姜黄素通过上调骨形态发生蛋白-7在体内抑制前列腺癌骨转移

Thambi Dorai, Janane Diouri, Orla O'Shea, Stephen B Doty
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引用次数: 34

摘要

许多研究都集中在姜黄素(异丙醇甲烷,用于南亚烹饪和传统医学)的有益特性上,例如化学预防癌症。最近的研究也表明,这种材料对治疗癌症有显著的好处,目前正在进行几次临床试验。我们一直对这种化合物作为晚期前列腺癌的治疗剂的应用很感兴趣,特别是这种恶性肿瘤的骨骼并发症。我们早期的工作表明,该化合物可以通过干扰转移性肿瘤微环境中这些癌细胞与骨细胞(即成骨细胞和破骨细胞)之间的共同点来抑制去势抵抗性前列腺癌细胞的拟骨特性。我们预测姜黄素可以打破导致骨基质不受控制的骨溶解的相互刺激的恶性循环。在这项工作中,我们在一个已建立的动物模型中评估了该化合物抑制激素难治性前列腺癌细胞骨转移的潜力。我们的研究结果强烈表明,姜黄素通过上调转移抑制骨形态发生蛋白7 (BMP- 7)来调节由于骨基质降解而发生的TGF-β信号。肿瘤微环境中TGF-β在TGF-β背景下的BMP-7的增强被证明可以促进间质向上皮的转变。最重要的是,我们发现由于BMP-7的上调,一种新的棕色/米色脂肪生成分化程序也被上调,该程序在抑制骨转移中起作用。我们的研究结果表明,姜黄素可能会破坏TGF-β信号传导到另一种脂肪生成分化程序中,从而在化学预防和治疗环境中抑制骨转移过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Curcumin Inhibits Prostate Cancer Bone Metastasis by Up-Regulating Bone Morphogenic Protein-7 <i>in Vivo.</i>

Curcumin Inhibits Prostate Cancer Bone Metastasis by Up-Regulating Bone Morphogenic Protein-7 <i>in Vivo.</i>

Curcumin Inhibits Prostate Cancer Bone Metastasis by Up-Regulating Bone Morphogenic Protein-7 <i>in Vivo.</i>

Curcumin Inhibits Prostate Cancer Bone Metastasis by Up-Regulating Bone Morphogenic Protein-7 in Vivo.

A number of studies have focused on the beneficial properties of Curcumin (diferuloyl methane, used in South Asian cuisine and traditional medicine) such as the chemoprevention of cancer. Recent studies have also indicated that this material has significant benefits for the treatment of cancer and is currently undergoing several clinical trials. We have been interested in the application of this compound as a therapeutic agent for advanced prostate cancer, particularly the skeletal complications in this malignancy. Our earlier work indicated that this compound could inhibit the osteomimetic properties which occur in castration resistant prostate cancer cells, by interfering with the common denominators between these cancer cells and the bone cells in the metastatic tumor microenvironment, namely the osteoblasts and the osteoclast. We predicted that curcumin could break the vicious cycle of reciprocal stimulation that results in uncontrolled osteolysis in the bony matrix. In this work, we have evaluated the potential of this compound in inhibiting the bone metastasis of hormone refractory prostate cancer cells in an established animal model. Our results strongly suggest that curcumin modulates the TGF-β signaling that occurs due to bone matrix degradation by up-regulating the metastasis inhibitory bone morphogenic protein-7 (BMP- 7). This enhancement of BMP-7 in the context of TGF-βin the tumor microenvironment is shown to enhance the mesenchymal-to-epithelial transition. Most importantly, we show that as a result of BMP-7 up-regulation, a novel brown/beige adipogenic differentiation program is also up-regu- lated which plays a role in the inhibition of bone metastasis. Our results suggest that curcumin may subvert the TGF-βsignaling to an alternative adipogenic differentiation program in addition to the previously established interference with the osteomimetic properties, thus inhibiting the bone metastatic processes in a chemopreventive as well as therapeutic setting.

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