CNRS, UMR 7244, NBD-CSPBAT, Laboratoire de Chimie, Structures et Propriétés de Biomatériaux et d'Agents Thérapeutiques Université Paris 13, Sorbonne Paris Nord, Bobigny, France.
Department of Hepatobiliary Surgery, Guangdong Provincial Key Laboratory of Regional Immunity and Diseases & Carson International Cancer Center, Shenzhen University General Hospital & Shenzhen University Clinical Medical Academy Center, Shenzhen University, Shenzhen, China.
Nanotheranostics. 2021 Apr 22;5(4):405-416. doi: 10.7150/ntno.59290. eCollection 2021.
Flavin adenine dinucleotide (FAD) is engaged in several metabolic diseases. Its main role is being a cofactor essential for the activity of many flavoproteins, which play a crucial role in electron transport pathways in living systems. The aim of this study was to apply a pegylated flavins formulation named FAD-PEG diacide complex as theranostic pathway in cancer therapy. For this purpose, a mouse liver cancer model induced by Hepa1-6 cells was used to evaluate the therapeutic efficacy of FAD (named NP1) and FAD-PEG diacide complex (named NP2). The cytokines were applied to screen the serum inflammatory factors, to establish the blood cell content of different groups of nude mice. The highlights follows that FAD formulations (NP1; NP2) significantly suppressed the tumor growth and reduced the tumor index without effects on the body weight of mice. Furthermore, NP2 significantly reduced the serum levels of cytokines IL-6, TNF-α and IL-12 (P70). The reported results provide the proof-of-concept for the synthesis of a smart adjuvant for liver cancer therapy and support their further development in the field of nanomedicine.
黄素腺嘌呤二核苷酸(FAD)参与多种代谢疾病。它的主要作用是作为许多黄素蛋白活性所必需的辅助因子,黄素蛋白在生命系统的电子传递途径中起着至关重要的作用。本研究旨在应用一种名为 FAD-PEG 二酸复合物的聚乙二醇化黄素制剂作为癌症治疗的治疗策略。为此,使用 Hepa1-6 细胞诱导的小鼠肝癌模型来评估 FAD(命名为 NP1)和 FAD-PEG 二酸复合物(命名为 NP2)的治疗效果。细胞因子用于筛选血清炎症因子,建立不同组裸鼠的血细胞含量。主要结果表明,FAD 制剂(NP1;NP2)显著抑制肿瘤生长并降低肿瘤指数,而对小鼠体重无影响。此外,NP2 显著降低了血清细胞因子 IL-6、TNF-α 和 IL-12(P70)的水平。报道的结果为合成用于肝癌治疗的智能佐剂提供了概念验证,并支持它们在纳米医学领域的进一步发展。