TY - JOUR
T1 - Linker-based GnRHh-PE chimeric proteins inhibit cancer growth in nude mice
AU - Ben-Yehudah, Ahmi
AU - Yarkoni, Shai
AU - Nechushtan, Amotz
AU - Belostotsky, Ruth
AU - Lorberboum-Galski, Haya
PY - 1999/4
Y1 - 1999/4
N2 - 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 (gly4ser)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.
AB - 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 (gly4ser)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.
KW - Cancer
KW - Chimeric proteins
KW - Gonadotropin releasing hormone (GnRH)
KW - Pseudomonas exotoxin A (PE)
KW - Targeting
UR - http://www.scopus.com/inward/record.url?scp=0032589064&partnerID=8YFLogxK
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C2 - 10382941
AN - SCOPUS:0032589064
SN - 0736-0118
VL - 16
SP - 38
EP - 45
JO - Medical Oncology
JF - Medical Oncology
IS - 1
ER -