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Human anti-nucleolin recombinant immunoagent for cancer therapy.
Palmieri, Dario; Richmond, Timothy; Piovan, Claudia; Sheetz, Tyler; Zanesi, Nicola; Troise, Fulvia; James, Cindy; Wernicke, Dorothee; Nyei, Fata; Gordon, Timothy J; Consiglio, Jessica; Salvatore, Francesco; Coppola, Vincenzo; Pichiorri, Flavia; De Lorenzo, Claudia; Croce, Carlo M.
Afiliación
  • Palmieri D; Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
  • Richmond T; Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
  • Piovan C; Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
  • Sheetz T; Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
  • Zanesi N; Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
  • Troise F; Centro di Ingegneria Genetica (CEINGE) Biotecnologie Avanzate, 80145 Naples, Italy;
  • James C; Department of Mass Spectroscopy and Proteomics, The Ohio State University, Columbus, OH 43210;
  • Wernicke D; Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
  • Nyei F; Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
  • Gordon TJ; Department of Veterinary Biosciences, The Ohio State University, Columbus, OH 43210;
  • Consiglio J; Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
  • Salvatore F; Centro di Ingegneria Genetica (CEINGE) Biotecnologie Avanzate, 80145 Naples, Italy;
  • Coppola V; Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210;
  • Pichiorri F; Department of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH 43210;
  • De Lorenzo C; Centro di Ingegneria Genetica (CEINGE) Biotecnologie Avanzate, 80145 Naples, Italy; Department of Molecular Medicine and Medical Biotechnologies, University of Napoli "Federico II", 80131 Naples, Italy carlo.croce@osumc.edu cladelor@unina.it.
  • Croce CM; Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210; carlo.croce@osumc.edu cladelor@unina.it.
Proc Natl Acad Sci U S A ; 112(30): 9418-23, 2015 Jul 28.
Article en En | MEDLINE | ID: mdl-26170308
Nucleolin (NCL) is a nucleocytoplasmic protein involved in many biological processes, such as ribosomal assembly, rRNA processing, and mRNA stabilization. NCL also regulates the biogenesis of specific microRNAs (miRNAs) involved in tumor development and aggressiveness. Interestingly, NCL is expressed on the surface of actively proliferating cancer cells, but not on their normal counterparts. Therefore, NCL is an attractive target for antineoplastic treatments. Taking advantage of phage-display technology, we engineered a fully human single-chain fragment variable, named 4LB5. This immunoagent binds NCL on the cell surface, it is translocated into the cytoplasm of target cells, and it abrogates the biogenesis of NCL-dependent miRNAs. Binding of 4LB5 to NCL on the cell surface of a variety of breast cancer and hepatocellular carcinoma cell lines, but not to normal-like MCF-10a breast cells, dramatically reduces cancer cell viability and proliferation. Finally, in orthotopic breast cancer mouse models, 4LB5 administration results in a significant reduction of the tumor volume without evident side effects. In summary, here we describe, to our knowledge, the first anti-NCL single-chain fragment variable displaying antineoplastic activity against established solid tumors, which could represent the prototype of novel immune-based NCL-targeting drugs with clinical potential as diagnostic and therapeutic tools in a wide variety of human cancers.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fosfoproteínas / Proteínas de Unión al ARN / Anticuerpos de Cadena Única / Neoplasias / Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2015 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fosfoproteínas / Proteínas de Unión al ARN / Anticuerpos de Cadena Única / Neoplasias / Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2015 Tipo del documento: Article Pais de publicación: Estados Unidos