A P16(INK4A)-INSENSITIVE CDK4 MUTANT TARGETED BY CYTOLYTIC T-LYMPHOCYTES IN A HUMAN-MELANOMA

被引:887
作者
WOLFEL, T
HAUER, M
SCHNEIDER, J
SERRANO, M
WOLFEL, C
KLEHMANNHIEB, E
DEPLAEN, E
HANKELN, T
ZUMBUSCHENFELDE, KHM
BEACH, D
机构
[1] COLD SPRING HARBOR LAB, HOWARD HUGHES MED INST, COLD SPRING HARBOR, NY 11724 USA
[2] CATHOLIC UNIV LEUVEN, LUDWIG INST CANC RES, B-1200 BRUSSELS, BELGIUM
[3] UNIV MAINZ, INST MOLEK GENET, D-55099 MAINZ, GERMANY
关键词
D O I
10.1126/science.7652577
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
A mutated cyclin-dependent kinase 4 (CDK4) was identified as a tumor-specific antigen recognized by HL4-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 p16(INK4a), but not of p21 or of p27(KIP1). 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 p16(INK4a).
引用
收藏
页码:1281 / 1284
页数:4
相关论文
共 50 条
[1]   A ROLE FOR SUNLIGHT IN SKIN-CANCER - UV-INDUCED P53 MUTATIONS IN SQUAMOUS-CELL CARCINOMA [J].
BRASH, DE ;
RUDOLPH, JA ;
SIMON, JA ;
LIN, A ;
MCKENNA, GJ ;
BADEN, HP ;
HALPERIN, AJ ;
PONTEN, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (22) :10124-10128
[2]   THE TYROSINASE GENE CODES FOR AN ANTIGEN RECOGNIZED BY AUTOLOGOUS CYTOLYTIC T-LYMPHOCYTES ON HLA-A2 MELANOMAS [J].
BRICHARD, V ;
VANPEL, A ;
WOLFEL, T ;
WOLFEL, C ;
DEPLAEN, E ;
LETHE, B ;
COULIE, P ;
BOON, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (02) :489-495
[3]   FREQUENT SOMATIC MUTATIONS AND HOMOZYGOUS DELETIONS OF THE P16 (MTS1) GENE IN PANCREATIC ADENOCARCINOMA [J].
CALDAS, C ;
HAHN, SA ;
DACOSTA, LT ;
REDSTON, MS ;
SCHUTTE, M ;
SEYMOUR, AB ;
WEINSTEIN, CL ;
HRUBAN, RH ;
YEO, CJ ;
KERN, SE .
NATURE GENETICS, 1994, 8 (01) :27-32
[4]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[5]   A NEW GENE CODING FOR A DIFFERENTIATION ANTIGEN RECOGNIZED BY AUTOLOGOUS CYTOLYTIC T-LYMPHOCYTES ON HLA-A2 MELANOMAS [J].
COULIE, PG ;
BRICHARD, V ;
VANPEL, A ;
WOLFEL, T ;
SCHNEIDER, J ;
TRAVERSARI, C ;
MATTEI, S ;
DEPLAEN, E ;
LURQUIN, C ;
SZIKORA, JP ;
RENAULD, JC ;
BOON, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (01) :35-42
[6]   AN INTRACISTERNAL A-PARTICLE SEQUENCE CODES FOR AN ANTIGEN RECOGNIZED BY SYNGENEIC CYTOLYTIC T-LYMPHOCYTES ON A MOUSE SPONTANEOUS LEUKEMIA [J].
DEBERGEYCK, V ;
DEPLAEN, E ;
CHOMEZ, P ;
BOON, T ;
VANPEL, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (09) :2203-2212
[7]   ALLELE-SPECIFIC MOTIFS REVEALED BY SEQUENCING OF SELF-PEPTIDES ELUTED FROM MHC MOLECULES [J].
FALK, K ;
ROTZSCHKE, O ;
STEVANOVIC, S ;
JUNG, G ;
RAMMENSEE, HG .
NATURE, 1991, 351 (6324) :290-296
[8]   VACCINATION WITH CYTOTOXIC T-LYMPHOCYTE EPITOPE-CONTAINING PEPTIDE PROTECTS AGAINST A TUMOR-INDUCED BY HUMAN PAPILLOMAVIRUS TYPE-16-TRANSFORMED CELLS [J].
FELTKAMP, MCW ;
SMITS, HL ;
VIERBOOM, MPM ;
MINNAAR, RP ;
DEJONGH, BM ;
DRIJFHOUT, JW ;
TERSCHEGGET, J ;
MELIEF, CJM ;
KAST, WM .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (09) :2242-2249
[9]   INHIBITION OF CDK2 ACTIVITY IN-VIVO BY AN ASSOCIATED 20K REGULATORY SUBUNIT [J].
GU, Y ;
TURCK, CW ;
MORGAN, DO .
NATURE, 1993, 366 (6456) :707-710
[10]   P15(INK4B) IS A POTENTIAL EFFECTOR OF TGF-BETA-INDUCED CELL-CYCLE ARREST [J].
HANNON, GJ ;
BEACH, D .
NATURE, 1994, 371 (6494) :257-261