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Updated: May 22, 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
Cancer peptide vaccine therapy developed from oncoantigens identified through genome-wide expression profile analysis
Wataru Obara1, Ryuji Ohsawa, Mitsugu Kanehira
1Department of Urology, Iwate Medical University School of Medicine, 19-1 Uchimaru, Morioka 020-8505, Japan. watao@iwate-med.ac.jp
Objective:
The field of cancer vaccine therapy is currently expected to become the fourth option in the treatment of cancer after surgery, chemotherapy and radiation therapy. We developed a novel cancer peptide vaccine therapy for bladder cancer through a genome-wide expression profile analysis.
Methods:
Among a number of oncoproteins that are transactivated in cancer cells, we focused on M phase phosphoprotein 1 and DEP domain containing 1, both of which are cancer-testis antigens playing critical roles in the growth of bladder cancer cells, as candidate molecules for the development of drugs for bladder cancer. In an attempt to identify the peptide epitope from these oncoantigens, we conducted a clinical trial using these peptides for patients with advanced bladder cancer.
Results:
We identified HLA-A24-restricted peptide epitopes corresponding to parts of M phase phosphoprotein 1 and DEP domain containing 1 proteins, which could induce peptide-specific cytotoxic T lymphocytes. Using these peptides, we found that M phase phosphoprotein 1- and DEP domain containing 1-derived peptide vaccines could be well tolerated without any serious adverse events, and effectively induced peptide-specific cytotoxic T lymphocytes in vivo.
Conclusions:
The novel approach adopted in the treatment with peptide vaccines is considered to be a promising therapy for bladder cancer.
Insights
A novel peptide vaccine therapy for bladder cancer shows promise as a new treatment option. This therapy, targeting specific cancer-testis antigens, was well-tolerated and effectively stimulated immune responses in patients.
Area of Science:
- Oncology
- Immunotherapy
- Genomics
Background:
- Cancer vaccine therapy is emerging as a significant treatment modality alongside surgery, chemotherapy, and radiation.
- Bladder cancer treatment requires novel therapeutic strategies to improve patient outcomes.
Purpose of the Study:
- To develop a novel peptide vaccine therapy for bladder cancer.
- To identify potential therapeutic targets through genome-wide expression profile analysis.
Main Methods:
- Genome-wide expression profile analysis identified M phase phosphoprotein 1 and DEP domain containing 1 as key oncoproteins in bladder cancer.
- Clinical trials were conducted using peptides derived from these cancer-testis antigens to identify effective epitopes.
Main Results:
- HLA-A24-restricted peptide epitopes from M phase phosphoprotein 1 and DEP domain containing 1 were identified.
- These peptide vaccines were well-tolerated in patients with advanced bladder cancer, with no serious adverse events.
- The peptide vaccines effectively induced peptide-specific cytotoxic T lymphocytes in vivo.
Conclusions:
- The developed peptide vaccine therapy represents a promising new approach for bladder cancer treatment.
- This novel immunotherapy strategy warrants further investigation for its clinical application in bladder cancer.
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