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Advances in research on the carcinogenic mechanisms and therapeutic potential of YAP1 in bladder cancer (Review).
- Source :
-
Oncology reports [Oncol Rep] 2025 Jan; Vol. 53 (1). Date of Electronic Publication: 2024 Nov 14. - Publication Year :
- 2025
-
Abstract
- Bladder cancer is the most common malignant tumor of the urinary system with high morbidity and no clear pathogenesis. The Hippo signaling pathway is an evolutionarily conserved pathway that regulates organ size and maintains tissue homeostasis. Yes‑associated protein 1 (YAP1) is a key effector of this pathway and regulates downstream target genes by binding to transcriptional co‑activators with PDZ binding sequences (TAZ). Several studies have demonstrated that YAP1 is overexpressed in bladder cancer and is involved in adverse outcomes such as bladder cancer occurrence, progression, resistance to cisplatin and the recurrence of tumours. The present review summarized the involvement of YAP1 in bladder cancer disease onset and progression, and the mechanism of YAP1 involvement in bladder cancer treatment. In addition, this study further explored the potential of YAP1 in the diagnosis and treatment of bladder cancer. This study aimed to explore the potential mechanism of YAP1 in the treatment of bladder cancer.
- Subjects :
- Humans
Phosphoproteins genetics
Phosphoproteins metabolism
Signal Transduction
Drug Resistance, Neoplasm
Carcinogenesis genetics
Hippo Signaling Pathway
Disease Progression
Urinary Bladder Neoplasms genetics
Urinary Bladder Neoplasms metabolism
Urinary Bladder Neoplasms pathology
Urinary Bladder Neoplasms drug therapy
YAP-Signaling Proteins
Adaptor Proteins, Signal Transducing genetics
Adaptor Proteins, Signal Transducing metabolism
Transcription Factors genetics
Transcription Factors metabolism
Gene Expression Regulation, Neoplastic
Subjects
Details
- Language :
- English
- ISSN :
- 1791-2431
- Volume :
- 53
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Oncology reports
- Publication Type :
- Academic Journal
- Accession number :
- 39540392
- Full Text :
- https://doi.org/10.3892/or.2024.8843