Paciotti G F, Tamarkin L
Clinical Psychobiology Branch, NIMH, Bethesda, Maryland 20892.
Anticancer Res. 1988 Nov-Dec;8(6):1233-9.
Direct in vitro and in vivo effects of the lymphokine, interleukin-2 (IL-2), on hormone-dependent (MCF-7) and- independent (MDA-231) human breast cancer cell proliferation were investigated. In vitro, picomolar concentrations of IL-2 directly inhibited MCF-7 cell proliferation after 12 days of culture, while nanomolar doses of IL-2 significantly stimulated MCF-7 cell growth over the same time period. In addition, micromolar concentrations of IL-2 had virtually no effect on the in vitro proliferation of MCF-7 cells. In parallel in vitro growth experiments, the hormone-independent cells, MDA-231, were not affected by IL-2 regardless of concentration. IL-2 treatment of overiectomized, estrogen-treated nude mice, burdened with MCF-7 or MDA-231 tumors, inhibited MCF-7 tumor growth, but had no effect on MDA-231 tumors. Examination of T, B and natural killer (NK) cell function in these animals indicated that the interleukin-2-mediated effect on MCF-7 cell growth in vivo is independent of the proliferative abilities of these lymphoid cells, suggesting that IL-2 may directly affect the growth of these hormone-dependent human breast cancer cells.
研究了淋巴因子白细胞介素-2(IL-2)对激素依赖性(MCF-7)和激素非依赖性(MDA-231)人乳腺癌细胞增殖的直接体外和体内作用。在体外,培养12天后,皮摩尔浓度的IL-2直接抑制MCF-7细胞增殖,而纳摩尔剂量的IL-2在同一时期显著刺激MCF-7细胞生长。此外,微摩尔浓度的IL-2对MCF-7细胞的体外增殖几乎没有影响。在平行的体外生长实验中,激素非依赖性细胞MDA-231不受IL-2浓度的影响。用IL-2处理荷有MCF-7或MDA-231肿瘤的去卵巢、雌激素处理的裸鼠,可抑制MCF-7肿瘤生长,但对MDA-231肿瘤无影响。对这些动物的T、B和自然杀伤(NK)细胞功能进行检测表明,白细胞介素-2在体内对MCF-7细胞生长的作用独立于这些淋巴细胞的增殖能力,这表明IL-2可能直接影响这些激素依赖性人乳腺癌细胞的生长。