Ingelfinger Rebecca, Henke Marina, Roser Luise, Ulshöfer Thomas, Calchera Anjuli, Singh Garima, Parnham Michael J, Geisslinger Gerd, Fürst Robert, Schmitt Imke, Schiffmann Susanne
Faculty of Biochemistry, Institute of Pharmaceutical Biology, Chemistry and Pharmacy, Goethe University Frankfurt, Frankfurt, Germany.
LOEWE Center Translational Biodiversity Genomics, Frankfurt, Germany.
Front Pharmacol. 2020 Sep 4;11:1322. doi: 10.3389/fphar.2020.01322. eCollection 2020.
Lichen-forming fungi are symbiotic organisms that synthesize unique natural products with potential for new drug leads. Here, we explored the pharmacological activity of six lichen extracts (, , , , , in the context of cancer and inflammation using a comprehensive set of 11 functional and biochemical screening assays. We assayed intracellular Ca levels and cell migration. For cancer, we measured tumor cell proliferation, cell cycle distribution and apoptosis, as well as the angiogenesis-associated proliferation of endothelial cells (ECs). Targeting inflammation, we assayed leukocyte adhesion onto ECs, EC adhesion molecule expression, as well as nitric oxide production and prostaglandin (PG)E synthesis in leukocytes. Remarkably, none of the lichen extracts showed any detrimental influence on the viability of ECs. We showed for the first time that extracts of induce Ca signaling. Furthermore, extracts from , , , and reduced cell migration. Interestingly, extracts strongly decreased tumor cell survival. The proliferation of ECs was significantly reduced by , , and extracts. The extracts did not inhibit the activity of inflammatory processes in ECs. However, the pro-inflammatory activation of leukocytes was inhibited by extracts from , , , and . After revealing the potential biological activities of lichen extracts by an array of screening tests, a correlation analysis was performed to evaluate particular roles of abundant lichen secondary metabolites, such as atranorin, physodic acid, and protocetraric acid as well as usnic acid in various combinations. Overall, some of the lichen extracts tested in this study exhibit significant pharmacological activity in the context of inflammation and/or cancer, indicating that the group lichen-forming fungi includes promising members for further testing.
地衣形成真菌是共生生物,能合成具有新药开发潜力的独特天然产物。在此,我们使用一套全面的11种功能和生化筛选试验,探讨了六种地衣提取物(,,,,,)在癌症和炎症方面的药理活性。我们检测了细胞内钙水平和细胞迁移。对于癌症,我们测量了肿瘤细胞增殖、细胞周期分布和凋亡,以及内皮细胞(ECs)的血管生成相关增殖。针对炎症,我们检测了白细胞在ECs上的黏附、EC黏附分子表达,以及白细胞中一氧化氮的产生和前列腺素(PG)E的合成。值得注意的是,没有一种地衣提取物对ECs的活力显示出任何有害影响。我们首次表明提取物可诱导钙信号。此外,,,,和的提取物可减少细胞迁移。有趣的是,提取物能显著降低肿瘤细胞存活率。,和的提取物可显著降低ECs的增殖。这些提取物并未抑制ECs中炎症过程的活性。然而,,,,和的提取物可抑制白细胞的促炎激活。通过一系列筛选试验揭示了地衣提取物的潜在生物活性后,进行了相关性分析,以评估丰富的地衣次生代谢产物,如阿特拉诺林、物理德酸、原岛衣酸以及松萝酸以各种组合形式所起的特定作用。总体而言,本研究中测试的一些地衣提取物在炎症和/或癌症方面表现出显著的药理活性,表明地衣形成真菌类群中有值得进一步测试的有前景的成员。