Related Experiment Video
Updated: Jul 2, 2026

Induction of Invasive Transitional Cell Bladder Carcinoma in Immune Intact Human MUC1 Transgenic Mice: A Model for Immunotherapy Development
Published on: October 30, 2013
p53 and chemosensitivity in bladder cancer
Hiroyuki Nishiyama1, Jun Watanabe, Osamu Ogawa
1Department of Urology, Kyoto University Graduate School of Medicine, 54 Shogoin Kawahara-cho, Sakyo-ku, Kyoto, Japan. nishiuro@kuhp.kyoto-u.ac.jp
Alterations in the p53 pathway are common in invasive urothelial carcinoma, impacting tumor progression, prognosis, and treatment response. Understanding these changes is crucial for improving patient outcomes in bladder cancer.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- Urothelial carcinoma is a common genitourinary malignancy with significant clinical challenges.
- Progression to invasive disease, poor prognosis, and variable chemosensitivity are key issues.
- The tumor suppressor gene p53 plays a critical role in various cellular functions.
Purpose of the Study:
- To review the role of p53 pathways in bladder cancer development.
- To discuss recent findings on p53 alterations in urothelial carcinoma.
- To explore the clinical significance of p53 pathway abrogation in treatment.
Main Methods:
- Literature review of p53's functions and alterations in urothelial carcinoma.
- Analysis of recent research findings from multiple groups.
- Discussion of clinical implications based on current evidence.
Main Results:
- p53 alterations are frequent in invasive urothelial carcinoma.
- These alterations are linked to tumor progression, prognosis, and chemosensitivity.
- p53's functions include cell-cycle arrest, apoptosis, DNA repair, and antioxidant activity.
Conclusions:
- p53 pathway abrogation is a significant factor in urothelial carcinoma.
- Understanding p53's role is vital for developing effective therapeutic strategies.
- Targeting p53 pathways may offer new treatment avenues for bladder cancer.
Related Concept Videos
Abnormal Proliferation
DNA Damage can Stall the Cell Cycle
DNA Damage Can Stall the Cell Cycle
Negative Regulator Molecules
