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Published in: Current Osteoporosis Reports 1/2012

01-03-2012 | Future Therapeutics (P Miller, Section Editor)

Inhibition of Cathepsin K for Treatment of Osteoporosis

Authors: Steven Boonen, Elizabeth Rosenberg, Frank Claessens, Dirk Vanderschueren, Socrates Papapoulos

Published in: Current Osteoporosis Reports | Issue 1/2012

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Abstract

Cathepsin K is the protease that is primarily responsible for the degradation of bone matrix by osteoclasts. Inhibitors of cathepsin K are in development for treatment of osteoporosis. Currently available antiresorptive drugs interfere with osteoclast function. They inhibit both bone resorption and formation, due to the coupling between these processes. Cathepsin K inhibitors, conversely, target the resorption process itself and may not interfere with osteoclast stimulation of bone formation. In fact, when cathepsin K is absent or inhibited in mice, rabbits, or monkeys, bone formation is maintained or increased. In humans, inhibition of cathepsin K is associated with sustained reductions in bone resorption markers but with smaller and transient reductions in bone formation markers. The usefulness of cathepsin K inhibitors in osteoporosis is now being examined in phase 2 and phase 3 clinical trials of postmenopausal osteoporotic women.
Literature
1.
3.
go back to reference Cummings SR, Melton LJ. Epidemiology and outcomes of osteoporotic fractures. Lancet. 2002;359:1761–7.PubMedCrossRef Cummings SR, Melton LJ. Epidemiology and outcomes of osteoporotic fractures. Lancet. 2002;359:1761–7.PubMedCrossRef
4.
go back to reference Fast Facts. nof.org/node/40. Accessed 7 June 2011. Fast Facts. nof.org/node/40. Accessed 7 June 2011.
6.
go back to reference Vaananen HK, Laitala-Leinonen T. Osteoclast lineage and function. Arch Biochem Biophys. 2008;473:132–8.PubMedCrossRef Vaananen HK, Laitala-Leinonen T. Osteoclast lineage and function. Arch Biochem Biophys. 2008;473:132–8.PubMedCrossRef
7.
go back to reference Lecaille F, Bromme D, Lalmanach G. Biochemical properties and regulation of cathepsin K activity. Biochimie. 2008;90:208–26.PubMedCrossRef Lecaille F, Bromme D, Lalmanach G. Biochemical properties and regulation of cathepsin K activity. Biochimie. 2008;90:208–26.PubMedCrossRef
8.
go back to reference Karsdal MA, Martin TJ, Bollerslev J, et al. Are nonresorbing osteoclasts sources of bone anabolic activity? J Bone Miner Res. 2007;22:487–94.PubMedCrossRef Karsdal MA, Martin TJ, Bollerslev J, et al. Are nonresorbing osteoclasts sources of bone anabolic activity? J Bone Miner Res. 2007;22:487–94.PubMedCrossRef
9.
go back to reference Henriksen K, Neutzsky-Wulff AV, Bonewald LF, Karsdal MA. Local communication on and within bone controls bone remodeling. Bone. 2009;44:1026–33.PubMedCrossRef Henriksen K, Neutzsky-Wulff AV, Bonewald LF, Karsdal MA. Local communication on and within bone controls bone remodeling. Bone. 2009;44:1026–33.PubMedCrossRef
10.
11.
go back to reference Boyce BF, Xing L. Functions of RANKL/RANK/OPG in bone modeling and remodeling. Arch Biochem Biophys. 2008;473:139–46.PubMedCrossRef Boyce BF, Xing L. Functions of RANKL/RANK/OPG in bone modeling and remodeling. Arch Biochem Biophys. 2008;473:139–46.PubMedCrossRef
12.
go back to reference Fuller K, Lawrence KM, Ross JL, et al. Cathepsin K inhibitors prevent matrix-derived growth factor degradation by human osteoclasts. Bone. 2008;42:200–11.PubMedCrossRef Fuller K, Lawrence KM, Ross JL, et al. Cathepsin K inhibitors prevent matrix-derived growth factor degradation by human osteoclasts. Bone. 2008;42:200–11.PubMedCrossRef
13.
go back to reference Tang Y, Wu X, Lei W, et al. TGF-beta1-induced migration of bone mesenchymal stem cells couples bone resorption with formation. Nat Med. 2009;15:757–65.PubMedCrossRef Tang Y, Wu X, Lei W, et al. TGF-beta1-induced migration of bone mesenchymal stem cells couples bone resorption with formation. Nat Med. 2009;15:757–65.PubMedCrossRef
14.
