The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
PLoS One. 2011 Apr 29;6(4):e19390. doi: 10.1371/journal.pone.0019390.
The aggressiveness of pancreatic ductal adenocarcinoma (PDA) is characterized by its high metastatic potential and lack of effective therapies, which is the result of a lack of understanding of the mechanisms involved in promoting PDA metastases. We identified Annexin A2 (ANXA2), a member of the Annexin family of calcium-dependent phospholipid binding proteins, as a new molecule that promotes PDA invasion and metastases. We found ANXA2 to be a PDA-associated antigen recognized by post-treatment sera of patients who demonstrated prolonged survival following treatment with a PDA-specific vaccine. Cell surface ANXA2 increases with PDA development and progression. Knockdown of ANXA2 expression by RNA interference or blocking with anti-ANXA2 antibodies inhibits in vitro invasion of PDA cells. In addition, post-vaccination patient sera inhibits in vitro invasion of PDA cells, suggesting that therapeutic anti-ANXA2 antibodies are induced by the vaccine. Furthermore, cell-surface localization of ANXA2 is tyrosine 23 phosphorylation-dependent; and tyrosine 23 phosphorylation is required for PDA invasion. We demonstrated that tyrosine 23 phosphorylation resulting in surface expression of ANXA2 is required for TGFβ-induced, Rho-mediated epithelial-mesenchymal transition (EMT), linking the cellular function of ANXA2 which was previously shown to be associated with small GTPase-regulated cytoskeletal rearrangements, to the EMT process in PDA. Finally, using mouse PDA models, we showed that shRNA knock-down of ANXA2, a mutation at tyrosine 23, or anti-ANXA2 antibodies, inhibit PDA metastases and prolong mouse survival. Thus, ANXA2 is part of a novel molecular pathway underlying PDA metastases and a new target for development of PDA therapeutics.
胰腺导管腺癌 (PDA) 的侵袭性特征是其高转移性潜能和缺乏有效治疗方法,这是由于缺乏对促进 PDA 转移的机制的理解。我们发现 Annexin A2(ANXA2),钙依赖性磷脂结合蛋白 Annexin 家族的一个成员,是促进 PDA 侵袭和转移的新分子。我们发现 ANXA2 是 PDA 相关抗原,被接受 PDA 特异性疫苗治疗后具有延长生存时间的患者的治疗后血清识别。细胞表面 ANXA2 随 PDA 的发展和进展而增加。通过 RNA 干扰敲低 ANXA2 表达或用抗 ANXA2 抗体阻断可抑制 PDA 细胞的体外侵袭。此外,疫苗接种后的患者血清可抑制 PDA 细胞的体外侵袭,表明治疗性抗 ANXA2 抗体是由疫苗诱导的。此外,ANXA2 的细胞表面定位依赖于酪氨酸 23 磷酸化;并且酪氨酸 23 磷酸化是 PDA 侵袭所必需的。我们证明,导致 ANXA2 表面表达的酪氨酸 23 磷酸化是 TGFβ 诱导的 Rho 介导的上皮间质转化 (EMT) 所必需的,将 ANXA2 的细胞功能与先前显示与小 GTPase 调节的细胞骨架重排相关联,与 PDA 中的 EMT 过程联系起来。最后,使用小鼠 PDA 模型,我们表明 ANXA2 的 shRNA 敲低、酪氨酸 23 突变或抗 ANXA2 抗体可抑制 PDA 转移并延长小鼠生存时间。因此,ANXA2 是 PDA 转移的新分子途径的一部分,也是开发 PDA 治疗方法的新靶点。