Yusifova Yagut, Choudhary M Iqbal, Siddiqui Mahwish, Khan Nisha, Atif Muhammad, Zafar Humaira, Ibadullayeva Sayyara J, Aghayeva Dilzara N
Institute of Botany, Ministry of Science and Education of the Republic of Azerbaijan, Baku AZ1004, Azerbaijan.
Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi 75270, Pakistan; Institute of Molecular Biology and Biochemistry, University of Lahore, Lahore 54000, Pakistan.
Steroids. 2025 Sep;221:109647. doi: 10.1016/j.steroids.2025.109647. Epub 2025 Jun 6.
Certain mushrooms are used as low-calorie food supplements due to their excellent taste, and presence of a variety of essential vitamins, minerals and secondary metabolites. Some of them have therapeutic significance, and used in traditional medicines. Mushrooms cells can also be used as biocatalysts for the derivatization of organic compounds. During the current study, 3β-hydroxy-24-methylenelanost-8-en-21-oic acid (1) was isolated from Laetiporus sulphureus (Bull.) Murrill. The cell culture of the same mushroom was used for the biotransformation of breast cancer drug, exemestane (2) into a new analogue, 18-hydroxy-6-methylene-androsta-1,4-diene-3,17-dione (3). Compounds 1, and 3 were purified by using various chromatographic techniques, and their structures were determined with the help of 1D- and 2D-NMR, HREI-MS, and IR spectroscopic techniques. Since compound 1 also has a steroidal skeleton (like aromatase inhibiting drug exemestane (2)), the metabolite 1 was also evaluated for its aromatase inhibitory potential, along with a new transformed product 3. Aromatase plays a crucial role in estrogen biosynthesis, and therefore its inhibition is a key approach for the treatment of estrogen receptor-positive (ER+) breast cancers. Compounds 1 and 3 demonstrated a significant aromatase inhibition, with IC values of 590 ± 0.03 nM and 337.5 ± 0.01 nM, respectively, relative to exemestane's IC of 210.0 ± 0.16 nM. Furthermore, in silico studies predicted that these inhibitors 1-3 were able to occupy the active site and interacted with catalytically important residues of the enzyme. While molecular dynamic simulation predicted the stability of aromatase- ligand complexes. The studies identified that metabolites 1 and 3 can serve as drug candidate after further development.
某些蘑菇因其绝佳的口感以及含有多种必需维生素、矿物质和次生代谢产物,而被用作低热量食品补充剂。其中一些蘑菇具有治疗意义,被用于传统药物中。蘑菇细胞还可用作有机化合物衍生化的生物催化剂。在本研究中,从硫黄多孔菌(Laetiporus sulphureus (Bull.) Murrill)中分离出了3β-羟基-24-亚甲基羊毛甾-8-烯-21-酸(1)。将同一蘑菇的细胞培养物用于将乳腺癌药物依西美坦(2)生物转化为一种新的类似物18-羟基-6-亚甲基雄甾-1,4-二烯-3,17-二酮(3)。通过各种色谱技术对化合物1和3进行了纯化,并借助一维和二维核磁共振、高分辨电子电离质谱和红外光谱技术确定了它们的结构。由于化合物1也具有甾体骨架(如芳香酶抑制药物依西美坦(2)),因此还评估了代谢物1以及新的转化产物3的芳香酶抑制潜力。芳香酶在雌激素生物合成中起关键作用,因此抑制芳香酶是治疗雌激素受体阳性(ER+)乳腺癌的关键方法。化合物1和3表现出显著的芳香酶抑制作用,其IC值分别为590±0.03 nM和337.5±0.01 nM,而依西美坦的IC值为210.0±0.16 nM。此外,计算机模拟研究预测,这些抑制剂1 - 3能够占据活性位点并与该酶的催化重要残基相互作用。同时分子动力学模拟预测了芳香酶 - 配体复合物的稳定性。这些研究表明,代谢物1和3经过进一步开发后可作为候选药物。