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Development of PEA-15 using a potent non-viral vector for therapeutic application in breast cancer

机译:使用有效的非病毒载体开发PEA-15在乳腺癌中的治疗应用

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摘要

Advanced breast cancer requires systemic treatment, therefore developing an efficient and safe strategy is urgently needed. To ensure the success of target therapy, we have developed a breast cancer-specific construct (T-VISA) composed of the human telomerase reverse transcriptase (hTERT; T) promoter and a versatile transgene amplification vector VISA (VP16-GAL4-WPRE integrated systemic amplifier) to target PEA-15 (Phosphoprotein enriched in astrocytes) in advanced breast tumors. PEA-15 contains a death effector domain that sequesters extracellular signal-regulated kinase (ERK) in cytoplasm, thereby inhibiting cell proliferation and inducing apoptosis. T-VISA-PEA-15 was found to be highly specific, selectively express PEA-15 in breast cancer cells, and induce cancer-cell killing in vitro and in vivo without affecting normal cells. Moreover, intravenously treatment with T-VISA-PEA-15 coupled with liposome nanoparticles attenuated tumor growth and prolonged survival in mice bearing advanced breast tumors. Importantly, there was virtually no severe toxicity when PEA-15 is expressed by our T-VISA system compared with cytomegalovirus (CMV) promoter. Thus, our findings demonstrate an effective cancer-targeted therapy that is worthy of development in clinical trials eradicating advanced breast cancer.
机译:晚期乳腺癌需要系统治疗,因此迫切需要开发有效且安全的策略。为确保目标疗法的成功,我们开发了由人端粒酶逆转录酶(hTERT; T)启动子和多功能转基因扩增载体VISA(VP16-GAL4-WPRE整合而成的系统)组成的乳腺癌特异性构建体(T-VISA)放大器)靶向晚期乳腺癌中的PEA-15(富含星形胶质细胞的磷酸蛋白)。 PEA-15包含一个死亡效应域,该域隔离细胞质中的细胞外信号调节激酶(ERK),从而抑制细胞增殖并诱导细胞凋亡。发现T-VISA-PEA-15是高度特异性的,在乳腺癌细胞中选择性表达PEA-15,并在不影响正常细胞的情况下在体内和体外诱导癌细胞杀伤。此外,用T-VISA-PEA-15结合脂质体纳米颗粒进行静脉内治疗可减缓患有晚期乳腺肿瘤的小鼠的肿瘤生长并延长其生存期。重要的是,与巨细胞病毒(CMV)启动子相比,当我们的T-VISA系统表达PEA-15时,几乎没有严重的毒性。因此,我们的发现证明了一种有效的针对癌症的疗法,值得在根除晚期乳腺癌的临床试验中进行开发。

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