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

被引:0
|
作者
Shu Fen Wen
Vikas Mahavni
Erlinda Quijano
Jeremy Shinoda
Michael Grace
Mary Lynn Musco-Hobkinson
Tong-Yuan Yang
Yuetian Chen
Ingo Runnenbaum
JoAnn Horowitz
Dan Maneval
Beth Hutchins
Richard Buller
机构
[1] Canji,
[2] Inc.,undefined
[3] The University of Iowa Hospital and Clinic,undefined
[4] Schering-Plough Research Institute,undefined
[5] Kenilworth and Union,undefined
[6] Universitäts-Frauenklinik,undefined
来源
Cancer Gene Therapy | 2003年 / 10卷
关键词
rAd-p53; ovarian cancer; gene therapy; QPCR; SCH 58500;
D O I
暂无
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学科分类号
摘要
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.
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页码:224 / 238
页数:14
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