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Soluble RANKL is physiologically dispensable but accelerates tumour metastasis to bone.
- Source :
-
Nature metabolism [Nat Metab] 2019 Sep; Vol. 1 (9), pp. 868-875. Date of Electronic Publication: 2019 Sep 02. - Publication Year :
- 2019
-
Abstract
- Receptor activator of NF-κB ligand (RANKL) is a multifunctional cytokine known to affect immune and skeletal systems, as well as oncogenesis and metastasis <superscript>1-4</superscript> . RANKL is synthesized as a membrane-bound molecule, and cleaved into its soluble form by proteases <superscript>5-7</superscript> . As the soluble form of RANKL does not contribute greatly to bone remodelling or ovariectomy-induced bone loss <superscript>8</superscript> , whether soluble RANKL has a role in pathological settings remains unclear. Here we show that soluble RANKL promotes the formation of tumour metastases in bone. Mice that selectively lack soluble RANKL (Tnfsf11 <superscript>ΔS/ΔS</superscript> ) <superscript>5-7,9</superscript> have normal bone homoeostasis and develop a normal immune system but display markedly reduced numbers of bone metastases after intracardiac injection of RANK-expressing melanoma and breast cancer cells. Deletion of soluble RANKL does not affect osteoclast numbers in metastatic lesions or tumour metastasis to non-skeletal tissues. Therefore, soluble RANKL is dispensable for physiological regulation of bone and immune systems, but has a distinct and pivotal role in the promotion of bone metastases.
- Subjects :
- Animals
Bone Remodeling physiology
Cell Differentiation physiology
Female
Humans
Male
Mice
Mice, Knockout
Neoplasm Metastasis
Osteoclasts cytology
Receptor Activator of Nuclear Factor-kappa B genetics
Bone Neoplasms secondary
Neoplasms pathology
Receptor Activator of Nuclear Factor-kappa B physiology
Subjects
Details
- Language :
- English
- ISSN :
- 2522-5812
- Volume :
- 1
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Nature metabolism
- Publication Type :
- Academic Journal
- Accession number :
- 32694743
- Full Text :
- https://doi.org/10.1038/s42255-019-0104-1