Vidal Isabel, Torres-Vargas José Antonio, Sánchez José María, Trigal Mónica, García-Caballero Melissa, Medina Miguel Ángel, Quesada Ana R
Department of Molecular Biology and Biochemistry, Faculty of Sciences, University of Málaga, Andalucía Tech, and IBIMA Plataforma BIONAND, E-29071 Málaga, Spain.
Biomar Microbial Technologies, Parque Tecnológico de León, Parcela M-10.4, Armunia, 24009 León, Spain.
Antioxidants (Basel). 2023 May 15;12(5):1101. doi: 10.3390/antiox12051101.
The role played by a sustained angiogenesis in cancer and other diseases stimulates the interest in the search for new antiangiogenic drugs. In this manuscript, we provide evidence that 1,8- dihydroxy-9,10-anthraquinone (danthron), isolated from the fermentation broth of the marine fungus sp. (HL-114-33-R04), is a new inhibitor of angiogenesis. The results obtained with the in vivo CAM assay indicate that danthron is a potent antiangiogenic compound. In vitro studies with human umbilical endothelial cells (HUVEC) reveal that this anthraquinone inhibits certain key functions of activated endothelial cells, including proliferation, proteolytic and invasive capabilities and tube formation. In vitro studies with human breast carcinoma MDA-MB231 and fibrosarcoma HT1080 cell lines suggest a moderate antitumor and antimetastatic activity of this compound. Antioxidant properties of danthron are evidenced by the observation that it reduces the intracellular reactive oxygen species production and increases the amount of intracellular sulfhydryl groups in endothelial and tumor cells. These results support a putative role of danthron as a new antiangiogenic drug with potential application in the treatment and angioprevention of cancer and other angiogenesis-dependent diseases.
持续的血管生成在癌症及其他疾病中所起的作用激发了人们寻找新型抗血管生成药物的兴趣。在本论文中,我们提供了证据表明,从海洋真菌sp.(HL - 114 - 33 - R04)发酵液中分离得到的1,8 - 二羟基 - 9,10 - 蒽醌(丹蒽醌)是一种新型血管生成抑制剂。体内鸡胚绒毛尿囊膜试验所得结果表明,丹蒽醌是一种有效的抗血管生成化合物。对人脐静脉内皮细胞(HUVEC)进行的体外研究显示,这种蒽醌可抑制活化内皮细胞的某些关键功能,包括增殖、蛋白水解和侵袭能力以及管腔形成。对人乳腺癌MDA - MB231和纤维肉瘤HT1080细胞系进行的体外研究表明,该化合物具有一定的抗肿瘤和抗转移活性。观察发现丹蒽醌可减少内皮细胞和肿瘤细胞内活性氧的产生并增加细胞内巯基的含量,这证明了其抗氧化特性。这些结果支持了丹蒽醌作为一种新型抗血管生成药物的假定作用,其在癌症及其他血管生成依赖性疾病的治疗和血管预防中具有潜在应用价值。