Evidence map›Paper›PMID 39030175›Full record

ArticleOncogenesis2024

USP32 facilitates non-small cell lung cancer progression via deubiquitinating BAG3 and activating RAF-MEK-ERK signaling pathway.

Shuang Li, Lina Yang, Xiaoyan Ding, Hongxiao Sun, Xiaolei Dong, Fanghao Yang, Mengjun Wang, Huhu Zhang, Ya Li, Bing Li and 1 more

Abstract read
In one paragraph

Article in Oncogenesis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Deubiquitination of Vangl by USP6 and USP32 Regulates Planar Cell Polarity Signaling.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. BAG3Frontiers in immunology · 2026
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Deubiquitylating Enzymes in Hepatocellular Carcinoma.International journal of biological sciences · 2025
    Review
  13. 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

11 authors.

Shuang Li *Department of Genetics and Cell Biology, School of Basic Medicine, Qingdao University, 266071, Qingdao, China.ORCID http://orcid.org/0009-0000-0568-7698
Lina Yang *Department of Genetics and Cell Biology, School of Basic Medicine, Qingdao University, 266071, Qingdao, China.
Xiaoyan DingDepartment of Genetics and Cell Biology, School of Basic Medicine, Qingdao University, 266071, Qingdao, China.
Hongxiao SunHeart Center, Women and Children's Hospital, Qingdao University, 6 Tongfu Road, 266034, Qingdao, China.
Xiaolei DongDepartment of Genetics and Cell Biology, School of Basic Medicine, Qingdao University, 266071, Qingdao, China.
Fanghao YangDepartment of Genetics and Cell Biology, School of Basic Medicine, Qingdao University, 266071, Qingdao, China.
Mengjun WangDepartment of Genetics and Cell Biology, School of Basic Medicine, Qingdao University, 266071, Qingdao, China.
Huhu ZhangDepartment of Genetics and Cell Biology, School of Basic Medicine, Qingdao University, 266071, Qingdao, China.
Ya LiDepartment of Genetics and Cell Biology, School of Basic Medicine, Qingdao University, 266071, Qingdao, China.
Bing LiDepartment of Genetics and Cell Biology, School of Basic Medicine, Qingdao University, 266071, Qingdao, China. libing_516@qdu.edu.cn.ORCID http://orcid.org/0000-0002-5545-9674
Chunyan LiuDepartment of Genetics and Cell Biology, School of Basic Medicine, Qingdao University, 266071, Qingdao, China. Liuchy@qdu.edu.cn.ORCID http://orcid.org/0000-0002-5893-8507

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The regulatory significance of ubiquitin-specific peptidase 32 (USP32) in tumor is significant, nevertheless, the biological roles and regulatory mechanisms of USP32 in non-small cell lung cancer (NSCLC) remain unclear. According to our research, USP32 was strongly expressed in NSCLC cell lines and tissues and was linked to a bad prognosis for NSCLC patients. Interference with USP32 resulted in a significant inhibition of NSCLC cell proliferation, migration potential, and EMT development; on the other hand, USP32 overexpression had the opposite effect. To further elucidate the mechanism of action of USP32 in NSCLC, we screened H1299 cells for interacting proteins and found that USP32 interacts with BAG3 (Bcl2-associated athanogene 3) and deubiquitinates and stabilizes BAG3 in a deubiquitinating activity-dependent manner. Functionally, restoration of BAG3 expression abrogated the antitumor effects of USP32 silencing. Furthermore, USP32 increased the phosphorylation level of the RAF/MEK/ERK signaling pathway in NSCLC cells by stabilizing BAG3. In summary, these findings imply that USP32 is critical to the development of NSCLC and could offer a theoretical framework for the clinical diagnosis and management of NSCLC patients in the future.

Identifiers

PMID39030175
PMCPMC11271578

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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.