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人α、β和γ干扰素对人黑色素瘤细胞生长和侵袭潜能的抗肿瘤作用的体外比较研究

In vitro comparative study of the antitumor effects of human interferon-alpha, beta and gamma on the growth and invasive potential of human melanoma cells.

作者信息

Horikoshi T, Fukuzawa K, Hanada N, Ezoe K, Eguchi H, Hamaoka S, Tsujiya H, Tsukamoto T

机构信息

Department of Dermatology and Urology, School of Medicine, Sapporo Medical University, Japan.

出版信息

J Dermatol. 1995 Sep;22(9):631-6. doi: 10.1111/j.1346-8138.1995.tb03889.x.

Abstract

We have studied the effects of interferon (IFN)-alpha, beta, and gamma in vitro on the growth and invasive potential of human melanoma SK-MEL-118 cells. The antiproliferative effects of IFNs were assessed by a quantitative regrowth assay in which cells were treated with IFNs at concentrations of 10(2), 10(3) or 10(4) IU/ml for 3 days (until day 4) and then further incubated without IFNs for 7 days (until day 11). The growth inhibitory effect of each IFN on melanoma cells was dose- and time-dependent. Among these three types of IFNs, however, IFN-beta exerted the strongest inhibitory effect on cell growth. To assess the anti-invasive effect of each IFN on melanoma cells, we employed an in vitro assay system using matrigel-coated Transwell chambers. When cells were treated with 10(2), 10(3), or 10(4) IU/ml of the three types of IFNs for 24 hours, the amount of tritiated thymidine incorporated into melanoma cells were treated for 24 hours with 10(4) IU/ml of IFN-beta or gamma prior to the assay, the number of cells that invaded the filter decreased by 40%; this decrease was only 10% with the same amount of IFN-alpha. Simultaneous addition of IFNs during the invasion assay was not effective in any combination. Only when the cells were pretreated with IFNs, antiinvasive effects against melanoma cells were exerted. IFN-alpha was less inhibitory than IFN-beta or gamma on proliferation and not at all inhibitory on invasion. Considering both the antiproliferative and antiinvasive effects of IFNs, our results suggest that IFN-beta has the strongest antitumoral effect on human melanoma cells.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们在体外研究了α、β和γ干扰素对人黑色素瘤SK-MEL-118细胞生长和侵袭潜能的影响。通过定量再生长试验评估干扰素的抗增殖作用,即细胞分别用浓度为10²、10³或10⁴ IU/ml的干扰素处理3天(至第4天),然后在无干扰素的条件下继续培养7天(至第11天)。每种干扰素对黑色素瘤细胞的生长抑制作用呈剂量和时间依赖性。然而,在这三种类型的干扰素中,β干扰素对细胞生长的抑制作用最强。为了评估每种干扰素对黑色素瘤细胞的抗侵袭作用,我们采用了一种使用基质胶包被的Transwell小室的体外检测系统。当细胞用三种类型的干扰素(10²、10³或10⁴ IU/ml)处理24小时后,在检测前用10⁴ IU/ml的β或γ干扰素处理黑色素瘤细胞24小时,侵袭滤膜的细胞数量减少了40%;而相同剂量的α干扰素处理时,细胞数量仅减少10%。在侵袭试验中同时添加干扰素,无论何种组合均无效。只有当细胞用干扰素预处理时,才会对黑色素瘤细胞产生抗侵袭作用。α干扰素在增殖方面的抑制作用比β或γ干扰素弱,且对侵袭完全没有抑制作用。综合考虑干扰素的抗增殖和抗侵袭作用,我们的结果表明β干扰素对人黑色素瘤细胞具有最强的抗肿瘤作用。(摘要截断于250字)

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