Yang Wenyi, Lam Pearl, Kitching Richard, Kahn Harriette J, Yee Albert, Aubin Jane E, Seth Arun
Division of Molecular and Cellular Biology, Sunnybrook Research Institute, University of Toronto, Toronto, Ontario, Canada.
Cancer Biol Ther. 2007 Aug;6(8):1289-94. doi: 10.4161/cbt.6.8.4504. Epub 2007 May 25.
A major dilemma facing patients with breast cancer is how to decide between over treating indolent tumors and failing to adequately treat aggressive, potentially lethal cancers. Determination of the metastatic potential of a patient's breast cancer would clearly help guide those treatment decisions. Breast cancer commonly spreads to bone in 70% of women with advanced disease. However, the mechanism of bone metastasis is not well understood. One possibility is that the microenvironment within bone marrow, highly rich in growth factors and cytokines, is suitable for the proliferation of breast cancer cells. In this study, we developed a method for implanting human bone in NOD/SCID mice and show that the human bone implants are viable for more than 20 weeks. This human bone NOD/SCID mouse model provides an opportunity to functionally characterize human breast cancer cell behavior in an in vivo human microenvironment. Several breast tumor cell lines have been shown to grow in the human-bone-NOD/SCID model system, however each line has a different functional profile. Here we show that cotransplantation of GFP-MDA-MB-231 breast cancer cells with morcellized human bone allows for tissue specific metastasis to an initially tumor free bone implant. Furthermore, metastasis of breast tumor cells to implanted tumor-free human bone was seen when patient bone containing a metastatic breast tumor was implanted in the host mouse. With this model, we can distinguish between primary invasive breast tumors with and without bone metastatic potential.
乳腺癌患者面临的一个主要困境是如何在过度治疗惰性肿瘤和未能充分治疗侵袭性、潜在致命性癌症之间做出抉择。确定患者乳腺癌的转移潜能显然有助于指导这些治疗决策。在70%的晚期乳腺癌女性患者中,乳腺癌通常会扩散至骨骼。然而,骨转移的机制尚未完全明确。一种可能性是,富含生长因子和细胞因子的骨髓微环境适合乳腺癌细胞的增殖。在本研究中,我们开发了一种将人骨植入NOD/SCID小鼠的方法,并证明人骨植入物在20周以上仍具有活性。这种人骨NOD/SCID小鼠模型为在体内人微环境中对人乳腺癌细胞行为进行功能特性分析提供了一个机会。已有研究表明,几种乳腺癌细胞系可在人骨-NOD/SCID模型系统中生长,然而每个细胞系都有不同的功能特征。在此我们表明,将GFP-MDA-MB-231乳腺癌细胞与切碎的人骨共同移植,可使肿瘤特异性转移至最初无肿瘤的骨植入物。此外,当将含有转移性乳腺癌肿瘤的患者骨植入宿主小鼠时,可观察到乳腺肿瘤细胞转移至植入的无肿瘤人骨。利用该模型,我们可以区分具有和不具有骨转移潜能的原发性浸润性乳腺癌肿瘤。