Welch D R, Harper D E, Yohem K H
Department of Pathology, Pennsylvania State University College of Medicine, Hershey 17033.
Clin Exp Metastasis. 1993 Mar;11(2):201-12. doi: 10.1007/BF00114978.
Several cinnamoyl compounds have been shown to have antitumor activities, but not specifically anti-invasive or antimetastatic effects. U-77,863 (o-methyl cinnanamide) was originally isolated from a fermentation beer of Streptomyces griseoluteus and recently synthesized (Harper, DE and Welch DR. Journal of Antibiotics, in press). Based upon some differential activities of cinnanamides, in general, and U-77,863, specifically, we tested the hypothesis that U-77,863 could inhibit invasion and metastasis of human malignant melanoma cell lines C8161 and A375M. Pretreatment of melanoma cells in vitro with nontoxic doses of U-77,863 caused a dose-, and time-dependent, reversible reduction (IC50 = 12.5 micrograms/ml) of invasion through Matrigel-coated polycarbonate filters in the Membrane Invasion Culture System (MICS). Likewise, lung colonization was significantly (P < 0.05) inhibited when tumor cells were pretreated in vitro with U-77,863 prior to intravenous injection. Structure-activity analysis revealed that the acrylamide side-chain alone and cinnanamide were only slightly less potent than U-77,863, whereas cinnamic acid analogs did not inhibit tumor cell invasion at doses < or = 100 micrograms/ml. U-77,863 inhibits invasion and metastasis without decreasing growth rates or clonogenic potential. Adhesion to endothelial monolayers or extracellular matrices (Matrigel) is not affected by exposure to U-77,863. U-77,863 presumably inhibits metastasis by inhibiting tumor cell extravasation (invasion). U-77,863 is a lead compound for developing a novel class of anti-invasive/anti-metastatic drugs.
几种肉桂酰化合物已被证明具有抗肿瘤活性,但并非具有特异性的抗侵袭或抗转移作用。U-77863(邻甲基肉桂酰胺)最初是从灰色链霉菌的发酵啤酒中分离出来的,最近已被合成(哈珀,DE和韦尔奇DR。《抗生素杂志》,即将出版)。基于肉桂酰胺类化合物一般的以及U-77863特异性的一些差异活性,我们测试了U-77863能够抑制人恶性黑色素瘤细胞系C8161和A375M侵袭和转移的假说。在体外用无毒剂量的U-77863预处理黑色素瘤细胞,在膜侵袭培养系统(MICS)中导致通过基质胶包被的聚碳酸酯滤膜的侵袭呈剂量和时间依赖性的可逆性降低(IC50 = 12.5微克/毫升)。同样,当肿瘤细胞在静脉注射前在体外先用U-77863预处理时,肺转移明显(P < 0.05)受到抑制。构效分析表明单独的丙烯酰胺侧链和肉桂酰胺的效力仅略低于U-77863,而肉桂酸类似物在剂量≤100微克/毫升时不抑制肿瘤细胞侵袭。U-77863抑制侵袭和转移而不降低生长速率或克隆形成潜力。暴露于U-77863不影响对内皮单层或细胞外基质(基质胶)的粘附。U-77863可能通过抑制肿瘤细胞外渗(侵袭)来抑制转移。U-77863是开发新型抗侵袭/抗转移药物的先导化合物。