Sugarman B J, Lewis G D, Eessalu T E, Aggarwal B B, Shepard H M
Cancer Res. 1987 Feb 1;47(3):780-6.
Tumor necrosis factors (TNFs) are a class of cytokines secreted by activated effector cells involved in host defense against tumor progression. Epidermal growth factor (EGF) and recombinant human transforming growth factor-alpha (rHuTGF-alpha) were shown to interfere with the in vitro antiproliferative effects of recombinant human tumor necrosis factor-alpha (rHuTNF-alpha) and -beta on a human cervical carcinoma cell line, ME-180. The inhibitory effect could be observed at EGF or rHuTGF-alpha concentrations of 100 pg/ml, and was maximal between 1 and 10 ng/ml. This response was not due to down regulation of the TNF receptor or to alteration of the affinity of TNF-alpha for its receptor. Since the antiproliferative effect of recombinant human interferon-gamma was not significantly affected by the presence of EGF or rHuTGF-alpha, the inhibition was specific for recombinant TNFs and was not due solely to enhanced proliferation induced by the growth factors. Neither growth factor had a substantial protective effect on the synergistic cytotoxicity observed when tumor cells were exposed simultaneously to rHuTNF-alpha and recombinant human interferon-gamma. TGF-beta can also interfere with the antiproliferative effects of rHuTNF-alpha in vitro. At concentrations of less than 1 ng/ml, TGF-beta significantly antagonized the cytotoxic effects of rHuTNF-alpha on NIH 3T3 fibroblasts. Since EGF, platelet-derived growth factor, and TGF-beta all enhanced NIH 3T3 cell proliferation, but only TGF-beta interfered with rHuTNF-alpha cytotoxicity, the protective effects of TGF-beta were not related in a simple manner to enhanced cell proliferation. rHuTGF-alpha and TGF-beta did not have a significant protective effect against rHuTNF-alpha-mediated cytotoxicity on two other tumor cell lines, BT-20 and L-929 cells. Based upon these observations we suggest that growth factors might enhance tumor growth in vivo by a combination of distinct mechanisms: (a) by autocrine stimulation tumor cell growth; and/or (b) by interfering with normal effector mechanisms of host defense.
肿瘤坏死因子(TNFs)是一类由活化效应细胞分泌的细胞因子,参与宿主抵抗肿瘤进展的防御过程。表皮生长因子(EGF)和重组人转化生长因子-α(rHuTGF-α)已被证明可干扰重组人肿瘤坏死因子-α(rHuTNF-α)和-β对人宫颈癌细胞系ME-180的体外抗增殖作用。在EGF或rHuTGF-α浓度为100 pg/ml时即可观察到抑制作用,在1至10 ng/ml之间达到最大。这种反应并非由于TNF受体的下调或TNF-α与其受体亲和力的改变。由于重组人干扰素-γ的抗增殖作用不受EGF或rHuTGF-α存在的显著影响,因此这种抑制作用对重组TNFs具有特异性,并非仅仅由于生长因子诱导的增殖增强所致。当肿瘤细胞同时暴露于rHuTNF-α和重组人干扰素-γ时,两种生长因子对观察到的协同细胞毒性均无实质性保护作用。TGF-β在体外也可干扰rHuTNF-α的抗增殖作用。在浓度低于1 ng/ml时,TGF-β可显著拮抗rHuTNF-α对NIH 3T3成纤维细胞的细胞毒性。由于EGF、血小板衍生生长因子和TGF-β均可增强NIH 3T3细胞增殖,但只有TGF-β干扰rHuTNF-α细胞毒性,因此TGF-β的保护作用并非简单地与细胞增殖增强相关。rHuTGF-α和TGF-β对另外两种肿瘤细胞系BT-20和L-929细胞的rHuTNF-α介导的细胞毒性均无显著保护作用。基于这些观察结果,我们认为生长因子可能通过多种不同机制的组合在体内促进肿瘤生长:(a)通过自分泌刺激肿瘤细胞生长;和/或(b)通过干扰宿主防御的正常效应机制。