| Literature DB >> 26170308 |
Dario Palmieri1, Timothy Richmond1, Claudia Piovan1, Tyler Sheetz1, Nicola Zanesi1, Fulvia Troise2, Cindy James3, Dorothee Wernicke1, Fata Nyei1, Timothy J Gordon4, Jessica Consiglio1, Francesco Salvatore2, Vincenzo Coppola1, Flavia Pichiorri5, Claudia De Lorenzo6, Carlo M Croce7.
Abstract
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.Entities:
Keywords: cancer immunotherapy; microRNA; nucleolin; phage-display; scFv
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Year: 2015 PMID: 26170308 PMCID: PMC4522807 DOI: 10.1073/pnas.1507087112
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205