Linker-based GnRH-PE chimeric proteins inhibit cancer growth in nude mice

被引:21
作者
Ben-Yehudah, A [1 ]
Yarkoni, S [1 ]
Nechushtan, A [1 ]
Belostotsky, R [1 ]
Lorberboum-Galski, H [1 ]
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Sch, Dept Cellular Biochem, IL-91120 Jerusalem, Israel
关键词
gonadotropin releasing hormone (GnRH); Pseudomonas exotoxin A (PE); cancer; chimeric proteins; targeting;
D O I
10.1007/BF02787357
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Since the number of cancer-related deaths has not decreased in recent years, major efforts are being made to find new drugs for cancer treatment, In this report we introduce the gonadotropin releasing hormone-Pseudomonas exotoxin (GnRH-PE) based chimeric proteins L-GnRH-PE66 and L-GnRH-PE40. These proteins are composed of a GnRH moiety attached to modified forms of Pseudomonas exotoxin via a polylinker (gly(4)ser)(2). The chimeric proteins L-GnRH-PE66 and L-GnRH-PE40 have the ability to target and kill adenocarcinoma cell lines in vitro, whereas non-adenocarcinoma cell lines are not affected. We demonstrate that L-GnRH-PE66 and L-GnRH-PE40 efficiently inhibit cancer growth, Nude mice were injected subcutaneously with the SW-48 adenocarcinoma cell line to produce xenograft tumours. When the tumours were established and visible, the animals were injected with chimeric proteins for 10 days. At the end of this period, a reduction of up to 3-fold in tumor size was obtained in the treated mice, as compared with the control group, which received equivalent amounts of GnRH; the difference was even greater 13 days after termination of treatment. Thus, the chimeric proteins L-GnRH-PE66 and L-GnRH-PE40 are promising candidates for treatment of a variety of adenocarcinomas and their use in humans should be considered.
引用
收藏
页码:38 / 45
页数:8
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