Evidence map›Paper›PMID 42237021›Full record

ReviewBritish journal of cancer2026

Next-generation models for lymphoid malignancies: the rise of 3D culture systems in translational hematology.

Narimène Houmera, Laurent Genestier, Sarah Huet

Abstract readReview
In one paragraph

Review in British journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Narimène HoumeraTeam Lymphoma Immuno-Biology, Centre International de Recherche en Infectiologie, Lyon, France.
Laurent GenestierTeam Lymphoma Immuno-Biology, Centre International de Recherche en Infectiologie, Lyon, France.
Sarah HuetTeam Lymphoma Immuno-Biology, Centre International de Recherche en Infectiologie, Lyon, France. sarah.huet@chu-lyon.fr.ORCID http://orcid.org/0000-0002-3408-2783

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Traditional models used to study lymphoid malignancies, such as 2D cell cultures and murine systems, have significantly advanced our understanding of tumour biology and drug development. However, their limited capacity to recapitulate the tumour microenvironment and 3D anatomical structure restricts their translational relevance. In response to these challenges, three-dimensional (3D) culture systems have recently emerged as promising platforms to more accurately replicate the architecture and biological complexity of lymphoid tissues. A variety of 3D models have been developed, ranging from simple spheroids to advanced organ-on-chip technologies that allow for continuous perfusion and precise modulation of microenvironmental parameters. Current optimisation efforts aim to enhance these systems' ability to sustain lymphoma cell viability and mimic key in vivo features such as stromal integration, spatial organisation, and biomechanical cues. This review provides an overview of the current 3D models used to investigate mature lymphoid malignancies, with a particular focus on chronic lymphocytic leukaemia and lymphomas. We discuss their relevance, strengths, and limitations, especially in the context of therapeutic screening and the advancement of personalised treatment approaches.

Indexed as

Cell Culture Techniques, Three DimensionalHematologyLeukemia, Lymphocytic, Chronic, B-CellLymphomaAnimalsHumansMicrophysiological SystemsSpheroids, CellularTranslational Research, BiomedicalTumor Microenvironment

Identifiers

PMID42237021
PMCPMC13372818

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Registered trials

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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.