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Assessment of p53 gene transfer and biological activities in a clinical study of adenovirus-p53 gene therapy for recurrent ovarian cancer

机译:腺病毒p53基因治疗复发性卵巢癌的临床研究中对p53基因转移和生物学活性的评估

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A cohort study was designed to evaluate the efficiency of gene transfer and whether biological activity from the expressed therapeutic gene resulted after administration of a recombinant adenovirus containing the human wild-type p53 (p53wt) gene (rAd-p53 SCH 58500). The cohort study was conducted in five trial subjects with recurrent ovarian cancer. Each trial subject received multiple cycles of rAd-p53 SCH 58500, each cycle comprised of doses of 7.5 1013 particles on each of five consecutive days. Subjects were treated with rAd-p53 SCH 58500 alone during Cycle 1 and in combination with gemcitabine during the subsequent cycles. Both tumor biopsies and peritoneal aspirates were collected and evaluated for gene transfer and evidence of the biological activities of the expressed p53wt gene. Using quantitative PCR and RT-PCR, and in situ PCR, gene transfer and expression were documented in tumor biopsies (four of five patients) collected from Cycle 1. Furthermore, upregulation of p21/WAF1, bax and mdm-2, and downregulation of survivin were observed in these same tumor biopsy samples, suggesting that intraperitoneal administration of rAd-p53 SCH 58500 leads to detectable p53 biological activity in target tumor tissue. In addition, gene transfer and its expression were observed in cells obtained from peritoneal aspirates. These fluids were mainly comprised of polymorphonuclear neutrophils, indicating that successful gene transfer can be achieved by multiple cycle intraperitoneal administration of recombinant adenovirus.
机译:设计了一项队列研究,以评估基因转移的效率以及表达的治疗基因的生物学活性是否在施用含有人野生型p53(p53wt)基因的重组腺病毒后产生(rAd-p53 SCH 58500)。该队列研究是在五个患有复发性卵巢癌的试验对象中进行的。每个试验对象接受rAd-p53 SCH 58500的多个周期,每个周期包含连续五天中的7.5 1013颗粒剂量。在第1周期中仅用rAd-p53 SCH 58500治疗受试者,在随后的周期中与吉西他滨联合治疗。收集肿瘤活检和腹膜抽吸物并评估其基因转移和表达的p53wt基因生物学活性的证据。使用定量PCR和RT-PCR以及原位PCR,记录了从第1周期收集的肿瘤活检组织(5名患者中的4名)的基因转移和表达。此外,p21 / WAF1,bax和mdm-2的上调,以及p21 / WAF1,bax和mdm-2的下调。在这些相同的肿瘤活检样品中观察到survivin,表明腹膜内施用rAd-p53 SCH 58500可在靶肿瘤组织中检测到p53生物学活性。此外,在从腹膜抽吸物中获得的细胞中观察到基因转移及其表达。这些液体主要由多形核中性粒细胞组成,表明成功的基因转移可以通过重组腺病毒的多周期腹膜内给药来实现。

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