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Advances and Insights of APC-Asef Inhibitors for Metastatic Colorectal Cancer Therapy

机译:转移性结直肠癌治疗的APC-ASEF抑制剂的进展和见解

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In colorectal cancer, adenomatous polyposis coli (APC) directly interacts with the Rho guanine nucleotide exchange factor 4 (Asef) and releases its GEF activity. Activated Asef promotes the aberrant migration and invasion of colorectal cancer cell through a CDC42-mediated pathway. Knockdown of either APC or Asef significantly decreases the migration of colorectal cancer cells. Therefore, disrupting the APC - Asef interaction is a promising strategy for the treatment of invasive colorectal cancer. With the growth of structural information, APC-Asef inhibitors have been designed, providing hope for colorectal cancer therapy. Here, we will review the APC-Asef interaction in cancer biology, the structural complex of APC-Asef, two generations of peptide inhibitors of APC-Asef, and small molecule inhibitors of APC-Asef, focusing on research articles over the past 30 years. We posit that these advances in the discovery of APC-Asef inhibitors establish the protein-protein interaction (PPI) as targetable and provide a framework for other PPI programs.
机译:在结直肠癌中,腺瘤性息肉蛋白Coli(APC)直接与Rho鸟嘌呤核苷酸交换因子4(ASEF)相互作用并释放其GEF活性。活化的ASEF通过CDC42介导的途径促进了成直肠癌细胞的异常迁移和侵袭。 APC或ASEF的敲低显着降低结肠直肠癌细胞的迁移。因此,破坏APC - ASEF相互作用是治疗侵袭性结直肠癌的有希望的策略。随着结构信息的增长,设计了APC-ASEF抑制剂,为结肠直肠癌治疗提供了希望。在这里,我们将审查癌症生物学的APC-ASEF相互作用,APC-ASEF的结构络合物,APC-ASEF的两代肽抑制剂,以及APC-ASEF的小分子抑制剂,在过去30年中关注研究文章。我们在发现APC-ASEF抑制剂的发现中的这些进步建立蛋白质 - 蛋白质相互作用(PPI)作为靶向,并为其他PPI程序提供框架。

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