Vucenik I, Kalebic T, Tantivejkul K, Shamsuddin A M
Department of Medical and Research Technology, University of Maryland School of Medicine, Baltimore 21201, USA.
Anticancer Res. 1998 May-Jun;18(3A):1377-84.
Inositol hexaphosphate (IP6) is a naturally occurring polyphosphorylated carbohydrate that has been shown to suppress the growth of epithelial cancers, including those of breast and colon. The objective of this study was to investigate whether IP6 inhibits growth of rhabdomyosarcoma (RMS), a tumor of mesenchymal origin, which is the most common soft tissue sarcoma in children. We performed both in vitro and in vivo studies to evaluate the effect of IP6 on human RD cells growth. Our results show that IP6 suppresses growth of rhabdomyosarcoma cell line (RD) in vitro in a dose-dependent fashion. A 50% inhibition of cell growth (IC50) was induced by < 1.0 mM IP6. However, the removal of IP6 from the media, after 72 hours of treatment, allowed cells to recover their logarithmic growth. Exposure of RD cells to IP6 led to differentiation; cells became larger with abundant cytoplasm, expressing higher levels of muscle-specific actin. Consistent with in vitro observation, IP6 suppressed RD cell growth in vivo, in a xenografted nude mice model. When compared to controls, IP6-treated mice produced a 25 fold smaller tumors (p = 0.008), as observed after a two weeks treatment. In a second experiment, wherein the treatment period was extended to five weeks, a 49 fold (p = 0.001) reduction in tumor size was observed in mice treated with IP6. Histologically no evidence of tumor cell necrosis was observed. These data suggest a potential usefulness of this cytostatic, and non-cytotoxic, compound in novel therapeutic strategies for these types of tumor.
肌醇六磷酸(IP6)是一种天然存在的多磷酸化碳水化合物,已被证明可抑制上皮癌的生长,包括乳腺癌和结肠癌。本研究的目的是调查IP6是否能抑制横纹肌肉瘤(RMS)的生长,RMS是一种间充质起源的肿瘤,是儿童中最常见的软组织肉瘤。我们进行了体外和体内研究,以评估IP6对人RD细胞生长的影响。我们的结果表明,IP6在体外以剂量依赖的方式抑制横纹肌肉瘤细胞系(RD)的生长。<1.0 mM的IP6可诱导50%的细胞生长抑制(IC50)。然而,在处理72小时后从培养基中去除IP6,可使细胞恢复对数生长。将RD细胞暴露于IP6会导致分化;细胞变大,细胞质丰富,表达更高水平的肌肉特异性肌动蛋白。与体外观察结果一致,在异种移植裸鼠模型中,IP6在体内抑制了RD细胞的生长。与对照组相比,经IP6处理的小鼠在两周治疗后产生的肿瘤小25倍(p = 0.008)。在第二项实验中,治疗期延长至五周,经IP6处理的小鼠肿瘤大小减少了49倍(p = 0.001)。组织学上未观察到肿瘤细胞坏死的证据。这些数据表明这种具有细胞抑制作用且无细胞毒性的化合物在针对这类肿瘤的新型治疗策略中具有潜在的应用价值。