Cited by 63Adipokines, Inflammation, and Metabolic DiseasesDiabetes Treatment and ManagementPancreatic function and diabetes

SMOC1 is a glucose-responsive hepatokine and therapeutic target for glycemic control

Montgomery, Magdalene K., Bayliss, Jacqueline, Devereux, Camille, Bezawork-Geleta, Ayenachew, Roberts, David, Huang, Cheng, Schittenhelm, Ralf B., Ryan, Andrew +7 more·2020·Science Translational Medicine

Abstract

mice, without adverse effects on adiposity, liver histopathology, or inflammation. Furthermore, circulating SMOC1 correlated with hepatic and systemic insulin sensitivity and was decreased in obese, insulin-resistant humans. Together, these findings identify SMOC1 as a potential pharmacological target for the management of glycemic control in type 2 diabetes.

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Crossref · 10.1126/scitranslmed.aaz8048

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  • Administration of a long-lasting SMOC1-Fc fusion protein improves glycemic control, cholesterol, and NAFLD activity scores in lean and obese mice up to 4 weeks following final administration.

    “Administration of a long-lasting SMOC1-Fc fusion protein improved glycemic control, cholesterol, and NAFLD activity scores in lean and obese mice up to 4 weeks following the final administration of SMOC1-Fc [266].”
  • SMOC1 is a hepatokine recently identified to improve glucose homeostasis in rodents.

    “SPARC-related modular calcium-binding protein-1 (SMOC1) is a hepatokine recently identified to improve glucose homeostasis in rodents [266].”
  • SMOC1 regulates cell matrix interactions by binding to cell surface receptors, including laminins, C-reactive protein, and tenascin-C.

    “SMOC1 is known to regulate cell matrix interactions by binding to cell surface receptors, including laminins, C-reactive protein, and tenascin-C [266,268].”
  • SMOC1 is highly expressed and secreted by the liver and regulates glucose homeostasis.

    “However, SMOC1 is highly expressed and secreted by the liver and regulates glucose homeostasis [266].”
  • Numerous families of secreted signaling molecules bearing the suffix "-kines," such as myokines, osteokines, adipokines, and hepatokines, have been identified in more recent times.

    “Hormones were identified and subsequently leveraged for use as therapeutics throughout the 20th century but it is only in more recent times that numerous families of secreted signaling molecules bearing the suffix “‐kines” such as myokines, 243 osteokines, adipokines, 244 and hepatokines 245 have been identified. 242”

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References 50 · Cited by 63

Authors
Montgomery, M. K., Bayliss, J., Devereux, C., Bezawork-Geleta, A., Roberts, D., Huang, C., Schittenhelm, R. B., Ryan, A., Townley, S. L., Selth, L. A., Biden, T. J., Steinberg, G. R., Samocha-Bonet, D., Meex, R. C. R., & Watt, M. J.
Affiliations
  • The University of Melbourne (AU)
  • Department of Physiology, University of Melbourne, Melbourne, VIC 3010, Australia.
  • Monash University (AU)
  • TissuPath (AU)
  • Freemasons Foundation Centre for Men's Health (AU)
  • Flinders University (AU)
  • Garvan Institute of Medical Research (AU)
  • McMaster University (CA)
  • Diabetes and Metabolism Division, Garvan Institute of Medical Research, Sydney, NSW 2010, Australia.
  • Maastricht University Medical Centre (NL)
Corresponding author
Watt, Matthew J.
Venue
Science Translational Medicine
Published
2020-09-02
Volume
12
Issue
559
ISSN
  • 1946-6234 (ISSN-L)
  • 1946-6242
OpenAlex
W3082079601
Cited by
63
References
50
Citations by year
2026: 2 · 2025: 14 · 2024: 18 · 2023: 5 · 2022: 10 · 2021: 10 · 2020: 3 · 2012: 1
FWCI
5.02
Type
journal article
Language
en
Open access
closed
Locations
  • Science Translational Medicine (publishedVersion)
  • PubMed (publishedVersion)
  • Research Publications (Maastricht University) (publishedVersion)
  • Adelaide Research & Scholarship (AR&S) (University of Adelaide) (submittedVersion)
  • Research Publications (Maastricht University) (submittedVersion)
Funders
  • European Commission (H2020-MSCA-IF)
  • National Health and Medical Research Council (APP1144180, APP1143224, APP1077703)
  • Canada Research Chairs (950-232028)
Topics
  • Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
  • Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
Keywords
SMOC1, hepatokines, glucose responsiveness, glycemic control, type 2 diabetes, insulin sensitivity, insulin resistance, obesity, therapeutic target, circulating biomarkers
MeSH terms
Glycemic Control, Animals, Blood Glucose, Diabetes Mellitus, Type 2, Glucose, Insulin, Insulin Resistance, Liver, Mice, Inbred C57BL, Mice

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