Beijing Key Laboratory of Protein Posttranslational Modifications and Cell Function, Department of Biochemistry and Biophysics, School of Basic Medical Sciences, Peking University Health Science Center, Beijing 100191, China.
Department of Medical Genetics, Center for Medical Genetics, Peking University Health Science Center, Beijing 100191, China.
Int J Mol Sci. 2024 Oct 28;25(21):11578. doi: 10.3390/ijms252111578.
Angiogenesis, a vital physiological or pathological process regulated by complex molecular networks, is widely implicated in organismal development and the pathogenesis of various diseases. SIRT7, a member of the Sirtuin family of nicotinamide adenine dinucleotide + (NAD) dependent deacetylases, plays crucial roles in cellular processes such as transcriptional regulation, cell metabolism, cell proliferation, and genome stability maintenance. Characterized by its enzymatic activities, SIRT7 targets an array of substrates, several of which exert regulatory effects on angiogenesis. Experimental evidence from in vitro and in vivo studies consistently demonstrates the effects of SIRT7 in modulating angiogenesis, mediated through various molecular mechanisms. Consequently, understanding the regulatory role of SIRT7 in angiogenesis holds significant promise, offering novel avenues for therapeutic interventions targeting either SIRT7 or angiogenesis. This review delineates the putative molecular mechanisms by which SIRT7 regulates angiogenesis, taking its substrates as a clue, endeavoring to elucidate experimental observations by integrating knowledge of SIRT7 substrates and established angiogenenic mechanisms.
血管生成是一种受复杂分子网络调节的重要生理或病理过程,广泛涉及生物发育和各种疾病的发病机制。SIRT7 是烟酰胺腺嘌呤二核苷酸 +(NAD)依赖性去乙酰化酶 Sirtuin 家族的成员,在转录调控、细胞代谢、细胞增殖和基因组稳定性维持等细胞过程中发挥关键作用。SIRT7 的特征在于其酶活性,其靶向一系列底物,其中一些对血管生成具有调节作用。来自体外和体内研究的实验证据一致表明 SIRT7 通过多种分子机制调节血管生成。因此,了解 SIRT7 在血管生成中的调节作用具有重要意义,为针对 SIRT7 或血管生成的治疗干预提供了新的途径。本综述以 SIRT7 的底物为线索,阐述了 SIRT7 调节血管生成的可能分子机制,通过整合 SIRT7 底物和已建立的血管生成机制的知识,努力阐明实验观察结果。