TY - JOUR
T1 - Immunological detection of altered signaling molecules involved in melanoma development
AU - Kawakami, Yutaka
AU - Sumimoto, Hidetoshi
AU - Fujita, Tomonobu
AU - Matsuzaki, Yuriko
N1 - Funding Information:
A part of the work was supported by grants from Grants-in-Aid for Scientific Research from the Ministry of Education, Science, Sport and Culture of Japan, Grant-in-Aid for Cancer Research from the Ministry of Health and Welfare, and grants from Keio University. I thank many lab members who conducted a part of this work and Minako Yanai, and Ryoko Suzuki for secretarial assistance.
PY - 2005/6
Y1 - 2005/6
N2 - To understand immune responses to human cancer and develop more effective immunotherapy, human tumor antigens has been isolated using various immunological methods with tumor reactive T cells or antibodies obtained from patients with melanoma. During the process of tumor antigen isolation, various molecules with genetic alterations or over-expression in tumor cells, which may be involved in proliferation, differentiation, or survival of various cancer cells, were identified. In melanoma, abnormal molecules with mutations including β -catenin, CDK4, and BRAF, and molecules with increased expression including Survivin, were immunologically detected. Therefore, immunological isolation of human tumor antigens contributes to the identification of important molecules including altered signaling molecules involved in melanoma formation.
AB - To understand immune responses to human cancer and develop more effective immunotherapy, human tumor antigens has been isolated using various immunological methods with tumor reactive T cells or antibodies obtained from patients with melanoma. During the process of tumor antigen isolation, various molecules with genetic alterations or over-expression in tumor cells, which may be involved in proliferation, differentiation, or survival of various cancer cells, were identified. In melanoma, abnormal molecules with mutations including β -catenin, CDK4, and BRAF, and molecules with increased expression including Survivin, were immunologically detected. Therefore, immunological isolation of human tumor antigens contributes to the identification of important molecules including altered signaling molecules involved in melanoma formation.
KW - BRAF
KW - DNA expression cloning
KW - Immunotherapy
KW - MART-2/Ski
KW - Tumor antigens
KW - β-catenin
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U2 - 10.1007/s10555-005-1583-y
DO - 10.1007/s10555-005-1583-y
M3 - Article
C2 - 15986143
AN - SCOPUS:21544484604
SN - 0167-7659
VL - 24
SP - 357
EP - 366
JO - Cancer and Metastasis Reviews
JF - Cancer and Metastasis Reviews
IS - 2
ER -