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肌醇六磷酸的新型抗癌功能:体外对人乳腺癌细胞系的生长抑制和分化作用

Novel anti-cancer functions of IP6: growth inhibition and differentiation of human mammary cancer cell lines in vitro.

作者信息

Shamsuddin A M, Yang G Y, Vucenik I

机构信息

Department of Pathology, University of Maryland School of Medicine, Baltimore 21201-1192, USA.

出版信息

Anticancer Res. 1996 Nov-Dec;16(6A):3287-92.

PMID:9042302
Abstract

Inositol hexaphosphate (InsP6 or IP6) is an active ingredient of high fiber diet that has anti-cancer action in both in vitro and in vivo models. Recently we have demonstrated that InsP6 significantly inhibits DMBA-induced rat mammary cancer in vivo. To test the hypothesis that InsP6 mediates its function via inhibition of cell proliferation irrespective of hormonal dependence, its effect on growth inhibition and differentiation were studied in two human mammary carcinoma cell lines with different estrogen receptor status. Cell growth was measured by MTT incorporation assay, DNA synthesis by 3H-Tdr uptake and differentiation marker lactalbumin by immunocytochemistry. Dose-dependent growth inhibition was observed in both estrogen receptor-positive (MCF-7) and receptor-negative cells (MDA-MB-231). Statistically significant growth inhibition (p < 0.05) was observed starting at 1 mM InsP6 as early as after the first day of treatment and continued up to 6 days for both the cell lines. DNA synthesis in both the cell lines was suppressed by InsP6 occurring as early as 3 h after the beginning of treatment and continued up to 48 h; significant inhibition (p < 0.05) started at 1 mM InsP6 after 6 h of treatment. Compared to untreated cells, a 5-fold (p < 0.05) and 22-fold (p < 0.01) increase in expression of lactalbumin, associated with luminal cell differentiation was identified by immunocytochemistry after 48 h of treatment with 1 and 5 mM InsP6. Our data show that the inhibition of DNA synthesis and cell growth and induction of differentiation of human mammary cancer cell lines by InsP6 is independent of the estrogen receptor status of the cells. Taken together with results from in vivo studies, InsP6 may be an important candidate for the prevention and treatment of human breast cancer.

摘要

肌醇六磷酸(InsP6 或 IP6)是高纤维饮食中的一种活性成分,在体外和体内模型中均具有抗癌作用。最近我们证明,InsP6 在体内能显著抑制二甲基苯并蒽(DMBA)诱导的大鼠乳腺癌。为了验证 InsP6 通过抑制细胞增殖来介导其功能这一假说,且该功能与激素依赖性无关,我们在两种具有不同雌激素受体状态的人乳腺癌细胞系中研究了其对生长抑制和分化的影响。通过 MTT 掺入法测定细胞生长,通过 3H-Tdr 摄取测定 DNA 合成,并通过免疫细胞化学测定分化标志物乳白蛋白。在雌激素受体阳性(MCF-7)和受体阴性细胞(MDA-MB-231)中均观察到剂量依赖性生长抑制。早在治疗第一天,从 1 mM InsP6 开始就观察到具有统计学意义的生长抑制(p < 0.05),并且两种细胞系持续至 6 天。两种细胞系中的 DNA 合成在治疗开始后 3 小时就被 InsP6 抑制,并持续至 48 小时;治疗 6 小时后,1 mM InsP6 开始出现显著抑制(p < 0.05)。与未处理的细胞相比,用 1 和 5 mM InsP6 处理 48 小时后,通过免疫细胞化学鉴定,与管腔细胞分化相关的乳白蛋白表达分别增加了 5 倍(p < 0.05)和 22 倍(p < 0.01)。我们的数据表明,InsP6 对人乳腺癌细胞系的 DNA 合成、细胞生长的抑制以及分化的诱导与细胞的雌激素受体状态无关。结合体内研究结果,InsP6 可能是预防和治疗人类乳腺癌的重要候选物。

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