Institute of General Pathology and Pathophysiology, 8 Baltiyskaya Str., 125315 Moscow, Russia.
Institute for Regenerative Medicine, Sechenov First Moscow State Medical University, 8-2 Trubetskaya Str., 119991 Moscow, Russia.
Biomed Res Int. 2021 Jul 20;2021:8463161. doi: 10.1155/2021/8463161. eCollection 2021.
Meso-Xanthin (Meso-Xanthin F199™) is a highly active antiaging injection drug of the latest generation. The main acting compound is fucoxanthin, supplemented with several growth factors, vitamins, and hyaluronic acid. Previous examination of fucoxanthin on melanocytes showed its ability to inhibit skin pigmentation through different signaling pathways focused on suppression of melanogenic-stimulating receptors. In turn, the anticancer property of fucoxanthin is realized through MAPK and PI3K pathways. We aimed to evaluate the effect of fucoxanthin and supplemented growth factors on melanocyte growth and transformation at a proteomic level. The effect of fucoxanthin on melanocytes cultivated in three-dimensional (3D) condition was examined using high-throughput proteomic and system biology approaches to disclose key molecular events of the targeted action. Our results demonstrated significant inhibition of cell differentiation and ubiquitination processes. We found that the negative regulation of and largely determines the inhibition of NF-B and MAPK2. Besides, fucoxanthin selectively inhibits cell differentiation via negative regulation of Raf signaling and the upstream activation of IL-1 signaling. It is assumed that inhibition of Raf influences the Notch-4 signaling and switches off the MAPK/MAPK2 cascade. Blockage of MAPK/MAPK2 is feasible due to suppression of Ras and NF-B by the addressed action of , , and . Suggestively, Meso-Xanthin F199™ can manage processes of proliferative activity and inhibition of apoptosis due to composition of fucoxanthin and growth-stimulating factors, which may increase the risk of skin cancer development under certain condition.
美索黄酮(Meso-Xanthin F199 ™ )是一种最新一代的高活性抗衰老注射药物。主要活性化合物是岩藻黄质,辅以几种生长因子、维生素和透明质酸。先前对黑色素细胞中岩藻黄质的研究表明,它通过专注于抑制黑色素生成刺激受体的不同信号通路,具有抑制皮肤色素沉着的能力。相反,岩藻黄质的抗癌特性是通过 MAPK 和 PI3K 途径实现的。我们旨在从蛋白质组学水平评估岩藻黄质和补充生长因子对黑色素细胞生长和转化的影响。使用高通量蛋白质组学和系统生物学方法研究了岩藻黄质对三维(3D)培养的黑色素细胞的影响,以揭示靶向作用的关键分子事件。我们的研究结果表明,细胞分化和泛素化过程受到显著抑制。我们发现和的负调控在很大程度上决定了 NF-B 和 MAPK2 的抑制。此外,岩藻黄质通过 Raf 信号的负调控和 IL-1 信号的上游激活选择性抑制细胞分化。假设 Raf 的抑制会影响 Notch-4 信号并关闭 MAPK/MAPK2 级联。由于所涉及的、和的作用抑制 Ras 和 NF-B,因此可以阻断 MAPK/MAPK2。暗示 Meso-Xanthin F199 ™ 可以由于岩藻黄质和生长刺激因子的组成来管理增殖活性和抑制细胞凋亡的过程,这可能会在某些条件下增加皮肤癌发展的风险。