Literature DB >> 15118836

NY-ESO-1 expression and its serum immunoreactivity in esophageal cancer.

Argun Akcakanat1, Tatsuo Kanda, Yu Koyama, Michitoshi Watanabe, Eiji Kimura, Yutaka Yoshida, Shintarou Komukai, Satoru Nakagawa, Shoji Odani, Hiroshi Fujii, Katsuyoshi Hatakeyama.   

Abstract

PURPOSE: NY-ESO-1, a member of the cancer/testis antigen (CTA) family, elicits humoral and cellular immune responses in patients with advanced cancer. Unresectable or metastatic esophageal carcinoma patients do not benefit from the present multimodality treatment regimens in terms of survival. The objectives of this study were to analyze the antibody response to NY-ESO-1 antigen in patients with esophageal cancer and to determine the potential of NY-ESO-1 for use in tumor-specific immunotherapy.
METHODS: Serum from 69 patients with esophageal cancer was investigated for antibody production against NY-ESO-1 by Western blot analysis. Also analyzed by immunohistochemistry were 56 tissue samples from these patients for NY-ESO-1 protein expression.
RESULTS: NY-ESO-1 protein expression was found in 18 of 56 (32%) esophageal carcinomas. Serum immunoreactivity specific for NY-ESO-1 was found in 9 patients (13%) of whom 8 were in the advanced stage (stages III and IV). There was no relationship between clinicopathologic features and serum immunoreactivity for NY-ESO-1. NY-ESO-1 protein expression was detected in three of five antibody-positive patients whose tissue was available for analysis. Survival analysis showed no significant difference between antibody-positive and antibody-negative patient groups.
CONCLUSIONS: A humoral immune response to NY-ESO-1 antigen was established in patients with advanced esophageal cancer. NY-ESO-1 is a good candidate for vaccine-based immunotherapy for advanced esophageal carcinoma.

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Year:  2004        PMID: 15118836     DOI: 10.1007/s00280-004-0768-3

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  20 in total

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4.  Expression of MAGE-A and NY-ESO-1 in Primary and Metastatic Cancers.

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5.  MAGE-A is More Highly Expressed Than NY-ESO-1 in a Systematic Immunohistochemical Analysis of 3668 Cases.

Authors:  Sid P Kerkar; Zeng-Feng Wang; Jerzy Lasota; Tristen Park; Krishna Patel; Eric Groh; Steven A Rosenberg; Markku M Miettinen
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Journal:  Immunology       Date:  2018-06-13       Impact factor: 7.215

10.  A human monoclonal autoantibody to breast cancer identifies the PDZ domain containing protein GIPC1 as a novel breast cancer-associated antigen.

Authors:  Sergei Rudchenko; Matthew Scanlan; Gavreel Kalantarov; Victoria Yavelsky; Chen Levy; Alison Estabrook; Lloyd Old; Gerald L Chan; Leslie Lobel; Ilya Trakht
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