A p16INK4a-Insensitive CDK4 Mutant Targeted by Cytolytic T Lymphocytes in a Human Melanoma
T Wölfel, M Hauer, J Schneider, M Serrano, C Wölfel… - Science, 1995 - science.org
T Wölfel, M Hauer, J Schneider, M Serrano, C Wölfel, E Klehmann-Hieb, E De Plaen…
Science, 1995•science.orgA mutated cyclin-dependent kinase 4 (CDK4) was identified as a tumor-specific antigen
recognized by HLA-A2. 1-restricted autologous cytolytic T lymphocytes (CTLs) in a human
melanoma. The mutated CDK4 allele was present in autologous cultured melanoma cells
and metastasis tissue, but not in the patient's lymphocytes. The mutation, an arginine-to-
cysteine exchange at residue 24, was part of the CDK4 peptide recognized by CTLs and
prevented binding of the CDK4 inhibitor p16INK4a, but not of p21 or of p27KIP1. The same …
recognized by HLA-A2. 1-restricted autologous cytolytic T lymphocytes (CTLs) in a human
melanoma. The mutated CDK4 allele was present in autologous cultured melanoma cells
and metastasis tissue, but not in the patient's lymphocytes. The mutation, an arginine-to-
cysteine exchange at residue 24, was part of the CDK4 peptide recognized by CTLs and
prevented binding of the CDK4 inhibitor p16INK4a, but not of p21 or of p27KIP1. The same …
A mutated cyclin-dependent kinase 4 (CDK4) was identified as a tumor-specific antigen recognized by HLA-A2. 1-restricted autologous cytolytic T lymphocytes (CTLs) in a human melanoma. The mutated CDK4 allele was present in autologous cultured melanoma cells and metastasis tissue, but not in the patient's lymphocytes. The mutation, an arginine-to-cysteine exchange at residue 24, was part of the CDK4 peptide recognized by CTLs and prevented binding of the CDK4 inhibitor p16INK4a, but not of p21 or of p27KIP1. The same mutation was found in one additional melanoma among 28 melanomas analyzed. These results suggest that mutation of CDK4 can create a tumor-specific antigen and can disrupt the cell-cycle regulation exerted by the tumor suppressor p16INK4a.
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