Khachigian L M, Field S L, Crouch R, Chesterman C N
University of New South Wales Centre for Thrombosis and Vascular Research, Prince of Wales Hospital, Sydney, Australia.
Anticancer Res. 1995 Mar-Apr;15(2):337-41.
The expression of polypeptide growth factors and their receptors by certain malignant human cell lines and the ability to grow these tumors as xenografts in murine hosts provides a useful setting to investigate the efficacy of antitumor agents. Exon 6 of the platelet-derived growth factor A-chain predicts a highly basic region consisting of 18 amino acids. Previously, we demonstrated that a synthetic peptide bearing this sequence interacts with a large population of binding sites at the cell surface and inhibits the binding and mitogenesis stimulated by several polypeptide growth factors (Khachigian et al J Biol Chem 267: 1660-1666, 1992; Khachigian and Chesterman, J Biol Chem 267: 7478-7482, 1992). In this report, we show that the exon 6 peptide can inhibit the mitogenic response of cultured human U-118 malignant glioma cells to normal human serum. When these cells are grown as subcutaneous xenografts in athymic nude mice, repeated intratumoral administration of the peptide results in dose-dependent growth inhibition. Indeed, injection of 0.48 mg of peptide five times a week abrogated growth during the entire course of treatment. Mouse weight or behavior did not differ significantly between control and treatment groups. Moreover, histologic examination of the tumors following treatment did not indicate necrosis. Thus, the exon 6 peptide can inhibit glioma cell proliferation both in culture and in an animal model without apparent side effects.
某些人类恶性细胞系表达多肽生长因子及其受体,并且能够在鼠宿主中作为异种移植物生长这些肿瘤,这为研究抗肿瘤药物的疗效提供了一个有用的环境。血小板衍生生长因子A链的第6外显子预测有一个由18个氨基酸组成的高度碱性区域。以前,我们证明带有这个序列的合成肽与细胞表面大量的结合位点相互作用,并抑制几种多肽生长因子刺激的结合和有丝分裂(Khachigian等人,《生物化学杂志》267: 1660 - 1666, 1992;Khachigian和Chesterman,《生物化学杂志》267: 7478 - 7482, 1992)。在本报告中,我们表明第6外显子肽可以抑制培养的人U - 118恶性胶质瘤细胞对正常人血清的有丝分裂反应。当这些细胞作为皮下异种移植物在无胸腺裸鼠中生长时,在肿瘤内重复给予该肽会导致剂量依赖性生长抑制。确实,每周注射5次0.48毫克的肽在整个治疗过程中消除了肿瘤生长。对照组和治疗组之间小鼠体重或行为没有显著差异。此外,治疗后肿瘤的组织学检查未显示坏死。因此,第6外显子肽可以在培养和动物模型中抑制胶质瘤细胞增殖,且无明显副作用。