Evidence map›Paper›PMID 25385716›Full record

ReviewJournal of laboratory automation2015

Biomimetic 3D Tissue Models for Advanced High-Throughput Drug Screening.

Ki-Hwan Nam, Alec S T Smith, Saifullah Lone, Sunghoon Kwon, Deok-Ho Kim

Abstract readReview
In one paragraph

Review in Journal of laboratory automation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing 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

67 citing papers in PubMed.

  1. Review
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  11. A closed-loop modular multiorgan-on-chips platform for self-sustaining and tightly controlled oxygenation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Review
  13. The Evolution of Technology-Driven In Vitro Models for Neurodegenerative Diseases.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  14. Article
  15. Contribution of the ELRs to the development of advancedFrontiers in bioengineering and biotechnology · 2024
    Review
  16. Progress in bioprinting technology for tissue regeneration.Journal of artificial organs : the official journal of the Japanese Society for Artificial Organs · 2023
    Review
  17. Review
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  19. Article
  20. Review

7 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

5 authors.

Ki-Hwan NamDepartment of Bioengineering, University of Washington, Seattle, WA, USA Department of Electrical and Computer Engineering, Seoul National University, Seoul, Republic of Korea Center for Analytical Instrumentation Development, The Korea Basic Science Institute, Deajeon, Republic of Korea.
Alec S T SmithDepartment of Bioengineering, University of Washington, Seattle, WA, USA.
Saifullah LoneDepartment of Electrical and Computer Engineering, Seoul National University, Seoul, Republic of Korea.
Sunghoon KwonDepartment of Electrical and Computer Engineering, Seoul National University, Seoul, Republic of Korea.
Deok-Ho KimDepartment of Bioengineering, University of Washington, Seattle, WA, USA Center for Cardiovascular Biology, University of Washington, Seattle, WA, USA Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA, USA deokho@uw.edu.

Funding

Nanopatterned 3D Vascularized Functional Muscle PatchR21AR064395 · NIAMS · UNIVERSITY OF WASHINGTON · PI KIM, DEOK-HO · 2014 to 2015
$421k
NIAMS NIH HHS R21 AR064395
6 · The paper itself

Abstract

Most current drug screening assays used to identify new drug candidates are 2D cell-based systems, even though such in vitro assays do not adequately re-create the in vivo complexity of 3D tissues. Inadequate representation of the human tissue environment during a preclinical test can result in inaccurate predictions of compound effects on overall tissue functionality. Screening for compound efficacy by focusing on a single pathway or protein target, coupled with difficulties in maintaining long-term 2D monolayers, can serve to exacerbate these issues when using such simplistic model systems for physiological drug screening applications. Numerous studies have shown that cell responses to drugs in 3D culture are improved from those in 2D, with respect to modeling in vivo tissue functionality, which highlights the advantages of using 3D-based models for preclinical drug screens. In this review, we discuss the development of microengineered 3D tissue models that accurately mimic the physiological properties of native tissue samples and highlight the advantages of using such 3D microtissue models over conventional cell-based assays for future drug screening applications. We also discuss biomimetic 3D environments, based on engineered tissues as potential preclinical models for the development of more predictive drug screening assays for specific disease models.

Indexed as

BiomimeticsTissue EngineeringAnimalsDrug Evaluation, PreclinicalHigh-Throughput Screening AssaysHumansNanotechnologyOrgan Culture Techniquesbiomimetic microenvironmentbio-nanotechnologyhigh-throughput drug screeningmicroengineered 3D tissue modelsorgan-on-chip

Identifiers

PMID25385716
PMCPMC4459652

What OpenQuestion holds

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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.