Literature DB >> 10679095

Identification of a gene coding for a new squamous cell carcinoma antigen recognized by the CTL.

M Nakao1, S Shichijo, T Imaizumi, Y Inoue, K Matsunaga, A Yamada, M Kikuchi, N Tsuda, K Ohta, S Takamori, H Yamana, H Fujita, K Itoh.   

Abstract

Peptide-based specific immunotherapy has resulted in tumor regression in some melanoma patients. However, tumor Ags and peptides for specific immunotherapy, except for treatment of melanomas, have not yet been well identified. In this study, we report a gene encoding a new squamous cell carcinoma (SCC) Ag recognized by cells of the HLA-A24-restricted and tumor-specific CTL line. This gene with 3958-bp length was transcribed from the chromosome 6q22 with six exons, and its mRNA was ubiquitously expressed in both SCCs and normal tissues, and partly expressed in adenocarcinomas. The deduced 958-aa sequence encoded by this gene showed no similarity to any known amino acid sequences. This gene product had a characteristic of an endoplasmic reticulum-resident protein. A 100-kDa protein was detected in the vast majority of SCCs from various tissues, in majority of renal cell carcinomas and brain tumors, and in about one-third of melanomas and adenocarcinomas from various organs other than the breast. In contrast, it was not expressed at all in any of the normal cells or tissues tested, including the testis and fetal liver. Three different peptides at positions 93-101, 161-169, and 899-907 of this Ag were recognized by this CTL line, and all of them induced HLA-A24-restricted and tumor-specific CTLs from PBMCs of SCC patients. Therefore, these peptides may be useful for peptide-based specific immunotherapy of HLA-A24+ patients with SCC in various organs, as well as for treatment of other cancer.

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Year:  2000        PMID: 10679095     DOI: 10.4049/jimmunol.164.5.2565

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  34 in total

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2.  Dermatan sulfate is involved in the tumorigenic properties of esophagus squamous cell carcinoma.

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3.  Two dermatan sulfate epimerases form iduronic acid domains in dermatan sulfate.

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Journal:  J Biol Chem       Date:  2009-02-02       Impact factor: 5.157

Review 4.  Mobilizing the low-avidity T cell repertoire to kill tumors.

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Journal:  Semin Cancer Biol       Date:  2007-06-23       Impact factor: 15.707

5.  Dermatan sulfate epimerase 1-deficient mice have reduced content and changed distribution of iduronic acids in dermatan sulfate and an altered collagen structure in skin.

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6.  HLA-A2-restricted cytotoxic T lymphocyte epitopes from human heparanase as novel targets for broad-spectrum tumor immunotherapy.

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8.  Gene expression in uninvolved oral mucosa of OSCC patients facilitates identification of markers predictive of OSCC outcomes.

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Review 9.  Molecular signature induced by RNASET2, a tumor antagonizing gene, in ovarian cancer cells.

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10.  Aberrant expression and potency as a cancer immunotherapy target of alpha-methylacyl-coenzyme A racemase in prostate cancer.

Authors:  Ichiya Honma; Toshihiko Torigoe; Yoshihiko Hirohashi; Hiroshi Kitamura; Eiji Sato; Naoya Masumori; Yasuaki Tamura; Taiji Tsukamoto; Noriyuki Sato
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