Mutch D G, Massad L S, Kao M S, Collins J L
Department of Obstetrics and Gynecology, Washington University School of Medicine, St. Louis, MO 63110.
Am J Obstet Gynecol. 1990 Dec;163(6 Pt 1):1920-4. doi: 10.1016/0002-9378(90)90774-2.
Four human cell lines derived from cervical carcinomas (ME-180, SiHa, HT-3, and MS751) and three human cell lines derived from ovarian carcinomas (SK-OV-3, Caov-3, and NIH:OVCAR-3) were analyzed in vitro to determine the effect of recombinant interferon-gamma and recombinant human tumor necrosis factor-alpha on cell growth and survival. The effects of interferon-gamma, tumor necrosis factor-alpha, and both interferon-gamma and tumor necrosis factor-alpha on cell growth were measured after 24 and 72 hours of incubation by the incorporation of chromium 51. The results of this analysis showed that all seven cell lines were resistant to the antiproliferative action of tumor necrosis factor-alpha, that the growth of most cell lines was inhibited by interferon-gamma by 72 hours of incubation, and that after 72 hours of incubation all cell lines demonstrated a synergistic antiproliferative response to the combination of interferon-gamma and tumor necrosis factor-alpha. However, the effects of these cytokines on cell growth were found to differ among cell lines and varied with the concentration and the duration of incubation. The growth of one cell line (Caov-3) was stimulated by both tumor necrosis factor-alpha and interferon-gamma. These results suggest that the clinical effects of these cytokines on the growth of gynecologic cancers may be more complex than previously supposed.
对四种源自宫颈癌的人细胞系(ME - 180、SiHa、HT - 3和MS751)以及三种源自卵巢癌的人细胞系(SK - OV - 3、Caov - 3和NIH:OVCAR - 3)进行了体外分析,以确定重组干扰素 - γ和重组人肿瘤坏死因子 - α对细胞生长和存活的影响。在孵育24小时和72小时后,通过掺入铬51来测量干扰素 - γ、肿瘤坏死因子 - α以及干扰素 - γ和肿瘤坏死因子 - α两者对细胞生长的影响。该分析结果表明,所有七种细胞系均对肿瘤坏死因子 - α的抗增殖作用具有抗性,大多数细胞系的生长在孵育72小时后受到干扰素 - γ的抑制,并且在孵育72小时后,所有细胞系对干扰素 - γ和肿瘤坏死因子 - α的组合均表现出协同抗增殖反应。然而,发现这些细胞因子对细胞生长的影响在不同细胞系之间存在差异,并且随孵育浓度和持续时间而变化。一种细胞系(Caov - 3)的生长受到肿瘤坏死因子 - α和干扰素 - γ两者的刺激。这些结果表明,这些细胞因子对妇科癌症生长的临床影响可能比先前认为的更为复杂。