a The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine , Baltimore , MD , USA.
b Department of Oncology , Johns Hopkins University School of Medicine , Baltimore , MD , USA.
Cell Adh Migr. 2017 Sep 3;11(5-6):514-523. doi: 10.1080/19336918.2016.1259057. Epub 2017 Feb 6.
Pancreatic adenocarcinoma (PDA) is characterized by a dense desmoplastic reaction that comprises 60-90% of the tumor, while only 10-40% of the tumor is composed of malignant epithelial cells. This desmoplastic reaction is composed of stromal fibroblast cells, extracellular matrix proteins, and immune cells. Accumulating evidence has suggested that the stromal and epithelial cell compartments interact during the pathogenesis of this disease. Therefore, it is important to identify the signaling pathways responsible for this interaction to better understand the mechanisms by which PDA invades and metastasizes. Here, we show that secreted stromal factors induce invasion of PDA cells. Specifically, hedgehog signaling from the tumor cells induces tenascin C (TnC) secretion from the stromal cells that acts back upon the tumor cells in a paracrine fashion to induce the invasion of PDA cells through its' receptor annexin A2 (AnxA2). Therefore, blocking the interaction between TnC and AnxA2 has the potential to prevent liver metastasis in PDA.
胰腺导管腺癌(PDA)的特征是致密的纤维母细胞反应,占肿瘤的 60-90%,而只有 10-40%的肿瘤由恶性上皮细胞组成。这种纤维母细胞反应由间质成纤维细胞、细胞外基质蛋白和免疫细胞组成。越来越多的证据表明,在这种疾病的发病机制中,基质和上皮细胞区室相互作用。因此,重要的是要确定负责这种相互作用的信号通路,以更好地了解 PDA 侵袭和转移的机制。在这里,我们表明,分泌的基质因子诱导 PDA 细胞的侵袭。具体来说,肿瘤细胞中的 hedgehog 信号诱导基质细胞分泌 tenascin C(TnC),以旁分泌的方式作用于肿瘤细胞,通过其受体 annexin A2(AnxA2)诱导 PDA 细胞的侵袭。因此,阻断 TnC 和 AnxA2 之间的相互作用有可能预防 PDA 中的肝转移。