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A Spontaneous Assembling Lipopeptide Nanoconjugate Transporting the Anthracycline Drug N-Benzyladriamycin-14-valerate for Personalized Therapy of Ewing Sarcoma.
Sabnis, Nirupama; Raut, Sangram; Nagarajan, Bhavani; Kapic, Ammar; Dossou, Akpedje Serena; Lothstein, Leonard; Fudala, Rafal; Bunnell, Bruce A; Lacko, Andras G.
Affiliation
  • Sabnis N; Lipoprotein Drug Delivery Research Laboratory, Department of Microbiology, Immunology & Genetics, University of North Texas Health Science Center, Fort Worth, Texas 76107, United States.
  • Raut S; Department of Physiology and Anatomy, University of North Texas Health Science Center, Fort Worth, Texas 76107, United States.
  • Nagarajan B; North Texas Research Eye Institute, Department of Pharmacology and Neuroscience, University of North Texas Health Science Center, Fort Worth, Texas 76107, United States.
  • Kapic A; Lipoprotein Drug Delivery Research Laboratory, Department of Microbiology, Immunology & Genetics, University of North Texas Health Science Center, Fort Worth, Texas 76107, United States.
  • Dossou AS; Lipoprotein Drug Delivery Research Laboratory, Department of Microbiology, Immunology & Genetics, University of North Texas Health Science Center, Fort Worth, Texas 76107, United States.
  • Lothstein L; Department of Pathology and Laboratory Medicine, The University of Tennessee Health Science Center, Memphis, Tennessee 38103, United States.
  • Fudala R; Lipoprotein Drug Delivery Research Laboratory, Department of Microbiology, Immunology & Genetics, University of North Texas Health Science Center, Fort Worth, Texas 76107, United States.
  • Bunnell BA; Lipoprotein Drug Delivery Research Laboratory, Department of Microbiology, Immunology & Genetics, University of North Texas Health Science Center, Fort Worth, Texas 76107, United States.
  • Lacko AG; Lipoprotein Drug Delivery Research Laboratory, Department of Microbiology, Immunology & Genetics, University of North Texas Health Science Center, Fort Worth, Texas 76107, United States.
Bioconjug Chem ; 35(2): 187-202, 2024 02 21.
Article in En | MEDLINE | ID: mdl-38318778
ABSTRACT
To meet the current need for a tumor-selective, targeted therapy regimen associated with reduced toxicity, our laboratory has developed a spontaneously assembled nanostructure that resembles high-density lipoproteins (HDLs). These myristoyl-5A (MYR-5A) nanotransporters are designed to safely transport lipophilic pharmaceuticals, including a novel anthracycline drug (N-benzyladriamycin-14-valerate (AD198)). This formulation has been found to enhance the therapeutic efficacy and reduced toxicity of drugs in preclinical studies of 2D and 3D models of Ewing sarcoma (EWS) and cardiomyocytes. Our findings indicate that the MYR-5A/AD198 nanocomplex delivers its payload selectively to cancer cells via the scavenger receptor type B1 (SR-B1), thus providing a solid proof of concept for the development of an improved and highly effective, potentially personalized therapy for EWS while protecting against treatment-associated cardiotoxicity.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sarcoma, Ewing / Doxorubicin Type of study: Prognostic_studies Limits: Humans Language: En Journal: Bioconjug Chem Journal subject: BIOQUIMICA Year: 2024 Type: Article Affiliation country: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sarcoma, Ewing / Doxorubicin Type of study: Prognostic_studies Limits: Humans Language: En Journal: Bioconjug Chem Journal subject: BIOQUIMICA Year: 2024 Type: Article Affiliation country: United States