Byrne Jennifer A, Frost Sarah, Chen Yuyan, Bright Robert K
Molecular Oncology Laboratory, Children's Cancer Research Unit, Kids Research Institute, The Children's Hospital at Westmead, Locked Bag 4001, Westmead, 2145, NSW, Australia,
Tumour Biol. 2014 Aug;35(8):7369-82. doi: 10.1007/s13277-014-2006-x. Epub 2014 May 6.
The Tumor protein D52 (TPD52) gene was identified nearly 20 years ago through its overexpression in human cancer, and a substantial body of data now strongly supports TPD52 representing a gene amplification target at chromosome 8q21.13. This review updates progress toward understanding the significance of TPD52 overexpression and targeting, both in tumors known to be characterized by TPD52 overexpression/amplification, and those where TPD52 overexpression/amplification has been recently or variably reported. We highlight recent findings supporting microRNA regulation of TPD52 expression in experimental systems and describe progress toward deciphering TPD52's cellular functions, particularly in cancer cells. Finally, we provide an overview of TPD52's potential as a cancer biomarker and immunotherapeutic target. These combined studies highlight the potential value of genes such as TPD52, which are overexpressed in many cancer types, but have been relatively understudied.
肿瘤蛋白D52(TPD52)基因近20年前通过其在人类癌症中的过表达被鉴定出来,现在大量数据有力地支持TPD52是8号染色体q21.13上的一个基因扩增靶点。这篇综述更新了在理解TPD52过表达和靶向作用的意义方面所取得的进展,这些研究涉及已知以TPD52过表达/扩增为特征的肿瘤,以及最近或不同程度报道过TPD52过表达/扩增的肿瘤。我们强调了支持实验系统中TPD52表达受微小RNA调控的最新发现,并描述了在破解TPD52细胞功能方面所取得的进展,特别是在癌细胞中的功能。最后,我们概述了TPD52作为癌症生物标志物和免疫治疗靶点的潜力。这些综合研究突出了TPD52等基因的潜在价值,这些基因在许多癌症类型中过表达,但相对研究较少。