Evidence map›Paper›PMID 37682709›Full record

ArticleCell reports2023

PUF60 promotes cell cycle and lung cancer progression by regulating alternative splicing of CDC25C.

Nan Xu, Yunpeng Ren, Yufang Bao, Xianfeng Shen, Jiahui Kang, Ning Wang, Zixian Wang, Xinlu Han, Zhen Li, Ji Zuo and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
6.0field-weighted citation impact, top 3% of its field
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

36 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. RNA splicing in health and disease.Molecular biomedicine · 2026
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  10. International journal of molecular sciences · 2026
    Review
  11. Review
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  14. Joint analysis ofNAR genomics and bioinformatics · 2025
    Article
  15. Article
  16. Vitamin BResearch square · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. 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

16 authors at 5 institutions in 2 countries.

Nan XuDepartment of Cellular and Genetic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.
Yunpeng RenDepartment of Cellular and Genetic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.
Yufang BaoDepartment of Cellular and Genetic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.
Xianfeng ShenDepartment of Cellular and Genetic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.
Jiahui KangInstitute of Reproductive Medicine, Medical School, Nantong University, Qixiu Road 19, Nantong 226001, China.
Ning WangShanghai Institute of Nutrition and Health, Chinese Academy of Sciences, Shanghai 200031, China.
Zixian WangMOE Key Laboratory of Metabolism and Molecular Medicine & Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, and Fudan University Shanghai Cancer Center, Shanghai Medical College of Fudan University, Shanghai 200032, China.
Xinlu HanDepartment of Cellular and Genetic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.
Zhen LiDepartment of Cellular and Genetic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.
Ji ZuoDepartment of Cellular and Genetic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.
Gong-Hong WeiMOE Key Laboratory of Metabolism and Molecular Medicine & Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, and Fudan University Shanghai Cancer Center, Shanghai Medical College of Fudan University, Shanghai 200032, China.
Zefeng WangShanghai Institute of Nutrition and Health, Chinese Academy of Sciences, Shanghai 200031, China.
Wei-Xing ZongDepartment of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers-The State University of New Jersey, Piscataway, NJ 08854, USA.
Wen LiuDepartment of Cellular and Genetic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.
Gangcai XieInstitute of Reproductive Medicine, Medical School, Nantong University, Qixiu Road 19, Nantong 226001, China. Electronic address: gangcai@ntu.edu.cn.
Yongbo WangDepartment of Cellular and Genetic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China; Minhang Hospital & Institutes of Biomedical Sciences, Fudan University, Shanghai 200032, China; Shanghai Key Laboratory of Medical Imaging Computing and Computer Assisted Intervention, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China. Electronic address: wangyongbo@fudan.edu.cn.
Fudan University · CNShanghai Medical College of Fudan University · CNNantong University · CNRutgers, The State University of New Jersey · USShanghai Institute of Nutrition and Health · CN

Funding

Protein and redox homeostasis in cancer development and therapyR01CA129536 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI ZONG, WEI-XING · 2008 to 2022
$4.8M
NCI NIH HHS R01 CA129536
6 · The paper itself

Abstract

Alternative splicing (AS) has been implicated in cell cycle regulation and cancer, but the underlying mechanisms are poorly understood. The poly(U)-binding splicing factor 60 (PUF60) is essential for embryonic development and is overexpressed in multiple types of cancer. Here, we report that PUF60 promotes mitotic cell cycle and lung cancer progression by controlling AS of the cell division cycle 25C (CDC25C). Systematic analysis of splicing factors deregulated in lung adenocarcinoma (LUAD) identifies that elevated copy number and expression of PUF60 correlate with poor prognosis. PUF60 depletion inhibits LUAD cell-cycle G2/M transition, cell proliferation, and tumor development. Mechanistically, PUF60 knockdown leads to exon skipping enriched in mitotic cell cycle genes, including CDC25C. Exon 3 skipping in the full-length CDC25C results in nonsense-mediated mRNA decay and a decrease of CDC25C protein, thereby inhibiting cell proliferation. This study establishes PUF60 as a cell cycle regulator and an oncogenic splicing factor in lung cancer.

Indexed as

Adenocarcinoma of LungLung NeoplasmsAlternative Splicingcdc25 PhosphatasesCell CycleCell DivisionCell Line, TumorHumansRepressor ProteinsRNA Splicing FactorsCDC25C protein, humancdc25 Phosphatasespoly-U binding splicing factor 60KDaRepressor ProteinsRNA Splicing Factorsalternative splicingCDC25Ccell cycleCP: Cancerlung cancerPUF60

Identifiers

PMID37682709
PMCPMC13034450
OpenAlexW4386541215

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.