Futakuchi Mitsuru, Nannuru Kalyan C, Varney Michelle L, Sadanandam Anguraj, Nakao Kimihisa, Asai Kiyofumi, Shirai Tomoyuki, Sato Shin-ya, Singh Rakesh K
Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska 68198-5845, USA.
Cancer Sci. 2009 Jan;100(1):71-81. doi: 10.1111/j.1349-7006.2008.01012.x. Epub 2008 Nov 25.
Understanding the cellular and molecular changes in the bone microenvironment is important for developing novel therapeutics to control breast cancer bone metastasis. Although the underlying mechanism(s) of bone metastasis has been the focus of intense investigation, relatively little is known about complex molecular interactions between malignant cells and bone stroma. Using a murine syngeneic model that mimics osteolytic changes associated with human breast cancer, we examined the role of tumor-bone interaction in tumor-induced osteolysis and malignant growth in the bone microenvironment. We identified transforming growth factor-beta receptor 1 (TGF-betaRI) as a commonly upregulated gene at the tumor-bone (TB) interface. Moreover, TGF-betaRI expression and activation, analyzed by nuclear localization of phospho-Smad2, was higher in tumor cells and osteoclasts at the TB interface as compared to the tumor-alone area. Furthermore, attenuation of TGF-beta activity by neutralizing antibody to TGF-beta or TGF-betaRI kinase inhibitor reduced mammary tumor-induced osteolysis, TGF-betaRI expression and its activation. In addition, we demonstrate a potential role of TGF-beta as an important modifier of receptor activator of NF-kappaB ligand (RANKL)-dependent osteoclast activation and osteolysis. Together, these studies demonstrate that inhibition of TGF-betaRI signaling at the TB interface will be a therapeutic target in the treatment of breast cancer-induced osteolysis.
了解骨微环境中的细胞和分子变化对于开发控制乳腺癌骨转移的新型疗法至关重要。尽管骨转移的潜在机制一直是深入研究的重点,但对于恶性细胞与骨基质之间复杂的分子相互作用却知之甚少。利用一种模拟与人类乳腺癌相关的溶骨性变化的小鼠同基因模型,我们研究了肿瘤与骨相互作用在肿瘤诱导的骨溶解和骨微环境中恶性生长中的作用。我们确定转化生长因子-β受体1(TGF-βRI)是肿瘤与骨(TB)界面处普遍上调的基因。此外,通过磷酸化Smad2的核定位分析,与仅肿瘤区域相比,TB界面处的肿瘤细胞和破骨细胞中TGF-βRI的表达和激活更高。此外,用抗TGF-β中和抗体或TGF-βRI激酶抑制剂减弱TGF-β活性可减少乳腺肿瘤诱导的骨溶解、TGF-βRI表达及其激活。此外,我们证明了TGF-β作为核因子-κB受体激活配体(RANKL)依赖性破骨细胞激活和骨溶解的重要调节因子的潜在作用。总之,这些研究表明,抑制TB界面处的TGF-βRI信号将是治疗乳腺癌诱导的骨溶解的一个治疗靶点。