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PMID: 14522938 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

NY-ESO-1 and LAGE-1 cancer-testis antigens are potential targets for immunotherapy in epithelial ovarian cancer.

Cancer research ·Vol. 63 ·No. 18 ·2003-09-15 ·Pages 6076-83

Odunsi K, Jungbluth AA, Stockert E, Qian F, Gnjatic S, Tammela J, Intengan M, Beck A, Keitz B, Santiago D, Williamson B, Scanlan MJ, Ritter G, Chen YT, Driscoll D, Sood A, Lele S, Old LJ

Abstract

Cancer-testis (CT) antigens are expressed in a variety of cancers, but not in normal adult tissues, except for germ cells of the testis, and hence appear to be ideal targets for immunotherapy. In an effort to examine the potential of NY-ESO-1 and LAGE-1 CT antigens for immunotherapy in epithelial ovarian cancer (EOC), we examined the expression of these antigens by reverse transcription-PCR (RT-PCR) and immunohistochemistry (IHC) in a large panel of EOC tissues and cell lines. Sera from a subgroup of the patients were tested for NY-ESO-1/LAGE-1 antibody by ELISA. The data indicated that four ovarian cancer cell lines were positive for one or both CT antigens. Expression of NY-ESO-1 in EOC was demonstrated by RT-PCR and/or IHC in 82 of 190 (43%) specimens. NY-ESO-1 expression by IHC ranged from homogeneous to heterogeneous pattern. LAGE-1 mRNA expression was present in 22 of 107 (21%) tumor tissues. Overall, the expression of either NY-ESO-1 or LAGE-1 mRNA was present in 42 of 107 (40%) EOC specimens and coexpression of both antigens was demonstrated in 11% of specimens. Antibody to NY-ESO-1/LAGE-1 was present in 11 of 37 (30%) patients whose tumors expressed either NY-ESO-1 or LAGE-1. Detectable antibodies were present for up to 3 years after initial diagnosis. Although there was no statistically significant relation between expression of NY-ESO-1/LAGE-1 antigen and survival, the data showed aberrant expression of NY-ESO-1 and LAGE-1 by IHC/RT-PCR in a significant proportion of EOC patients. These findings indicate that NY-ESO-1 and LAGE-1 are attractive targets for antigen-specific immunotherapy in EOC.

MeSH Terms
Adult Aged Aged, 80 and over Antibodies, Neoplasm/biosynthesis,blood Antigens, Neoplasm Antigens, Surface Enzyme-Linked Immunosorbent Assay Female Gene Expression Humans Membrane Proteins Middle Aged Ovarian Neoplasms/genetics,immunology,metabolism,therapy Prognosis Protein Biosynthesis Proteins/genetics,immunology RNA, Messenger/biosynthesis,genetics
Chemicals
Antibodies, Neoplasm Antigens, Neoplasm Antigens, Surface CTAG1B protein, human CTAG2 protein, human Membrane Proteins Proteins RNA, Messenger
Authors & Affiliations
18 authors, click to expand affiliations / ORCID
Odunsi Kunle
Division of Gynecologic Oncology, Roswell Park Cancer Institute, Buffalo, New York 14263, USA.
Jungbluth Achim A
Stockert Elisabeth
Qian Feng
Gnjatic Sacha
Tammela Jonathan
Intengan Marilyn
Beck Amy
Keitz Bernadette
Santiago Darren
Williamson Barbara
Scanlan Matthew J
Ritter Gerd
Chen Yao-Tseng
Driscoll Deborah
Sood Ashwani
Lele Shashikant
Old Lloyd J
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
2003-09-15
Pages
6076-83
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
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