Wang Xiaosong, Zhao Haitao, Xu Qingwen, Jin Weibo, Liu Changning, Zhang Huagang, Huang Zhibin, Zhang Xinyu, Zhang Yu, Xin Dianqi, Simpson Andrew J G, Old Lloyd J, Na Yanqun, Zhao Yi, Chen Weifeng
Department of Immunology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing 100083, China.
Nucleic Acids Res. 2006 Jan 1;34(Database issue):D607-12. doi: 10.1093/nar/gkj082.
Tumor-associated antigens (TAAs) have been the most actively employed targets in the clinical diagnosis and treatment of human carcinoma, such as PSA in the diagnosis of prostate cancer and NY-ESO-1 in the immunotherapy of melanoma and other cancers. However, identification of TAAs has often been hampered by the complicated and laborsome laboratory procedures. In order to accelerate the process of tumor antigen discovery, and thereby improve diagnosis and treatment of human carcinoma, we have made an effort to establish a publicly available Human Potential Tumor Associated Antigen database (HPtaa) with potential TAAs identified by in silico computing (http://www.hptaa.org). Tumor specificity was chosen as the core of tumor antigen evaluation, together with other relevant clues. Various platforms of gene expression, including microarray, expressed sequence tag and SAGE data, were processed and integrated by several penalty algorithms. A total of 3518 potential TAAs have been included in the database, which is freely available to academic users. As far as we know, this database is the first one addressing human potential TAAs, and the first one integrating various kinds of expression platforms for one purpose.
肿瘤相关抗原(TAAs)一直是人类癌症临床诊断和治疗中最积极应用的靶点,例如前列腺特异性抗原(PSA)用于前列腺癌的诊断,而纽约食管鳞状细胞癌-1(NY-ESO-1)用于黑色素瘤及其他癌症的免疫治疗。然而,TAAs的鉴定常常受到复杂且繁琐的实验室程序的阻碍。为了加速肿瘤抗原发现的进程,从而改善人类癌症的诊断和治疗,我们努力建立了一个可公开获取的人类潜在肿瘤相关抗原数据库(HPtaa),其中的潜在TAAs是通过计算机计算鉴定出来的(http://www.hptaa.org)。肿瘤特异性与其他相关线索一起被选为肿瘤抗原评估的核心。包括微阵列、表达序列标签和基因表达连续分析(SAGE)数据在内的各种基因表达平台,通过几种惩罚算法进行处理和整合。该数据库共纳入了3518个潜在TAAs,学术用户可免费使用。据我们所知,这个数据库是首个针对人类潜在TAAs的数据库,也是首个为单一目的整合各类表达平台的数据库。