Literature DB >> 16596224

Expression of the MAGE-A4 and NY-ESO-1 cancer-testis antigens and T cell infiltration in non-small cell lung carcinoma and their prognostic significance.

Naofumi Yoshida1, Hiroyuki Abe, Takayuki Ohkuri, Daiko Wakita, Masayoshi Sato, Daisuke Noguchi, Masaki Miyamoto, Toshiaki Morikawa, Satoshi Kondo, Hiroaki Ikeda, Takashi Nishimura.   

Abstract

Cancer-testis (CT) antigens were identified as a group of highly attractive targets for cancer immunotherapy because of their expression in a variety of malignant tumors but solely in the testis among the normal adult tissues. To evaluate the potential of two members of this family, MAGE-A4 and NY-ESO-1 antigens, for cancer vaccine in non-small cell lung carcinoma (NSCLC), we examined the expression of these antigens and T cell infiltration in tumor tissue, and evaluated their prognostic significance. One hundred fifty-seven patients with NSCLC were studied. Reverse transcription-PCR was performed to evaluate MAGE-A4 and NY-ESO-1 expression. Immunohistochemistry was performed for NY-ESO-1 expression and T cell infiltration into the tumor site. Survival analysis was also performed. MAGE-A4 and NY-ESO-1 were expressed in 40 of 141 (28.4%) and 13 of 157 (8.3%) NSCLC respectively. Both CT antigens were more frequently expressed in squamous cell carcinoma (SCC) than in adenocarcinoma. An inverse correlation was found between MAGE-A4 expression and patient survival in advanced stage cancers. Combined infiltration of both CD4+ and CD8+ T cells into tumor nest predicted better survival. There was no correlation, however, between lymphocyte infiltration and antigen expression in the tumor. MAGE-A4 expression in advanced group and T cell infiltration may provide prognostic information. Lastly, these CT antigens, especially MAGE-A4, may represent potential targets for cancer immunotherapy in patients with NSCLC.

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Year:  2006        PMID: 16596224

Source DB:  PubMed          Journal:  Int J Oncol        ISSN: 1019-6439            Impact factor:   5.650


  33 in total

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2.  Rates of MAGE-A3 and PRAME expressing tumors in FFPE tissue specimens from bladder cancer patients: potential targets for antigen-specific cancer immunotherapeutics.

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Journal:  Int J Clin Exp Pathol       Date:  2015-08-01

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Journal:  Med Oncol       Date:  2011-11-25       Impact factor: 3.064

4.  Myeloid-derived suppressor cells enhance the expression of melanoma-associated antigen A4 in a Lewis lung cancer murine model.

Authors:  Guilan Shi; Huiru Wang; Xiufen Zhuang
Journal:  Oncol Lett       Date:  2015-11-13       Impact factor: 2.967

5.  The biology of cancer testis antigens: putative function, regulation and therapeutic potential.

Authors:  Elisabetta Fratta; Sandra Coral; Alessia Covre; Giulia Parisi; Francesca Colizzi; Riccardo Danielli; Hugues Jean Marie Nicolay; Luca Sigalotti; Michele Maio
Journal:  Mol Oncol       Date:  2011-02-18       Impact factor: 6.603

Review 6.  DNA vaccines, electroporation and their applications in cancer treatment.

Authors:  Si-Hyeong Lee; Sayyed Nilofar Danishmalik; Jeong-Im Sin
Journal:  Hum Vaccin Immunother       Date:  2015       Impact factor: 3.452

Review 7.  Predictive biomarkers of response to PD-1/PD-L1 immune checkpoint inhibitors in non-small cell lung cancer.

Authors:  Kazuhiko Shien; Vassiliki A Papadimitrakopoulou; Ignacio I Wistuba
Journal:  Lung Cancer       Date:  2016-06-21       Impact factor: 5.705

8.  Cancer-testis (CT) antigen expression in medulloblastoma.

Authors:  Sueli M Oba-Shinjo; Otavia L Caballero; Achim A Jungbluth; Sergio Rosemberg; Lloyd J Old; Andrew J G Simpson; Suely K N Marie
Journal:  Cancer Immun       Date:  2008-04-22

9.  Expression of cancer-testis antigens MAGE-A3/6 and NY-ESO-1 in non-small-cell lung carcinomas and their relationship with immune cell infiltration.

Authors:  Sang Hyun Kim; Sangyull Lee; Chang Hun Lee; Min Ki Lee; Young Dae Kim; Dong Hoon Shin; Kyung Un Choi; Jee Yeon Kim; Do Youn Park; Mee Young Sol
Journal:  Lung       Date:  2009-10-01       Impact factor: 2.584

10.  EarlyCDT®-Lung test: improved clinical utility through additional autoantibody assays.

Authors:  Caroline J Chapman; Graham F Healey; Andrea Murray; Peter Boyle; Chris Robertson; Laura J Peek; Jared Allen; Alison J Thorpe; Geoffrey Hamilton-Fairley; Celine B Parsy-Kowalska; Isabel K MacDonald; William Jewell; Paul Maddison; John F R Robertson
Journal:  Tumour Biol       Date:  2012-04-11
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