Ueno N T, Yu D, Hung M C
Department of Molecualr and Cellular Oncology, The University of Texas, M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Box 448, Houston, TX 77030, USA.
Breast Cancer. 2001;8(4):285-93. doi: 10.1007/BF02967526.
In the late 1980s, we have shown that the E1A gene can downregulate HER-2/neu overexpression, thus reversing the tumorigenic and metastatic phenotype. Further, E1A can function as a tumor suppressor gene by inducing apoptosis and inhibiting metastasis. At The University of Texas M. D. Anderson Cancer Center, we have been investigating the adenovirus type 5 E1A gene as a potential therapeutic gene in breast and ovarian cancer since 1995 by using cationic liposome as gene delivery system. In this chapter, we recount our development of E1A as a therapeutic gene.
在20世纪80年代后期,我们已经证明E1A基因可以下调HER-2/neu的过表达,从而逆转肿瘤发生和转移表型。此外,E1A可以通过诱导凋亡和抑制转移发挥肿瘤抑制基因的作用。自1995年以来,我们在德克萨斯大学MD安德森癌症中心,一直使用阳离子脂质体作为基因递送系统,研究5型腺病毒E1A基因作为乳腺癌和卵巢癌潜在治疗基因的可能性。在本章中,我们讲述了E1A作为治疗基因的发展历程。