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Updated: Aug 14, 2026

Tractable In Vivo Reprogramming of Tumor Cells to Type 1 Conventional Dendritic Cell-like Cells
Published on: August 1, 2025
Carbonic anhydrase II is a tumor vessel endothelium-associated antigen targeted by dendritic cell therapy
Kenta Yoshiura1, Takashi Nakaoka, Toshihide Nishishita
1Department of Advanced Medical Science, University of Tokyo, Japan. yoshiura-gi@umin.ac.jp.
Abstract:
Tumor-associated antigens are promising candidates as target molecules for immunotherapy and a wide variety of tumor-associated antigens have been discovered through the presence of serum antibodies in cancer patients. We previously conducted dendritic cell therapy on 10 malignant melanoma patients and shrinkage or disappearance of metastatic tumors with massive necrosis occurred in two patients. In this study, we found a 29-kDa protein against which antibody was elicited by dendritic cell therapy in one of the two patients. Matrix-assisted laser desorption ionization-time of flight/mass spectrometry analysis of the protein isolated by two-dimensional electrophoresis combined with Western blots revealed that the 29-kDa protein was carbonic anhydrase II (CA-II). Immunohistochemistry of the tumors and normal tissues showed that CA-II was expressed in the tumor vessel but not in normal vessel endothelium. CA-II expression in tumor endothelium was observed as well in other cancers including esophageal, renal, and lung cancers. In an in vitro angiogenesis model, CA-II expression of normal human vein endothelial cells was significantly up-regulated when cells were cultured in the acidic and hypoxic conditions indicative of a tumor environment. These findings suggest that CA-II is a tumor vessel endothelium-associated antigen in melanoma and other cancers, and elicitation of serum anti-CA-II antibody by dendritic cell therapy may be associated with good clinical outcome including tumor reduction.
Insights
Dendritic cell therapy may target carbonic anhydrase II (CA-II), a protein found on tumor blood vessels. This discovery offers a new avenue for cancer immunotherapy by potentially eliciting antibodies against CA-II.
Area of Science:
- Oncology
- Immunology
- Biochemistry
Background:
- Tumor-associated antigens are key targets for cancer immunotherapy.
- Previous dendritic cell therapy in melanoma patients showed promising tumor reduction in some cases.
Purpose of the Study:
- To identify the specific antigen targeted by dendritic cell therapy in melanoma patients.
- To investigate the expression and potential role of this antigen in various cancer types.
Main Methods:
- Matrix-assisted laser desorption ionization-time of flight/mass spectrometry (MALDI-TOF/MS) and Western blotting to identify a 29-kDa protein.
- Immunohistochemistry to analyze carbonic anhydrase II (CA-II) expression in tumor and normal tissues.
- In vitro angiogenesis model to assess CA-II expression under tumor-mimicking conditions.
Main Results:
- A 29-kDa protein, identified as carbonic anhydrase II (CA-II), was found to elicit an antibody response post-dendritic cell therapy.
- CA-II was specifically expressed in the endothelium of tumor vessels across melanoma, esophageal, renal, and lung cancers, but not in normal vessels.
- CA-II expression in endothelial cells was significantly upregulated under acidic and hypoxic conditions simulating a tumor microenvironment.
Conclusions:
- Carbonic anhydrase II (CA-II) is a tumor vessel endothelium-associated antigen relevant to multiple cancer types.
- The induction of anti-CA-II antibodies via dendritic cell therapy may correlate with positive clinical outcomes, including tumor regression.
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