Mutated mitogen-activated protein kinase: A tumor rejection antigen of mouse sarcoma

被引:91
作者
Ikeda, H
Ohta, N
Furukawa, K
Miyazaki, H
Wang, LJ
Furukawa, K
Kuribayashi, K
Old, LJ
Shiku, H
机构
[1] MIE UNIV, SCH MED, DEPT INTERNAL MED 2, TSU, MIE 514, JAPAN
[2] MIE UNIV, SCH MED, DEPT BIOCHEM, TSU, MIE 514, JAPAN
[3] MIE UNIV, SCH MED, DEPT BIOREGULAT, TSU, MIE 514, JAPAN
[4] NAGASAKI UNIV, SCH MED, DEPT ONCOL, NAGASAKI 852, JAPAN
[5] MEM SLOAN KETTERING CANC CTR, LUDWIG INST CANC RES, NEW YORK, NY 10021 USA
关键词
D O I
10.1073/pnas.94.12.6375
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The molecular basis of the polymorphic tumor rejection antigens of chemically induced sarcomas of inbred mice remains a mystery, despite the discovery of these antigens over 40 years ago and their critical importance to the foundation of tumor immunology. In an analysis of a panel of BALB/c 3-methylcholanthrene-induced tumors, we identified one tumor, CMS5, that elicited a strong cytotoxic T cell response with exquisite specificity for CMS5, A stable cloned line of T cells with this specificity (C18) was used to screen a CMS5 cDNA expression library, The gene encoding the C18-defined antigen was identified as a mutated form of a mouse mitogen-activated protein kinase, ERK2, and a peptide incorporating the resulting amino acid substitution (lysine to glutamine) was efficiently recognized by C18, Vaccination with this peptide elicited specific resistance to CMS5 challenge, Extensive efforts to isolate antigen-loss variants of CMS5 were unsuccessful, suggesting that the mutated mitogen-activated protein kinase is essential for maintenance of the malignant phenotype.
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页码:6375 / 6379
页数:5
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