Nano-Hydroxyapatite-Derived Drug and Gene Co-Delivery System for Anti-Angiogenesis Therapy of Breast Cancer

被引:27
作者
Zhao, Lina [1 ]
Zhao, Wenhui [2 ]
Liu, Ye [3 ]
Chen, Xue [1 ]
Wang, Yan [1 ]
机构
[1] Harbin Med Univ, Tumor Hosp, Dept Hematol, Harbin, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Tumor Hosp, Dept Internal Med, Harbin, Heilongjiang, Peoples R China
[3] Harbin Med Univ, Dept Immunol, Harbin, Heilongjiang, Peoples R China
来源
MEDICAL SCIENCE MONITOR | 2017年 / 23卷
关键词
Angiogenesis Inhibitors; Angiotensin II Type 1 Receptor Blockers; Genes; p53; Hydroxyapatites; Inflammatory Breast Neoplasms; II TYPE-1 RECEPTOR; TUMOR ANGIOGENESIS; IN-VIVO; CATIONIC MICELLES; UP-REGULATION; WILD-TYPE; NANOPARTICLES; GROWTH; INHIBITION; CELLS;
D O I
10.12659/MSM.902538
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Breast cancer is among the deadliest cancers across the world and is responsible for countless deaths. There is an urgent need for co-delivery systems which can simultaneously transport both drug and gene into a single cancer cell with low toxicity and high anti-angiogenesis efficiency. Material/Methods: In the present study, well-formed amine-functionalized hydroxyapatite nanoparticles based on combined angiogenesis therapy for breast cancer were successfully constructed for the simultaneous delivery of p53 and candesartan (CD) (p53/CD/NHAP). Results: In vitro and in vivo experiments revealed that p53/CD/NHAP can effectively transfer the p53 gene and deliver the loaded CD to achieve preferable anti-breast cancer effect both at the cellular level and in tumor-bearing mice. This may possibly be due to the combined anti-angiogenic mechanisms of p53 and CD via different pathways. Conclusions: p53/CD/NHAP might be a candidate carrier for efficient anti-angiogenesis therapy of breast cancer.
引用
收藏
页码:4723 / 4732
页数:10
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