ReviewJournal of pharmacy & bioallied sciences2024
Deubiquitinases and Cancer.
Review in Journal of pharmacy & bioallied sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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.
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.
Who cites it
5 citing papers in PubMed.
- Deubiquitinating Enzymes as Therapeutic Candidates in Hepatocellular Carcinoma and Other Liver Disease.International journal of molecular sciences · 2026Review
- Regulatory roles of five key USP family deubiquitinases in cancer: from mechanisms to targeted therapy advances.Frontiers in pharmacology · 2026Review
- The deubiquitinase USP35: from an oncogenic hub to a therapeutic target in human cancers.Frontiers in oncology · 2026Review
- Molecular regulation by ubiquitin-specific proteases (USPs) in HCC: cell cycle, oncogenic signaling, and beyond.Naunyn-Schmiedeberg's archives of pharmacology · 2025Review
- UCHL1 Promotes Gastric Cancer Progression by Regulating CIP2A Degradation.Pharmaceuticals (Basel, Switzerland) · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Deubiquitinases are involved in removing ubiquitin (UBQ) from ubiquitylated substrates to regulate their activity and stability. They are involved in various cellular functions including proteasome- and lysosome-dependent proteolysis, gene expression, cell cycle progression, chromosome segregation, kinase activation, histone modification, cell cycle regulation, cell differentiation, spermatogenesis, apoptosis, endocytosis, autophagy, localization, and DNA damage repair. On the other hand, it is also involved in the processes of carcinogenesis and cancer development. DUBs are related to different aspects of human cancer, including proliferation, cell cycle control, apoptosis, DNA damage response (DDR), tumor suppression, oncogenesis, and metastasis. Multiple processes involved in innate and adaptive immunity, such as antigen presentation, cell differentiation, immune defense, and inflammatory responses, are regulated by ubiquitination/deubiquitination. Dysregulation of DUBs is implicated in several human diseases, highlighting the importance of DUB function. This review also provides basic knowledge of DUBs in the development of cancers and highlights the importance of DUBs in T-cell development, apoptosis, and cancer with a specific emphasis on oral cancers. This review highlights the recent advances in the field of cancer biology with a specific role in DUBs in cellular functions. The aberrant expression and regulation of these enzymes have been shown to contribute to promote tumorigenesis, making them promising therapeutic targets for cancer therapy.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.