nanobiopolymer for direct targeting and inhibition of egfr expression in triple negative breast cancernanobiopolymer为直接目标和抑制表皮生长因子受体在三阴性乳腺癌.pdfVIP
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nanobiopolymer for direct targeting and inhibition of egfr expression in triple negative breast cancernanobiopolymer为直接目标和抑制表皮生长因子受体在三阴性乳腺癌
Nanobiopolymer for Direct Targeting and Inhibition of EGFR Expression in Triple Negative Breast Cancer 1 1 1 1 1 1 Satoshi Inoue , Rameshwar Patil , Jose Portilla-Arias , Hui Ding , Bindu Konda , Andres Espinoza , 2 1 1 1 1 Dmitriy Mongayt , Janet L. Markman , Adam Elramsisy , H. Westley Phillips , Keith L. Black , Eggehard 1 1 Holler , Julia Y. Ljubimova * 1 Department of Neurosurgery, Cedars-Sinai Medical Center, Los Angeles, California, United States of America, 2 Center for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, Massachusetts, United States of America Abstract Treatment options for triple negative breast cancer (TNBC) are generally limited to cytotoxic chemotherapy. Recently, anti- epidermal growth factor receptor (EGFR) therapy has been introduced for TNBC patients. We engineered a novel nanobioconjugate based on a poly(b-L-malic acid) (PMLA) nanoplatform for TNBC treatment. The nanobioconjugate carries anti-tumor nucleosome-specific monoclonal antibody (mAb) 2C5 to target breast cancer cells, anti-mouse transferrin receptor (TfR) antibody for drug delivery through the host endothelial system, and Morpholino antisense oligonucleotide (AON) to inhibit EGFR synthesis. The nanobioconjugates variants were: (1) P (BioPolymer) with AON, 2C5 and anti-TfR for tumor endothelial and cancer cell targeting, and EGFR suppression (P/AON/2C5/TfR), and (2) P with AON and 2C5 (P/AON/ 2C5). Controls included (3) P with 2C5 but without AON (P/2C5), (4) PBS, and (5) P with PEG and leucine
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