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改性柑橘果胶与两种植物复方制剂协同增效抑制人乳腺癌和前列腺癌细胞侵袭行为。

Synergistic and additive effects of modified citrus pectin with two polybotanical compounds, in the suppression of invasive behavior of human breast and prostate cancer cells.

机构信息

Indiana University Health, Indianapolis, IN, USA.

出版信息

Integr Cancer Ther. 2013 Mar;12(2):145-52. doi: 10.1177/1534735412442369. Epub 2012 Apr 24.

DOI:10.1177/1534735412442369
PMID:22532035
Abstract

AIM

The objective of this study was to evaluate the combined effect of a known galectin-3 inhibitor, PectaSol-C modified citrus pectin (MCP), and 2 novel integrative polybotanical compounds for breast and prostate health, BreastDefend (BD) and ProstaCaid (PC), on invasive behavior in human breast and prostate cancer cells in vitro, respectively.

METHODS

The effect of MCP and BD and of MCP and PC on invasiveness was assessed by cell adhesion, cell migration, and cell invasion assays. Secretion of urokinase plasminogen activator (uPA) was determined by Western blot analysis.

RESULTS

Although low concentrations of MCP (0.25-1.0 mg/mL) do not suppress cell adhesion of breast or prostate cancer cells, the combination of MCP with BD or PC synergistically inhibits adhesion of these cells. Dose-dependent inhibition of breast and prostate cancer cell migration by MCP (0.25-1.0 mg/mL) is synergistically enhanced by BD (20 µg/mL) and PC (10 µg/mL), respectively. BD or PC did not further inhibit the invasion of breast and prostate cancer cells by MCP; however, the combination of MCP with BD or PC suppressed secretion of uPA from breast and prostate cancer cells, respectively.

CONCLUSION

The combination of MCP with BD and of MCP with PC synergistically inhibits the metastatic phenotypes of human breast and prostate cancer cells, respectively. Further studies confirming these observations in animal models of breast and prostate cancer metastasis are warranted.

摘要

目的

本研究旨在评估一种已知半乳糖凝集素-3 抑制剂——果胶 MCP(PectaSol-C modified citrus pectin),以及两种新型综合植物化合物——乳腺健康宝(BreastDefend,BD)和前列腺健康宝(ProstaCaid,PC)对体外人乳腺癌和前列腺癌细胞侵袭行为的联合作用。

方法

通过细胞黏附、细胞迁移和细胞侵袭实验评估 MCP 和 BD 以及 MCP 和 PC 对侵袭性的影响。通过 Western blot 分析测定尿激酶纤溶酶原激活物(uPA)的分泌。

结果

尽管低浓度的 MCP(0.25-1.0 mg/mL)不会抑制乳腺癌或前列腺癌细胞的黏附,但 MCP 与 BD 或 PC 的联合使用可协同抑制这些细胞的黏附。MCP(0.25-1.0 mg/mL)剂量依赖性抑制乳腺癌和前列腺癌细胞的迁移,与 BD(20 µg/mL)和 PC(10 µg/mL)分别协同增强。BD 或 PC 并未进一步抑制 MCP 对乳腺癌和前列腺癌细胞的侵袭;然而,MCP 与 BD 或 PC 的联合使用抑制了乳腺癌和前列腺癌细胞 uPA 的分泌。

结论

MCP 与 BD 的联合使用以及 MCP 与 PC 的联合使用分别协同抑制了人乳腺癌和前列腺癌细胞的转移表型。进一步在乳腺癌和前列腺癌转移的动物模型中证实这些观察结果的研究是必要的。

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