Evidence map›Paper›PMID 35310996›Full record

ReviewFrontiers in cardiovascular medicine2022

3D Tissue-Engineered Vascular Drug Screening Platforms: Promise and Considerations.

Isra Marei, Tala Abu Samaan, Maryam Ali Al-Quradaghi, Asmaa A Farah, Shamin Hayat Mahmud, Hong Ding, Chris R Triggle

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cardiovascular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.3field-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

20 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Engineering in vitro vascular microsystems.Microsystems & nanoengineering · 2025
    Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Targeted Cancer Therapy-on-A-Chip.Advanced healthcare materials · 2024
    Review
  13. Plant Cellulose as a Substrate for 3D Neural Stem Cell Culture.Bioengineering (Basel, Switzerland) · 2023
    Article
  14. Review
  15. Review
  16. Article
  17. Cancer 3D Models for Metallodrug Preclinical Testing.International journal of molecular sciences · 2023
    Review
  18. Article
  19. Next-Generation Microfluidics for Biomedical Research and Healthcare Applications.Biomedical engineering and computational biology · 2023
    Review
  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

7 authors at 1 institution in 2 countries.

Isra MareiDepartment of Pharmacology, Weill Cornell Medicine-Qatar, Doha, Qatar.
Tala Abu SamaanDepartment of Pharmacology, Weill Cornell Medicine-Qatar, Doha, Qatar.
Maryam Ali Al-QuradaghiDepartment of Pharmacology, Weill Cornell Medicine-Qatar, Doha, Qatar.
Asmaa A FarahDepartment of Pharmacology, Weill Cornell Medicine-Qatar, Doha, Qatar.
Shamin Hayat MahmudDepartment of Pharmacology, Weill Cornell Medicine-Qatar, Doha, Qatar.
Hong DingDepartment of Pharmacology, Weill Cornell Medicine-Qatar, Doha, Qatar.
Chris R TriggleDepartment of Pharmacology, Weill Cornell Medicine-Qatar, Doha, Qatar.
Weill Cornell Medical College in Qatar · QA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the efforts devoted to drug discovery and development, the number of new drug approvals have been decreasing. Specifically, cardiovascular developments have been showing amongst the lowest levels of approvals. In addition, concerns over the adverse effects of drugs to the cardiovascular system have been increasing and resulting in failure at the preclinical level as well as withdrawal of drugs post-marketing. Besides factors such as the increased cost of clinical trials and increases in the requirements and the complexity of the regulatory processes, there is also a gap between the currently existing pre-clinical screening methods and the clinical studies in humans. This gap is mainly caused by the lack of complexity in the currently used 2D cell culture-based screening systems, which do not accurately reflect human physiological conditions. Cell-based drug screening is widely accepted and extensively used and can provide an initial indication of the drugs' therapeutic efficacy and potential cytotoxicity. However,

Indexed as

3D bioprinting3D drug screeningbioreactorspersonalizationscaffoldsself-organization and self-assemblystem cellstissue engineered blood vessels

Identifiers

PMID35310996
PMCPMC8931492
OpenAlexW4214861754

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.