| Literature DB >> 33557143 |
Yu-An Chen1,2,3, Yi-Ru Lai1, Hui-Yu Wu1, Yen-Ju Lo1, Yu-Fang Chang1, Chiu-Lien Hung4, Chun-Jung Lin3, U-Ging Lo3, Ho Lin2, Jer-Tsong Hsieh3,5, Cheng-Hsun Chiu1,6, Yu-Hsin Lin5,7, Chih-Ho Lai1,5,6,8.
Abstract
Prostate cancer (PCa) is one of the most commonly diagnosed cancers in men and usually becomes refractory because of recurrence and metastasis. CD44, a transmembrane glycoprotein, serves as a receptor for hyaluronic acid (HA). It has been found to be abundantly expressed in cancer stem cells (CSCs) that often exhibit a radioresistant phenotype. Cytolethal distending toxin (CDT), produced by Campylobacter jejuni, is a tripartite genotoxin composed of CdtA, CdtB, and CdtC subunits. Among the three, CdtB acts as a type I deoxyribonuclease (DNase I), which creates DNA double-strand breaks (DSBs). Nanoparticles loaded with antitumor drugs and specific ligands that recognize cancerous cell receptors are promising methods to overcome the therapeutic challenges. In this study, HA-decorated nanoparticle-encapsulated CdtB (HA-CdtB-NPs) were prepared and their targeted therapeutic activity in radioresistant PCa cells was evaluated. Our results showed that HA-CdtB-NPs sensitized radioresistant PCa cells by enhancing DSB and causing G2/M cell-cycle arrest, without affecting the normal prostate epithelial cells. HA-CdtB-NPs possess maximum target specificity and delivery efficiency of CdtB into the nucleus and enhance the effect of radiation in radioresistant PCa cells. These findings demonstrate that HA-CdtB-NPs exert target specificity accompanied with radiomimetic activity and can be developed as an effective strategy against radioresistant PCa.Entities:
Keywords: genotoxin; nanoparticles; prostate cancer; radioresistance
Year: 2021 PMID: 33557143 PMCID: PMC7913852 DOI: 10.3390/biomedicines9020151
Source DB: PubMed Journal: Biomedicines ISSN: 2227-9059