Evidence map›Paper›PMID 41922471›Full record

ArticleCommunications biology2026

A compatible gravity-driven organoid perfusion (GDOP) platform for drug screening with sensitivity and toxicity process evaluation.

Shun Wang, Xiaoliang Zhang, Houshi Ma, Linlin Lu, Huabin Jiang, Yuqiao Bai, Xiaoran Chang, Jinxian Wang, Tianhang Yang, Gangyin Luo

Abstract read
In one paragraph

Article in Communications biology, 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

10 authors.

Shun WangSuzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, China.
Xiaoliang ZhangSuzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, China.
Houshi MaSuzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, China.
Linlin LuThe First Affiliated Hospital of Soochow University, Suzhou, China.
Huabin JiangCollege of Life Sciences, Shandong Normal University, Jinan, China.
Yuqiao BaiSchool of Biomedical Engineering (Suzhou), Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.ORCID http://orcid.org/0000-0001-6835-4516
Xiaoran ChangSuzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, China.
Jinxian WangSuzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, China. wangjx@sibet.ac.cn.ORCID http://orcid.org/0000-0003-3566-6905
Tianhang YangSuzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, China. yangth@sibet.ac.cn.
Gangyin LuoSuzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, China. luogy@sibet.ac.cn.

Funding

Natural Science Foundation of Shandong Province (Shandong Provincial Natural Science Foundation) ZR2023QE236
6 · The paper itself

Abstract

High-throughput experiments, unidirectional fluid replacement, real-time process monitoring, and simultaneous drug sensitivity and toxicity tests are hard to achieve on most existing tumor organoid chips. Here, we developed a gravity-driven organoid perfusion (GDOP) platform facilitating scalable throughput and supporting drug sensitivity and toxicity assessment on organoids. The unidirectional perfusion capability and optimized operational parameters of the GDOP chip were validated through fluid dynamics simulations. Using this platform, we successfully established uniform on-chip triple-negative breast cancer (TNBC) organoids, with endpoint detection results aligning closely with clinical diagnosis. Throughout the drug treatment process, we monitored and then analyzed the morphological and grayscale changes of the organoids. The sensitivity and toxicity tests revealed the optimal concentration range for the 3 chemotherapeutic drugs. In addition, on-chip brain organoids were established, which lays a feasible foundation for future drug toxicity tests of complex organoids. The GDOP platform, combined with its integrated evaluation method, provides a powerful and reliable approach for advancing organoid-based researches.

Indexed as

Antineoplastic AgentsHigh-Throughput Screening AssaysOrganoidsPerfusionAnimalsDrug Evaluation, PreclinicalDrug Screening Assays, AntitumorFemaleGravitationHumansMicrophysiological SystemsTriple Negative Breast NeoplasmsAntineoplastic Agents

Identifiers

PMID41922471
PMCPMC13212913

What OpenQuestion holds

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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.