Evidence map›Paper›PMID 42764940›Full record

ReviewActa pharmaceutica Sinica. B2026

Emerging organoids and organoids-on-chip platforms for translational development of antibody‒drug conjugates and next-generation bioconjugates.

Zhuoliang Hu, Yuheng Liao, Mengxian Niu, Zhanghong Kong, Hugo Vankelecom, Jianjun Cheng, Michela Deleidi, Chenzhong Li, Zhengjin Jiang, Sumin Bian and 1 more

Abstract readReview
In one paragraph

Review in Acta pharmaceutica Sinica. B, 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

11 authors.

Zhuoliang HuState Key Laboratory of Bioactive Molecules and Druggability Assessment/Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs/Institute of Pharmaceutical Analysis, College of Pharmacy, Jinan University, Guangzhou 510632, China.
Yuheng LiaoState Key Laboratory of Bioactive Molecules and Druggability Assessment/Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs/Institute of Pharmaceutical Analysis, College of Pharmacy, Jinan University, Guangzhou 510632, China.
Mengxian NiuState Key Laboratory of Bioactive Molecules and Druggability Assessment/Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs/Institute of Pharmaceutical Analysis, College of Pharmacy, Jinan University, Guangzhou 510632, China.
Zhanghong KongState Key Laboratory of Bioactive Molecules and Druggability Assessment/Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs/Institute of Pharmaceutical Analysis, College of Pharmacy, Jinan University, Guangzhou 510632, China.
Hugo VankelecomLaboratory of Tissue Plasticity in Health and Disease, Cluster of Stem Cell and Developmental Biology, Department of Development and Regeneration, KU Leuven, Leuven 3000, Belgium.
Jianjun ChengSchool of Engineering, Westlake University, Hangzhou 310024, China.
Michela DeleidiImagine Institut, INSERM U1163, Paris Cite University, Paris 75015, France.
Chenzhong LiDepartment of Biomedical Engineering, School of Medicine, The Chinese University of Hong Kong (Shenzhen), Shenzhen 518172, China.
Zhengjin JiangState Key Laboratory of Bioactive Molecules and Druggability Assessment/Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs/Institute of Pharmaceutical Analysis, College of Pharmacy, Jinan University, Guangzhou 510632, China.
Sumin BianSchool of Engineering, Westlake University, Hangzhou 310024, China.
Qiqin WangState Key Laboratory of Bioactive Molecules and Druggability Assessment/Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs/Institute of Pharmaceutical Analysis, College of Pharmacy, Jinan University, Guangzhou 510632, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The rapid evolution of antibody‒drug conjugates (ADCs) and emerging X-drug conjugates (XDCs) has revolutionized targeted cancer therapy, yet their clinical translation is severely bottlenecked by the lack of human-relevant preclinical models. To bridge this translational gap, patient-derived organoids and organoids-on-chip (OoC) platforms recapitulate key features of human tumor biology, offering powerful tools for investigating cancer heterogeneity and improving the predictive evaluation of bioconjugated therapeutics. In this review, we systematically summarize the current landscape and challenges of ADCs and XDCs development across existing preclinical models, critically discuss the concepts, biological principles and application potential of organoid- and OoC-based systems, and highlight recent global policy developments and collaborative initiatives shaping their translational implementation. Finally, we highlight key challenges and future perspectives for leveraging organoids and OoCs in the druggability assessment, optimization, and translational development of ADCs and XDCs.

Indexed as

Antibody‒drug conjugatesDruggability assessment and drug screeningOrganoidsOrganoids-on-chipTargeted therapiesX-drug conjugates

Identifiers

PMID42764940
PMCPMC13589940

What Socratic holds

Textmetadata
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.