## Abstract Nude mice bearing xenografts of the androgen‐independent human prostate‐cancer cell line PC‐3 were treated for 4 weeks with somatostatin analog RC‐160, bombesin/gastrin‐releasing peptide (GRP) antagonist (RC‐3095), or the combination of both peptides. In the first experiment, treatment
Somatostatin analog RC-160 inhibits the growth of human osteosarcomas in nude mice
✍ Scribed by Jacek Pinski; Andrew V. Schally; Gabor Halmos; Karoly Szepeshazi; Kate Groot
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- French
- Weight
- 627 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
We investigated the effects of the potent somatostatin analog RC-160 on the growth of human osteosarcoma cell lines SK-ES-I and MNNG/HOS, transplanted into nude mice or cultured in vitro. Growth of SK-ES-I and MNNG/HOS tumors in nude mice was significantly inhibited after 4 weeks of treatment with daily S.C. injections of 100 pg RC-160, as measured by a reduction in tumor volume and weight. Histologically, the number of mitotic cells was decreased in the groups treated with RC-160. In mice bearing either tumor model, administration of RC-I60 significantly decreased serum growth hormone and insulin-like growth factor I (IGF-I) levels. Specific highaffinity receptors for somatostatin and epidermal growth factor were found on membranes of MNNG/HOS tumors but not on SK-ES-I tumors. Receptor analyses also demonstrated highaffinity binding sites for ICF-I on membranes of both tumors. In cell cultures, the proliferation rate of MNNG/HOS cells, but not of SK-ES-I, was significantly suppressed by RC-160. Our findings demonstrate that RC-I60 can significantly inhibit the growth of SK-ES-I and MNNG/HOS osteosarcomas in mice.
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