Department of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Department of Human and Molecular Genetics, Massey Cancer Center, VCU Institute of Molecular Medicine (VIMM), Virginia Commonwealth University, Richmond, VA 23298, USA.
Genes (Basel). 2021 Feb 22;12(2):308. doi: 10.3390/genes12020308.
Since its initial cloning in 2002, a plethora of studies in a vast number of cancer indications, has strongly established AEG-1 as a bona fide oncogene. In all types of cancer cells, overexpression and knockdown studies have demonstrated that AEG-1 performs a seminal role in regulating proliferation, invasion, angiogenesis, metastasis and chemoresistance, the defining cancer hallmarks, by a variety of mechanisms, including protein-protein interactions activating diverse oncogenic pathways, RNA-binding promoting translation and regulation of inflammation, lipid metabolism and tumor microenvironment. These findings have been strongly buttressed by demonstration of increased tumorigenesis in tissue-specific AEG-1 transgenic mouse models, and profound resistance of multiple types of cancer development and progression in total and conditional AEG-1 knockout mouse models. Additionally, clinicopathologic correlations of AEG-1 expression in a diverse array of cancers establishing AEG-1 as an independent biomarker for highly aggressive, chemoresistance metastatic disease with poor prognosis have provided a solid foundation to the mechanistic and mouse model studies. In this review a comprehensive analysis of the current and up-to-date literature is provided to delineate the clinical significance of AEG-1 in cancer highlighting the commonality of the findings and the discrepancies and discussing the implications of these observations.
自 2002 年首次克隆以来,大量针对多种癌症适应症的研究强烈证实 AEG-1 是一种真正的癌基因。在所有类型的癌细胞中,过表达和敲低研究表明,AEG-1 通过多种机制,包括激活各种致癌途径的蛋白-蛋白相互作用、促进翻译和调节炎症、脂质代谢和肿瘤微环境的 RNA 结合,在调节增殖、侵袭、血管生成、转移和化疗耐药性等癌症特征方面发挥着重要作用。这些发现得到了强有力的支持,即在组织特异性 AEG-1 转基因小鼠模型中观察到肿瘤发生增加,以及在总和条件性 AEG-1 敲除小鼠模型中观察到多种癌症的发展和进展的显著抵抗。此外,在多种癌症中 AEG-1 表达的临床病理相关性确立了 AEG-1 作为具有高度侵袭性、化疗耐药性和预后不良的转移性疾病的独立生物标志物,为机制和小鼠模型研究提供了坚实的基础。在这篇综述中,对当前和最新的文献进行了全面分析,以阐述 AEG-1 在癌症中的临床意义,突出了这些发现的共同点和差异,并讨论了这些观察结果的意义。