Evidence map›Paper›PMID 42449704›Full record

ArticleCancers2026

MKRN2-Mediated Degradation of IGF2BP3 Suppresses MYC and Enhances CDK4/6 Inhibitor Sensitivity in Bladder Cancer.

Qi Pan, Qing Shi, Yubo Zhao, Tianxi Yu, Shiyu Bai, Haoran Zhu, Wei Zhang, Yaowei Li, Ziyi Liu, Haonan Li and 2 more

Abstract read
In one paragraph

Article in Cancers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Qi PanDepartment of Urology, Shanghai General Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200080, China.
Qing ShiNHC Key Laboratory of Molecular Probe and Targeted Theranostics, Harbin Medical University Cancer Hospital, Harbin Medical University, Harbin 150001, China.
Yubo ZhaoDepartment of Urology, Second Affiliate Hospital of Harbin Medical University, Harbin 150001, China.
Tianxi YuNHC Key Laboratory of Molecular Probe and Targeted Theranostics, Harbin Medical University Cancer Hospital, Harbin Medical University, Harbin 150001, China.
Shiyu BaiDepartment of Pharmacology, College of Pharmacy, Harbin Medical University, Harbin 150001, China.
Haoran ZhuNHC Key Laboratory of Molecular Probe and Targeted Theranostics, Harbin Medical University Cancer Hospital, Harbin Medical University, Harbin 150001, China.
Wei ZhangDepartment of Urology, Second Affiliate Hospital of Harbin Medical University, Harbin 150001, China.
Yaowei LiNHC Key Laboratory of Molecular Probe and Targeted Theranostics, Harbin Medical University Cancer Hospital, Harbin Medical University, Harbin 150001, China.
Ziyi LiuNHC Key Laboratory of Molecular Probe and Targeted Theranostics, Harbin Medical University Cancer Hospital, Harbin Medical University, Harbin 150001, China.
Haonan LiNHC Key Laboratory of Molecular Probe and Targeted Theranostics, Harbin Medical University Cancer Hospital, Harbin Medical University, Harbin 150001, China.
Ziqi WangNHC Key Laboratory of Molecular Probe and Targeted Theranostics, Harbin Medical University Cancer Hospital, Harbin Medical University, Harbin 150001, China.
Zhichao TongNHC Key Laboratory of Molecular Probe and Targeted Theranostics, Harbin Medical University Cancer Hospital, Harbin Medical University, Harbin 150001, China.

Funding

Excellent Youth Project of Heilongjiang Provincial Natural Science Foundation YQ2024H023Heilongjiang Province Postdoctoral Foundation LBH-Z22030National Natural Science Foundation of China 81902569National Natural Science Foundation of China 82572347National Natural Science Foundation of China 82573847The Harbin Medical University Cancer Hospital Haiyan Foundation JJZD2024-24The Nn10 project at the Affiliated Cancer Hospital of Harbin Medical University Nn102024-01
6 · The paper itself

Abstract

backgroundCDK4/6 inhibitors induce G1/S cell-cycle arrest in bladder cancer; however, adaptive resistance limits their therapeutic efficacy. The role of the m

methodsTranscriptomic profiling was performed in palbociclib-treated bladder cancer cell lines (T24, RT112, and UMUC-3) to identify m

resultsIGF2BP3 was identified as the only m

conclusionsThese findings establish the MKRN2-IGF2BP3-MYC axis as a critical regulator of CDK4/6 inhibitor sensitivity in bladder cancer. Targeting IGF2BP3 or enhancing MKRN2 activity may represent a promising strategy to overcome adaptive resistance and improve the therapeutic efficacy of CDK4/6 inhibitors.

Indexed as

bladder cancerCDK4/6 inhibitionIGF2BP3MKRN2MYCproliferation

Identifiers

PMID42449704
PMCPMC13359444

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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.