Evidence map›Paper›PMID 42806000›Full record

ReviewActa pharmacologica Sinica2026

Dynamic centrosomes: functional diversity and remodeling across cell types.

Ning Ju, Hui-Jie Zhu, Jia-Rui Shi, Jin-Min Gao, Fei-Fei Qi

Abstract readReview
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In one paragraph

Review in Acta pharmacologica Sinica, 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

5 authors.

Ning Ju *Shandong Provincial Key Laboratory of Animal Resistance Biology, Collaborative Innovation Center of Cell Biology in Universities of Shandong, Institute of Biomedical Sciences, College of Life Sciences, Shandong Normal University, Ji-nan, 250014, China.
Hui-Jie Zhu *Shandong Provincial Key Laboratory of Animal Resistance Biology, Collaborative Innovation Center of Cell Biology in Universities of Shandong, Institute of Biomedical Sciences, College of Life Sciences, Shandong Normal University, Ji-nan, 250014, China.
Jia-Rui Shi *Shandong Provincial Key Laboratory of Animal Resistance Biology, Collaborative Innovation Center of Cell Biology in Universities of Shandong, Institute of Biomedical Sciences, College of Life Sciences, Shandong Normal University, Ji-nan, 250014, China.
Jin-Min GaoShandong Provincial Key Laboratory of Animal Resistance Biology, Collaborative Innovation Center of Cell Biology in Universities of Shandong, Institute of Biomedical Sciences, College of Life Sciences, Shandong Normal University, Ji-nan, 250014, China.
Fei-Fei QiShandong Provincial Key Laboratory of Animal Resistance Biology, Collaborative Innovation Center of Cell Biology in Universities of Shandong, Institute of Biomedical Sciences, College of Life Sciences, Shandong Normal University, Ji-nan, 250014, China. feifeiqi@sdnu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The centrosome is an evolutionarily conserved, microtubule-based organelle that has pronounced cell type-specific functions. In somatic cells, it serves as the primary microtubule-organizing center (MTOC), regulating chromosome segregation and contributing to asymmetric cell division and ciliogenesis. Although traditionally considered structurally stable, increasing evidence indicates that centrosomes can undergo extensive remodeling or even complete elimination in specialized cell types. Recent studies have begun to elucidate the molecular basis of these processes. For example, during oogenesis, CDK1-mediated phosphorylation of SAS-6 disrupts its phase separation, thus promoting cartwheel disassembly and centriole elimination. Building on these advances, this review summarizes the dynamic behaviors and fates of centrosomes across diverse cell types, with a particular focus on oogenesis, spermatogenesis, and neurodevelopment, and discusses the emerging molecular mechanisms that regulate centrosome remodeling. We further highlight the potential links between dysregulated centrosome dynamics and human diseases, including cancer, neurodevelopmental disorders, and infertility, and discuss centrosome regulators as potential therapeutic targets. A deeper understanding of centrosome dynamics is expected to provide new insights into both fundamental cell biology and the development of targeted interventions.

Indexed as

centriole eliminationcentrosome remodelingneurodevelopmentoogenesisspermatogenesistherapeutic targets

Identifiers

PMID42806000

What OpenQuestion holds

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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 OpenQuestion graph.