Oncogenic cancer/testis antigens: prime candidates for immunotherapy

被引:252
作者
Gjerstorff, Morten F. [1 ]
Andersen, Mads H. [2 ]
Ditzel, Henrik J. [1 ,3 ]
机构
[1] Univ Southern Denmark, Dept Canc & Inflammat Res, Odense, Denmark
[2] Copenhagen Univ Hosp, Ctr Canc Immune Therapy CCIT, Dept Haematol, Herlev, Denmark
[3] Odense Univ Hosp, Dept Oncol, DK-5000 Odense, Denmark
关键词
cancer/testis antigen; oncogenesis; immunotherapy; CANCER-TESTIS ANTIGENS; MEIOSIS-SPECIFIC GENES; DOUBLE-STRAND BREAKS; MAGE-A; T-CELLS; MULTIPLE-MYELOMA; MESSENGER-RNA; MESENCHYMAL TRANSITION; CONFERS RESISTANCE; PROTEIN EXPRESSION;
D O I
10.18632/oncotarget.4694
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent developments have set the stage for immunotherapy as a supplement to conventional cancer treatment. Consequently, a significant effort is required to further improve efficacy and specificity, particularly the identification of optimal therapeutic targets for clinical testing. Cancer/testis antigens are immunogenic, highly cancer-specific, and frequently expressed in various types of cancer, which make them promising candidate targets for cancer immunotherapy, including cancer vaccination and adoptive T-cell transfer with chimeric T-cell receptors. Our current understanding of tumor immunology and immune escape suggests that targeting oncogenic antigens may be beneficial, meaning that identification of cancer/testis antigens with oncogenic properties is of high priority. Recent work from our lab and others provide evidence that many cancer/testis antigens, in fact, have oncogenic functions, including support of growth, survival and metastasis. This novel insight into the function of cancer/testis antigens has the potential to deliver more effective cancer vaccines. Moreover, immune targeting of oncogenic cancer/testis antigens in combination with conventional cytotoxic therapies or novel immunotherapies such as checkpoint blockade or adoptive transfer, represents a highly synergistic approach with the potential to improve patient survival.
引用
收藏
页码:15772 / 15787
页数:16
相关论文
共 121 条
[11]   Tumor antigen expression in melanoma varies according to antigen and stage [J].
Barrow, C ;
Browning, J ;
MacGregor, D ;
Davis, ID ;
Sturrock, S ;
Jungbluth, AA ;
Cebon, J .
CLINICAL CANCER RESEARCH, 2006, 12 (03) :764-771
[12]   MAGE-C2 Promotes Growth and Tumorigenicity of Melanoma Cells, Phosphorylation of KAP1, and DNA Damage Repair [J].
Bhatia, Neehar ;
Xiao, Tony Z. ;
Rosenthal, Kimberly A. ;
Siddiqui, Imtiaz A. ;
Thiyagarajan, Saravanan ;
Smart, Brendan ;
Meng, Qiao ;
Zuleger, Cindy L. ;
Mukhtar, Hasan ;
Kenney, Shannon C. ;
Albertini, Mark R. ;
Longley, B. Jack .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2013, 133 (03) :759-767
[13]   Effects of CT-Xp Gene Knock down in Melanoma Cell Lines [J].
Caballero, Otavia L. ;
Cohen, Tzeela ;
Gurung, Sita ;
Chua, Ramon ;
Lee, Peishan ;
Chen, Yao-Tseng ;
Jat, Parmjit ;
Simpson, Andrew J. G. .
ONCOTARGET, 2013, 4 (04) :531-541
[14]   Identification of a Titin-Derived HLA-A1-Presented Peptide as a Cross-Reactive Target for Engineered MAGE A3-Directed T Cells [J].
Cameron, Brian J. ;
Gerry, Andrew B. ;
Dukes, Joseph ;
Harper, Jane V. ;
Kannan, Vivekanandan ;
Bianchi, Frayne C. ;
Grand, Francis ;
Brewer, Joanna E. ;
Gupta, Minnal ;
Plesa, Gabriela ;
Bossi, Giovanna ;
Vuidepot, Annelise ;
Powlesland, Alex S. ;
Legg, Alison ;
Adams, Katherine J. ;
Bennett, Alan D. ;
Pumphrey, Nicholas J. ;
Williams, Daniel D. ;
Binder-Scholl, Gwendolyn ;
Kulikovskaya, Irina ;
Levine, Bruce L. ;
Riley, James L. ;
Varela-Rohena, Angel ;
Stadtmauer, Edward A. ;
Rapoport, Aaron P. ;
Linette, Gerald P. ;
June, Carl H. ;
Hassan, Namir J. ;
Kalos, Michael ;
Jakobsen, Bent K. .
SCIENCE TRANSLATIONAL MEDICINE, 2013, 5 (197)
[15]   Multiple Cancer Testis Antigens Function To Support Tumor Cell Mitotic Fidelity [J].
Cappell, Kathryn M. ;
Sinnott, Rebecca ;
Taus, Patrick ;
Maxfield, Kimberly ;
Scarbrough, Moriah ;
Whitehurst, Angelique W. .
MOLECULAR AND CELLULAR BIOLOGY, 2012, 32 (20) :4131-4140
[16]  
Chen Yao-Tseng, 2005, Cancer Immun, V5, P9
[17]   Cancer/testis antigen CT45: Analysis of mRNA and protein expression in human cancer [J].
Chen, Yao-Tseng ;
Hsu, Melinda ;
Lee, Peishan ;
Shin, Sandra J. ;
Mhawech-Fauceglia, Paulette ;
Odunsi, Kunle ;
Altorki, Nasser K. ;
Song, Chao-Jun ;
Jin, Bo-Quan ;
Simpson, Andrew J. ;
Old, Lloyd J. .
INTERNATIONAL JOURNAL OF CANCER, 2009, 124 (12) :2893-2898
[18]   Identification of multiple cancer/testis antigens by allogeneic antibody screening of a melanoma cell line library [J].
Chen, YT ;
Güre, AO ;
Tsang, S ;
Stockert, E ;
Jäger, E ;
Knuth, A ;
Old, LJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (12) :6919-6923
[19]   Identification of cancer/testis-antigen genes by massively parallel signature sequencing [J].
Chen, YT ;
Scanlan, MJ ;
Venditti, CA ;
Chua, R ;
Theiler, G ;
Stevenson, BJ ;
Iseli, C ;
Gure, AO ;
Vasicek, T ;
Strausberg, RL ;
Jongeneel, CV ;
Old, LJ ;
Simpson, AJG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (22) :7940-7945
[20]   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