부산대학교 도서관

Tumour necrosis factor receptor-associated factor 6 (TRAF6) has been implicated in breast cancer and osteoclastic bone destruction. Here, we report that 6877002, a verified small-molecule inhibitor of TRAF6, reduced metastasis, osteolysis and osteoclastogenesis in models of osteotropic human and mouse breast cancer. First, we observed that TRAF6 is highly expressed in osteotropic breast cancer cells and its level of expression was higher in patients with bone metastasis. Pre-exposure of osteoclasts and osteoblasts to non-cytotoxic concentrations of 6877002 inhibited cytokine-induced NFκB activation and osteoclastogenesis, and reduced the ability of osteotropic human MDA-MB-231 and mouse 4T1 breast cancer cells to support bone cell activity. 6877002 inhibited human MDA-MB-231-induced osteolysis in the mouse calvaria organ system, and reduced soft tissue and bone metastases in immuno-competent mice following intra-cardiac injection of mouse 4T1-Luc2 cells. Of clinical relevance, combined administration of 6877002 with Docetaxel reduced metastasis and inhibited osteolytic bone damage in mice bearing 4T1-Luc2 cells. Thus, TRAF6 inhibitors such as 6877002 – alone or in combination with conventional chemotherapy - show promise for the treatment of metastatic breast cancer. • TRAF6/NFκB signalling is implicated in bone remodelling and breast cancer. • TRAF6/NFκB inhibitor reduced breast cancer cell-induced osteolysis. • TRAF6/NFκB inhibitor and docetaxel reduced breast cancer bone metastasis in mice. • TRAF6 inhibitors and chemotherapy show promise for breast cancer treatment. [ABSTRACT FROM AUTHOR]