| Literature DB >> 27786455 |
Wen-Ying Huang1, Jia-Ni Lin2, Jer-Tsong Hsieh3, Shen-Chieh Chou2, Chih-Ho Lai4, Eun-Jin Yun3, U-Ging Lo3, Rey-Chen Pong3, Jui-Hsiang Lin5, Yu-Hsin Lin2,3.
Abstract
Prostate cancer is one of the leading causes of cancer death in adult men and is a multistage disease with therapeutic challenges of local recurrent advanced tumors and distant metastatic disease. CD44 is a multifunctional and multistructural cell surface glycoprotein that is involved in cell-cell interactions, cell proliferation, and cell migration. In the study, we produced negatively charged and biocompatible hyaluronic acid-based nanoparticles as a therapeutic system for targeting CD44-positive cancer cells. Subsequently, we confirmed the delivery of bioactive epigallocatechin-3-gallate and site-specific inhibition of prostate tumor growth. In this study, hyaluronic acid-based nanoparticles successfully encapsulated epigallocatechin-3-gallate and were efficiently internalized into cancer cells via CD44 ligand receptor recognition, induced cell cycle arrest at G2/M phase, and inhibited prostate cancer cell growth. Furthermore, in vivo assays indicated that these nanoparticles specifically bind CD44 receptors and increase apoptosis of cancer cells, leading to significant decreases in prostate tumor activity and tumor tissue inflammation.Entities:
Keywords: CD44; epigallocatechin-3-gallate; hyaluronic acid; nanoparticles; prostate cancer
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Year: 2016 PMID: 27786455 DOI: 10.1021/acsami.6b10029
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229