| Literature DB >> 25304382 |
Xinhua Xie1,2, Hailin Tang1,2, Yanan Kong1,2, Minqing Wu1,2, Xiangsheng Xiao1,2, Lu Yang1,2, Jie Gao1,2, Weidong Wei1,2, Jangsoon Lee3, Chandra Bartholomeusz3, Naoto T Ueno3, Xiaoming Xie1,2.
Abstract
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 the 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, intravenous 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.Entities:
Keywords: Breast cancer; PEA-15; T-VISA system; Target therapy
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Year: 2014 PMID: 25304382 PMCID: PMC4571276 DOI: 10.1016/j.canlet.2014.09.033
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679