15.
go back to reference Zhao C, Irie N, Takada Y, et al. Bidirectional ephrinB2-EphB4 signaling controls bone homeostasis. Cell Metab. 2006;4:111–21.PubMedCrossRef Zhao C, Irie N, Takada Y, et al. Bidirectional ephrinB2-EphB4 signaling controls bone homeostasis. Cell Metab. 2006;4:111–21.PubMedCrossRef
16.
go back to reference Segovia-Silvestre T, Neutzsky-Wulff AV, Sorensen MG, et al. Advances in osteoclast biology resulting from the study of osteopetrotic mutations. Hum Genet. 2009;124:561–77.PubMedCrossRef Segovia-Silvestre T, Neutzsky-Wulff AV, Sorensen MG, et al. Advances in osteoclast biology resulting from the study of osteopetrotic mutations. Hum Genet. 2009;124:561–77.PubMedCrossRef
17.
go back to reference Drake FH, Dodds RA, James IE, et al. Cathepsin K, but not cathepsins B, L, or S, is abundantly expressed in human osteoclasts. J Biol Chem. 1996;271:12511–6.PubMedCrossRef Drake FH, Dodds RA, James IE, et al. Cathepsin K, but not cathepsins B, L, or S, is abundantly expressed in human osteoclasts. J Biol Chem. 1996;271:12511–6.PubMedCrossRef
18.
go back to reference Bromme D, Okamoto K, Wang BB, Biroc S. Human cathepsin O2, a matrix protein-degrading cysteine protease expressed in osteoclasts. Functional expression of human cathepsin O2 in Spodoptera frugiperda and characterization of the enzyme. J Biol Chem. 1996;271:2126–32.PubMedCrossRef Bromme D, Okamoto K, Wang BB, Biroc S. Human cathepsin O2, a matrix protein-degrading cysteine protease expressed in osteoclasts. Functional expression of human cathepsin O2 in Spodoptera frugiperda and characterization of the enzyme. J Biol Chem. 1996;271:2126–32.PubMedCrossRef
19.
go back to reference Garnero P, Borel O, Byrjalsen I, et al. The collagenolytic activity of cathepsin K is unique among mammalian proteinases. J Biol Chem. 1998;273:32347–52.PubMedCrossRef Garnero P, Borel O, Byrjalsen I, et al. The collagenolytic activity of cathepsin K is unique among mammalian proteinases. J Biol Chem. 1998;273:32347–52.PubMedCrossRef
20.
go back to reference Gelb BD, Shi GP, Chapman HA, Desnick RJ. Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency. Science. 1996;273:1236–8.PubMedCrossRef Gelb BD, Shi GP, Chapman HA, Desnick RJ. Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency. Science. 1996;273:1236–8.PubMedCrossRef
21.
go back to reference Schilling AF, Mulhausen C, Lehmann W, et al. High bone mineral density in pycnodysostotic patients with a novel mutation in the propeptide of cathepsin K. Osteoporos Int. 2007;18:659–69.PubMedCrossRef Schilling AF, Mulhausen C, Lehmann W, et al. High bone mineral density in pycnodysostotic patients with a novel mutation in the propeptide of cathepsin K. Osteoporos Int. 2007;18:659–69.PubMedCrossRef
22.
go back to reference Ho N, Punturieri A, Wilkin D, et al. Mutations of CTSK result in pycnodysostosis via a reduction in cathepsin K protein. J Bone Miner Res. 1999;14:1649–53.PubMedCrossRef Ho N, Punturieri A, Wilkin D, et al. Mutations of CTSK result in pycnodysostosis via a reduction in cathepsin K protein. J Bone Miner Res. 1999;14:1649–53.PubMedCrossRef
23.
