Department of Gastroenterology, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, 1665 Kongjiang Road, Shanghai, 200092, China.
Sci Rep. 2017 Apr 3;7:45895. doi: 10.1038/srep45895.
Transmembrane-4-L-six-family-1(TM4SF1), a four-transmembrane L6 family member, is highly expressed in various pancreatic cancer cell lines and promotes cancer cells metastasis. However, the TM4SF1-associated signaling network in metastasis remains unknown. In the present study, we found that TM4SF1 affected the formation and function of invadopodia. Silencing of TM4SF1 reduced the expression of DDR1 significantly in PANC-1 and AsPC-1 cells. Through double fluorescence immuno-staining and Co-immunoprecipitation, we also found that TM4SF1 colocalized with DDR1 and had an interaction with DDR1. In addition, upregulating the expression of DDR1 rescued the inhibitory effects of cell migration and invasion, the expression of MMP2 and MMP9 and the formation and function of invadopodia when TM4SF1 silenced. In pancreatic cancer tissues, qRT-PCR and scatter plots analysis further determined that TM4SF1 had a correlation with DDR1. Collectively, our study provides a novel regulatory pathway involving TM4SF1, DDR1, MMP2 and MMP9, which promotes the formation and function of invadopodia to support cell migration and invasion in pancreatic cancer.
跨膜 4 结构域家族 1(TM4SF1)是四跨膜 L6 家族成员,在各种胰腺癌细胞系中高度表达,并促进癌细胞转移。然而,转移过程中 TM4SF1 相关的信号网络尚不清楚。在本研究中,我们发现 TM4SF1 影响了侵袭伪足的形成和功能。沉默 TM4SF1 可显著降低 PANC-1 和 AsPC-1 细胞中 DDR1 的表达。通过双荧光免疫染色和共免疫沉淀,我们还发现 TM4SF1 与 DDR1 共定位并与 DDR1 相互作用。此外,上调 DDR1 的表达可挽救 TM4SF1 沉默时对细胞迁移和侵袭、MMP2 和 MMP9 表达以及侵袭伪足形成和功能的抑制作用。在胰腺癌组织中,qRT-PCR 和散点图分析进一步确定 TM4SF1 与 DDR1 相关。总之,我们的研究提供了一个涉及 TM4SF1、DDR1、MMP2 和 MMP9 的新的调节途径,该途径促进侵袭伪足的形成和功能,从而支持胰腺癌中的细胞迁移和侵袭。