Computational Biology, Bioinformatics and Genomics Program, Department of Biological Sciences, University of Maryland, College Park, MD 20742, USA.
International Cancer Center, Shenzhen University Medical School, Shenzhen 518054, China.
Molecules. 2023 Sep 27;28(19):6819. doi: 10.3390/molecules28196819.
Human cell surface receptor CD58, also known as lymphocyte function-associated antigen 3 (LFA-3), plays a critical role in the early stages of immune response through interacting with CD2. Recent research identified CD58 as a surface marker of colorectal cancer (CRC), which can upregulate the Wnt pathway and promote self-renewal of colorectal tumor-initiating cells (CT-ICs) by degradation of Dickkopf 3. In addition, it was also shown that knockdown of CD58 significantly impaired tumor growth. In this study, we developed a structure-based virtual screening pipeline using Autodock Vina and binding analysis and identified a group of small molecular compounds having the potential to bind with CD58. Five of them significantly inhibited the growth of the SW620 cell line in the following in vitro studies. Their proposed binding models were further verified by molecular dynamics (MD) simulations, and some pharmaceutically relevant chemical and physical properties were predicted. The hits described in this work may be considered interesting leads or structures for the development of new and more efficient CD58 inhibitors.
人类细胞表面受体 CD58,也称为淋巴细胞功能相关抗原 3(LFA-3),通过与 CD2 相互作用,在免疫反应的早期阶段发挥关键作用。最近的研究将 CD58 鉴定为结直肠癌(CRC)的表面标志物,它可以通过降解 Dickkopf 3 上调 Wnt 通路并促进结直肠肿瘤起始细胞(CT-IC)的自我更新。此外,还表明敲低 CD58 可显著抑制肿瘤生长。在这项研究中,我们使用 Autodock Vina 开发了一种基于结构的虚拟筛选管道,并进行了结合分析,鉴定出了一组具有与 CD58 结合潜力的小分子化合物。其中 5 种在随后的体外研究中显著抑制了 SW620 细胞系的生长。通过分子动力学(MD)模拟进一步验证了它们的建议结合模型,并预测了一些与药物相关的化学和物理性质。本文描述的这些化合物可能被认为是开发新型、更有效的 CD58 抑制剂的有趣先导化合物或结构。