| Literature DB >> 24996756 |
Dangge Wang1, Zhiai Xu2, Haijun Yu3, Xianzhi Chen1, Bing Feng1, Zhirui Cui1, Bin Lin2, Qi Yin1, Zhiwen Zhang1, Chunying Chen4, Jun Wang5, Wen Zhang2, Yaping Li6.
Abstract
Despite the exciting advances in cancer therapy over past decades, tumor metastasis remains the dominate reason for cancer-related mortality. In present work, DNA-wrapped gold nanorods with doxorubicin (DOX)-loading (GNR@DOX) were developed for treatment of metastatic breast cancer via a combination of chemotherapy and photothermal ablation. The GNR@DOX nanoparticles induced significant temperature elevation and DOX release upon irradiation with near infrared (NIR) light as shown in the test tube studies. It was found that GNR@DOX nanoparticles in combination with laser irradiation caused higher cytotoxicity than free DOX in 4T1 breast cancer cells. Animal experiment with an orthotropic 4T1 mammary tumor model demonstrated that GNR@DOX nanoplatform significantly reduced the growth of primary tumors and suppressed their lung metastasis. The Hematoxylin and Eosin (H&E) and immunohistochemistry (IHC) staining assays confirmed that the tumor growth inhibition and metastasis prevention of GNR@DOX nanoparticles were attributed to their abilities to induce cellular apoptosis/necrosis and ablate intratumoral blood vessels. All these results suggested a considerable potential of GNR@DOX nanoplatform for treatment of metastatic breast cancer.Entities:
Keywords: Chemotherapy; Doxorubicin; Gold nanorods; Metastatic breast cancer; Photothermal ablation
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Year: 2014 PMID: 24996756 DOI: 10.1016/j.biomaterials.2014.05.094
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479