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首页> 外文期刊>British Journal of Cancer >Synthesis of somatostatin by breast cancer cells and their inhibition by exogenous somatostatin and sandostatin
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Synthesis of somatostatin by breast cancer cells and their inhibition by exogenous somatostatin and sandostatin

机译:乳腺癌细胞生长抑素的合成及其对外源生长抑素和沙司他汀的抑制作用

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Three human breast cancer cell lines ZR-75-1, MDA-MB-436 and MCF-7 were found to contain respectively, 3.06, 2.69 and 1.86 fmol of somatostatin-like immunoreactivity (SLI) per 10(6) cells. Since SLI is undetectable in the passaging media it must, therefore, be synthesised by the cells. In the presence of fetal calf serum the cells were growth inhibited by addition of somatostatin or its long-lasting analogue, Sandostatin, but only after 3 days of continuous exposure. A 1-day exposure to either peptide had little or no effect on subsequent cell growth in peptide-free medium. Inhibition of cell proliferation is not due to cytotoxic effects of the dose used (500 ng ml-1, each) since both peptides caused short-term stimulation of growth in the absence of serum.
机译:发现三个人乳腺癌细胞系ZR-75-1,MDA-MB-436和MCF-7每10(6)个细胞分别含有3.06、2.69和1.86 fmol生长抑素样免疫反应性(SLI)。由于SLI在传代培养基中无法检测到,因此必须由细胞合成。在胎牛血清存在的情况下,通过添加生长抑素或其持久类似物Sandostatin抑制细胞生长,但仅在连续暴露3天后才能进行。暴露于任一肽的1天对无肽培养基中的后续细胞生长几乎没有影响。细胞增殖的抑制不是由于所用剂量(每个500 ng ml-1)的细胞毒性作用所致,因为这两种肽均可在缺乏血清的情况下引起短期的生长刺激。

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