Shang B, Gao A, Pan Y, Zhang G, Tu J, Zhou Y, Yang P, Cao Z, Wei Q, Ding Y, Zhang J, Zhao Y, Zhou Q
Cyrus Tang Hematology Center, Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Key Laboratory of Thrombosis and Hemostasis, Ministry of Health, Soochow University, Suzhou, Jiangsu, China.
The Second Affiliated Hospital of Soochow University, Soochow University, Suzhou, Jiangsu, China.
Cell Death Dis. 2014 Jun 5;5(6):e1285. doi: 10.1038/cddis.2014.244.
Cancer/testis antigen (CTA)-45 family (CT45) belongs to a new family of genes in phylogenetics and is absent in normal tissues except for testis, but is aberrantly overexpressed in various cancer types. Whether CT45 and other CTAs act as proto-oncogenes has not been determined. Using breast cancer as a model, we found that CT45A1, a representative CT45 family member, alone had a weak tumorigenic effect. However, its neoplastic potency was greatly enhanced in the presence of growth factors. Overexpression of CT45A1 in breast cancer cells markedly upregulated various oncogenic and metastatic genes, constitutively activated ERK and CREB signaling pathways, promoted epithelial-mesenchymal transition, and increased cell stemness, tumorigenesis, invasion, and metastasis, whereas silencing CT45A1 significantly reduced cancer cell migration and invasion. We propose that CT45A1 functions as a novel proto-oncogene to trigger oncogenesis and metastasis. CT45A1 and other CT45 members are therefore excellent targets for anticancer drug discovery and targeted tumor therapy, and valuable genes in the study of a molecular phylogenetic tree.
癌/睾丸抗原(CTA)-45家族(CT45)在系统发育学上属于一个新的基因家族,除睾丸外,在正常组织中不存在,但在多种癌症类型中异常高表达。CT45和其他CTA是否作为原癌基因尚未确定。以乳腺癌为模型,我们发现CT45家族的代表性成员CT45A1单独具有较弱的致瘤作用。然而,在生长因子存在的情况下,其致瘤能力大大增强。CT45A1在乳腺癌细胞中的过表达显著上调了各种致癌和转移基因,持续激活ERK和CREB信号通路,促进上皮-间质转化,并增加细胞干性、肿瘤发生、侵袭和转移,而沉默CT45A1则显著降低癌细胞的迁移和侵袭。我们提出CT45A1作为一种新型原癌基因发挥作用,触发肿瘤发生和转移。因此,CT45A1和其他CT45成员是抗癌药物发现和靶向肿瘤治疗的优秀靶点,也是分子系统发育树研究中有价值的基因。