Evidence map›Paper›PMID 34469054›Full record

ArticleJournal of cellular and molecular medicine2021

Pharmacological inhibition of USP7 suppresses growth and metastasis of melanoma cells in vitro and in vivo.

Minmin Xiang, Long Liang, Xinwei Kuang, Zuozhong Xie, Jing Liu, Shuang Zhao, Juan Su, Xiang Chen, Hong Liu

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
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

9 authors at 1 institution in 1 country.

Minmin XiangDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha, China.
Long LiangDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha, China.
Xinwei KuangDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha, China.
Zuozhong XieDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha, China.
Jing LiuMedical Genetics & School of Life Sciences, Central South University, Changsha, China.ORCID 0000-0002-9317-774X
Shuang ZhaoDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha, China.
Juan SuDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha, China.
Xiang ChenDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha, China.
Hong LiuDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0002-2083-0103
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanoma is a highly aggressive type of skin cancer. The development of diverse resistance mechanisms and severe adverse effects significantly limit the efficiency of current therapeutic approaches. Identification of the new therapeutic targets involved in the pathogenesis will benefit the development of novel therapeutic strategies. The deubiquitinase ubiquitin-specific protease-7, a potential target for cancer treatment, is deregulated in types of cancer, but its role in melanoma is still unclear. We investigated the role and the inhibitor P22077 of ubiquitin-specific protease-7 in melanoma treatment. We found that ubiquitin-specific protease-7 was overexpressed and correlated with poor prognosis in melanoma. Further, pharmacological inhibition of ubiquitin-specific protease-7 by P22077 can effectively inhibit proliferation, and induce cell cycle arrest and apoptosis via ROS accumulation-induced DNA damage in melanoma cells. Inhibition of ubiquitin-specific protease-7 by P22077 also inhibits melanoma tumour growth in vivo. Moreover, inhibition of ubiquitin-specific protease-7 prevented migration and invasion of melanoma cells in vitro and in vivo by decreasing the Wnt/β-catenin signalling pathway. Taken together, our study revealed that ubiquitin-specific protease-7 acted as an oncogene involved in melanoma cell proliferation and metastasis. Therefore, ubiquitin-specific protease-7 may serve as potential candidates for the treatment of melanoma.

Indexed as

AnimalsApoptosisCell Cycle CheckpointsCell Line, TumorCell MovementCell ProliferationCell SurvivalDisease Models, AnimalDNA DamageHumansImmunohistochemistryMelanomaMelanoma, ExperimentalMiceReactive Oxygen SpeciesThiophenes1-(5-((2,4-difluorophenyl)thio)-4-nitrothiophen-2-yl)ethanoneReactive Oxygen SpeciesThiophenesUbiquitin-Specific Peptidase 7USP7 protein, humanapoptosisinvasionmelanomaROSUSP7

Identifiers

PMID34469054
PMCPMC8500953
OpenAlexW3197813906

What OpenQuestion holds

Textmetadata
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.