go back to reference Saftig P, Hunziker E, Wehmeyer O, et al. Impaired osteoclastic bone resorption leads to osteopetrosis in cathepsin-K-deficient mice. Proc Natl Acad Sci U S A. 1998;95:13453–8.PubMedCrossRef Saftig P, Hunziker E, Wehmeyer O, et al. Impaired osteoclastic bone resorption leads to osteopetrosis in cathepsin-K-deficient mice. Proc Natl Acad Sci U S A. 1998;95:13453–8.PubMedCrossRef
24.
go back to reference Gowen M, Lazner F, Dodds R, et al. Cathepsin K knockout mice develop osteopetrosis due to a deficit in matrix degradation but not demineralization. J Bone Miner Res. 1999;14:1654–63.PubMedCrossRef Gowen M, Lazner F, Dodds R, et al. Cathepsin K knockout mice develop osteopetrosis due to a deficit in matrix degradation but not demineralization. J Bone Miner Res. 1999;14:1654–63.PubMedCrossRef
25.
go back to reference Li CY, Jepsen KJ, Majeska RJ, et al. Mice lacking cathepsin K maintain bone remodeling but develop bone fragility despite high bone mass. J Bone Miner Res. 2006;21:865–75.PubMedCrossRef Li CY, Jepsen KJ, Majeska RJ, et al. Mice lacking cathepsin K maintain bone remodeling but develop bone fragility despite high bone mass. J Bone Miner Res. 2006;21:865–75.PubMedCrossRef
26.
go back to reference Pennypacker B, Shea M, Liu Q, et al. Bone density, strength, and formation in adult cathepsin K (-/-) mice. Bone. 2009;44:199–207.PubMedCrossRef Pennypacker B, Shea M, Liu Q, et al. Bone density, strength, and formation in adult cathepsin K (-/-) mice. Bone. 2009;44:199–207.PubMedCrossRef
27.
go back to reference Kiviranta R, Morko J, Uusitalo H, et al. Accelerated turnover of metaphyseal trabecular bone in mice overexpressing cathepsin K. J Bone Miner Res. 2001;16:1444–52.PubMedCrossRef Kiviranta R, Morko J, Uusitalo H, et al. Accelerated turnover of metaphyseal trabecular bone in mice overexpressing cathepsin K. J Bone Miner Res. 2001;16:1444–52.PubMedCrossRef
28.
go back to reference Yasuda Y, Kaleta J, Bromme D. The role of cathepsins in osteoporosis and arthritis: rationale for the design of new therapeutics. Adv Drug Deliv Rev. 2005;57:973–93.PubMedCrossRef Yasuda Y, Kaleta J, Bromme D. The role of cathepsins in osteoporosis and arthritis: rationale for the design of new therapeutics. Adv Drug Deliv Rev. 2005;57:973–93.PubMedCrossRef
29.
go back to reference Stoch SA, Wagner JA. Cathepsin K inhibitors: a novel target for osteoporosis therapy. Clin Pharmacol Ther. 2008;83:172–6.PubMedCrossRef Stoch SA, Wagner JA. Cathepsin K inhibitors: a novel target for osteoporosis therapy. Clin Pharmacol Ther. 2008;83:172–6.PubMedCrossRef
30.
go back to reference Yamashita DS, Marquis RW, Xie R, et al. Structure activity relationships of 5-, 6-, and 7-methyl-substituted azepan-3-one cathepsin K inhibitors. J Med Chem. 2006;49:1597–612.PubMedCrossRef Yamashita DS, Marquis RW, Xie R, et al. Structure activity relationships of 5-, 6-, and 7-methyl-substituted azepan-3-one cathepsin K inhibitors. J Med Chem. 2006;49:1597–612.PubMedCrossRef
31.
go back to reference Gauthier JY, Chauret N, Cromlish W, et al. The discovery of odanacatib (MK-0822), a selective inhibitor of cathepsin K. Bioorg Med Chem Lett. 2008;18:923–8.PubMedCrossRef Gauthier JY, Chauret N, Cromlish W, et al. The discovery of odanacatib (MK-0822), a selective inhibitor of cathepsin K. Bioorg Med Chem Lett. 2008;18:923–8.PubMedCrossRef
32.
go back to reference Adami S, Supronik J, Hala T, et al. Effect of 1 year treatment with the Cathepsin-K inhibitor, balicatib, on bone mineral density (BMD) in postmenopausal women with osteopenia/osteoporosis. J Bone Miner Res. 2006;21(Suppl S1):S24. Abstract 1085. Adami S, Supronik J, Hala T, et al. Effect of 1 year treatment with the Cathepsin-K inhibitor, balicatib, on bone mineral density (BMD) in postmenopausal women with osteopenia/osteoporosis. J Bone Miner Res. 2006;21(Suppl S1):S24. Abstract 1085.
