Overexpression of melanoma-associated antigen D4 is an independent prognostic factor in squamous cell carcinoma of the esophagus

被引:21
作者
Oya, H. [1 ]
Kanda, M. [1 ]
Takami, H. [1 ]
Hibino, S. [1 ]
Shimizu, D. [1 ]
Niwa, Y. [1 ]
Koike, M. [1 ]
Nomoto, S. [1 ]
Yamada, S. [1 ]
Nishikawa, Y. [1 ]
Asai, M. [1 ]
Fujii, T. [1 ]
Nakayama, G. [1 ]
Sugimoto, H. [1 ]
Fujiwara, M. [1 ]
Kodera, Y. [1 ]
机构
[1] Nagoya Univ, Grad Sch Med, Dept Gastroenterol Surg Surg 2, Nagoya, Aichi 4668550, Japan
关键词
esophageal cancer; expression; MAGE-D4; progression; MAGE GENE FAMILY; HEPATOCELLULAR-CARCINOMA; CHROMOSOMAL LOCALIZATION; BIOLOGICAL FUNCTIONS; BREAST-CANCER; MYELOMA CELLS; LUNG-CANCER; EXPRESSION; IDENTIFICATION; APOPTOSIS;
D O I
10.1111/dote.12156
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
To pursue an urgently needed treatment target for esophageal cancer (EC), we investigated the function of the recently discovered melanoma-associated antigen (MAGE)-D4 in squamous cell EC. MAGE-D4 messenger RNA (mRNA) expression was analyzed in nine EC cell lines using quantitative reverse transcription polymerase chain reaction. In 65 surgical specimens of squamous cell EC with no prior neoadjuvant therapy, MAGE-D4mRNA expression in EC tissues and corresponding normal tissues was analyzed and compared, and evaluated in terms of clinicopathological factors. In representative cases, MAGE-D4 protein distribution was analyzed immunohistochemically. The heterogeneity of MAGE-D4mRNA expression was confirmed in EC cell lines by quantitative reverse transcription polymerase chain reaction. In surgical specimens, MAGE-D4mRNA expression was significantly higher in EC tissues than in corresponding normal tissues (P<0.001). Patients with the highest MAGE-D4mRNA expression in EC tissues (top quartile, n = 17) had significantly shorter overall survival than patients with low expression (2-year survival: 44% and 73%, respectively, P = 0.006). Univariate analysis identified age (65 years), lymphatic involvement, and high MAGE-D4mRNA expression as significant prognostic factors; high MAGE-D4mRNA expression was also an independent prognostic factor in multivariable analysis (hazard ratio: 2.194; P = 0.039) and was significantly associated with Brinkman index (P = 0.008) and preoperative carcinoembryonic antigen level (P = 0.002). Immunohistochemical MAGE-D4b expression was consistent with MAGE-D4mRNA profiling. Our results suggest that MAGE-D4 overexpression influences tumor progression, and MADE-D4 can be a prognostic marker and a potential molecular target in squamous cell EC.
引用
收藏
页码:188 / 195
页数:8
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