
Lawrence Scott Levin
· M.D.VerifiedUniversity of Pennsylvania · Rehabilitation Medicine
Active 1900–2024
Research topics
- Medicine
- Pathology
- Family medicine
- Surgery
- Cancer research
- Anatomy
Selected publications
Tips and Tricks in Plastic Surgery
Springer eBooks · 2021 · 8 citations
- Medicine
- Surgery
- Family medicine
Targeting cartilage EGFR pathway for osteoarthritis treatment
Science Translational Medicine · 2021 · 175 citations
- Medicine
- Cancer research
- Pathology
Osteoarthritis (OA) is a widespread joint disease for which there are no disease-modifying treatments. Previously, we found that mice with cartilage-specific epidermal growth factor receptor (EGFR) deficiency developed accelerated knee OA. To test whether the EGFR pathway can be targeted as a potential OA therapy, we constructed two cartilage-specific EGFR overactivation models in mice by overexpressing heparin binding EGF-like growth factor (HBEGF), an EGFR ligand. Compared to wild type, Col2-Cre HBEGF-overexpressing mice had persistently enlarged articular cartilage from adolescence, due to an expanded pool of chondroprogenitors with elevated proliferation ability, survival rate, and lubricant production. Adult Col2-Cre HBEGF-overexpressing mice and Aggrecan-CreER HBEGF-overexpressing mice were resistant to cartilage degeneration and other signs of OA after surgical destabilization of the medial meniscus (DMM). Treating mice with gefitinib, an EGFR inhibitor, abolished the protective action against OA in HBEGF-overexpressing mice. Polymeric micellar nanoparticles (NPs) conjugated with transforming growth factor-α (TGFα), a potent EGFR ligand, were stable and nontoxic and had long joint retention, high cartilage uptake, and penetration capabilities. Intra-articular delivery of TGFα-NPs effectively attenuated surgery-induced OA cartilage degeneration, subchondral bone plate sclerosis, and joint pain. Genetic or pharmacologic activation of EGFR revealed no obvious side effects in knee joints and major vital organs in mice. Together, our studies demonstrate the feasibility of using nanotechnology to target EGFR signaling for OA treatment.
Frequent coauthors
- 234 shared
Stephen J. Kovach
University of Pennsylvania
- 140 shared
Detlev Erdmann
Duke Medical Center
- 101 shared
Scott T. Hollenbeck
Duke Medical Center
- 91 shared
Ines C. Lin
University of Pennsylvania
- 80 shared
Benjamin B. Chang
Children's Hospital of Philadelphia
- 79 shared
Eugenia H. Cho
Keimyung University
- 66 shared
Martin J. Carney
Yale University
- 61 shared
Jason M. Weissler
Mayo Clinic in Arizona
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