Department of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, 08826, South Korea; Tumor Microenvironment Global Core Research Center, College of Pharmacy, Seoul National University, Seoul, 08826, South Korea.
Tumor Microenvironment Global Core Research Center, College of Pharmacy, Seoul National University, Seoul, 08826, South Korea.
Biochem Biophys Res Commun. 2020 Dec 17;533(4):995-1003. doi: 10.1016/j.bbrc.2020.08.015. Epub 2020 Oct 2.
PIN1, the peptidyl-prolyl isomerase (PPIase), is an enzyme that changes the conformation of phosphoproteins. The conformational change induced by PIN1 alters the function and stability of the target proteins. PIN1 is overexpressed in many different types of malignancies, including breast, lung, cervical, brain and colorectal tumors. PIN1 overexpression has been associated with activation of multiple oncogenic signaling pathways during tumor development. Hypoxia-inducible factor 2α (HIF-2α), a transcription factor activated in hypoxia, plays a role in erythropoiesis, glycolysis, tissue invasion, metastasis and angiogenesis. In this study, we found the direct interaction between HIF-2α and PIN1 in colorectal cancer HCT116 cells. Notably, serine 16 and lysine 63 residues of PIN1 were critical for its interaction with HIF-2α. When PIN1 protein was silenced by transient transfection of PIN1 short interfering RNA, the expression of HIF-2α was attenuated under a hypoxic condition. Moreover, genetic and pharmacologic inhibition of PIN1 abrogated the expression of vascular endothelial growth factor and angiogenesis. The cycloheximide chase experiment revealed the stabilization of HIF-2α by PIN1. Both WW and PPIase domains of PIN1 appear to be critical for its interaction with HIF-2α.
PIN1 是一种肽基脯氨酰顺反异构酶(PPIase),能够改变磷酸化蛋白的构象。PIN1 诱导的构象变化改变了靶蛋白的功能和稳定性。PIN1 在许多不同类型的恶性肿瘤中过度表达,包括乳腺癌、肺癌、宫颈癌、脑癌和结直肠癌。在肿瘤发生发展过程中,PIN1 的过表达与多种致癌信号通路的激活有关。缺氧诱导因子 2α(HIF-2α)是一种在缺氧时被激活的转录因子,在红细胞生成、糖酵解、组织侵袭、转移和血管生成中发挥作用。在本研究中,我们在结直肠癌细胞 HCT116 中发现了 HIF-2α 与 PIN1 的直接相互作用。值得注意的是,PIN1 的丝氨酸 16 和赖氨酸 63 残基对于其与 HIF-2α 的相互作用至关重要。当通过瞬时转染 PIN1 短发夹 RNA 沉默 PIN1 蛋白时,在缺氧条件下 HIF-2α 的表达减弱。此外,PIN1 的遗传和药理学抑制消除了血管内皮生长因子和血管生成的表达。环己酰亚胺追踪实验显示 PIN1 稳定了 HIF-2α。PIN1 的 WW 和 PPIase 结构域似乎都对其与 HIF-2α 的相互作用至关重要。