Cargando…
Nanobiopolymer for Direct Targeting and Inhibition of EGFR Expression in Triple Negative Breast Cancer
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(β-L-malic acid) (PMLA) nanoplatform...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3280290/ https://www.ncbi.nlm.nih.gov/pubmed/22355336 http://dx.doi.org/10.1371/journal.pone.0031070 |
_version_ | 1782223809524269056 |
---|---|
author | Inoue, Satoshi Patil, Rameshwar Portilla-Arias, Jose Ding, Hui Konda, Bindu Espinoza, Andres Mongayt, Dmitriy Markman, Janet L. Elramsisy, Adam Phillips, H. Westley Black, Keith L. Holler, Eggehard Ljubimova, Julia Y. |
author_facet | Inoue, Satoshi Patil, Rameshwar Portilla-Arias, Jose Ding, Hui Konda, Bindu Espinoza, Andres Mongayt, Dmitriy Markman, Janet L. Elramsisy, Adam Phillips, H. Westley Black, Keith L. Holler, Eggehard Ljubimova, Julia Y. |
author_sort | Inoue, Satoshi |
collection | PubMed |
description | 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(β-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 ester (LOEt) for endosomal escape (P/mPEG/LOEt). Drugs were injected intravenously to MDA-MB-468 TNBC bearing mice. Tissue accumulation of injected nanobioconjugates labeled with Alexa Fluor 680 was examined by Xenogen IVIS 200 (live imaging) and confocal microscopy of tissue sections. Levels of EGFR, phosphorylated and total Akt in tumor samples were detected by western blotting. In vitro western blot showed that the leading nanobioconjugate P/AON/2C5/TfR inhibited EGFR synthesis significantly better than naked AON. In vivo imaging revealed that 2C5 increased drug-tumor accumulation. Significant tumor growth inhibition was observed in mice treated with the lead nanobioconjugate (1) [P = 0.03 vs. controls; P<0.05 vs. nanobioconjugate variant (2)]. Lead nanobioconjugate (1) also showed stronger inhibition of EGFR expression and Akt phosphorylation than other treatments. Treatment of TNBC with the new nanobioconjugate results in tumor growth arrest by inhibiting EGFR and its downstream signaling intermediate, phosphorylated Akt. The nanobioconjugate represents a new generation of nanodrugs for treatment of TNBC. |
format | Online Article Text |
id | pubmed-3280290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32802902012-02-21 Nanobiopolymer for Direct Targeting and Inhibition of EGFR Expression in Triple Negative Breast Cancer Inoue, Satoshi Patil, Rameshwar Portilla-Arias, Jose Ding, Hui Konda, Bindu Espinoza, Andres Mongayt, Dmitriy Markman, Janet L. Elramsisy, Adam Phillips, H. Westley Black, Keith L. Holler, Eggehard Ljubimova, Julia Y. PLoS One Research Article 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(β-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 ester (LOEt) for endosomal escape (P/mPEG/LOEt). Drugs were injected intravenously to MDA-MB-468 TNBC bearing mice. Tissue accumulation of injected nanobioconjugates labeled with Alexa Fluor 680 was examined by Xenogen IVIS 200 (live imaging) and confocal microscopy of tissue sections. Levels of EGFR, phosphorylated and total Akt in tumor samples were detected by western blotting. In vitro western blot showed that the leading nanobioconjugate P/AON/2C5/TfR inhibited EGFR synthesis significantly better than naked AON. In vivo imaging revealed that 2C5 increased drug-tumor accumulation. Significant tumor growth inhibition was observed in mice treated with the lead nanobioconjugate (1) [P = 0.03 vs. controls; P<0.05 vs. nanobioconjugate variant (2)]. Lead nanobioconjugate (1) also showed stronger inhibition of EGFR expression and Akt phosphorylation than other treatments. Treatment of TNBC with the new nanobioconjugate results in tumor growth arrest by inhibiting EGFR and its downstream signaling intermediate, phosphorylated Akt. The nanobioconjugate represents a new generation of nanodrugs for treatment of TNBC. Public Library of Science 2012-02-15 /pmc/articles/PMC3280290/ /pubmed/22355336 http://dx.doi.org/10.1371/journal.pone.0031070 Text en Inoue et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Inoue, Satoshi Patil, Rameshwar Portilla-Arias, Jose Ding, Hui Konda, Bindu Espinoza, Andres Mongayt, Dmitriy Markman, Janet L. Elramsisy, Adam Phillips, H. Westley Black, Keith L. Holler, Eggehard Ljubimova, Julia Y. Nanobiopolymer for Direct Targeting and Inhibition of EGFR Expression in Triple Negative Breast Cancer |
title | Nanobiopolymer for Direct Targeting and Inhibition of EGFR Expression in Triple Negative Breast Cancer |
title_full | Nanobiopolymer for Direct Targeting and Inhibition of EGFR Expression in Triple Negative Breast Cancer |
title_fullStr | Nanobiopolymer for Direct Targeting and Inhibition of EGFR Expression in Triple Negative Breast Cancer |
title_full_unstemmed | Nanobiopolymer for Direct Targeting and Inhibition of EGFR Expression in Triple Negative Breast Cancer |
title_short | Nanobiopolymer for Direct Targeting and Inhibition of EGFR Expression in Triple Negative Breast Cancer |
title_sort | nanobiopolymer for direct targeting and inhibition of egfr expression in triple negative breast cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3280290/ https://www.ncbi.nlm.nih.gov/pubmed/22355336 http://dx.doi.org/10.1371/journal.pone.0031070 |
work_keys_str_mv | AT inouesatoshi nanobiopolymerfordirecttargetingandinhibitionofegfrexpressionintriplenegativebreastcancer AT patilrameshwar nanobiopolymerfordirecttargetingandinhibitionofegfrexpressionintriplenegativebreastcancer AT portillaariasjose nanobiopolymerfordirecttargetingandinhibitionofegfrexpressionintriplenegativebreastcancer AT dinghui nanobiopolymerfordirecttargetingandinhibitionofegfrexpressionintriplenegativebreastcancer AT kondabindu nanobiopolymerfordirecttargetingandinhibitionofegfrexpressionintriplenegativebreastcancer AT espinozaandres nanobiopolymerfordirecttargetingandinhibitionofegfrexpressionintriplenegativebreastcancer AT mongaytdmitriy nanobiopolymerfordirecttargetingandinhibitionofegfrexpressionintriplenegativebreastcancer AT markmanjanetl nanobiopolymerfordirecttargetingandinhibitionofegfrexpressionintriplenegativebreastcancer AT elramsisyadam nanobiopolymerfordirecttargetingandinhibitionofegfrexpressionintriplenegativebreastcancer AT phillipshwestley nanobiopolymerfordirecttargetingandinhibitionofegfrexpressionintriplenegativebreastcancer AT blackkeithl nanobiopolymerfordirecttargetingandinhibitionofegfrexpressionintriplenegativebreastcancer AT hollereggehard nanobiopolymerfordirecttargetingandinhibitionofegfrexpressionintriplenegativebreastcancer AT ljubimovajuliay nanobiopolymerfordirecttargetingandinhibitionofegfrexpressionintriplenegativebreastcancer |