Evidence map›Paper›PMID 34328185›Full record

ReviewEssays in biochemistry2021

3D bioprinting: novel approaches for engineering complex human tissue equivalents and drug testing.

Judith Hagenbuchner, Daniel Nothdurfter, Michael J Ausserlechner

Open access · hybridAbstract readReview
In one paragraph

Review in Essays in biochemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. AlternativeExpert reviews in molecular medicine · 2026
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Targeted Cancer Therapy-on-A-Chip.Advanced healthcare materials · 2024
    Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Generation of a Perfusable 3D Lung Cancer Model by Digital Light Processing.International journal of molecular sciences · 2023
    Article
  17. Review
  18. Article
  19. Article
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.

Judith HagenbuchnerDepartment of Pediatrics II, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0003-1396-3407
Daniel NothdurfterDepartment of Pediatrics I, Medical University of Innsbruck, Innsbruck, Austria.
Michael J AusserlechnerDepartment of Pediatrics I, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0002-1015-2302
Innsbruck Medical University · AT

Funding

Austrian Science Fund FWF I 3089
6 · The paper itself

Abstract

Conventional approaches in drug development involve testing on 2D-cultured mammalian cells, followed by experiments in rodents. Although this is the common strategy, it has significant drawbacks: in 2D cell culture with human cells, the cultivation at normoxic conditions on a plastic or glass surface is an artificial situation that significantly changes energy metabolism, shape and intracellular signaling, which in turn directly affects drug response. On the other hand, rodents as the most frequently used animal models have evolutionarily separated from primates about 100 million years ago, with significant differences in physiology, which frequently leads to results not reproducible in humans. As an alternative, spheroid technology and micro-organoids have evolved in the last decade to provide 3D context for cells similar to native tissue. However, organoids used for drug testing are usually just in the 50-100 micrometers range and thereby too small to mimic micro-environmental tissue conditions such as limited nutrient and oxygen availability. An attractive alternative offers 3D bioprinting as this allows fabrication of human tissue equivalents from scratch with hollow structures for perfusion and strict spatiotemporal control over the deposition of cells and extracellular matrix proteins. Thereby, tissue surrogates with defined geometry are fabricated that offer unique opportunities in exploring cellular cross-talk, mechanobiology and morphogenesis. These tissue-equivalents are also very attractive tools in drug testing, as bioprinting enables standardized production, parallelization, and application-tailored design of human tissue, of human disease models and patient-specific tissue avatars. This review, therefore, summarizes recent advances in 3D bioprinting technology and its application for drug screening.

Indexed as

BioprintingAnimalsCells, CulturedHumansMammalsPrinting, Three-DimensionalTissue EngineeringTissue Scaffoldsbioinkextrusion printingmicrojetreplacement of animal experimentstissue engineeringtissue on chip

Identifiers

PMID34328185
PMCPMC8365325
OpenAlexW3186560229

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.