Literature DB >> 10463614

A new MAGE gene with ubiquitous expression does not code for known MAGE antigens recognized by T cells.

S Lucas1, F Brasseur, T Boon.   

Abstract

A number of genes of the MAGE family have been shown to code for antigens that are recognized on many human tumors by autologous CTLs. These antigens should be strictly tumor specific because the encoding MAGE genes are not expressed in normal adult cells, except for male germ-line cells, which lack HLA expression. Here, we report that a distant relative of the previously identified MAGE genes is expressed in many, if not all, normal tissues. This gene, which was named MAGE-D, is located in Xp11. Its exon-intron structure is completely different from that of the other MAGE genes. None of the 20 MAGE antigenic peptides presently known to be recognized by T lymphocytes is encoded by the new MAGE gene. It appears, therefore, that this new finding leaves intact the tumor specificity of the antigens encoded by the MAGE genes that are expressed only in tumor and germ-line cells.

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Year:  1999        PMID: 10463614

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  16 in total

1.  Characterization of a cancer/testis (CT) antigen gene family capable of eliciting humoral response in cancer patients.

Authors:  Raphael B Parmigiani; Fabiana Bettoni; Maria D Vibranovski; Marilene H Lopes; Waleska K Martins; Isabela W Cunha; Fernando A Soares; Andrew J G Simpson; Sandro J de Souza; Anamaria A Camargo
Journal:  Proc Natl Acad Sci U S A       Date:  2006-11-17       Impact factor: 11.205

2.  Large-scale cDNA transfection screening for genes related to cancer development and progression.

Authors:  Dafang Wan; Yi Gong; Wenxin Qin; Pingping Zhang; Jinjun Li; Lin Wei; Xiaomei Zhou; Hongnian Li; Xiaokun Qiu; Fei Zhong; Liping He; Jian Yu; Genfu Yao; Huiqiu Jiang; Lianfang Qian; Ye Yu; Huiqun Shu; Xianlian Chen; Huili Xu; Minglei Guo; Zhimei Pan; Yan Chen; Chao Ge; Shengli Yang; Jianren Gu
Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-21       Impact factor: 11.205

Review 3.  Tumour antigens recognized by T lymphocytes: at the core of cancer immunotherapy.

Authors:  Pierre G Coulie; Benoît J Van den Eynde; Pierre van der Bruggen; Thierry Boon
Journal:  Nat Rev Cancer       Date:  2014-02       Impact factor: 60.716

Review 4.  Insights into the processing of MHC class I ligands gained from the study of human tumor epitopes.

Authors:  Nathalie Vigneron; Benoît J Van den Eynde
Journal:  Cell Mol Life Sci       Date:  2011-03-09       Impact factor: 9.261

5.  MAGE-A1 interacts with adaptor SKIP and the deacetylase HDAC1 to repress transcription.

Authors:  Sandra Laduron; Rachel Deplus; Sifang Zhou; Olga Kholmanskikh; Danièle Godelaine; Charles De Smet; S Diane Hayward; François Fuks; Thierry Boon; Etienne De Plaen
Journal:  Nucleic Acids Res       Date:  2004-08-17       Impact factor: 16.971

Review 6.  Complex roles of NRAGE on tumor.

Authors:  Ge Zhang; Huandi Zhou; Xiaoying Xue
Journal:  Tumour Biol       Date:  2016-05-21

Review 7.  Biological functions of melanoma-associated antigens.

Authors:  Jiang Xiao; Hong-Song Chen
Journal:  World J Gastroenterol       Date:  2004-07-01       Impact factor: 5.742

Review 8.  Emerging roles of the MAGE protein family in stress response pathways.

Authors:  Rebecca R Florke Gee; Helen Chen; Anna K Lee; Christina A Daly; Benjamin A Wilander; Klementina Fon Tacer; Patrick Ryan Potts
Journal:  J Biol Chem       Date:  2020-09-13       Impact factor: 5.157

9.  MAGE1 is expressed by a subset of pancreatic endocrine neoplasms and associated lymph node and liver metastases.

Authors:  Donna E Hansel; Michael G House; Raheela Ashfaq; Ayman Rahman; Charles J Yeo; Anirban Maitra
Journal:  Int J Gastrointest Cancer       Date:  2003

10.  In silico analysis of human Telomerase Reverse Transcriptase (hTERT) gene: identification of a distant homolog of Melanoma Antigen Family Gene (MAGE).

Authors:  Ruhul Amin; Hasan Jamil; M Anwar Hossain
Journal:  Cancer Inform       Date:  2009-11-24
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