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人甲胎蛋白对不同类型肿瘤细胞和正常细胞的生长调节活性

Growth-regulative activity of human alpha-fetoprotein for different types of tumor and normal cells.

作者信息

Dudich E, Semenkova L, Gorbatova E, Dudich I, Khromykh L, Tatulov E, Grechko G, Sukhikh G

机构信息

Institute of Engineering Immunology, Moscow Region, Russia.

出版信息

Tumour Biol. 1998;19(1):30-40. doi: 10.1159/000029972.

Abstract

The dose-dependent alpha-fetoprotein (AFP) reactivity of different types of tumor cells and normal embryonal fibroblasts, which are capable of taking up AFP, was investigated. High doses (more than 100 micrograms/ml) of purified human AFP were shown to induce strongly dose-dependent growth inhibition of human hepatoma HepG2 cells, human lymphoblastoma MT4 cells, lymphoma Jurkat cells and murine fibroblastoma L929 cells. Human mammary carcinoma MCF-7 cells also revealed a growth inhibitory response to AFP, although to a lesser extent. Equivalent doses of human serum albumin (HSA) demonstrated no effect on these cells. On the contrary, normal embryonal fibroblasts of different organ origin showed dose-dependent stimulation (50-90%) of proliferation in response to AFP. A similar stimulative effect was obtained when embryonal fibroblasts were treated with the same doses of HSA. The myeloblastoma cell line U-937 and the normal epidermal fibroblast cell line M19 were shown to be resistant to the AFP action over a wide range of protein concentrations. It was demonstrated that growth factor deprivation (i.e. low serum concentration) could stimulate U-937 cell proliferation in response to high doses of AFP. It was also shown that intensive washing of U-937 and MCF-7 cells with fresh medium to remove secreted cytokines and growth factors distinctly increased cell sensitivity to high-dose-AFP-induced growth-inhibitory activity. Low AFP concentrations (less than 100 micrograms/ml) failed to induce growth inhibition in all studied cells and rather showed a slight stimulative effect. These findings demonstrate that physiological levels of AFP can exhibit a dose-dependent growth-regulatory activity toward sensitive tumor or developing cells. Our data demonstrated that AFP could reveal either stimulative or inhibitory growth activity, depending on the relative concentration of AFP and on exogenous or endogenous cytokines and growth factors in the cell culture medium. A growth-stimulative activity in normal embryonal fibroblasts and certain tumor cell lines exhibited by low AFP concentrations is supposed to result from the synergistic effects of AFP and various other secreted growth factors.

摘要

研究了不同类型能够摄取甲胎蛋白(AFP)的肿瘤细胞和正常胚胎成纤维细胞的剂量依赖性AFP反应性。结果显示,高剂量(超过100微克/毫升)的纯化人AFP可强烈诱导人肝癌HepG2细胞、人成淋巴细胞瘤MT4细胞、淋巴瘤Jurkat细胞和鼠成纤维细胞瘤L929细胞的剂量依赖性生长抑制。人乳腺癌MCF-7细胞对AFP也有生长抑制反应,尽管程度较小。等量的人血清白蛋白(HSA)对这些细胞无影响。相反,不同器官来源的正常胚胎成纤维细胞对AFP呈剂量依赖性增殖刺激(50 - 90%)。用相同剂量的HSA处理胚胎成纤维细胞时也获得了类似的刺激效果。髓母细胞瘤细胞系U - 937和正常表皮成纤维细胞系M19在广泛的蛋白质浓度范围内对AFP作用具有抗性。结果表明,生长因子剥夺(即低血清浓度)可刺激U - 937细胞对高剂量AFP作出增殖反应。还表明,用新鲜培养基对U - 937和MCF - 7细胞进行密集洗涤以去除分泌的细胞因子和生长因子,可明显增加细胞对高剂量AFP诱导的生长抑制活性的敏感性。低AFP浓度(低于100微克/毫升)在所有研究细胞中均未诱导生长抑制,反而显示出轻微的刺激作用。这些发现表明,AFP的生理水平可对敏感肿瘤细胞或发育中的细胞表现出剂量依赖性生长调节活性。我们的数据表明,AFP可根据AFP的相对浓度以及细胞培养基中外源性或内源性细胞因子和生长因子的情况,表现出刺激或抑制生长的活性。低AFP浓度在正常胚胎成纤维细胞和某些肿瘤细胞系中表现出的生长刺激活性被认为是AFP与其他各种分泌生长因子协同作用的结果。

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