for lung cancer.Frontiers in bioengineering and biotechnology · 2024
    Review
  7. Review
  8. Article
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  11. Article
  12. Review
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  14. Article
  15. Article
  16. Biosensing in Smart Engineered Probiotics.Biotechnology journal · 2020
    Review
  17. Article
  18. Article
  19. Article
  20. 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.

Colin L WalshDepartment of Chemical Engineering, University of Massachusetts, 159 Goessmann Laboratory, 686 North Pleasant Street. Amherst, MA 01003-9303, USA.
Brett M Babin
Rachel W Kasinskas
Jean A Foster
Marissa J McGarry
Neil S Forbes
University of Massachusetts Amherst · US

Funding

Engineering Salmonella to be a targeted intratumoral anti-cancer therapeuticR01CA120825 · NCI · UNIVERSITY OF MASSACHUSETTS AMHERST · PI FORBES, NEIL S. · 2008 to 2011
$1.2M
Microelectrode oxygenation control of tumor necrosisR21CA112335 · NCI · UNIVERSITY OF MASSACHUSETTS AMHERST · PI FORBES, NEIL S · 2005 to 2006
$332k
NCI NIH HHS 1R01CA120825-01A1NCI NIH HHS 1R21CA112335-01ANCI NIH HHS R01 CA120825NCI NIH HHS R21 CA112335
6 · The paper itself

Abstract

The heterogeneity of cellular microenvironments in tumors severely limits the efficacy of most cancer therapies. We have designed a microfluidic device that mimics the microenvironment gradients present in tumors that will enable the development of more effective cancer therapies. Tumor cell masses were formed within micron-scale chambers exposed to medium perfusion on one side to create linear nutrient gradients. The optical accessibility of the PDMS and glass device enables quantitative transmitted and fluorescence microscopy of all regions of the cell masses. Time-lapse microscopy was used to measure the growth rate and show that the device can be used for long-term efficacy studies. Fluorescence microscopy was used to demonstrate that the cell mass contained viable, apoptotic, and acidic regions similar to in vivo tumors. The diffusion coefficient of doxorubicin was accurately measured, and the accumulation of therapeutic bacteria was quantified. The device is simple to construct, and it can easily be reproduced to create an array of in vitro tumors. Because microenvironment gradients and penetration play critical roles controlling drug efficacy, we believe that this microfluidic device will be vital for understanding the behavior of common cancer drugs in solid tumors and designing novel intratumorally targeted therapeutics.

Indexed as

Antineoplastic AgentsBacteriaCell Culture TechniquesCell Growth ProcessesCell Line, TumorDiffusionDoxorubicinDrug Screening Assays, AntitumorEquipment DesignHumansMicrofluidic Analytical TechniquesAntineoplastic AgentsDoxorubicin

Identifiers

PMID19190790
PMCPMC2855303
OpenAlexW2168090230

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.