Modulation of Colorectal Tumor Behavior via lncRNA TP53TG1-Lipidic Nanosystem

• Published in: Pharmaceutics Vol. 13; no. 9; p. 1507
• Main Authors: Masoumi, Farimah, Saraiva, Sofia M., Bouzo, Belén L., López-López, Rafael, Esteller, Manel, Díaz-Lagares, Ángel, de la Fuente, María
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 18.09.2021; MDPI
• Subjects: Acids; Cancer therapies; Cloning; Colorectal cancer; Cytotoxicity; DNA methylation; emulsions; Epigenetics; epigenomics; Gene expression; Gene therapy; Lipids; long non-coding RNAs; nanocarriers; Particle size; Tumors; United Kingdom > UK; United States > US; Madrid Spain; Germany; Spain
• ISSN: 1999-4923; 1999-4923
• DOI: 10.3390/pharmaceutics13091507

Long non-coding RNAs (lncRNAs) are an emerging group of RNAs with a crucial role in cancer pathogenesis. In gastrointestinal cancers, TP53 target 1 (TP53TG1) is an epigenetically regulated lncRNA that represents a promising therapeutic target due to its tumor suppressor properties regulating the p53-mediated DNA damage and the intracellular localization of the oncogenic YBX1 protein. However, to translate this finding into the clinic as a gene therapy, it is important to develop effective carriers able to deliver exogenous lncRNAs to the targeted cancer cells. Here, we propose the use of biocompatible sphingomyelin nanosystems comprising DOTAP (DSNs) to carry and deliver a plasmid vector encoding for TP53TG1 (pc(TP53TG1)-DSNs) to a colorectal cancer cell line (HCT-116). DSNs presented a high association capacity and convenient physicochemical properties. In addition, pc(TP53TG1)-DSNs showed anti-tumor activities in vitro, specifically a decrease in the proliferation rate, a diminished colony-forming capacity, and hampered migration and invasiveness of the treated cancer cells. Consequently, the proposed strategy displays a high potential as a therapeutic approach for colorectal cancer.