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Induction of apoptosis and sensitization of head and neck squamous carcinoma cells to cisplatin by targeting survivin gene expression

机译:靶向survivin基因表达诱导头颈部鳞状细胞凋亡和敏化顺铂

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摘要

Survivin is known to be highly-expressed in various carcinomas; and is associated with their biologically aggressive characteristics and drug resistance. We have previously reported survivin as an important anti-apototic protein involved in head and neck squamous cell carcinoma (HNSCC) tumorigenesis and providing resistance to conventional cancer therapies. The purpose of present study was to investigate the potential of survivin as a therapeutic target in HNSCC. This study was designed to explore the effect(s) of survivin-siRNA therapy on the apoptosis in HNSCC cells, and its influence on cisplatin-sensitivity. Lentivirus vector was developed to deliver survivin specific siRNA into cancer cells. The data indicates that silencing of survivin-mediated by Lentivirus-siRNA therapy effectively suppressed cancer cell proliferation and induced caspase-dependent apoptosis in HNSCC cells. The study also shows that the response of HNSCC cells to cisplatin drug treatment at clinically relevant level was limited. We observed survivin to be a key factor involved in this cisplatin-resistance mechanism, and down-regulation of survivin significantly increased sensitivity of cancer cells to cisplatin-mediated apoptosis. Thus, this combination therapy acts as a multimodality regimen with significant potential to improve clinical outcomes in head and neck cancers.
机译:已知Survivin在多种癌中高表达;并与其生物学攻击性和耐药性有关。我们以前曾报道过生存素是一种重要的抗凋亡蛋白,参与头颈部鳞状细胞癌(HNSCC)的肿瘤发生并提供对常规癌症治疗的抗性。本研究的目的是研究生存素在HNSCC中作为治疗靶标的潜力。本研究旨在探讨survivin-siRNA治疗对HNSCC细胞凋亡的影响及其对顺铂敏感性的影响。开发了慢病毒载体以将survivin特异性siRNA递送到癌细胞中。数据表明,由慢病毒-siRNA治疗介导的存活蛋白沉默可有效抑制癌细胞增殖,并诱导HNSCC细胞中caspase依赖性凋亡。研究还表明,在临床相关水平上,HNSCC细胞对顺铂药物治疗的反应有限。我们观察到生存素是参与这种顺铂耐药机制的关键因素,而survivin的下调显着增加了癌细胞对顺铂介导的细胞凋亡的敏感性。因此,这种联合疗法可作为多模式疗法,具有改善头颈癌临床疗效的巨大潜力。

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