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Polymalic Acid-based Nano Biopolymers for Targeting of Multiple Tumor Markers: An Opportunity for Personalized Medicine?
Published on: June 13, 2014
Nanobiopolymer for direct targeting and inhibition of EGFR expression in triple negative breast cancer
Satoshi Inoue1, Rameshwar Patil, Jose Portilla-Arias
1Department of Neurosurgery, Cedars-Sinai Medical Center, Los Angeles, California, 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(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.
Insights
A novel nanobioconjugate effectively treats triple-negative breast cancer (TNBC) by inhibiting EGFR synthesis and downstream signaling. This targeted therapy shows significant tumor growth inhibition in preclinical models, offering a promising new treatment for TNBC.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Oncology
Background:
- Triple-negative breast cancer (TNBC) has limited treatment options, primarily relying on cytotoxic chemotherapy.
- Anti-epidermal growth factor receptor (EGFR) therapy is an emerging option for TNBC patients.
- Developing targeted nanomedicines is crucial for improving TNBC treatment efficacy.
Purpose of the Study:
- To engineer and evaluate a novel nanobioconjugate for targeted TNBC treatment.
- To assess the nanobioconjugate's efficacy in inhibiting EGFR synthesis and downstream signaling pathways.
- To investigate the nanobioconjugate's therapeutic potential in a preclinical TNBC model.
Main Methods:
- A poly(β-L-malic acid) (PMLA) nanoplatform was functionalized with an anti-EGFR antibody (2C5), an anti-transferrin receptor (TfR) antibody, and an antisense oligonucleotide (AON) to inhibit EGFR.
- Nanobioconjugate variants were intravenously administered to MDA-MB-468 TNBC-bearing mice.
- Tumor accumulation, EGFR expression, and Akt phosphorylation were analyzed using in vivo imaging, western blotting, and confocal microscopy.
Main Results:
- The lead nanobioconjugate (P/AON/2C5/TfR) demonstrated superior inhibition of EGFR synthesis in vitro compared to naked AON.
- In vivo imaging confirmed that the 2C5 antibody enhanced drug accumulation in tumors.
- Significant tumor growth inhibition was observed with the lead nanobioconjugate, outperforming other variants and controls, with reduced EGFR expression and Akt phosphorylation.
Conclusions:
- The novel nanobioconjugate effectively inhibits tumor growth in TNBC by targeting EGFR and its downstream signaling pathway (Akt).
- This nanobioconjugate represents a new generation of nanodrugs with significant therapeutic potential for TNBC treatment.
- Targeted delivery and inhibition of key oncogenic pathways offer a promising strategy for TNBC management.
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