Evidence map›Paper›PMID 30428372›Full record

ArticleiScience2018

Bioprinted 3D Primary Human Intestinal Tissues Model Aspects of Native Physiology and ADME/Tox Functions.

Lauran R Madden, Theresa V Nguyen, Salvador Garcia-Mojica, Vishal Shah, Alex V Le, Andrea Peier, Richard Visconti, Eric M Parker, Sharon C Presnell, Deborah G Nguyen and 1 more

Abstract read
In one paragraph

Article in iScience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing 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

69 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 3D Bioprinting Strategies in Autoimmune Disease Models.International journal of molecular sciences · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Extrusion bioprinting: meeting the promise of human tissue biofabrication?Progress in biomedical engineering (Bristol, England) · 2025
    Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Rising role of 3D-printing in delivery of therapeutics for infectious disease.Journal of controlled release : official journal of the Controlled Release Society · 2024
    Review
  18. Article
  19. Recent Advances in Cell-Based In Vitro Models to Recreate Human Intestinal Inflammation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Review
  20. Article

9 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.

Lauran R MaddenOrganovo, Inc., San Diego, CA 92121, USA.
Theresa V NguyenDepartment of Pharmacokinetics, Merck & Co., Inc., Rahway, NJ 07065, USA.
Salvador Garcia-MojicaOrganovo, Inc., San Diego, CA 92121, USA.
Vishal ShahOrganovo, Inc., San Diego, CA 92121, USA.
Alex V LeOrganovo, Inc., San Diego, CA 92121, USA.
Andrea PeierDepartment of Pharmacology, Merck & Co., Inc., Kenilworth, NJ 07033, USA.
Richard ViscontiDepartment of Pharmacology, Merck & Co., Inc., Kenilworth, NJ 07033, USA.
Eric M ParkerDepartment of Pharmacology, Merck & Co., Inc., Kenilworth, NJ 07033, USA.
Sharon C PresnellOrganovo, Inc., San Diego, CA 92121, USA.
Deborah G NguyenOrganovo, Inc., San Diego, CA 92121, USA.
Kelsey N RettingOrganovo, Inc., San Diego, CA 92121, USA. Electronic address: kretting@organovo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human intestinal mucosa is a critical site for absorption, distribution, metabolism, and excretion (ADME)/Tox studies in drug development and is difficult to recapitulate in vitro. Using bioprinting, we generated three-dimensional (3D) intestinal tissue composed of human primary intestinal epithelial cells and myofibroblasts with architecture and function to model the native intestine. The 3D intestinal tissue demonstrates a polarized epithelium with tight junctions and specialized epithelial cell types and expresses functional and inducible CYP450 enzymes. The 3D intestinal tissues develop physiological barrier function, distinguish between high- and low-permeability compounds, and have functional P-gp and BCRP transporters. Biochemical and histological characterization demonstrate that 3D intestinal tissues can generate an injury response to compound-induced toxicity and inflammation. This model is compatible with existing preclinical assays and may be implemented as an additional bridge to clinical trials by enhancing safety and efficacy prediction in drug development.

Indexed as

BioengineeringIn Vitro Toxicology Including 3D CultureTissue Engineering

Identifiers

PMID30428372
PMCPMC6135981

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.