Evidence map›Paper›PMID 40202486›Full record

ArticleThe Journal of cell biology2025

Plasticity of mitotic cyclins in promoting the G2-M transition.

Adrijana Crncec, Ho Wai Lau, Lau Yan Ng, Hoi Tang Ma, Joyce P Y Mak, Hon Fung Choi, Tsz Kwan Yeung, Randy Yat Choi Poon

Abstract read
In one paragraph

Article in The Journal of cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Countervailing effects of cyclin isoforms A and B during mitosis.bioRxiv : the preprint server for biology · 2026
    Article
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

8 authors.

Adrijana Crncec *Division of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong.ORCID 0000-0003-2076-1707
Ho Wai Lau *Division of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong.ORCID 0000-0002-0735-144X
Lau Yan Ng *Division of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong.ORCID 0000-0002-9098-8352
Hoi Tang MaDepartment of Pathology, The University of Hong Kong, Pok Fu Lam, Hong Kong.ORCID 0000-0001-5876-0107
Joyce P Y MakDivision of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong.ORCID 0000-0002-1366-2084
Hon Fung ChoiDivision of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong.ORCID 0000-0002-5996-7107
Tsz Kwan YeungDivision of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong.ORCID 0000-0003-4101-4671
Randy Yat Choi PoonDivision of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong.ORCID 0000-0001-5571-6231

Funding

Hong Kong University of Science and TechnologyInnovation and Technology Commission ITCPD/17-9Research Grants Council 16100417
6 · The paper itself

Abstract

Cyclins and cyclin-dependent kinases (CDKs) orchestrate key events in the cell cycle. However, the uniqueness of individual mitotic cyclins has been a long-standing puzzle. By rapidly removing cyclins in G2 human cells, we found that deficiency of B-type cyclins attenuates mitotic onset and uncouples the G2-M kinase network from mitosis, resulting in sustained activation of PLK1 and cyclin A-CDK1. This culminates in mitotic slippage without completing nuclear envelope breakdown. Remarkably, elevating cyclin A several-fold above its endogenous level is adequate to restore mitosis, allowing cells to survive without B-type cyclins. In contrast, cyclin A is rate-limiting but not essential for G2-M due to compensation by endogenous cyclin B1-CDK2, a non-canonical pair. These findings challenge the traditional indispensable roles of different cyclins and highlight their plasticity. Due to the high malleability of the A- and B-type cyclins, cancer cells may be able to place different weights on different cyclins, while maintaining sufficient CDK activities for successful mitosis.

Indexed as

Cyclin ACyclinsG2 PhaseMitosisCDC2 Protein KinaseCell Cycle ProteinsCyclin BCyclin B1Cyclin-Dependent Kinase 2HeLa CellsHumansPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsCDC2 Protein KinaseCDK1 protein, humanCDK2 protein, humanCell Cycle ProteinsCyclin ACyclin BCyclin B1Cyclin-Dependent Kinase 2CyclinsPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene Proteins

Identifiers

PMID40202486
PMCPMC11980681

What OpenQuestion holds

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LicenceCC BY
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.