Expression of cancer testis antigens in thymic epithelial tumors. 2021

Tadashi Sakane, and Takayuki Murase, and Katsuhiro Okuda, and Ayako Masaki, and Ryoichi Nakanishi, and Hiroshi Inagaki
Department of Pathology and Molecular Diagnostics, Nagoya City University Graduate School of Medical Sciences, Aichi, Japan.

Cancer testis antigens (CTAs) are detected in cancer cells but not in healthy normal tissues, with the exception of gametogenic tissues. However, to our knowledge, expression of the antigens in thymic epithelial tumors has not been examined yet. We examined the immunohistochemical expression of five CTAs (MAGE-A, NY-ESO-1, MAGE-C1, SAGE and GAGE7) in 192 cases of thymic epithelial tumor. The CTAs were variably expressed in the thymic epithelial tumors. Type B component of type AB thymomas, type B1/B2/B3 thymomas, and thymic carcinomas showed a generally positive correlation between the malignancy grades and positive expression rates in four CTAs other than MAGE-C1. In thymic squamous cell carcinomas (SqCCs), four antigens except for MAGE-C1 showed high expression rates ranging from 23.1% to 43.6%. In the prognostic analysis, a positive expression of SAGE (P = 0.0485) and GAGE7 (P = 0.0289) were associated with a shorter overall survival in type B2/B3 thymomas, respectively. In thymic SqCC, a positive MAGE-A expression was significantly associated with an increased level of programmed death ligand in tumor-infiltrating lymphocytes (P = 0.0181). We showed (i) a frequent CTA expression, (ii) a general correlation of CTA expression with tumor malignancy grades and (iii) a prognostic impact in some of the CTAs.

UI MeSH Term Description Entries
D007150 Immunohistochemistry Histochemical localization of immunoreactive substances using labeled antibodies as reagents. Immunocytochemistry,Immunogold Techniques,Immunogold-Silver Techniques,Immunohistocytochemistry,Immunolabeling Techniques,Immunogold Technics,Immunogold-Silver Technics,Immunolabeling Technics,Immunogold Silver Technics,Immunogold Silver Techniques,Immunogold Technic,Immunogold Technique,Immunogold-Silver Technic,Immunogold-Silver Technique,Immunolabeling Technic,Immunolabeling Technique,Technic, Immunogold,Technic, Immunogold-Silver,Technic, Immunolabeling,Technics, Immunogold,Technics, Immunogold-Silver,Technics, Immunolabeling,Technique, Immunogold,Technique, Immunogold-Silver,Technique, Immunolabeling,Techniques, Immunogold,Techniques, Immunogold-Silver,Techniques, Immunolabeling
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D009375 Neoplasms, Glandular and Epithelial Neoplasms composed of glandular tissue, an aggregation of epithelial cells that elaborate secretions, and of any type of epithelium itself. The concept does not refer to neoplasms located in the various glands or in epithelial tissue. Epithelial Cell Neoplasms,Glandular Cell Neoplasms,Epithelial Neoplasms,Glandular Neoplasms,Glandular and Epithelial Neoplasms,Neoplasms, Epithelial,Neoplasms, Glandular,Neoplasms, Glandular Epithelial,Cell Neoplasm, Epithelial,Cell Neoplasm, Glandular,Cell Neoplasms, Epithelial,Epithelial Cell Neoplasm,Epithelial Neoplasm,Epithelial Neoplasm, Glandular,Glandular Cell Neoplasm,Glandular Epithelial Neoplasm,Glandular Epithelial Neoplasms,Glandular Neoplasm,Neoplasm, Epithelial,Neoplasm, Epithelial Cell,Neoplasm, Glandular,Neoplasm, Glandular Cell,Neoplasm, Glandular Epithelial
D011379 Prognosis A prediction of the probable outcome of a disease based on a individual's condition and the usual course of the disease as seen in similar situations. Prognostic Factor,Prognostic Factors,Factor, Prognostic,Factors, Prognostic,Prognoses
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D000368 Aged A person 65 years of age or older. For a person older than 79 years, AGED, 80 AND OVER is available. Elderly
D000951 Antigens, Neoplasm Proteins, glycoprotein, or lipoprotein moieties on surfaces of tumor cells that are usually identified by monoclonal antibodies. Many of these are of either embryonic or viral origin. Neoplasm Antigens,Tumor Antigen,Tumor Antigens,Antigen, Tumor,Antigens, Tumor

Related Publications

Tadashi Sakane, and Takayuki Murase, and Katsuhiro Okuda, and Ayako Masaki, and Ryoichi Nakanishi, and Hiroshi Inagaki
August 2014, Lung cancer (Amsterdam, Netherlands),
Tadashi Sakane, and Takayuki Murase, and Katsuhiro Okuda, and Ayako Masaki, and Ryoichi Nakanishi, and Hiroshi Inagaki
June 2017, Gynecologic oncology,
Tadashi Sakane, and Takayuki Murase, and Katsuhiro Okuda, and Ayako Masaki, and Ryoichi Nakanishi, and Hiroshi Inagaki
May 2019, Clinical lung cancer,
Tadashi Sakane, and Takayuki Murase, and Katsuhiro Okuda, and Ayako Masaki, and Ryoichi Nakanishi, and Hiroshi Inagaki
July 2005, Chest,
Tadashi Sakane, and Takayuki Murase, and Katsuhiro Okuda, and Ayako Masaki, and Ryoichi Nakanishi, and Hiroshi Inagaki
August 1982, Human immunology,
Tadashi Sakane, and Takayuki Murase, and Katsuhiro Okuda, and Ayako Masaki, and Ryoichi Nakanishi, and Hiroshi Inagaki
September 2011, The American journal of surgical pathology,
Tadashi Sakane, and Takayuki Murase, and Katsuhiro Okuda, and Ayako Masaki, and Ryoichi Nakanishi, and Hiroshi Inagaki
January 2014, PloS one,
Tadashi Sakane, and Takayuki Murase, and Katsuhiro Okuda, and Ayako Masaki, and Ryoichi Nakanishi, and Hiroshi Inagaki
January 1991, Developmental and comparative immunology,
Tadashi Sakane, and Takayuki Murase, and Katsuhiro Okuda, and Ayako Masaki, and Ryoichi Nakanishi, and Hiroshi Inagaki
October 2002, Zhongguo fei ai za zhi = Chinese journal of lung cancer,
Tadashi Sakane, and Takayuki Murase, and Katsuhiro Okuda, and Ayako Masaki, and Ryoichi Nakanishi, and Hiroshi Inagaki
October 2003, Lung cancer (Amsterdam, Netherlands),
Copied contents to your clipboard!