Lu Dong, Zhang Hao, Fu Jiale, Qi Yanhua, Wang Xu, Wu Shishuang, Zhou Xiuping, Yu Rutong
Institute of Nervous System Diseases, Xuzhou Medical University, Xuzhou, China.
Brain Hospital, Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Cell Physiol Biochem. 2018;47(6):2445-2457. doi: 10.1159/000491618. Epub 2018 Jul 10.
BACKGROUND/AIMS: Golgi phosphoprotein 3 (GOLPH3) plays pro-malignancy roles in several types of cancer. However, the molecular mechanism underlying GOLPH3 promoting tumor progression remains poorly understood.
The expression of GOLPH3 and Wntless (Wls) in glioma tissues was examined by western blotting and immunohistochemistry. EdU incorporation assay and colony formation assay was used to examine the cell growth ability. The effect of GOLPH3 on Wls recycling, Wnt secretion and β-catenin activity was detected using western blotting, immunofluorescence, RT-PCR, ELISA or luciferase assay.
The protein levels of GOLPH3 and Wls were upregulated and positively correlated with each other in human glioma tissues. The promoting effect of GOLPH3 on glioma cell proliferation was partially mediated by Wls. In addition, GOLPH3 interacted with Wls and GOLPH3 down-regulation drove Wls into lysosome for degradation, inhibiting its recycling to golgi and the plasma membrane. Importantly, GOLPH3 down-regulation inhibited Wnt2b secretion and decreased β-catenin level and transcription activity.
This study provides a brand new evidence that GOLPH3 promotes glioma cell proliferation by facilitating Wls recycling and Wnt/β-catenin signaling. Our findings suggest a rationale for targeting the GOLPH3-Wls-Wnt axis as a promising therapeutic approach for glioblastoma.
背景/目的:高尔基体磷蛋白3(GOLPH3)在多种癌症中发挥促癌作用。然而,GOLPH3促进肿瘤进展的分子机制仍知之甚少。
采用蛋白质免疫印迹法和免疫组织化学法检测胶质瘤组织中GOLPH3和无翅型MMTV整合位点家族成员(Wls)的表达。采用EdU掺入法和集落形成试验检测细胞生长能力。采用蛋白质免疫印迹法、免疫荧光法、逆转录-聚合酶链反应、酶联免疫吸附测定法或荧光素酶测定法检测GOLPH3对Wls循环、Wnt分泌和β-连环蛋白活性的影响。
在人脑胶质瘤组织中,GOLPH3和Wls的蛋白水平上调且呈正相关。GOLPH3对胶质瘤细胞增殖的促进作用部分由Wls介导。此外,GOLPH3与Wls相互作用,GOLPH3下调促使Wls进入溶酶体降解,抑制其循环至高尔基体和质膜。重要的是,GOLPH3下调抑制Wnt2b分泌,降低β-连环蛋白水平和转录活性。
本研究提供了全新的证据,表明GOLPH3通过促进Wls循环和Wnt/β-连环蛋白信号传导促进胶质瘤细胞增殖。我们的研究结果为靶向GOLPH3-Wls-Wnt轴作为胶质母细胞瘤一种有前景的治疗方法提供了理论依据。