Flavin Adenine Dinucleotide (FAD) Pegylated (PEG)-Complexes: Proof of Concept (PoC) of theranostic tool on a Murine Breast Cancer Model.

Q1 Pharmacology, Toxicology and Pharmaceutics
Celia Arib, Hui Liu, Qiqian Liu, Anne-Marie Cieutat, Didier Paleni, Xiaowu Li, Jolanda Spadavecchia
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引用次数: 1

Abstract

Flavin adenine dinucleotide (FAD) plays a key role in an extensive range of cellular oxidation-reduction reactions, which is engaged in metabolic pathways. The purpose of this study was to realize pegylated flavins formulation, named FAD and FAD-PEG diacid complex as theranostic tool in cancer therapy. For this objective, a murine breast cancer model, which was induced by mouse-derived4T1 breast cancer cells was studied to assess the therapeutic efficacy of FAD (named NP1) and FAD-PEG diacid complex (named NP2). The cytokines were monitored to evaluate the serum inflammatory factors to develop the blood cell content of different groups of nude mice. The experimental model shows that an intravenous injection of FAD (NP1) can significantly reduce tumour volume, tumour index and thymus index, and decrease neutrophils (NE), monocytes (MO), eosinophils (EO), and basophils (BA). At the same time, the content of IL-1α, IL-12P70, TNF α, IL-1β and IL-6 was significantly reduced, and the content of IL-10 was significantly increased. These results provide the proof-of-concept for FAD as a smart adjuvant for cancer therapy and encourages their further development in the field of Nanomedicine.

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黄素腺嘌呤二核苷酸(FAD)聚乙二醇化(PEG)复合物:小鼠乳腺癌模型治疗工具的概念验证(PoC)。
黄素腺嘌呤二核苷酸(Flavin adenine dinucleotide, FAD)在广泛的细胞氧化还原反应中起关键作用,参与代谢途径。本研究的目的是实现聚乙二醇黄酮制剂,命名为FAD和FAD- peg二酸配合物,作为癌症治疗的治疗工具。为此,我们建立了小鼠源性4t1乳腺癌细胞诱导的小鼠乳腺癌模型,以评估FAD(命名为NP1)和FAD- peg二酸复合物(命名为NP2)的治疗效果。监测各组裸鼠血清中细胞因子的变化,评价各组裸鼠血清中炎性因子的含量。实验模型显示,静脉注射FAD (NP1)可显著降低肿瘤体积、肿瘤指数和胸腺指数,降低中性粒细胞(NE)、单核细胞(MO)、嗜酸性粒细胞(EO)和嗜碱性粒细胞(BA)。同时,IL-1α、IL-12P70、TNF α、IL-1β、IL-6含量显著降低,IL-10含量显著升高。这些结果为FAD作为一种智能辅助癌症治疗提供了概念证明,并鼓励其在纳米医学领域的进一步发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nanotheranostics
Nanotheranostics Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
10.40
自引率
0.00%
发文量
37
审稿时长
12 weeks
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