Evidence map›Paper›PMID 41368202›Full record

ReviewAnimal cells and systems2026

Sumoylation of cyclin and its therapeutic potential for cancer.

Hong-Yeoul Ryu, Mark Hochstrasser

Abstract readReview
In one paragraph

Review in Animal cells and systems, 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

2 authors.

Hong-Yeoul RyuKNU G-LAMP Project Group, KNU Institute of Basic Sciences, School of Life Sciences, BK21 FOUR KNU Creative BioResearch Group, College of Natural Sciences, Kyungpook National University, Daegu, 41566, South Korea.
Mark HochstrasserDepartment of Molecular Biophysics & Biochemistry, Yale University, New Haven, CT, 06520, USA.

Funding

Mechanisms of Cell Regulation and Manipulation by the Ubiquitin SystemR35GM136325 · NIGMS · YALE UNIVERSITY · PI Mark W Hochstrasser · 2020 to 2026
$6.5M
NIGMS NIH HHS R35 GM136325
6 · The paper itself

Abstract

The precision of the cell cycle is essential for organismal development, tissue homeostasis, and the prevention of malignancies. Cyclins and cyclin-dependent kinases (CDKs) play pivotal roles in regulating cell cycle progression. Recent studies have underscored the importance of post-translational modifications, particularly sumoylation, in modulating the functions of cyclins. Sumoylation profoundly influences the stability, localization, and activity of cyclins D and E, which are crucial for the G1/S transition and DNA replication. Dysregulation of these processes is a hallmark of various cancers, where aberrant sumoylation enhances the oncogenic potential of cyclins. This review examines how sumoylation governs cyclin dynamics, maintains cell division fidelity, and contributes to cancer progression. Moreover, advances in targeting the SUMO pathway offer new therapeutic opportunities for treating cyclin-related malignancies, positioning sumoylation-based strategies as promising tools in precision medicine. Gaining a deeper understanding of how sumoylation regulates cyclins may ultimately transform therapeutic approaches for cyclin-dependent diseases.

Indexed as

cancerCDKCyclin Dcyclin Esumoylation

Identifiers

PMID41368202
PMCPMC12683770

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.