El Hassab Mahmoud A, Eldehna Wagdy M, Hassan Ghaneya S, Abou-Seri Sahar M
Department of Medicinal Chemistry, Faculty of Pharmacy, King Salman International University (KSIU), South Sinai, Ras Sudr, 46612, Egypt.
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Kafrelsheikh University, P.O. Box 33516, Kafrelsheikh, Egypt.
BMC Chem. 2025 Feb 1;19(1):30. doi: 10.1186/s13065-025-01389-2.
Presently, humanity is confronted with a range of diseases that have high death rates, especially those linked to cancerous growths. Several enzymes and proteins have been discovered as highly attractive targets for cancer treatment. The PARP family consists of 17 members and plays a crucial role in repairing DNA damage, which enables the survival of cancer cells. PARP-1 and, to a lesser extent, PARP-2 display above 90% activity in response to DNA damage, thereby distinguishing them apart from other members of the PARP family. Elevated levels of PARP-1 were observed in many types of tumor cells, such as breast, lung, ovarian, prostate, and melanomas. In an attempt to provide a future guide for developing selective inhibitors for PARP-1 over PARP-2 to minimize the resulting side effects from PARP-2 inhibitors, we constructed a structure-based virtual screening approach (SBVS). Firstly. A 3D pharmacophore was constructed based on the interaction of the selective inhibitor compound IV. After that, a database of nearly 450,000 phthalimide-containing inhibitors was screened through the validated pharmacophore, and 165 compounds were retrieved. The retrieved compounds were docked into the active site of PARP-1 where only 5 compounds MWGS-1-5 achieved a favorable docking score than the reference IV (-16.8 Kcal/mol). Redocking of the five compounds should have excellent selectivity for PARP-1 over PARP-2, especially compound MWGS-1. Further endorsement via molecular dynamics has proven higher affinity and selectivity for MWGS-1 towards PARP-1 over PARP-2, in which PARP-1- MWGS-1 and PARP-1- MWGS-1 achieved RMSD values of 1.42 and 2.8 Å, respectively.
目前,人类面临着一系列死亡率很高的疾病,尤其是那些与癌性生长相关的疾病。已经发现几种酶和蛋白质是极具吸引力的癌症治疗靶点。PARP家族由17个成员组成,在修复DNA损伤中起关键作用,这使得癌细胞得以存活。PARP-1以及在较小程度上的PARP-2在响应DNA损伤时显示出90%以上的活性,从而将它们与PARP家族的其他成员区分开来。在许多类型的肿瘤细胞中都观察到PARP-1水平升高,如乳腺癌、肺癌、卵巢癌、前列腺癌和黑色素瘤。为了为开发对PARP-1比对PARP-2具有选择性的抑制剂提供未来指导,以尽量减少PARP-2抑制剂产生的副作用,我们构建了一种基于结构的虚拟筛选方法(SBVS)。首先,基于选择性抑制剂化合物IV的相互作用构建了一个3D药效团。之后,通过经过验证的药效团筛选了一个近450,000种含邻苯二甲酰亚胺抑制剂的数据库,检索到165种化合物。将检索到的化合物对接至PARP-1的活性位点,其中只有5种化合物MWGS-1-5获得了比参考化合物IV(-16.8千卡/摩尔)更好的对接分数。这五种化合物的重新对接应该对PARP-1比对PARP-2具有优异的选择性,尤其是化合物MWGS-1。通过分子动力学的进一步验证证明,MWGS-1对PARP-1比对PARP-2具有更高的亲和力和选择性,其中PARP-1-MWGS-1和PARP-1-MWGS-1的均方根偏差(RMSD)值分别为1.42和2.8 Å。