Zhang Hong, Sun Jia-Dong, Yan Ling-Jian, Zhao Xiao-Peng
Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Stomatology, Guangzhou, China.
Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, China; Department of Oral and Maxillofacial Surgery, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Biochem Biophys Res Commun. 2016 Sep 16;478(2):845-51. doi: 10.1016/j.bbrc.2016.08.035. Epub 2016 Aug 6.
Platelet-derived growth factor D (PDGF-D) signaling plays significant roles during the development and progression of human malignancies via interacting with the receptor of PDGF-D (PDGFR). Meanwhile, the majority of human tumor metastasis is closely associated with epithelial-mesenchymal transition (EMT). However, the underlying mechanism between PDGF-D/PDGFR signaling and EMT which involved in tumor metastasis remain dismal. This study aimed to investigate the role of PDGF-D signaling during EMT process of tongue squamous cell carcinoma (TSCC). In our study, the expression of PDGF-D and PDGFR were examined in primary TSCC samples and the expression of PDGF-D was also determined in TSCC cell lines. In addition, the correlation between PDGF-D expression and TSCC aggressive histopathological features was analyzed. Our results implied that upregulation of PDGFRβ in UM1 cells induced with exogenous PDGF-D can remarkably promote tumor cells invasiveness; conversely, when using small interfering RNA (siRNA), the invasiveness can be severely prohibited. Furthermore, PDGF-D downstream signal molecules p38, AKT, ERK and EMT biomarkers (E-cadherin, N-cadherin, Vimentin and snail) were measured using Western blot. Our results showed that PDGF-D can induce p38, AKT and ERK phosphorylation; downregulate epithelial markers and upregulate mesenchymal markers. On the contrary, PDGFRβ siRNA significantly prohibited p38, AKT and ERK phosphorylation; inhibited EMT process. Function analysis revealed that PDGFRβ siRNA obviously interfered with UM1 cell migration and invasion, according to transwell and wound healing assay. In conclusion, this study suggested that EMT process can be triggered by the PDGF-D/PDGFRβ axis in TSCC, and then involved in the tumor cell invasion via activation of p38/AKT/ERK/EMT pathway.
血小板衍生生长因子D(PDGF-D)信号通过与PDGF-D受体(PDGFR)相互作用,在人类恶性肿瘤的发生发展过程中发挥重要作用。同时,大多数人类肿瘤转移与上皮-间质转化(EMT)密切相关。然而,PDGF-D/PDGFR信号与参与肿瘤转移的EMT之间的潜在机制仍不清楚。本研究旨在探讨PDGF-D信号在舌鳞状细胞癌(TSCC)EMT过程中的作用。在我们的研究中,检测了原发性TSCC样本中PDGF-D和PDGFR的表达,并在TSCC细胞系中测定了PDGF-D的表达。此外,分析了PDGF-D表达与TSCC侵袭性组织病理学特征之间的相关性。我们的结果表明,外源性PDGF-D诱导的UM1细胞中PDGFRβ的上调可显著促进肿瘤细胞的侵袭性;相反,使用小干扰RNA(siRNA)时,侵袭性可被严重抑制。此外,使用蛋白质免疫印迹法检测了PDGF-D下游信号分子p38、AKT、ERK和EMT生物标志物(E-钙黏蛋白、N-钙黏蛋白、波形蛋白和蜗牛蛋白)。我们的结果表明,PDGF-D可诱导p38、AKT和ERK磷酸化;下调上皮标志物并上调间质标志物。相反,PDGFRβ siRNA显著抑制p38、AKT和ERK磷酸化;抑制EMT过程。功能分析表明,根据Transwell和伤口愈合试验,PDGFRβ siRNA明显干扰了UM1细胞的迁移和侵袭。总之,本研究表明,TSCC中EMT过程可由PDGF-D/PDGFRβ轴触发,然后通过激活p38/AKT/ERK/EMT途径参与肿瘤细胞侵袭。