Departments of Gastroenterology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.
Departments of Cardiovascular, Zigong First People's Hospital, Sichuan 643000, China.
Aging (Albany NY). 2021 Sep 13;13(17):21571-21586. doi: 10.18632/aging.203497.
Early metastasis of pancreatic cancer (PC) leads to high mortality, and the underlying mechanism of metastasis remains unclear. Tumor necrosis factor superfamily member 9 (TNFSF9) is associated with poor prognosis in PC. Here, we investigated the effect of TNFSF9 on PC proliferation and apoptosis, and focused on the effect of TNFSF9 on PC metastasis and its potential mechanism. We found that TNFSF9 promotes PC metastasis and , and may be partially dependent on the Wnt/Snail signaling pathway. In addition, TNFSF9 also regulates the release of cytokines IL-10 and transforming growth factor-β (TGF-β) in pancreatic cancer cells through Wnt signaling to induce the M2 polarization of macrophages and promote the migration of PC cells. Overall, our study found that TNFSF9 may directly promote PC metastasis or indirectly promote PC metastasis through macrophage M2 polarization. Our study provides a new costimulatory target for the treatment of PC.
早期胰腺癌(PC)转移导致高死亡率,转移的潜在机制仍不清楚。肿瘤坏死因子超家族成员 9(TNFSF9)与 PC 的不良预后相关。在这里,我们研究了 TNFSF9 对 PC 增殖和凋亡的影响,并重点研究了 TNFSF9 对 PC 转移的影响及其潜在机制。我们发现 TNFSF9 促进 PC 转移,并可能部分依赖于 Wnt/Snail 信号通路。此外,TNFSF9 还通过 Wnt 信号调节胰腺癌细胞中细胞因子白细胞介素 10(IL-10)和转化生长因子-β(TGF-β)的释放,诱导巨噬细胞 M2 极化,并促进 PC 细胞的迁移。总的来说,我们的研究发现 TNFSF9 可能通过直接促进 PC 转移或通过巨噬细胞 M2 极化间接促进 PC 转移。我们的研究为 PC 的治疗提供了一个新的共刺激靶点。