| Literature DB >> 29405062 |
Liujiang Song1, Xiaojun Tao1, Li Lin2, Chao Chen1, Hui Yao1, Guangchun He1, Guangyang Zou2, Zhong Cao2, Shichao Yan1, Lu Lu1, Huimei Yi1, Di Wu1, Siyuan Tan1, Wanxin Ouyang1, Zhifei Dai2, Xiyun Deng1.
Abstract
Triple-negative breast cancer (TNBC) is a subtype of breast cancer with a higher risk in younger women and a poorer prognosis and without targeted therapies available currently. Cancer stem cells (CSCs) are increasingly recognized as the main cause of treatment failure and tumor recurrence. The present paper reports the encapsulation of lovastatin (LV) into cerasomes. Compared with free LV, cerasome-encapsulated LV (C-LV) nanohybrids showed cytotoxicity to MDA-MB-231 CSCs in a dose- and time-dependent manner. Furthermore, intravenous injection of C-LV nanohybrids resulted in a significant tumor size reduction in a dose-dependent manner in xenograft tumors derived from subcutaneous inoculation of MDA-MB-231 cells. Furthermore, histopathological and/or immunohistochemical analysis revealed that C-LV nanohybrids significantly induced mammary gland formation and apoptosis and inhibited angiogenesis, the CSC phenotype, and the epithelial-to-mesenchymal transition in xenograft tumors. Most importantly, C-LV nanohybrids were found to be more effective than free LV in inhibiting the growth of breast cancer xenografts and the stemness properties in vivo. To the best of our knowledge, ours is the first demonstration of nanohybrids for efficient inhibition of CSCs derived from TNBC, offering a new option for the TNBC treatment.Entities:
Keywords: cancer stem cells; cerasome; epithelial-to-mesenchymal transition; lovastatin; triple-negative breast cancer
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Year: 2018 PMID: 29405062 DOI: 10.1021/acsami.8b01633
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229