SBIR/STTR Research Award

Development of R-Spondin 1 as an Anabolic Agent for the Treatment of Estrogen Deficiency-induced Bone Loss

Award identifier a8834297ccd6083b582afda390f66787394613804ca657a4ca720f911df4184eAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$228,977

Program and phase

SBIR · Phase I

Award year

2015

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
VIBE PHARMACEUTICALS LLC
Proposal award date
2015-09-30
Contract end date
2017-02-28
UEI
Not reported
Solicitation number
PA14-071
Topic code
NIA

Research abstract

DESCRIPTION provided by applicant Development of R Spondin as an anabolic agent for the treatment of estrogen deficiency induced bone loss A major challenge in the elderly is osteoporosis and the associated high risk of fracture One in two women and one in four men andgt years will have an osteoporosis related fracture in their lifetimes Age related bone conditions cause significant morbidity worldwide particularly among the elderly and include systemic bone loss e g postmenopausal osteoporosis focal bone loss and fractures Bone is continuously remodeled and this remodeling process couples osteoclastic bone resorption and osteoblastic bone formation Various therapeutics are currently used for the treatment of low bone mass osteopenia or osteoporosis with the vast majority being antiresorptive agents e g bisphosphonates that act by limiting osteoclast mediated bone resorption However these agents cannot replace bone that has been lost and the successful development of therapeutics that can stimulate bone formation would have tremendous implications for achieving increased bone mass and bone strength Such bone rebuilding anabolic agents could thus provide important treatment options not only for conditions of low bone mass but also for fracture healing and other orthopedic applications Bone tissue adapts to its functional environment by optimizing its morphology for mechanical demand Among the mechanosensitive cells that recognize and respond to forces in the skeleton are osteocytes osteoblasts and mesenchymal progenitor cells MPCs Therefore the ability to use mechanical signals to improve bone health through exercise and devices that deliver mechanical signals is an attractive approach to age related bone loss however the extracellular or circulating mediators of such signals are largely unknown Using SDS PAGE separation of proteins secreted by MPCs in response to low magnitude mechanical signals and in gel trypsin digestion followed by HPLC and mass spectroscopy we identified secreted proteins up regulated by vibratory stimulation We exploited a cell senescence associated secretory phenotype screen and reasoned that a subset of vibration induced proteins with diminished secretion by senescent MPCs will have the capacity to promote bone formation in vivo We identified one such vibration induced bone enhancing vibe gene as R Spondin a Wnt pathway modulator and demonstrated that it has the capacity to promote bone formation in three mouse models of age related bone loss By virtue of their secretory status some vibe proteins including R Spondin may be candidates for pre clinical development as anabolic agents for the treatment of osteoporosis The goals of this application are to establish R Spondin as a pivotal regulator of bone formation in the aging skeleton and provide evidence that R spondin represents a promising new therapeutic approach for the anabolic treatment of bone related disorders such as post menopausal osteoporosis The specific aims of this proposal are to demonstrate a reversal of estrogen deficiency induced bone loss after treatment with R Spondin and determine possible short term adverse effects of R Spondin on organ function PUBLIC HEALTH RELEVANCE Development of R Spondin as an anabolic agent for the treatment of estrogen deficiency induced bone loss A major challenge in the elderly is osteoporosis and the associated high risk of fracture Various therapeutics are currently used for the treatment of low bone mass osteopenia or osteoporosis with the vast majority being antiresorptive agents e g bisphosphonates However these agents cannot replace bone that has been lost and the successful development of therapeutics that can stimulate bone formation would have tremendous implications for achieving increased bone mass and bone strength Such bone rebuilding anabolic agents could thus provide important treatment options not only for conditions of low bone mass but also for fracture healing and other orthopedic applications The ability to use mechanical signals to improve bone health through exercise and devices that deliver mechanical signals is an attractive approach to age related bone loss however the extracellular or circulating mediators of such signals are largely unknown We identified one such circulating mediator as R Spondin and demonstrated that it has the capacity to promote bone formation in three mouse models of age related bone loss Therefore R Spondin is an exceptionally strong candidate for pre clinical development as anabolic agents for the treatment of bone loss The major goal of this application is to provide evidence that R spondin represents a promising new therapeutic approach for the anabolic treatment of bone related disorders such as post menopausal osteoporosis The specific aims of this proposal are to demonstrate a reversal of estrogen deficiency induced bone loss after treatment with R Spondin and determine possible short term adverse effects of R Spondin on organ function

Technology keywords

Not reported

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Agency intelligence

Department of Health and Human Services

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