Targeted destruction of cancer stem cells using multifunctional magnetic nanoparticles that enable combined hyperthermia and chemotherapy

Autor: Mengsu Yang, Siu-Kie Au, Yu Zhu, Shubin Wang, Dandan Liu, Yingcai Hong, Tak-Chun Yip, Yaping Li, Chi-Chun Fong, Weimao Wang, Chong Hu, Wai-Kin Yu
Rok vydání: 2019
Předmět:
Hyperthermia
Lung Neoplasms
medicine.medical_treatment
Medicine (miscellaneous)
Mice
Nude

Antineoplastic Agents
02 engineering and technology
Metastasis
Multifunctional nanoparticle
03 medical and health sciences
Mice
In vivo
Cancer stem cell
Cell Line
Tumor

medicine
Animals
Humans
Lung cancer stem cell
Magnetite Nanoparticles
Pharmacology
Toxicology and Pharmaceutics (miscellaneous)

Thermotherapy and chemotherapy
030304 developmental biology
0303 health sciences
Chemotherapy
Drug Carriers
Mice
Inbred BALB C

Alternating magnetic field
business.industry
Mesenchymal Stem Cells
Hyperthermia
Induced

021001 nanoscience & nanotechnology
medicine.disease
Combined Modality Therapy
Small Cell Lung Carcinoma
In vitro
Cancer research
Neoplastic Stem Cells
Magnetic nanoparticles
Nanomedicine
Neoplasm Recurrence
Local

0210 nano-technology
business
Research Paper
Zdroj: Theranostics
ISSN: 1838-7640
Popis: Cancer stem cells (CSCs) have been implicated in cancer recurrence and therapy resistance. Therefore, a CSC-targeted therapy that disrupts the maintenance and survival of CSCs may offer an effective approach in killing tumor cells in primary tumors and preventing the metastasis caused by CSCs. Nanoparticles (NPs)-based thermotherapy and/or chemotherapy are promising therapeutic methods for cancer treatment. Methods: A silica-based multifunctional NP system was present, which encapsulated a chemotherapeutic agent and magnetic cores and coated with a specific antibody against the lung CSCs. The efficacy of this novel therapeutic strategy was systematically studied both in vitro and in vivo by simultaneous activating the combined thermotherapy and chemotherapy via CSC-targeted NPs. Results: These NPs were systematically administered and activated for targeted chemotherapy and thermotherapy by using an externally applied alternating magnetic field (AMF). The antibody-modified NPs targeted to lung CSCs with enhanced cellular uptake in vitro and extended accumulation in tumor in vivo. Up to 98% of lung CSCs was killed in vitro with 30-min application of AMF, due to the combined effects of hyperthermia and chemotherapeutic drug treatment. In in vivo models, this combined therapy significantly suppressed tumor growth and metastasis in lung CSC xenograft-bearing mice, with minimal side effects and adverse effects. Conclusion: With good biocompatibility and targeting capability, the nanodrug delivery system may offer a promising clinical platform for the combined thermotherapy and chemotherapy. This work demonstrated the feasibility of developing multifunctional nanomedicine targeting CSCs for effective cancer treatment.
Databáze: OpenAIRE