Mhashilkar A M, Schrock R D, Hindi M, Liao J, Sieger K, Kourouma F, Zou-Yang X H, Onishi E, Takh O, Vedvick T S, Fanger G, Stewart L, Watson G J, Snary D, Fisher P B, Saeki T, Roth J A, Ramesh R, Chada S
Introgen Therapeutics Inc, Houston, TX 77030, USA.
Mol Med. 2001 Apr;7(4):271-82.
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.
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).
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.
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.
mda - 7基因(黑色素瘤分化相关基因 - 7)是一种新型肿瘤抑制基因。此前已有关于MDA - 7抗增殖活性的报道。在本报告中,我们分析了Ad - mda7在多种癌细胞系中的抗肿瘤疗效。
对经Ad - mda7转导的癌细胞或正常细胞系进行细胞增殖检测(氚标记胸腺嘧啶核苷掺入试验、阿拉玛蓝试验和台盼蓝排斥试验)、凋亡检测(TUNEL法以及通过荧光显微镜或流式细胞术分析可视化的膜联蛋白V染色)和细胞周期调控检测(碘化丙啶染色和流式细胞术分析)。
用Ad - mda7处理肿瘤细胞会导致其生长受到抑制并出现凋亡,且呈时间和剂量依赖性。这些细胞中的抗肿瘤作用与p53、RB、p16、ras、bax和半胱天冬酶3的基因组状态无关。此外,正常细胞系对Ad - mda7未表现出增殖抑制或凋亡反应。而且,经Ad - mda7转导的癌细胞分泌一种可溶性形式的MDA - 7蛋白。因此,Ad - mda7可能是一种用于治疗多种癌症的新型基因治疗药物。
Ad - mda7对癌细胞具有强大且选择性的杀伤活性,而对正常细胞无此作用,这使得该载体成为癌症基因治疗的一个潜在候选者。