1. Corrigendum
- Author
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Mariana Brait, Xiaofei Chang, Wayne M. Koch, David Sidransky, Nissim Silanikove, Masamichi Hayashi, Vui Pham, Rajani Ravi, Keren Paz, and Gilson Baia
- Subjects
Oncology ,Cancer Research ,medicine.medical_specialty ,Antineoplastic Agents ,Triple Negative Breast Neoplasms ,Immunocompromised Host ,Colloid ,Drug Delivery Systems ,Breast cancer ,Cell Line, Tumor ,Internal medicine ,medicine ,Animals ,Humans ,Colloids ,Cancer biology ,Melanoma ,Pharmacology ,Drug Carriers ,business.industry ,medicine.disease ,Corrigenda ,Xenograft Model Antitumor Assays ,Mice, Inbred C57BL ,Milk ,Doxorubicin ,Drug delivery ,Nanoparticles ,Molecular Medicine ,Female ,business - Abstract
Triple negative breast cancer has an extremely poor prognosis when chemotherapy is no longer effective. To overcome drug resistance, novel drug delivery systems based on nanoparticles have had remarkable success. We produced a novel nanoparticle component 'MDC' from milk-derived colloid. In order to evaluate the anti-cancer effect of MDC, we conducted in vitro and in vivo experiments on cancer cell lines and a primary tumor derived breast xenograft. Doxorubicin (Dox) conjugated to MDC (MDC-Dox) showed higher cancer cell growth inhibition than MDC alone especially in cell lines with high EGFR expression. In a mouse melanoma model, MDC-Dox significantly suppressed tumor growth when compared with free Dox. Moreover, in a primary tumor derived breast xenograft, one of the mice treated with MDC-Dox showed partial regression, while mice treated with free Dox failed to show any suppression of tumor growth. We have shown that a novel nanoparticle compound made of simple milk-derived colloid has the capability for drug conjugation, and serves as a tumor-specific carrier of anti-cancer drugs. Further research on its safety and ability to carry various anti-cancer drugs into multiple drug-resistant primary breast models is warranted.
- Published
- 2015
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