Evidence map›Paper›PMID 23172153›Full record

ArticleIntegrative biology : quantitative biosciences from nano to macro2013

Screening therapeutic EMT blocking agents in a three-dimensional microenvironment.

Amir R Aref, Ruby Yun-Ju Huang, Weimiao Yu, Kian-Ngiap Chua, Wei Sun, Ting-Yuan Tu, Jing Bai, Wen-Jing Sim, Ioannis K Zervantonakis, Jean Paul Thiery and 1 more

Abstract read
In one paragraph

Article in Integrative biology : quantitative biosciences from nano to macro, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing 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

90 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. BIOPRINTING OF MICRODISSECTED TUMOR "CUBOIDS" IN HYDROGELS.bioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Targeted Cancer Therapy-on-A-Chip.Advanced healthcare materials · 2024
    Review
  10. Review
  11. Review
  12. Engineering Heterogeneous Tumor Models for Biomedical Applications.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  13. Reaching the Tumor: Mobility of Polymeric Micelles Inside anACS applied materials & interfaces · 2023
    Article
  14. Review
  15. Review
  16. Article
  17. The Applications and Challenges of the Development ofCellular and molecular bioengineering · 2023
    Review
  18. Review
  19. 3D cancer models: One step closer toFrontiers in immunology · 2023
    Review
  20. Article

30 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

11 authors.

Amir R ArefBioSystems and Micromechanics IRG, S16-07, SMART, Singapore 117543, Singapore.
Ruby Yun-Ju Huang
Weimiao Yu
Kian-Ngiap Chua
Wei Sun
Ting-Yuan Tu
Jing Bai
Wen-Jing Sim
Ioannis K Zervantonakis
Jean Paul Thiery
Roger D Kamm

Funding

Microfluidic 3D Assays for Metastatic CancerR33CA174550 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI KAMM, ROGER D · 2013 to 2015
$1.1M
NCI NIH HHS R33 CA174550
6 · The paper itself

Abstract

Epithelial-mesenchymal transition (EMT) plays a critical role in the early stages of dissemination of carcinoma leading to metastatic tumors, which are responsible for over 90% of all cancer-related deaths. Current therapeutic regimens, however, have been ineffective in the cure of metastatic cancer, thus an urgent need exists to revisit existing protocols and to improve the efficacy of newly developed therapeutics. Strategies based on preventing EMT could potentially contribute to improving the outcome of advanced stage cancers. To achieve this goal new assays are needed to identify targeted drugs capable of interfering with EMT or to revert the mesenchymal-like phenotype of carcinoma to an epithelial-like state. Current assays are limited to examining the dispersion of carcinoma cells in isolation in conventional 2-dimensional (2D) microwell systems, an approach that fails to account for the 3-dimensional (3D) environment of the tumor or the essential interactions that occur with other nearby cell types in the tumor microenvironment. Here we present a microfluidic system that integrates tumor cell spheroids in a 3D hydrogel scaffold, in close co-culture with an endothelial monolayer. Drug candidates inhibiting receptor activation or signal transduction pathways implicated in EMT have been tested using dispersion of A549 lung adenocarcinoma cell spheroids as a metric of effectiveness. We demonstrate significant differences in response to drugs between 2D and 3D, and between monoculture and co-culture.

Indexed as

Antineoplastic AgentsCell CommunicationCell Line, TumorDrug DiscoveryDrug Evaluation, PreclinicalEndothelial CellsEpithelial-Mesenchymal TransitionEquipment DesignEquipment Failure AnalysisHumansLung NeoplasmsMicrofluidic Analytical TechniquesTumor MicroenvironmentAntineoplastic Agents

Identifiers

PMID23172153
PMCPMC4039387

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.