Evidence map›Paper›PMID 38702734›Full record

ReviewMolecular cancer2024

Drug resistance mechanisms and treatment strategies mediated by Ubiquitin-Specific Proteases (USPs) in cancers: new directions and therapeutic options.

Hongli Gao, Zhuo Xi, Jingwei Dai, Jinqi Xue, Xin Guan, Liang Zhao, Zhiguang Chen, Fei Xing

Abstract readReview
In one paragraph

Review in Molecular cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
–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

50 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  15. Role of histone modifications in gastric cancer (Review).International journal of oncology · 2026
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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

8 authors.

Hongli Gao *Department of Oncology, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Zhuo Xi *Department of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Jingwei Dai *Department of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Jinqi XueDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Xin GuanDepartment of Gastroenterology, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Liang ZhaoDepartment of General Surgery, Shengjing Hospital of China Medical University, Shenyang, 110004, China. 1203517217@qq.com.
Zhiguang ChenDepartment of Emergency Medicine, Shengjing Hospital of China Medical University, Shenyang, 110004, China. Chencmuchenzg@163.com.
Fei XingDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, 110004, China. xingfshengjing@sina.com.

Funding

National Natural Science Foundation of China No. 81701570Science and Technology Plan Joint Plan Project of Liaoning Province 2023JH2/101700153
6 · The paper itself

Abstract

Drug resistance represents a significant obstacle in cancer treatment, underscoring the need for the discovery of novel therapeutic targets. Ubiquitin-specific proteases (USPs), a subclass of deubiquitinating enzymes, play a pivotal role in protein deubiquitination. As scientific research advances, USPs have been recognized as key regulators of drug resistance across a spectrum of treatment modalities, including chemotherapy, targeted therapy, immunotherapy, and radiotherapy. This comprehensive review examines the complex relationship between USPs and drug resistance mechanisms, focusing on specific treatment strategies and highlighting the influence of USPs on DNA damage repair, apoptosis, characteristics of cancer stem cells, immune evasion, and other crucial biological functions. Additionally, the review highlights the potential clinical significance of USP inhibitors as a means to counter drug resistance in cancer treatment. By inhibiting particular USP, cancer cells can become more susceptible to a variety of anti-cancer drugs. The integration of USP inhibitors with current anti-cancer therapies offers a promising strategy to circumvent drug resistance. Therefore, this review emphasizes the importance of USPs as viable therapeutic targets and offers insight into fruitful directions for future research and drug development. Targeting USPs presents an effective method to combat drug resistance across various cancer types, leading to enhanced treatment strategies and better patient outcomes.

Indexed as

Antineoplastic AgentsDrug Resistance, NeoplasmNeoplasmsUbiquitin-Specific ProteasesAnimalsApoptosisDNA RepairHumansMolecular Targeted TherapyAntineoplastic AgentsUbiquitin-Specific ProteasesDrug resistanceImmunotherapyUbiquitin-specific proteases (USPs)USP inhibitors

Identifiers

PMID38702734
PMCPMC11067278

What OpenQuestion holds

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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.