Ad-MDA-7; INGN 241: a review of preclinical and clinical experience

被引:43
作者
Eager, Robert [1 ,2 ]
Harle, Lindsey [1 ,3 ]
Nemunaitis, John [1 ,4 ,5 ,6 ]
机构
[1] Mary Crowley Canc Res Ctr, Dallas, TX 75201 USA
[2] Univ Hawaii, Dept Internal Med, Honolulu, HI 96822 USA
[3] Univ Hawaii, Dept Pathol, Honolulu, HI 96822 USA
[4] Gradalis Inc, Dallas, TX USA
[5] Texas Oncol PA, Dallas, TX USA
[6] Baylor Sammons Canc Ctr, Dallas, TX USA
基金
美国国家卫生研究院;
关键词
adenoviris; APC apoptosis; beta-catenin; bcl receptor; bystander; cancer gene therapy; cytokine; E-cadherin; GSK-3; beta; IL-10; IL-20; IL-22; IL-24; intratumoral; MDA-7; PI3K; PTEN; targeted;
D O I
10.1517/14712598.8.10.1633
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The melanoma differentiation-associated gene-7 (MDA-7) was isolated while screening for upregulated genes in terminally differentiated melanoma cell lines. Preclinical studies attempted to test the theory that oncogenesis arises from a cellular differentiation process culminating in dysregulation of the cell cycle and ultimately malignancy. The MDA-7 gene (gene symbol IL-24) has been classified as part of the IL-10 family of cytokines demonstrating significant anticancer potential. Preclinical studies have shown that MDA-7/IL-24 is effective in inducing cancer cell death by several pathways in various tumor models. A Phase I clinical trial studying intratumoral injections of solid tumors showed evidence of clinical activity with limited toxicity. This small trial suggested therapeutic potential. Results are reviewed. Future opportunities involve combination with different gene delivery systems with systemic potential.
引用
收藏
页码:1633 / 1643
页数:11
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