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肌醇六磷酸抑制PC-3人前列腺癌细胞的生长并诱导其分化。

Inositol hexaphosphate inhibits growth and induces differentiation of PC-3 human prostate cancer cells.

作者信息

Shamsuddin A M, Yang G Y

机构信息

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

出版信息

Carcinogenesis. 1995 Aug;16(8):1975-9. doi: 10.1093/carcin/16.8.1975.

Abstract

We investigated the effects of inositol hexaphosphate (InsP6) on growth inhibition and differentiation of human prostate cancer cells PC-3 in vitro. A significant dose- and time-dependent growth inhibition was observed as tested by the MTT-incorporation assay (P < 0.05 at 1 mM InsP6 after 24 h treatment, P < 0.01 at 0.1 mM after 3 days). DNA synthesis as determined by [3H]thymidine incorporation assay was also suppressed by InsP6 in a dose-dependent manner, occurring as early as 3 h after treatment and continuing up to 48 h (P < 0.01 at 1 mM InsP6). A 9- to 10-fold increase (P < 0.01) in expression of HLA class I molecule associated with tumor immunosurveillance and cell differentiation was induced by InsP6. The marker for prostatic cell differentiation, prostate acid phosphatase, was significantly (P < 0.05) increased after 48 h treatment at 0.5-5 mM InsP6. Since InsP6 strongly inhibits growth and induces differentiation in human prostate cancer cells in vitro, in vivo studies using a tumor xenograft model and a prostate carcinogenesis model are warranted to validate the efficacy of InsP6 in the treatment and prevention of prostate cancer.

摘要

我们研究了肌醇六磷酸(InsP6)对人前列腺癌细胞PC-3体外生长抑制和分化的影响。通过MTT掺入试验检测,观察到显著的剂量和时间依赖性生长抑制(24小时处理后1 mM InsP6时P < 0.05,3天后0.1 mM时P < 0.01)。通过[3H]胸苷掺入试验测定的DNA合成也被InsP6以剂量依赖性方式抑制,最早在处理后3小时出现并持续至48小时(1 mM InsP6时P < 0.01)。InsP6诱导与肿瘤免疫监视和细胞分化相关的HLA I类分子表达增加9至10倍(P < 0.01)。在0.5 - 5 mM InsP6处理48小时后,前列腺细胞分化标志物前列腺酸性磷酸酶显著增加(P < 0.05)。由于InsP6在体外强烈抑制人前列腺癌细胞的生长并诱导其分化,因此有必要使用肿瘤异种移植模型和前列腺癌发生模型进行体内研究,以验证InsP6在前列腺癌治疗和预防中的疗效。

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