De Giovanni C, Melani C, Nanni P, Landuzzi L, Nicoletti G, Frabetti F, Griffoni C, Colombo M P, Lollini P L
Istituto di Cancerologia, Università di Bologna, Italy.
Br J Cancer. 1995 Nov;72(5):1224-9. doi: 10.1038/bjc.1995.490.
Three human rhabdomyosarcoma cell lines were used to investigate the presence of autocrine loops based on the production of insulin-like growth factor (IGF)-II, basic fibroblast growth factor (bFGF) and epidermal growth factor (EGF)/transforming growth factor (TGF)-alpha and of their corresponding receptors, and whether these loops affect cell proliferation and myogenic differentiation. Two cell lines, RD/18 and CCA, deriving from tumours of the embryonal histotype, showed the presence of both growth factors and receptors which make possible three different autocrine loops, while the alveolar RMZ-RC2 cell line lacked that based on the EGF receptor. Culture of rhabdomyosarcoma cells in the presence of specific blocking antibodies, directed to a component of single autocrine loops, inhibited cell proliferation (up to 50%), without inducing myogenic differentiation. Suramin, a drug which non-selectively interferes with the binding of growth factors to their cellular receptors, was used to block all the autocrine loops simultaneously. In CCA and RMZ-RC2 cells suramin was able to induce a significant increase (up to 3-fold) in the proportion of myosin-positive cells over control cultures. Therefore rhabdomyosarcoma cells of embryonal and alveolar histotype can show a redundancy of growth-sustaining autocrine loops. Suramin could interfere with them by acting on both growth inhibition and induction of myogenic differentiation.
使用三种人横纹肌肉瘤细胞系来研究基于胰岛素样生长因子(IGF)-II、碱性成纤维细胞生长因子(bFGF)和表皮生长因子(EGF)/转化生长因子(TGF)-α及其相应受体的自分泌环的存在,以及这些环是否影响细胞增殖和肌源性分化。源自胚胎组织学类型肿瘤的两种细胞系RD/18和CCA显示同时存在生长因子和受体,这使得三种不同的自分泌环成为可能,而肺泡型RMZ-RC2细胞系缺乏基于EGF受体的自分泌环。在存在针对单个自分泌环成分的特异性阻断抗体的情况下培养横纹肌肉瘤细胞,可抑制细胞增殖(高达50%),而不诱导肌源性分化。苏拉明是一种非选择性干扰生长因子与其细胞受体结合的药物,用于同时阻断所有自分泌环。在CCA和RMZ-RC2细胞中,与对照培养物相比,苏拉明能够使肌球蛋白阳性细胞的比例显著增加(高达3倍)。因此,胚胎型和肺泡型组织学类型的横纹肌肉瘤细胞可显示维持生长的自分泌环的冗余性。苏拉明可通过抑制生长和诱导肌源性分化来干扰这些自分泌环。