Harper Cancer Research Institute, University of Notre Dame, South Bend, IN 46556, USA; Integrated Biomedical Sciences Program, University of Notre Dame, South Bend, IN 46556, USA.
Harper Cancer Research Institute, University of Notre Dame, South Bend, IN 46556, USA; Department of Biological Sciences, University of Notre Dame, South Bend, IN 46556, USA.
Neoplasia. 2018 Jan;20(1):12-24. doi: 10.1016/j.neo.2017.10.004. Epub 2017 Nov 23.
Pancreatic ductal adenocarcinoma (PDAC) presents at metastatic stage in over 50% of patients. With a survival rate of just 2.7% for patients presenting with distant disease, it is imperative to uncover novel mechanisms capable of suppressing metastasis in PDAC. Previously, we reported that the loss of metastasis suppressor protein 1 (MTSS1) in PDAC cells results in significant increase in cellular migration and invasion. Conversely, we also found that overexpressing MTSS1 in metastatic PDAC cell lines corresponds with not only decreased metastatic phenotype, but also greater overall survival. While it is known that MTSS1 is downregulated in late-stage PDAC, the mechanism behind that loss has not yet been elucidated. Here, we build off our previous findings to present a novel regulatory mechanism for the stabilization of MTSS1 via the tumor suppressor protein phosphatase and tensin homolog (PTEN). We show that PTEN loss in PDAC cells results in a decrease in MTSS1 expression and increased metastatic potential. Additionally, we demonstrate that PTEN forms a complex with MTSS1 in order to stabilize and protect it from proteasomal degradation. Finally, we show that the inflammatory tumor microenvironment, which makes up over 90% of PDAC tumor bulk, is capable of downregulating PTEN expression through secretion of miRNA-23b, potentially uncovering a novel extrinsic mechanism of MTSS1 regulation. Collectively, these data offer new insight into the role and regulation of MTSS1in suppressing tumor cell invasion and migration and help shed light as to what molecular mechanisms could be leading to early cell dissemination in PDAC.
胰腺导管腺癌(PDAC)在超过 50%的患者中处于转移阶段。对于远处转移的患者,生存率仅为 2.7%,因此迫切需要发现能够抑制 PDAC 转移的新机制。先前,我们报道了 PDAC 细胞中转移抑制蛋白 1(MTSS1)的缺失会导致细胞迁移和侵袭显著增加。相反,我们还发现,转移性 PDAC 细胞系中 MTSS1 的过表达不仅与转移性表型降低有关,而且与总生存期延长有关。虽然已知 MTSS1 在晚期 PDAC 中下调,但导致其缺失的机制尚未阐明。在这里,我们根据之前的研究结果,提出了一个通过肿瘤抑制蛋白磷酸酶和张力蛋白同源物(PTEN)稳定 MTSS1 的新调控机制。我们表明,PDAC 细胞中 PTEN 的缺失会导致 MTSS1 表达减少和转移潜能增加。此外,我们证明了 PTEN 与 MTSS1 形成复合物,以稳定和保护其免受蛋白酶体降解。最后,我们表明,占 PDAC 肿瘤块 90%以上的炎症肿瘤微环境能够通过分泌 miRNA-23b 下调 PTEN 表达,这可能揭示了 MTSS1 调控的一种新的外在机制。总的来说,这些数据为 MTSS1 在抑制肿瘤细胞侵袭和迁移中的作用和调控提供了新的见解,并有助于阐明哪些分子机制可能导致 PDAC 中早期细胞扩散。