33.
go back to reference Peroni A, Zini A, Braga V, et al. Drug-induced morphea: report of a case induced by balicatib and review of the literature. J Am Acad Dermatol. 2008;59:125–9.PubMedCrossRef Peroni A, Zini A, Braga V, et al. Drug-induced morphea: report of a case induced by balicatib and review of the literature. J Am Acad Dermatol. 2008;59:125–9.PubMedCrossRef
35.
go back to reference Pennypacker BL, Duong lT, Cusick TE, et al. Cathepsin K inhibitors prevent bone loss in estrogen-deficient rabbits. J Bone Miner Res. 2011;26:252–62.PubMedCrossRef Pennypacker BL, Duong lT, Cusick TE, et al. Cathepsin K inhibitors prevent bone loss in estrogen-deficient rabbits. J Bone Miner Res. 2011;26:252–62.PubMedCrossRef
36.
go back to reference Stroup GB, Kumar S, Jerome CP. Treatment with a potent cathepsin K inhibitor preserves cortical and trabecular bone mass in ovariectomized monkeys. Calcif Tissue Int. 2009;85:344–55.PubMedCrossRef Stroup GB, Kumar S, Jerome CP. Treatment with a potent cathepsin K inhibitor preserves cortical and trabecular bone mass in ovariectomized monkeys. Calcif Tissue Int. 2009;85:344–55.PubMedCrossRef
37.
go back to reference • Masarachia PJ, Pennypacker B, Pickarski M, et al. Odanacatib reduces bone turnover and increases bone mass in lumbar spine of skeletally mature ovariectomized rhesus monkeys. J Bone Miner Res. 2011, in press. Uses non-human primates to explore the mechanism of action of cathepsin K inhibitors for osteoporosis. • Masarachia PJ, Pennypacker B, Pickarski M, et al. Odanacatib reduces bone turnover and increases bone mass in lumbar spine of skeletally mature ovariectomized rhesus monkeys. J Bone Miner Res. 2011, in press. Uses non-human primates to explore the mechanism of action of cathepsin K inhibitors for osteoporosis.
38.
go back to reference Yamada H, Mori H, Kunishige A, et al. Efficacy of ONO-5334, a cathepsin K inhibitor, on bone turnover markers and bone mineral density in ovariectomized cynomolgus monkeys. Presented at European Calicified Tissue International, Glasgow, Scottland; 2010. Yamada H, Mori H, Kunishige A, et al. Efficacy of ONO-5334, a cathepsin K inhibitor, on bone turnover markers and bone mineral density in ovariectomized cynomolgus monkeys. Presented at European Calicified Tissue International, Glasgow, Scottland; 2010.
39.
go back to reference Yamada H, Ochi Y, Kunishige A, et al. Efficacy of ONO-5334, a cathepsin K inhibitor, on bone mass and strength in ovariectomized cynomolgus monkeys. Bone. 2011;48:S221.CrossRef Yamada H, Ochi Y, Kunishige A, et al. Efficacy of ONO-5334, a cathepsin K inhibitor, on bone mass and strength in ovariectomized cynomolgus monkeys. Bone. 2011;48:S221.CrossRef
40.
go back to reference Ochi Y, Yamada H, Kunishige ANS, et al. Efficacy of ONO-5334, a cathepsin K inhibitor, on bone turnover and cortical geometry in ovariectomized cynolmolgus monkeys. Bone. 2011;48:S72.CrossRef Ochi Y, Yamada H, Kunishige ANS, et al. Efficacy of ONO-5334, a cathepsin K inhibitor, on bone turnover and cortical geometry in ovariectomized cynolmolgus monkeys. Bone. 2011;48:S72.CrossRef
41.
