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Melanoma differentiation associated gene-7 (mda-7): a novel anti-tumor gene for cancer gene therapy.

机译:黑色素瘤分化相关基因7(mda-7):一种用于癌症基因治疗的新型抗肿瘤基因。

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摘要

BACKGROUND: The mda-7 gene (melanoma differentiation associated gene-7) is a novel tumor suppressor gene. The anti-proliferative activity of MDA-7 has been previously reported. In this report, we analyze the anti-tumor efficacy of Ad-mda7 in a broad spectrum of cancer lines. MATERIALS AND METHODS: Ad-mda7-transduced cancer or normal cell lines were assayed for cell proliferation (tritiated thymidine incorporation assay, Alamar blue assay, and trypan-blue exclusion assay), apoptosis (TUNEL, and Annexin V staining visualized by fluorescent microscopy or FACs analysis), and cell cycle regulation (Propidium Iodide staining and FACs analysis). RESULTS: Ad-mda7 treatment of tumor cells resulted in growth inhibition and apoptosis in a temporal and dose-dependent manner. The anti-tumor effects were independent of the genomic status of p53, RB, p16, ras, bax, and caspase 3 in these cells. In addition, normal cell lines did not show inhibition of proliferation or apoptotic response to Ad-mda7. Moreover, Ad-mda7-transduced cancer cells secreted a soluble form of MDA-7 protein. Thus, Ad-mda7 may represent a novel gene-therapeutic agent for the treatment of a variety of cancers. CONCLUSIONS: The potent and selective killing activity of Ad-mda7 in cancer cells but not in normal cells makes this vector a potential candidate for cancer gene therapy.
机译:背景:mda-7基因(黑色素瘤分化相关基因7)是一种新型的肿瘤抑制基因。先前已经报道了MDA-7的抗增殖活性。在本报告中,我们分析了Ad-mda7在多种癌症细胞系中的抗肿瘤功效。材料与方法:检测Ad-mda7转导的癌症或正常细胞系的细胞增殖(tri标记的胸苷掺入测定,Alamar蓝测定和锥虫蓝排除测定),凋亡(TUNEL和膜联蛋白V染色,通过荧光显微镜或FACs分析)和细胞周期调控(碘化丙锭染色和FACs分析)。结果:Ad-mda7处理肿瘤细胞导致生长抑制和凋亡的时间和剂量依赖性。在这些细胞中,抗​​肿瘤作用与p53,RB,p16,ras,bax和caspase 3的基因组状态无关。另外,正常细胞系未显示出对Ad-mda7的增殖或凋亡反应的抑制。此外,Ad-mda7转导的癌细胞分泌MDA-7蛋白的可溶性形式。因此,Ad-mda7可能代表一种新型的基因治疗剂,用于治疗多种癌症。结论:Ad-mda7在癌细胞中而不是在正常细胞中的强效和选择性杀伤活性使该载体成为癌症基因治疗的潜在候选者。

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