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基因放疗克服肿瘤对细胞毒性药物的耐药性。

Genetic radiotherapy overcomes tumor resistance to cytotoxic agents.

作者信息

Seung L P, Mauceri H J, Beckett M A, Hallahan D E, Hellman S, Weichselbaum R R

机构信息

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

出版信息

Cancer Res. 1995 Dec 1;55(23):5561-5.

PMID:7585635
Abstract

We report that radiation enhances gene therapy of a radioresistant tumor by upregulating the induction of a chimeric gene encoding a radiosensitizing protein, tumor necrosis factor alpha (TNF-alpha). We ligated the radiation-inducible CArG elements of the radiation-inducible Egr-1 promoter/enhancer region upstream to the transcriptional start site of the human TNF cDNA (pE425-TNF). This construct was transfected using cationic liposomes into the variant murine fibrosarcoma cell line, P4L. The P4L cell line was both radioresistant (D0 = 188) and resistant to TNF. After a single intratumoral injection of 10 micrograms of pE425-TNF in cationic liposomes and two 20-Gy doses of irradiation, mean tumor volumes were significantly reduced in P4L tumors as compared to those receiving either pE425-TNF in liposomes or radiation alone (P = 0.01). TNf protein in P4L tumors was induced by radiation as high as 29 times control levels and remained detectable for 14 days. Our data indicate that combined gene therapy using liposomes, together with ionizing radiation to locally activate the induction of a radiosensitizing protein, is successful at overcoming resistance to both TNF and radiation.

摘要

我们报告称,辐射通过上调编码放射增敏蛋白肿瘤坏死因子α(TNF-α)的嵌合基因的诱导来增强对放射抗拒肿瘤的基因治疗。我们将辐射诱导型Egr-1启动子/增强子区域的辐射诱导型CArG元件连接到人类TNF cDNA(pE425-TNF)转录起始位点的上游。使用阳离子脂质体将该构建体转染到变异的小鼠纤维肉瘤细胞系P4L中。P4L细胞系既对辐射有抗性(D0 = 188),又对TNF有抗性。在瘤内单次注射10微克阳离子脂质体包裹的pE425-TNF并给予两次20 Gy剂量的辐射后,与单独接受脂质体包裹的pE425-TNF或单独接受辐射的P4L肿瘤相比,其平均肿瘤体积显著减小(P = 0.01)。P4L肿瘤中的TNF蛋白被辐射诱导至对照水平的29倍之高,并在14天内均可检测到。我们的数据表明,脂质体联合基因治疗与电离辐射一起局部激活放射增敏蛋白的诱导,在克服对TNF和辐射的抗性方面是成功的。

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