go back to reference Mayhew PM, Thomas CD, Clement JG, et al. Relation between age, femoral neck cortical stability, and hip fracture risk. Lancet. 2005;366:129–35.PubMedCrossRef Mayhew PM, Thomas CD, Clement JG, et al. Relation between age, femoral neck cortical stability, and hip fracture risk. Lancet. 2005;366:129–35.PubMedCrossRef
42.
go back to reference • Jerome C, Missbach M, Gamse R. Balicatib, a cathepsin K inhibitor, stimulates periosteal bone formation in monkeys. Osteoporos Int. 2011. • Jerome C, Missbach M, Gamse R. Balicatib, a cathepsin K inhibitor, stimulates periosteal bone formation in monkeys. Osteoporos Int. 2011.
43.
go back to reference • Cusick T, Chen CM, Pennypacker BL, et al. Odanacatib treatment increases Hi bone mass and cortical thickness by preserving endocortical bone formation and stimulating periosteal bone formation in ovariectomized adult rhesus monkey. J Bone Miner Res. 2011, in press. Uses non-human primates to explore the mechanism of action of cathepsin K inhibitors for osteoporosis. • Cusick T, Chen CM, Pennypacker BL, et al. Odanacatib treatment increases Hi bone mass and cortical thickness by preserving endocortical bone formation and stimulating periosteal bone formation in ovariectomized adult rhesus monkey. J Bone Miner Res. 2011, in press. Uses non-human primates to explore the mechanism of action of cathepsin K inhibitors for osteoporosis.
44.
go back to reference •• Bone HG, McClung MR, Roux C, et al. Odanacatib, a cathepsin-K inhibitor for osteoporosis: a two-year study in postmenopausal women with low bone density. J Bone Miner Res. 2010;25:937–47. Reports clinical results of drugs in development that use the novel mechanism of action of inhibition of cathepsin K.PubMed •• Bone HG, McClung MR, Roux C, et al. Odanacatib, a cathepsin-K inhibitor for osteoporosis: a two-year study in postmenopausal women with low bone density. J Bone Miner Res. 2010;25:937–47. Reports clinical results of drugs in development that use the novel mechanism of action of inhibition of cathepsin K.PubMed
45.
go back to reference •• Eisman JA, Bone HG, Hosking DJ, et al. Odanacatib in the treatment of postmenopausal women with low bone mineral density: three-year continued therapy and resolution of effect. J Bone Miner Res. 2011;26:242–51. Reports clinical results of drugs in development that use the novel mechanism of action of inhibition of cathepsin K.PubMedCrossRef •• Eisman JA, Bone HG, Hosking DJ, et al. Odanacatib in the treatment of postmenopausal women with low bone mineral density: three-year continued therapy and resolution of effect. J Bone Miner Res. 2011;26:242–51. Reports clinical results of drugs in development that use the novel mechanism of action of inhibition of cathepsin K.PubMedCrossRef
46.
go back to reference Binkley N, Bone H, Gilcrist N, et al. Treatment with the cathepsin K inhibitor odanacatib in postmenopausal women with low BMD: 5 year results of a phase 2 trial. Presented at the American Society of Bone and Mineral Research, San Diego, CA; 2011. Binkley N, Bone H, Gilcrist N, et al. Treatment with the cathepsin K inhibitor odanacatib in postmenopausal women with low BMD: 5 year results of a phase 2 trial. Presented at the American Society of Bone and Mineral Research, San Diego, CA; 2011.
47.
go back to reference Bone H, Dempster D, Eisman J, et al. Phase 3 fracture trial of odanacatib for osteoporosis - study design. Presented at the Endocrine Society meeting, San Diego, CA; 2010. Bone H, Dempster D, Eisman J, et al. Phase 3 fracture trial of odanacatib for osteoporosis - study design. Presented at the Endocrine Society meeting, San Diego, CA; 2010.
