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Grant: Collaborative Health Research Projects

University of British Columbia

$238,000.00

Side effect-free cathepsin K targeting drugs for skeletal diseases

FY 2019-20

Summary
Arthritic diseases affect 15 % of the population and bone cancer is a frequent metastatic sideeffect of the most common breast and prostate cancer. Aside from human suffering enormousfinancial health care costs are added to the treatment of these diseases. Current treatmentshave various shortcomings and side effects, which include increased cancer risks, atypicalfractures, bone necrosis, infections, and vascular problems. There is clearly a need for moreeffective and safer treatments. Unfortunately, little progress has been made in recent years.Most treatments attack rather non-specifically entire cells or block complex pathways, whichis likely causing the side effects. In contrast, the protease, cathepsin K, is solely responsiblefor the bone degradation and significantly contributes to joint erosion. Its inhibition has beenshown to effectively reduce fracture rates in post-menopausal women. However, thistreatment also had severe side effects leading to the termination of the further development ofcathepsin K inhibitors. Our research has identified and verified a novel type of cathepsin Kinhibitors without causing any of the side effects seen in clinical trials. Interestingly, a majorsource of these compounds are certain Chinese herbs traditionally used in skeletal diseases.Recently, we have shown the efficacy of one of these compounds in an osteoporosis modelwithout any observable side effects. This project will expand this approach and will generatemore potent and druggable derivatives from the herbal compounds. Compounds will beanalyzed in arthritis and bone cancer mouse models. We anticipate that these compounds willhave a superior efficacy with no or fewer side effects than current treatment regimes. Thisproject requires a strong interdisciplinary collaboration between chemists, pharmaceuticalscientists, biochemists, and animal model researchers and will provide an excellentopportunity for the training of students.
Program
Collaborative Health Research Projects
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
523434-2018
Name nom
Bromme, Dieter
Department département
Oral Biological & Medical Sciences
Organization id
2
Institution établissement
University of British Columbia
Province en
British Columbia
Province fr
Colombie-Britannique
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2019
Competition year année de concours
2018
Award amount
238000
Program id
CHRPJ
Program name en
Collaborative Health Research Projects
Program name fr
Projets de recherche concertée sur la santé
Group en
RESEARCH PARTNERSHIPS
Group fr
PARTENARIATS DE RECHERCHE
Committee code
360
Committee name en
Collaborative Health Research Projects Selection Panel
Committee name fr
Comité de sélection de projets de recherche concertée sur la santé
Area of application code
9999
Area of application group en
Not available
Area of application group fr
Non disponible
Area of application en
Not available
Area of application fr
Non disponible
Research subject code
5400
Research subject group en
Biochemistry
Research subject group fr
Biochimie
Research subject en
Biochemistry
Research subject fr
Biochimie
Installment
inst:2 - 3
Partie
2
Nb partie
3
Application title
Side effect-free cathepsin K targeting drugs for skeletal diseases
Keyword
NSERC
Application summary
Arthritic diseases affect 15 % of the population and bone cancer is a frequent metastatic sideeffect of the most common breast and prostate cancer. Aside from human suffering enormousfinancial health care costs are added to the treatment of these diseases. Current treatmentshave various shortcomings and side effects, which include increased cancer risks, atypicalfractures, bone necrosis, infections, and vascular problems. There is clearly a need for moreeffective and safer treatments. Unfortunately, little progress has been made in recent years.Most treatments attack rather non-specifically entire cells or block complex pathways, whichis likely causing the side effects. In contrast, the protease, cathepsin K, is solely responsiblefor the bone degradation and significantly contributes to joint erosion. Its inhibition has beenshown to effectively reduce fracture rates in post-menopausal women. However, thistreatment also had severe side effects leading to the termination of the further development ofcathepsin K inhibitors. Our research has identified and verified a novel type of cathepsin Kinhibitors without causing any of the side effects seen in clinical trials. Interestingly, a majorsource of these compounds are certain Chinese herbs traditionally used in skeletal diseases.Recently, we have shown the efficacy of one of these compounds in an osteoporosis modelwithout any observable side effects. This project will expand this approach and will generatemore potent and druggable derivatives from the herbal compounds. Compounds will beanalyzed in arthritis and bone cancer mouse models. We anticipate that these compounds willhave a superior efficacy with no or fewer side effects than current treatment regimes. Thisproject requires a strong interdisciplinary collaboration between chemists, pharmaceuticalscientists, biochemists, and animal model researchers and will provide an excellentopportunity for the training of students.
University of British Columbia - $238,000 Grant (2019… | Canada Spends