Fatal attraction: why breast cancer cells home to bone.

Osteolytic metastases due to breast cancer are serious events. The interactions between breast cancer cells with the microenvironment of bone have been thought to provide an ideal milieu for cancer cells. Recent data now indicate that migration of breast cancer cells into bone and their subsequent growth into metastases depends upon the interaction of the receptor activator of NF-kappaB ligand (RANKL) with its receptor RANK.

Bone metastases represent a frequent and severe complication of advanced breast cancer, and are associated with pathological fractures, intractable pain, and reduced quality of life. Most skeletal metastases due to breast cancer are osteolytic with histological evidence of an increased number and activity of bone-resorbing osteoclasts [1]. That osteoclasts are actively involved in tumour-induced skeletal destruction has been noted for decades, and a vicious circle has been suggested (Figure 1). Tumour cells activate osteoclasts by producing the putative 'osteoclast activating factor'. Osteoclasts in turn resorb bone and release factors embedded in the bone matrix, including parathyroid hormone-related peptide (PTHrP), IL-6, and transforming growth factor (TGF)-β, which serve as tumour survival factors [1].

Figure 1

Breast cancer-bone interactions in skeletal metastasis using the receptor activator of NF-κB ligand (RANKL)/RANK pathway. Expression of RANK enables breast cancer cells to migrate to bone where the cognate ligand RANKL is abundantly expressed by osteoblasts. Some tumour cells express RANKL, whereas others further enhance RANKL expression by cell-to-cell contact of tumour cells with osteoblastic lineage cells. This enables breast cancer cells to enter a vicious circle where they stimulate bone-destroying osteoclasts that express RANK (first loop). Bone degradation by osteoclasts creates further space for expansive tumour growth within the bone microenvironment and releases a variety of growth factors and cytokines that have been deposited by osteoblasts, including parathyroid hormone-related peptide (PTHrP), IL-6, and transforming-growth factor (TGF)-β, and that serve as tumour survival factors (second loop). OAF, osteoclast activating factor.

A major breakthrough in bone cell biology was the identification of receptor activator of NF-κB ligand (RANKL), the stem cell factor for osteoclasts [2,3]. RANKL, which is abundantly produced by osteoblasts, stimulates osteoclastic lineage commitment, promotes cellular maturation and functions, and prolongs survival, which together enhance bone resorption [3]. RANKL binds to RANK, a member of the tumour necrosis factor receptor superfamily that is expressed on osteoclastic lineage cells [2,3]. The effects of RANKL are counter-balanced by the endogenous decoy receptor osteoprotegerin (OPG), also produced by osteoblasts [4]. Alterations of the RANKL/OPG balance have been implicated in a spectrum of skeletal diseases characterised by excessive osteoclastic activity, including osteoporosis, rheumatoid arthritis, and bone metastases.

Earlier studies suggested that RANKL may be the long sought-after osteoclast activating factor, the critical factor expressed by breast cancer cells that functions as the stem cell factor for osteoclasts (Figure 1) [5]. When challenged by PTHrP, the human breast cancer cell line MCF-7 expressed RANKL, enhanced osteoclastic activity, and caused skeletal lesions and hypercalcemia after injection into mice [5]. Another human breast cancer cell line, MDA-MB-231, spontaneously expressed RANKL and grew bone metastases when transferred into susceptible mice [6]. Of note, skeletal lesions in these mice were reduced after blockade of RANKL by an OPG analogue [6]. These studies indicated that a local increase of the RANKL-to-OPG ratio is key for skeletal growth of breast cancer metastases and a potential target for therapeutic intervention. Other local factors released from bone matrix by osteoclasts or directly produced by osteoblasts, such as PTHrP, IL-6, TGF-β and TGF superfamily members as well as activators and inhibitors of the Wnt signalling pathway, can directly modulate tumour biology of skeletal metastases. This involves direct receptor-mediated effects and paracrine effects converging at the RANKL/OPG level.

The RANKL/RANK pathway may direct breast cancer cells to preferentially migrate into bone, the crucial requirement and initial step for skeletal metastasis. Epithelial cells from normal mammary glands express RANK, and RANKL-RANK signalling is required for the development of lactating mammary glands during pregnancy [7]. Both RANKL- and RANK-deficient mice lack lactating mammary glands and cannot feed their off-spring [7]. Based on high constitutive RANK expression in breast cancer specimens and cell lines, recent data now indicate that the RANK expression status of cancer cells determines whether tumours predominantly migrate into bone, where the corresponding ligand RANKL is abundantly expressed [8]. The correlation of high RANK expression with osteotropism in murine models was demonstrated across diverse tumour cell types, including breast cancer and melanoma [8]. Blocking RANKL-RANK signalling in these mice by OPG administration reduced the skeletal tumour burden by 50% and prevented tumour-induced paralysis [8].

What are the clinical lessons to be learned from these discoveries? The ménage à trois of breast cancer cells, osteoblasts, and osteoclasts is linked through the RANKL/RANK/OPG system, which explains why tumour cells home to bone and later on destroy it. It will be important to know whether high-risk patients for skeletal metastases can be identified based on high RANK expression in their primary breast tumours. Currently, women with skeletal metastases due to breast cancer are treated by chemotherapy, radiotherapy, and intravenous bisphosphonates, or combinations thereof. Of these, bisphosphonates inhibit certain osteoclast functions and promote osteoclast apoptosis. Recently, a fully human monoclonal antibody against RANKL (denosumab) has been developed and is currently being evaluated in clinical trials. Denosumab interferes with RANK signalling by blocking RANKL and, just like OPG, preventing RANK activation. Denosumab protected against bone loss in postmenopausal women with low bone mass based on biochemical markers of bone turnover and measurements of bone mineral density [9]. Moreover, RANKL inhibition also suppressed biochemical markers of bone turnover and skeletal-related events such as fractures, spinal cord compression, or the need to perform surgery or radiotherapy in women with breast cancer [10]. Long-term data on denosumab will show whether our detailed knowledge of bone cell biology and the RANKL/RANK pathway can be translated to prevent skeletal migration and metastases in women suffering from breast cancer.

Abbreviations

IL = interleukin; OPG = osteoprotegerin; PTHrP = parathyroid hormone-related peptide; RANK = receptor activator of NF-κB; RANKL = RANK ligand; TGF = transforming growth factor.

Competing interests

The authors declare that they have no competing interests.