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放射性和化学诱导型TNFerade载体在人类癌症治疗中的转化应用。

Translation of the radio- and chemo-inducible TNFerade vector to the treatment of human cancers.

作者信息

Weichselbaum R R, Kufe D

机构信息

Department of Radiation and Cellular Oncology, The University of Chicago, Chicago, IL 60637, USA.

出版信息

Cancer Gene Ther. 2009 Aug;16(8):609-19. doi: 10.1038/cgt.2009.37. Epub 2009 May 15.

Abstract

Radiotherapy is a widely used treatment for localized malignancies that is often delivered in combination with cytotoxic chemotherapeutic agents. The concept that treatment of localized tumors can be improved with a radio- and chemo-inducible gene therapy strategy has been investigated in the laboratory and now translated to the clinic. The TNFerade (Ad.Egr-TNF11D) adenoviral vector was engineered by inserting radio- and chemo-inducible elements from the Egr-1 promoter upstream to a cDNA encoding tumor necrosis factor-alpha (TNF-alpha). Transduction of tumor cells with TNFerade and then treatment with radiation or chemotherapy is associated with spatial and temporal control of TNF-alpha secretion and enhanced antitumor activity. TNFerade has been evaluated in trials for patients with sarcomas, melanomas and cancers of the pancreas, esophagus, rectum and head and neck. If the ongoing phase III trial for pancreatic cancer is successful, TNFerade will likely become the first gene therapy approved for cancer in the United States.

摘要

放射疗法是一种广泛用于治疗局部恶性肿瘤的方法,通常与细胞毒性化疗药物联合使用。在实验室中已经研究了通过放射和化学诱导基因治疗策略来改善局部肿瘤治疗的概念,并且现在已转化到临床应用。TNFerade(Ad.Egr-TNF11D)腺病毒载体是通过将来自Egr-1启动子的放射和化学诱导元件插入到编码肿瘤坏死因子-α(TNF-α)的cDNA上游而构建的。用TNFerade转导肿瘤细胞,然后进行放射治疗或化疗,与TNF-α分泌的时空控制和增强的抗肿瘤活性相关。TNFerade已在肉瘤、黑色素瘤以及胰腺癌、食管癌、直肠癌和头颈癌患者的试验中进行了评估。如果正在进行的胰腺癌III期试验成功,TNFerade可能会成为美国首个获批用于癌症治疗的基因疗法。

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