48.
go back to reference •• Eastell R, Nagase S, Ohyama M, et al. Safety and efficacy of the Cathepsin K inhibitor, ONO-5334, in postmenopausal osteoporosis - the OCEAN study. J Bone Miner Res. 2011;26:1303–12. Reports clinical results of drugs in development that use the novel mechanism of action of inhibition of cathepsin K.PubMedCrossRef •• Eastell R, Nagase S, Ohyama M, et al. Safety and efficacy of the Cathepsin K inhibitor, ONO-5334, in postmenopausal osteoporosis - the OCEAN study. J Bone Miner Res. 2011;26:1303–12. Reports clinical results of drugs in development that use the novel mechanism of action of inhibition of cathepsin K.PubMedCrossRef
49.
go back to reference Eastell R, Nagase S, Small M, et al. Effect of the cathepsin K inhibitor ONO-5334 on biochemical markers of bone turnover in the treatment of postmennopausal osteopenia or osteoporosis: 2-year results from the OCEAN atudy. J Bone Miner Res. 2011. Eastell R, Nagase S, Small M, et al. Effect of the cathepsin K inhibitor ONO-5334 on biochemical markers of bone turnover in the treatment of postmennopausal osteopenia or osteoporosis: 2-year results from the OCEAN atudy. J Bone Miner Res. 2011.
50.
go back to reference Harris ST, Watts NB, Genant HK, et al. Effects of risedronate treatment on vertebral and nonvertebral fractures in women with postmenopausal osteoporosis: a randomized controlled trial. Vertebral Efficacy With Risedronate Therapy (VERT) Study Group. JAMA. 1999;282:1344–52.PubMedCrossRef Harris ST, Watts NB, Genant HK, et al. Effects of risedronate treatment on vertebral and nonvertebral fractures in women with postmenopausal osteoporosis: a randomized controlled trial. Vertebral Efficacy With Risedronate Therapy (VERT) Study Group. JAMA. 1999;282:1344–52.PubMedCrossRef
51.
go back to reference Black DM, Schwartz AV, Ensrud KE, et al. Effects of continuing or stopping alendronate after 5 years of treatment: the Fracture Intervention Trial Long-term Extension (FLEX): a randomized trial. JAMA. 2006;296:2927–38.PubMedCrossRef Black DM, Schwartz AV, Ensrud KE, et al. Effects of continuing or stopping alendronate after 5 years of treatment: the Fracture Intervention Trial Long-term Extension (FLEX): a randomized trial. JAMA. 2006;296:2927–38.PubMedCrossRef
52.
go back to reference Gallagher JC, Rapuri PB, Haynatzki G, Detter JR. Effect of discontinuation of estrogen, calcitriol, and the combination of both on bone density and bone markers. J Clin Endocrinol Metab. 2002;87:4914–23.PubMedCrossRef Gallagher JC, Rapuri PB, Haynatzki G, Detter JR. Effect of discontinuation of estrogen, calcitriol, and the combination of both on bone density and bone markers. J Clin Endocrinol Metab. 2002;87:4914–23.PubMedCrossRef
53.
go back to reference Miller PD, Bolognese MA, Lewiecki EM, et al. Effect of denosumab on bone density and turnover in postmenopausal women with low bone mass after long-term continued, discontinued, and restarting of therapy: a randomized blinded phase 2 clinical trial. Bone. 2008;43:222–9.PubMedCrossRef Miller PD, Bolognese MA, Lewiecki EM, et al. Effect of denosumab on bone density and turnover in postmenopausal women with low bone mass after long-term continued, discontinued, and restarting of therapy: a randomized blinded phase 2 clinical trial. Bone. 2008;43:222–9.PubMedCrossRef
54.
go back to reference Stakkestad JA, Lakatos P, Lorenc R, et al. Monthly oral ibandronate is effective and well tolerated after 3 years: the MOBILE long-term extension. Clin Rheumatol. 2008;27:955–60.PubMedCrossRef Stakkestad JA, Lakatos P, Lorenc R, et al. Monthly oral ibandronate is effective and well tolerated after 3 years: the MOBILE long-term extension. Clin Rheumatol. 2008;27:955–60.PubMedCrossRef
Metadata
Title
Inhibition of Cathepsin K for Treatment of Osteoporosis
Authors
Steven Boonen
Elizabeth Rosenberg
Frank Claessens
Dirk Vanderschueren
Socrates Papapoulos
Publication date
01-03-2012
Publisher
Current Science Inc.
Published in
Current Osteoporosis Reports / Issue 1/2012
Print ISSN: 1544-1873
Electronic ISSN: 1544-2241
DOI
https://doi.org/10.1007/s11914-011-0085-9

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