Bacterial Genotoxin-Coated Nanoparticles for Radiotherapy Sensitization in Prostate Cancer.
Yu-An ChenYi-Ru LaiHui-Yu WuYen-Ju LoYu-Fang ChangChiu-Lien HungChun-Jung LinU-Ging LoChung-Jung LinJer-Tsong HsiehCheng-Hsun ChiuYu-Hsin LinChih-Ho LaiPublished in: Biomedicines (2021)
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.
Keyphrases
- cell cycle arrest
- prostate cancer
- cell death
- induced apoptosis
- pi k akt
- hyaluronic acid
- cancer stem cells
- radical prostatectomy
- drug delivery
- early stage
- oxidative stress
- endoplasmic reticulum stress
- cancer therapy
- signaling pathway
- stem cells
- oxide nanoparticles
- radiation therapy
- pseudomonas aeruginosa
- cell proliferation
- squamous cell carcinoma
- biofilm formation
- rectal cancer
- circulating tumor
- staphylococcus aureus
- single molecule
- bone marrow
- candida albicans
- antimicrobial resistance
- cystic fibrosis
- mesenchymal stem cells
- cell free
- iron oxide
- childhood cancer