Naka Norifumi, Joyama Susumu, Tsukamoto Yoshitane, Yoshioka Kiyoko, Hashimoto Nobuyuki, Ujiiye Takeshi, Hayashi Tsukasa, Kawase Masako, Mano Masayuki, Ishiguro Shingo, Myoui Akira, Ueda Takafumi, Yoshikawa Hideki, Araki Nobuhito, Itoh Kazuyuki
Department of Orthopedic Surgery, Osaka Medical Center for Cancer and Cardiovascular Diseases, 1-3-2 Nakamichi, Higashinari-ku, Osaka 537-8511, Japan.
J Mol Diagn. 2005 May;7(2):187-97. doi: 10.1016/S1525-1578(10)60545-4.
The SSX family proteins have been considered new members of the cancer/testis antigens because of the restricted expression in testis among normal tissues and the activation in a wide range of cancers. Thus, they would be potential molecular targets for immunotherapeutic strategies. We have developed a competitive nucleic acid sequence-based amplification (NASBA) assay to analyze SSX mRNA expression in 211 bone and soft tissue tumors. The copy numbers of SSX mRNA per mug of total RNA in tumor tissues were widely distributed, ranging logarithmically from 0.6 to 6.6. We found that malignant tumors showed significantly higher expression of SSX mRNA than benign tumors (P < 0.0001). Further, SSX mRNA expression in stage III tumors was significantly higher than that in stage I or II tumors (P < 0.005). This NASBA assay was also more sensitive compared to immunohistochemistry using newly affinity-purified polyclonal antibody against SSX. Collectively, these results suggest that the SSX quantitative NASBA assay could provide useful information to select eligible patients for SSX-specific cancer vaccines.
由于在正常组织中SSX家族蛋白仅在睾丸中表达受限,而在多种癌症中被激活,因此被认为是癌胚抗原的新成员。因此,它们可能是免疫治疗策略的潜在分子靶点。我们开发了一种基于竞争性核酸序列扩增(NASBA)的检测方法,以分析211例骨和软组织肿瘤中SSX mRNA的表达情况。肿瘤组织中每微克总RNA的SSX mRNA拷贝数分布广泛,对数范围为0.6至6.6。我们发现恶性肿瘤中SSX mRNA的表达明显高于良性肿瘤(P < 0.0001)。此外,III期肿瘤中SSX mRNA的表达明显高于I期或II期肿瘤(P < 0.005)。与使用新亲和纯化的抗SSX多克隆抗体进行免疫组织化学相比,这种NASBA检测方法也更灵敏。总体而言,这些结果表明,SSX定量NASBA检测可为选择适合使用SSX特异性癌症疫苗的患者提供有用信息。