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Logo of jclinpathJournal of Clinical PathologyCurrent TOCInstructions for authors
J Clin Pathol. Nov 2002; 55(11): 877–878.
PMCID: PMC1769799

Tumour cells produce receptor activator of NF-κB ligand (RANKL) in skeletal metastases

Osteolytic bone destruction is a common complication of tumours that metastasise to bone. Several solid tumours, most notably breast carcinoma, lung carcinoma, and prostate carcinoma, commonly metastasise to bone in patients with advanced disease, where they cause osteolysis and associated pain, hypercalcemia, and fracture. It is generally accepted that osteoclasts are the only cells capable of resorbing mineralised bone. In osteolytic metastases, it has been shown that tumour cells direct osteoclastic bone resorption through a vicious cycle1,2: in particular, tumour cell produced parathyroid hormone related protein (PTH-rP) facilitates bone resorption and, as a consequence, transforming growth factor β is released from the bone matrix and promotes the progression of bone metastases by further inducing PTH-rP production by tumour cells. Other tumour cell products, such as macrophage colony stimulating factor, interleukin 6 (IL-6), IL-11, and tumour necrosis factor α, have also been reported to be associated with tumour induced osteolysis.

However, with the identification and characterisation of a direct stimulator of osteoclastogenesis—the receptor activator of NF-kB ligand (RANKL,3,4 also known as ODF, OPGL, and TRANCE)—a possible final common pathway for osteoclastic bone destruction has emerged. A variety of osteotropic factors, such as 1,25-dihydroxyvitamin D3, prostaglandin E2, parathyroid hormone, IL-6, and IL-11, have been shown to mediate osteoclast differentiation through the upregulation of RANKL expression or the downregulation of osteoprotegerin (OPG; the decoy receptor of RANKL) expression in osteoblast/stromal cells.5 There is also experimental evidence that tumour produced PTH-rP may stimulate osteoclastic bone resorption by enhancing RANKL expression and reducing OPG expression in the osteoblast.6 However, whether tumour cells directly produce RANKL, which subsequently mediates osteolysis in metastatic skeletal lesions, has not been determined.

To this end, we have investigated the expression of RANKL in the skeletal lesions of patients with carcinomas that had metastasised to bone. Sixteen cases, including breast carcinoma (four cases), lung carcinoma (six cases), prostate carcinoma (two cases), and follicular thyroid carcinoma (four cases), were collected during surgery of pathological fractures. Histological confirmation of the diagnosis in each case was based on the review of routinely prepared paraffin wax embedded tissue sections in conjunction with knowledge of the clinical and radiological findings. All patients presented with aggressive osteolytic lesions and pathological fracture, and adenocarcinoma was the predominant histological subtype (table 11).). The expression of RANKL mRNA and protein was assessed using in situ hybridisation (digoxenin labelled RANKL antisense riboprobe, 0.5 ng/ml)7 and immunohistochemistry (mouse antihuman TRANCE monoclonal antibody from R&D, Minneapolis, Minnesota, USA; StreptABComplex/horseradish peroxidase mouse/rabbit system from Dako, Carpinteria, California, USA), respectively, on paraffin wax embedded tissue sections. Typical histological appearances of neoplastic cells in various bone metastatic tumours were revealed by haematoxylin and eosin staining (fig 11,, H&E). The neoplastic cells of breast carcinoma, lung carcinoma, prostate carcinoma, and thyroid carcinoma showed strong positive hybridisation signals with RANKL riboprobes (fig 11,, ISH), and also strong positive staining with anti-RANKL antibodies (fig 11,, IHC). RANKL mRNA and protein were also present in osteoblasts and fibroblasts in surrounding tissues (fig 11).). Table 11 summarises the percentages of tumour cells exhibiting immunoreactivity for RANKL and the intensity of immunostaining in all 16 specimens. In short, we found that both RANKL mRNA and protein were present in more than 90% and in some cases 100% of metastatic tumour cells in lesions of breast, lung, prostate, and thyroid adenocarcinoma. Therefore, we conclude that in osteolytic skeletal secondaries, metastatic tumour cells, regardless of origin, express RANKL, and may directly stimulate osteoclastic bone destruction. In support of our observations, Zhang and colleagues8 have recently provided evidence that tumour cells of prostate cancer are capable of inducing osteoclastogenesis in vitro, directly through the production of soluble RANKL.

Figure 1
Expression of RANKL mRNA and protein in bone metastatic tumours. Signals are dark blue in colour. RANKL mRNA was present in the neoplastic cells of various metastatic tumours. Positive signals are brown in colour. RANKL protein was present at different ...
Table 1
A list of tumour bone metastases and RANKL immunoreactivity

Bone resorption is a necessary priming event for the establishment and propagation of tumour metastasis in bone. Our study has been conducted on the metastatic component of the primary carcinoma in the skeleton, and we did not have access to tissues of the primary site. Indeed, there is a paucity of studies that compare RANKL expression in the primary and metastatic tumours of the same patients. Brown and colleagues9 reported that RANKL was heterogeneously expressed in 10 of 11 prostate carcinoma specimens, and the proportion of tumour cells expressing RANKL was significantly increased in all bone metastases in comparison with non-osseous metastases or the primary prostatic tumour. Whether RANKL expression in the primary tumour is predictive of a possible propensity towards skeletal metastasis remains to be seen and could be the focus of future studies.

Acknowledgments

This study was fully supported by a grant of the Research Grants Council of the Hong Kong SAR (CUHK/4142/00M).

References

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3. Yasuda H, Shima N, Nakagawa N, et al. Osteoclast differentiation factor is a ligand for osteoprotegerin/osteoclastogenesis-inhibitory factor and is identical to TRANCE/RANKL. Proc Natl Acad Sci U S A 1998;95:3597–602. [PMC free article] [PubMed]
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6. Thomas RJ, Guise TA, Yin JJ, et al. Breast cancer cells interact with osteoblasts to support osteoclast formation. Endocrinology 1999;140:4451–8. [PubMed]
7. Huang L, Xu J, Wood DJ, et al. Gene expression of osteoprotegerin ligand, osteoprotegerin, and receptor activator of NF-kappaB in giant cell tumor of bone: possible involvement in tumor cell-induced osteoclast-like cell formation. Am J Pathol 2000;156:761–7. [PMC free article] [PubMed]
8. Zhang J, Dai J, Qi Y, et al. Osteoprotegerin inhibits prostate cancer-induced osteoclastogenesis and prevents prostate tumor growth in the bone. J Clin Invest 2001;107:1235–44. [PMC free article] [PubMed]
9. Brown JM, Corey E, Lee ZD, et al. Osteoprotegerin and rank ligand expression in prostate cancer. Urology 2001;57:611–16. [PubMed]

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