Evidence map›Paper›PMID 40266756›Full record

ArticleMolecular biology of the cell2025

M phase-specific generation of supernumerary centrioles in cancer cells.

Byungho Shin, Myungse Kim, Yejoo Lee, Kunsoo Rhee

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2025. 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

4 authors.

Byungho ShinDepartment of Biological Sciences, Seoul National University, Seoul, South Korea 08826.
Myungse KimDepartment of Biological Sciences, Seoul National University, Seoul, South Korea 08826.
Yejoo LeeDepartment of Biological Sciences, Seoul National University, Seoul, South Korea 08826.
Kunsoo RheeDepartment of Biological Sciences, Seoul National University, Seoul, South Korea 08826.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many cancer cells maintain supernumerary centrioles, despite the potential risks associated with catastrophic outcomes during mitosis. In this study, we searched for cancer cell lines in which supernumerary centrioles are generated during the M phase and identified a few cell lines among the dozen examined. PLK4 activity is also required for M phase-specific generation of supernumerary centrioles. We observed that mitotic centrioles prematurely separate in many cancer cells when levels of pericentriolar material (PCM) proteins, such as PCNT and CEP215, are low. Furthermore, the presence of supernumerary centrioles was correlated with reduced mitotic PCM levels. Notably, overexpression of PCNT led to a reduction in supernumerary centrioles in MDA-MB-157 cells. These findings suggest that diminution of mitotic PCM may be a cause of M phase-specific generation of supernumerary centrioles in selected cancer cells.

Indexed as

CentriolesNeoplasmsCell Cycle ProteinsCell Line, TumorHumansMitosisProtein Serine-Threonine KinasesCell Cycle ProteinsPLK4 protein, humanProtein Serine-Threonine Kinases

Identifiers

PMID40266756
PMCPMC12206510

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.