Targeting Engineered Nanoparticles for Breast Cancer Therapy.
Kumar GanesanYan WangFei GaoQingqing LiuChen ZhangPeng LiJinming ZhangJianping ChenPublished in: Pharmaceutics (2021)
Breast cancer (BC) is the second most common cancer in women globally after lung cancer. Presently, the most important approach for BC treatment consists of surgery, followed by radiotherapy and chemotherapy. The latter therapeutic methods are often unsuccessful in the treatment of BC because of their various side effects and the damage incurred to healthy tissues and organs. Currently, numerous nanoparticles (NPs) have been identified and synthesized to selectively target BC cells without causing any impairments to the adjacent normal tissues or organs. Based on an exploratory study, this comprehensive review aims to provide information on engineered NPs and their payloads as promising tools in the treatment of BC. Therapeutic drugs or natural bioactive compounds generally incorporate engineered NPs of ideal sizes and shapes to enhance their solubility, circulatory half-life, and biodistribution, while reducing their side effects and immunogenicity. Furthermore, ligands such as peptides, antibodies, and nucleic acids on the surface of NPs precisely target BC cells. Studies on the synthesis of engineered NPs and their impact on BC were obtained from PubMed, Science Direct, and Google Scholar. This review provides insights on the importance of engineered NPs and their methodology for validation as a next-generation platform with preventive and therapeutic effects against BC.
Keyphrases
- induced apoptosis
- gene expression
- oxide nanoparticles
- early stage
- public health
- healthcare
- minimally invasive
- squamous cell carcinoma
- oxidative stress
- type diabetes
- locally advanced
- bone marrow
- metabolic syndrome
- papillary thyroid
- insulin resistance
- adipose tissue
- pet ct
- skeletal muscle
- atrial fibrillation
- positron emission tomography
- drug induced
- lymph node metastasis
- percutaneous coronary intervention