首页> 美国卫生研究院文献>Annals of Surgery >Gene therapy of metastatic pancreas cancer with intraperitoneal injections of concentrated retroviral herpes simplex thymidine kinase vector supernatant and ganciclovir.
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Gene therapy of metastatic pancreas cancer with intraperitoneal injections of concentrated retroviral herpes simplex thymidine kinase vector supernatant and ganciclovir.

机译:腹膜内注射浓缩的逆转录病毒疱疹胸苷激酶载体上清液和更昔洛韦治疗转移性胰腺癌的基因治疗。

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摘要

OBJECTIVE: The objective of this study was to determine the efficacy of intraperitoneal (IP) injections of a new concentrated herpes simplex thymidine kinase (HS-tk) retroviral vector and ganciclovir (GCV) for peritoneal metastases from pancreas cancer. SUMMARY BACKGROUND DATA: Metastatic pancreas cancer is fatal. Gene therapy may provide a novel approach for this disease. Gene therapy with adeno- or retroviral-mediated transfer of the HS-tk gene into tumor cells renders the cells susceptible to GCV. Intratumoral or intracavity injections of retroviral vectors have been ineffective in previous studies. METHODS: Pancreatic cancer B x PC3 cells (3 x 10(7)) were injected into the tail of pancreas in nude mice. Mice received IP injections of a concentrated HS-tk vector (5 x 10(7)) cfu/mliters) or a control vector (G1Na) without the tk gene for 10 days and GCV (100 mg/kg) for 14 days. To determine whether the vector would survive in the milieu of the peritoneal cavity, the authors examined the effects of ascitic fluid on the vector. Pancreas cancer cells were transduced in vitro with HS-tk vector in presence of media or ascitic fluid and treated with GCV. RESULTS: Highly significant reductions in the mass of metastatic peritoneal tumor deposits were found in HS-tk-treated group (124 +/- 27 mg; n = 11) compared with G1Na vector controls (910 +/- 168 mg; n = 8; p < 0.0001). Results of polymerase chain reaction analysis demonstrated integration of the vector in the tumors, and on immunohistochemistry, expression of the TK protein was seen in the number of surviving colonies (representing nontransduced cells) were similar in both groups, suggesting that the vector effectively transduced tumor cells bathed in the ascitic fluid. CONCLUSIONS: Results demonstrate that IP administration of concentrated retroviral HS-tk vectors is effective treatment for pancreas cancer metastatic to the peritoneal cavity; furthermore, the vector is active in the presence of ascitic fluid. Intraperitoneal retroviral HS-tk may provide a novel approach to treatment of metastatic pancreas cancer.
机译:目的:本研究的目的是确定腹膜内(IP)注射新的浓缩单纯疱疹胸苷激酶(HS-tk)逆转录病毒载体和更昔洛韦(GCV)对胰腺癌腹膜转移的疗效。摘要背景数据:转移性胰腺癌是致命的。基因治疗可能为这种疾病提供一种新颖的方法。用腺病毒或逆转录病毒介导的HS-tk基因转移到肿瘤细胞的基因疗法使细胞对GCV敏感。在先前的研究中,肿瘤内或腔内注射逆转录病毒载体无效。方法:将胰腺癌B x PC3细胞(3 x 10(7))注射入裸鼠胰腺尾部。小鼠接受IP注射浓缩的HS-tk载体(5 x 10(7)cfu / ml)或没有tk基因的对照载体(G1Na)10天,GCV(100 mg / kg)注射14天。为了确定载体是否能在腹膜腔环境中存活,作者检查了腹水对载体的影响。在培养基或腹水存在的情况下,用HS-tk载体体外转导胰腺癌细胞,并用GCV处理。结果:与G1Na载体对照组(910 +/- 168 mg; n = 8)相比,HS-tk治疗组(124 +/- 27 mg; n = 11)发现转移性腹膜肿瘤沉积物的质量显着降低。 ; p <0.0001)。聚合酶链反应分析的结果表明该载体已整合到肿瘤中,并且在免疫组织化学中,两组存活的菌落(代表未转导的细胞)中TK蛋白的表达均相似,这表明该载体已有效地转导了肿瘤。细胞浸入腹水中。结论:结果表明,浓缩逆转录病毒HS-tk载体的IP给药可有效治疗转移至腹膜腔的胰腺癌。此外,该载体在腹水存在下具有活性。腹膜内逆转录病毒HS-tk可能提供一种治疗转移性胰腺癌的新方法。

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