Identification of a meiosis-specific protein as a member of the class of cancer/testis antigens

被引:215
作者
Türeci, O
Sahin, U [1 ]
Zwick, C
Koslowski, M
Seitz, G
Pfreundschuh, M
机构
[1] Univ Saarlandes Kliniken, Med Klin 1, D-66421 Homburg, Germany
[2] Klinikum Bamberg, Inst Pathol, Bamberg, Germany
关键词
D O I
10.1073/pnas.95.9.5211
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
Little is known about the function of human cancer/testis antigens (CTAs), such as MAGE, BAGE, GAGE, HOM-MEL-40, and NY-ESO-1, the expression of which is restricted to human malignancies and testis, When screening a cDNA expression library enriched for testis-specific representative long transcripts for reactivity with high-titered IgG antibodies from the serum of a patient with renal cell carcinoma, one repeatedly detected antigen, designated HOMTES-14, turned out to be encoded by the synaptonemal complex protein 1 (SCP-1) gene. SCP-1 is known to be selectively expressed during the meiotic prophase of spermatocytes and is involved in the pairing of homologous chromosomes, an essential step for the generation of haploid cells in meiosis I. Investigation of a broad spectrum of normal and malignant tissues revealed expression of SCP-1 transcripts and antigen selectively in a variety of neoplastic tissues and tumor cell lines. Immunofluorescence microscopy analysis with specific antiserum showed a cell cycle phase-independent nuclear expression of SCP-1 protein in cancer cells. SCP-1 differs from other members of the class of CTA by its localization on chromosome 1 and its frequent expression in malignant gliomas, breast, renal cell, and ovarian cancer. The aberrant expression of SCP-l in tumors might contribute to their genomic instability and suggests that the functional role of other CTA might also relate to meiosis.
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页码:5211 / 5216
页数:6
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共 37 条
[1]  
ALTINGMEES MA, 1992, METHOD ENZYMOL, V216, P483
[2]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[3]   MELANOMA-CELLS AND NORMAL MELANOCYTES SHARE ANTIGENS RECOGNIZED BY HLA-A2-RESTRICTED CYTOTOXIC T-CELL CLONES FROM MELANOMA PATIENTS [J].
ANICHINI, A ;
MACCALLI, C ;
MORTARINI, R ;
SALVI, S ;
MAZZOCCHI, A ;
SQUARCINA, P ;
HERLYN, M ;
PARMIANI, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (04) :989-998
[4]  
BAIROCH A, 1994, NUCLEIC ACIDS RES, V22, P3583
[5]   MELANOCYTE LINEAGE-SPECIFIC ANTIGEN GP100 IS RECOGNIZED BY MELANOMA-DERIVED TUMOR-INFILTRATING LYMPHOCYTES [J].
BAKKER, ABH ;
SCHREURS, MWJ ;
DEBOER, AJ ;
KAWAKAMI, Y ;
ROSENBERG, SA ;
ADEMA, GJ ;
FIGDOR, CG .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (03) :1005-1009
[6]   TUMOR-ANTIGENS RECOGNIZED BY T-LYMPHOCYTES [J].
BOON, T ;
CEROTTINI, JC ;
VANDENEYNDE, B ;
VANDERBRUGGEN, P ;
VANPEL, A .
ANNUAL REVIEW OF IMMUNOLOGY, 1994, 12 :337-365
[7]   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
[8]   GENE CONVERSION, RECOMBINATION NODULES, AND THE INITIATION OF MEIOTIC SYNAPSIS [J].
CARPENTER, ATC .
BIOESSAYS, 1987, 6 (05) :232-236
[9]   A testicular antigen aberrantly expressed in human cancers detected by autologous antibody screening [J].
Chen, YT ;
Scanlan, MJ ;
Sahin, U ;
Tureci, O ;
Gure, AO ;
Tsang, SL ;
Williamson, B ;
Stockert, E ;
Pfreundschuh, M ;
Old, LJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (05) :1914-1918
[10]   DEMETHYLATION OF SOMATIC AND TESTIS-SPECIFIC HISTONE H2A AND H2B GENES IN F9 EMBRYONAL CARCINOMA-CELLS [J].
CHOI, YC ;
CHAE, CB .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (09) :5538-5548