Evidence map›Paper›PMID 35930221›Full record

ReviewDrug delivery and translational research2023

Modelling acute myeloid leukemia (AML): What's new? A transition from the classical to the modern.

Annachiara Dozzo, Aoife Galvin, Jae-Won Shin, Santo Scalia, Caitriona M O'Driscoll, Katie B Ryan

Abstract readReview
In one paragraph

Review in Drug delivery and translational research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
–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

25 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  16. Investigation methylation status of tumor suppressor geneMolecular biology research communications · 2025
    Article
  17. Review
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  20. Roles ofClinical Medicine Insights. Oncology · 2024
    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

6 authors.

Annachiara DozzoSchool of Pharmacy, University College Cork, Cork, Ireland.ORCID 0000-0003-1352-3305
Aoife GalvinSchool of Pharmacy, University College Cork, Cork, Ireland.
Jae-Won ShinDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago College of Medicine, 909 S. Wolcott Ave, Chicago, IL, 5091 COMRB, USA.ORCID 0000-0003-4823-6373
Santo ScaliaUniversità degli Studi di Ferrara, Via Luigi Borsari 46, 44121, Ferrara, Italy.
Caitriona M O'DriscollSchool of Pharmacy, University College Cork, Cork, Ireland.ORCID 0000-0002-6915-6201
Katie B RyanSchool of Pharmacy, University College Cork, Cork, Ireland. Katie.ryan@ucc.ie.ORCID 0000-0002-6236-2977

Funding

Encapsulation of mesenchymal stromal cells in engineered microgels for resolution of lung fibrosisR01HL141255 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SHIN, JAE-WON · 2019 to 2023
$2.0M
NHLBI NIH HHS R01 HL141255
6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a heterogeneous malignancy affecting myeloid cells in the bone marrow (BM) but can spread giving rise to impaired hematopoiesis. AML incidence increases with age and is associated with poor prognostic outcomes. There has been a disconnect between the success of novel drug compounds observed in preclinical studies of hematological malignancy and less than exceptional therapeutic responses in clinical trials. This review aims to provide a state-of-the-art overview on the different preclinical models of AML available to expand insights into disease pathology and as preclinical screening tools. Deciphering the complex physiological and pathological processes and developing predictive preclinical models are key to understanding disease progression and fundamental in the development and testing of new effective drug treatments. Standard scaffold-free suspension models fail to recapitulate the complex environment where AML occurs. To this end, we review advances in scaffold/matrix-based 3D models and outline the most recent advances in on-chip technology. We also provide an overview of clinically relevant animal models and review the expanding use of patient-derived samples, which offer the prospect to create more "patient specific" screening tools either in the guise of 3D matrix models, microphysiological "organ-on-chip" tools or xenograft models and discuss representative examples.

Indexed as

Leukemia, Myeloid, AcuteAnimalsBone MarrowDisease Models, AnimalHumans3D modelAML, cancerBiomaterialsBone marrowMatrixOrgan-on-chipPreclinical modelsScaffoldXenograft

Identifiers

PMID35930221
PMCPMC10315355

What Socratic 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 Socratic graph.