Department of Biomedical Engineering, Tufts University, Medford, MA 02155, USA.
J Tissue Eng Regen Med. 2010 Dec;4(8):590-9. doi: 10.1002/term.268. Epub 2010 Sep 23.
Prostate cancer cases and deaths have increased for years, yet the mechanisms involved in prostate cancer metastasis to bone remain poorly understood. To address this need, an effective and relevant in vitro model for the study of prostate cancer bone metastases would be useful. Therefore, a 3D in vitro tissue system was established using prostate cancer cells (PC3), suitable culture conditions and a 3D silk scaffold biomaterial to provide mechanically robust and slow degrading matrices to support the tissues for extended time frames. The role of BMP-2 on the progression of prostate cancer was investigated using this 3D tissue system. The results suggest that BMP-2 stimulates the migration of PC3 cells, suggesting insight into mechanisms involved in this critical step in the disease. The data support the conclusion that this in vitro system mimics aspects of prostate cancer metastasis in the presence of BMP-2, thus the system can be utilized as a starting point as an in vitro model for further studies of prostate cancer development and metastasis, as well as in the screening of new therapeutic treatments.
前列腺癌病例和死亡人数多年来一直在增加,但前列腺癌转移到骨骼的相关机制仍知之甚少。为了满足这一需求,建立一种用于研究前列腺癌骨转移的有效且相关的体外模型将非常有用。因此,我们使用前列腺癌细胞(PC3)、合适的培养条件和 3D 丝素支架生物材料建立了一种 3D 体外组织系统,为组织提供机械强度高且降解缓慢的基质,以支持组织在较长时间内的生长。我们使用该 3D 组织系统研究了 BMP-2 对前列腺癌进展的作用。结果表明,BMP-2 可刺激 PC3 细胞的迁移,这提示我们对该疾病关键步骤中涉及的机制有了更深入的了解。数据支持以下结论:该体外系统在存在 BMP-2 的情况下模拟了前列腺癌转移的某些方面,因此该系统可以用作进一步研究前列腺癌发生和转移以及筛选新的治疗方法的体外模型的起点。