Evidence map›Paper›PMID 33846536›Full record

ArticleCell death and differentiation2021

USP24 promotes drug resistance during cancer therapy.

Shao-An Wang, Ming-Jer Young, Yi-Chang Wang, Shu-Hui Chen, Chia-Yu Liu, Yao-An Lo, Hung-Hsiang Jen, Kai-Cheng Hsu, Jan-Jong Hung

Open access · hybridAbstract read
In one paragraph

Article in Cell death and differentiation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

21 citing papers in PubMed, 28 citations in OpenAlex.

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

9 authors at 2 institutions in 1 country.

Shao-An Wang *Department of Biotechnology and Bioindustry Sciences, National Cheng Kung University, Tainan, Taiwan.ORCID http://orcid.org/0000-0002-5473-4195
Ming-Jer Young *Department of Biotechnology and Bioindustry Sciences, National Cheng Kung University, Tainan, Taiwan.ORCID http://orcid.org/0000-0003-2638-6813
Yi-Chang WangDepartment of Biotechnology and Bioindustry Sciences, National Cheng Kung University, Tainan, Taiwan.ORCID http://orcid.org/0000-0001-9346-5234
Shu-Hui ChenDepartment of Chemistry, College of Science, National Cheng Kung University, Tainan, Taiwan.
Chia-Yu LiuDepartment of Biotechnology and Bioindustry Sciences, National Cheng Kung University, Tainan, Taiwan.ORCID http://orcid.org/0000-0003-1823-190X
Yao-An LoDepartment of Biotechnology and Bioindustry Sciences, National Cheng Kung University, Tainan, Taiwan.ORCID http://orcid.org/0000-0003-1960-5846
Hung-Hsiang JenDepartment of Chemistry, College of Science, National Cheng Kung University, Tainan, Taiwan.ORCID http://orcid.org/0000-0002-6378-8961
Kai-Cheng HsuGraduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.ORCID http://orcid.org/0000-0002-9022-6673
Jan-Jong HungDepartment of Biotechnology and Bioindustry Sciences, National Cheng Kung University, Tainan, Taiwan. petehung@mail.ncku.edu.tw.ORCID http://orcid.org/0000-0001-5772-8877
National Cheng Kung University · TWTaipei Medical University · TW

Funding

Ministry of Science and Technology, Taiwan (Ministry of Science and Technology of Taiwan) 104-2923-B-038-002-MY3Ministry of Science and Technology, Taiwan (Ministry of Science and Technology of Taiwan) 106-2320-B-006-020-MY3Ministry of Science and Technology, Taiwan (Ministry of Science and Technology of Taiwan) 106-2320-B-006-065-MY3Ministry of Science and Technology, Taiwan (Ministry of Science and Technology of Taiwan) 109-2320-B-038 -011 -MY2Taipei Medical University (TMU) TMU108-AE1-B15
6 · The paper itself

Abstract

Drug resistance has remained an important issue in the treatment and prevention of various diseases, including cancer. Herein, we found that USP24 not only repressed DNA-damage repair (DDR) activity by decreasing Rad51 expression to cause the tumor genomic instability and cancer stemness, but also increased the levels of the ATP-binding cassette (ABC) transporters P-gp, ABCG2, and ezrin to enhance the pumping out of Taxol from cancer cells, thus resulted in drug resistance during cancer therapy. A novel USP24 inhibitor, NCI677397, was screened for specific inhibiting the catalytic activity of USP24. This inhibitor was identified to suppress drug resistance via decreasing genomic instability, cancer stemness, and the pumping out of drugs from cancer cells. Understanding the role and molecular mechanisms of USP24 in drug resistance will be beneficial for the future development of a novel USP24 inhibitor. Our studies provide a new insight of USP24 inhibitor for clinically implication of blocking drug resistance during chemotherapy.

Indexed as

AnimalsDrug DevelopmentDrug Resistance, NeoplasmHumansMiceMice, SCIDNeoplasmsTransfectionUbiquitin ThiolesteraseUbiquitin ThiolesteraseUsp24 protein, mouse

Identifiers

PMID33846536
PMCPMC8408266
OpenAlexW3153330875

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.