Dual-targeted therapy in HER2-positive breast cancer cells with the combination of carbon dots/HER3 siRNA and trastuzumab
Autor: | Yan Wu, Chulang Yu, Feng Gao, Guili He, Nantao Hu, Mengjun Shu, Yanjie Su, Zhi Yang, Zhihua Zhou, Min Zeng, Lin Xu |
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Rok vydání: | 2020 |
Předmět: |
Small interfering RNA
Materials science Receptor ErbB-3 Cell Survival medicine.medical_treatment Down-Regulation Bioengineering Breast Neoplasms 02 engineering and technology Gene delivery 010402 general chemistry 01 natural sciences Targeted therapy Trastuzumab Cell Line Tumor Antineoplastic Combined Chemotherapy Protocols Chlorocebus aethiops medicine Animals Humans General Materials Science Electrical and Electronic Engineering RNA Small Interfering skin and connective tissue diseases Cell Proliferation Cell growth Mechanical Engineering Cell Cycle Drug Synergism General Chemistry Transfection 021001 nanoscience & nanotechnology Carbon 0104 chemical sciences body regions Gene Expression Regulation Neoplastic Mechanics of Materials Cell culture Drug Resistance Neoplasm Cancer cell COS Cells Cancer research Female 0210 nano-technology medicine.drug |
Zdroj: | Nanotechnology. 31(33) |
ISSN: | 1361-6528 |
Popis: | Dual-targeted therapy in HER2-positive breast cancer cells with the combination of carbon dots/HER3 siRNA and trastuzumab resulted in enhanced antitumor activity, which overcomes the resistance to trastuzumab monotherapy. Herein, we have developed branched polyethylenimine-functionalized carbon dot (BP-CD) nanocarriers, which exhibited efficient green fluorescent protein gene delivery and expression. The positively charged BP-CDs allowed for effective nucleic acid binding and displayed a highly efficient small interfering RNA (siRNA)-mediated delivery targeting of cancer cells. The transfection of BP-CDs and HER3 siRNA complexes down-regulated HER3 protein expression and induced significant cell growth inhibition in BT-474 cells. BP-CDs/HER3 siRNA complexes induced cell death of BT-474 cells through G0/G1 cell cycle arrest and apoptosis. The combined treatment of BP-CDs/HER3 siRNA complexes and trastuzumab caused greater cell growth suppression in BT-474 cells when compared to either agent alone. The findings suggest that this dual-targeted therapy with the combination of BP-CDs/HER3 siRNA and trastuzumab represents a promising approach in breast cancer. |
Databáze: | OpenAIRE |
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