Rodriguez-Gonzalez Agustin, Lin Tara, Ikeda Alan K, Simms-Waldrip Tiffany, Fu Cecilia, Sakamoto Kathleen M
Division of Hematology-Oncology, Mattel Children's Hospital, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California 90095-1752, USA.
Cancer Res. 2008 Apr 15;68(8):2557-60. doi: 10.1158/0008-5472.CAN-07-5989.
Misfolded or aggregated proteins have two fates: they are either refolded with the help of chaperones or degraded by the proteasome. Cells also have an alternative pathway that involves intracellular "storage bins" for misfolded intracellular proteins known as aggresomes. Aggresomes recruit motor proteins that transport misfolded or aggregated proteins to chaperones and proteasomes for subsequent destruction. There is emerging evidence that inhibiting the aggresome pathway leads to accumulation of misfolded proteins and apoptosis in tumor cells through autophagy. We discuss the role of aggresomes in cancer and the potential to target this pathway for therapy.
它们要么在伴侣蛋白的帮助下重新折叠,要么被蛋白酶体降解。细胞还有一条替代途径,涉及细胞内错误折叠的细胞内蛋白质的“储存库”,即聚集体。聚集体招募驱动蛋白,将错误折叠或聚集的蛋白质运输到伴侣蛋白和蛋白酶体进行后续破坏。越来越多的证据表明,抑制聚集体途径会导致肿瘤细胞中错误折叠蛋白质的积累,并通过自噬导致细胞凋亡。我们讨论了聚集体在癌症中的作用以及针对该途径进行治疗的潜力。