Sakamoto K, Venkatraman G, Shamsuddin A M
Department of Pathology, University of Maryland School of Medicine, Baltimore 21201.
Carcinogenesis. 1993 Sep;14(9):1815-9. doi: 10.1093/carcin/14.9.1815.
Inositol hexaphosphate (InsP6 or phytic acid) has been shown to have antineoplastic action in in vivo models of colon carcinogenesis. We therefore investigated its effect on proliferation and differentiation of the human colon cancer cell line HT-29 in vitro. Proliferation was evaluated by neutral red incorporation assay, and differentiation was assessed by expression of the markers, cytokeratin, carcinoembryonic antigen (CEA) and beta-D-galactose-[1-->3]-N-acetyl-galactosamine (Gal-GalNAc). InsP6 in the culture media (0.66-10 mM) inhibited cell proliferation in a dose-dependent manner (P < 0.001), while inositol or inositol hexasulfate used as controls or media without InsP6 did not show any suppressive effect. The expression of the tumor marker, Gal-GalNac, was augmented (100.7% increase) by low dose (0.66 mM) of InsP6 but was subsequently suppressed with higher concentrations of InsP6. The expression of cytokeratin and CEA were both augmented by either InsP6 or inositol at all concentrations tested, although the degree of augmentation was milder with inositol than with InsP6. The combination of InsP6 and inositol (both 0.66 mm) resulted in augmentation (P < 0.001) of cytokeratin expression, while that of CEA remained unchanged. The inhibitory effect of InsP6 on cell proliferation was not altered by combination with additional inositol at any concentrations tested. Our results show that InsP6 inhibits cell proliferation and concomitantly increases differentiation and is therefore a candidate chemopreventive and chemotherapeutic agent for human large intestinal cancer.
肌醇六磷酸(InsP6或植酸)已被证明在结肠癌发生的体内模型中具有抗肿瘤作用。因此,我们研究了其对人结肠癌细胞系HT - 29体外增殖和分化的影响。通过中性红摄取试验评估增殖,通过细胞角蛋白、癌胚抗原(CEA)和β - D - 半乳糖 - [1→3] - N - 乙酰半乳糖胺(Gal - GalNAc)标志物的表达评估分化。培养基中的InsP6(0.66 - 10 mM)以剂量依赖性方式抑制细胞增殖(P < 0.001),而用作对照的肌醇或肌醇六硫酸盐或不含InsP6的培养基未显示任何抑制作用。低剂量(0.66 mM)的InsP6可使肿瘤标志物Gal - GalNac的表达增加(增加100.7%),但随后随着InsP6浓度升高而受到抑制。在所有测试浓度下,InsP6或肌醇均可使细胞角蛋白和CEA的表达增加,尽管肌醇的增加程度比InsP6轻。InsP6和肌醇(均为0.66 mM)联合使用可使细胞角蛋白表达增加(P < 0.001),而CEA的表达保持不变。在任何测试浓度下,InsP6与额外的肌醇联合使用均未改变其对细胞增殖的抑制作用。我们的结果表明,InsP6抑制细胞增殖并同时增加分化,因此是人类大肠癌化学预防和化疗的候选药物。