Evidence map›Paper›PMID 39135915›Full record

ArticleMedComm2024

Ubiquitin-specific protease 22 controls melanoma metastasis and vulnerability to ferroptosis through targeting SIRT1/PTEN/PI3K signaling.

Huiyan Sun, Yu Meng, Lei Yao, Songtao Du, Yayun Li, Qian Zhou, Yihuang Liu, Yating Dian, Yuming Sun, Xiaomin Wang and 4 more

Abstract read
In one paragraph

Article in MedComm, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. PTEN enhances the radiosensitivity of melanoma by inhibiting DNA-PKcs.Frontiers in cell and developmental biology · 2025
    Article
  10. Review
  11. Potential role of SIRT1 in cell ferroptosis.Frontiers in cell and developmental biology · 2025
    Review
  12. Article
  13. Review
  14. Review
  15. 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

14 authors.

Huiyan SunDepartment of Dermatology Xiangya Hospital Central South University Changsha China.
Yu MengDepartment of Dermatology Xiangya Hospital Central South University Changsha China.
Lei YaoDepartment of Liver Surgery Xiangya Hospital Central South University Changsha China.
Songtao DuDepartment of Colorectal Surgical Oncology The Tumor Hospital of Harbin Medical University Harbin China.
Yayun LiDepartment of Dermatology The Third Xiangya Hospital Central South University Changsha China.
Qian ZhouDepartment of Dermatology Xiangya Hospital Central South University Changsha China.
Yihuang LiuDepartment of Dermatology Xiangya Hospital Central South University Changsha China.
Yating DianDepartment of Dermatology Xiangya Hospital Central South University Changsha China.
Yuming SunDepartment of Plastic and Cosmetic Surgery Xiangya Hospital Central South University Changsha China.
Xiaomin WangDepartment of Breast Surgery Xiangya Hospital Central South University Changsha China.
Xiao-Wei LiangDepartment of Dermatology Xiangya Hospital Central South University Changsha China.
Guangtong DengDepartment of Dermatology Xiangya Hospital Central South University Changsha China.ORCID https://orcid.org/0000-0002-4424-9727
Xiang ChenDepartment of Dermatology Xiangya Hospital Central South University Changsha China.
Furong ZengDepartment of Oncology Xiangya Hospital Central South University Changsha China.ORCID https://orcid.org/0000-0001-6621-8131

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastasis is a major contributing factor that affects the prognosis of melanoma patients. Nevertheless, the underlying molecular mechanisms involved in melanoma metastasis are not yet entirely understood. Here, we identified ubiquitin-specific protease 22 (USP22) as a pro-oncogenic protein in melanoma through screening the survival profiles of 52 ubiquitin-specific proteases (USPs). USP22 demonstrates a strong association with poor clinical outcomes and is significantly overexpressed in melanoma. Ablation of USP22 expression remarkably attenuates melanoma migration, invasion, and epithelial-mesenchymal transition in vitro and suppresses melanoma metastasis in vivo. Mechanistically, USP22 controls melanoma metastasis through the SIRT1/PTEN/PI3K pathway. In addition, we conducted an United States Food and Drug Administration-approved drug library screening and identified topotecan as a clinically applicable USP22-targeting molecule by promoting proteasomal degradation of USP22. Finally, we found that both pharmacological and genetic silence of USP22 sensitize RSL3-induced ferroptosis through suppressing the PI3K/Akt/mTOR pathway and its downstream SCD, and ferroptosis inhibitor could partly rescued the decreased lung metastasis by topotecan in vivo. Overall, our findings reveal a prometastatic role of USP22 and identify topotecan as a potent USP22-targeting drug to limit melanoma metastasis.

Indexed as

ferroptosismelanomametastasistopotecanUSP22

Identifiers

PMID39135915
PMCPMC11318338

What OpenQuestion holds

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Registered trials

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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.