Evidence map›Paper›PMID 41732277›Full record

ArticleiScience2026

Contrastive learning of dynamic processing body formation reveals undefined mechanisms of approved compounds.

Dexin Shen, Qionghua Zhu, Xiquan Pang, Dongzhen Pan, Maria Camila Copo Amador, Mengyang Zhang, Yanping Li, Zhiyuan Sun, Zemin Cao, Xian Yang and 3 more

Abstract read
In one paragraph

Article in iScience, 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

13 authors.

Dexin ShenInstitute of Biopharmaceutical and Health Engineering, Tsinghua Shenzhen International Graduate School, Shenzhen 518055, China.
Qionghua ZhuShenzhen Key Laboratory of Gene Regulation and Systems Biology, School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055, China.
Xiquan PangInstitute of Biopharmaceutical and Health Engineering, Tsinghua Shenzhen International Graduate School, Shenzhen 518055, China.
Dongzhen PanDepartment of Systems Biology, School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055, China.
Maria Camila Copo AmadorInstitute of Biopharmaceutical and Health Engineering, Tsinghua Shenzhen International Graduate School, Shenzhen 518055, China.
Mengyang ZhangDepartment of Systems Biology, School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055, China.
Yanping LiDepartment of Systems Biology, School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055, China.
Zhiyuan SunDepartment of Systems Biology, School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055, China.
Zemin CaoDepartment of Systems Biology, School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055, China.
Xian YangInstitute of Biopharmaceutical and Health Engineering, Tsinghua Shenzhen International Graduate School, Shenzhen 518055, China.
Liang FangShenzhen Key Laboratory of Gene Regulation and Systems Biology, School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055, China.
Wei ChenShenzhen Key Laboratory of Gene Regulation and Systems Biology, School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055, China.
Tatsuhisa TsuboiInstitute of Biopharmaceutical and Health Engineering, Tsinghua Shenzhen International Graduate School, Shenzhen 518055, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Membraneless organelles (MLOs) are liquid-like compartments that organize cellular functions through liquid-liquid phase separation of proteins and RNA. Their regulation is crucial for RNA metabolism, stress response, and signaling, yet leveraging their full spatial and quantitative diversity for phenotypic screening remains challenging. Here, we present processing body (PB)-scope, an unsupervised deep-learning framework for imaging-based screening of PBs, a representative MLO. The model was trained on >400,000 single-cell confocal images from a colon cancer cell line treated with 280 compounds. PB-scope enabled precise drug classification based on multiple PB features, including number, size, and spatial distribution. This approach uncovered phenotypic patterns that were previously obscured by the subtle and dynamic nature of PBs and highlighted a set of compounds that converge on Janus kinase (JAK) signaling as a regulator of PB dynamics. PB-scope is readily extensible to other MLOs, offering broad applicability in this emerging field of cell biology.

Indexed as

BiochemistryBiological sciencesCell biologyComputational ScienceDrug ScreeningImage analysisNatural sciences

Identifiers

PMID41732277
PMCPMC12925565

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.