Takagi Kohji, Shimomura Akiko, Imura Johji, Mori Hisashi, Noguchi Akira, Tanaka Shinichi, Minamisaka Takashi, Nishida Takeshi, Hatta Hideki, Nakajima Takahiko
Department of Diagnostic Pathology, Faculty of Medicine, Academic Assembly, University of Toyama, Toyama 930-0194, Japan.
Department of Molecular Neuroscience, Faculty of Medicine, Academic Assembly, University of Toyama, Toyama 930-0194, Japan.
Oncol Lett. 2022 Jan;23(1):14. doi: 10.3892/ol.2021.13132. Epub 2021 Nov 11.
Pancreatic cancer is a malignant neoplasm with high invasiveness and poor prognosis. In a previous study, a highly invasive pancreatic cancer cell line was established and found to feature enhanced interleukin-32 (IL-32) expression. However, whether IL-32 promotes the invasiveness by enhancing or suppressing the expression of IL-32 through regulating downstream molecules was unclear. To investigate the effect of IL-32, cells were established with high levels of expression or downregulated IL-32; their invasive ability was measured using a real-time measurement system and the expression of some candidate downstream molecules involved in invasion was evaluated in the two cell types. The morphological changes in both cell types and the localization of IL-32 expression in pancreatic cancer tissues were studied using immunohistochemistry. Among the several splice variants of IL-32, cells transfected with the ε isoform had increased invasiveness, whereas the IL-32-suppressed cells had reduced invasiveness. Several downstream molecules, whose expression was changed in the two cell types, were monitored. Notably, changes of E-cadherin, CLDN1, CD44, CTGF and Wnt were documented. The morphologies of the two cell types differed from the original cell line. Immunohistochemically, the expression of IL-32 was observed only in tumor cells and not in normal pancreatic cells. In conclusion, IL-32 was found to promote the invasiveness of pancreatic cancer cells by regulating downstream molecules.
胰腺癌是一种具有高侵袭性和不良预后的恶性肿瘤。在先前的一项研究中,建立了一种高侵袭性的胰腺癌细胞系,并发现其白细胞介素-32(IL-32)表达增强。然而,IL-32是通过增强还是抑制IL-32的表达来调节下游分子从而促进侵袭性尚不清楚。为了研究IL-32的作用,构建了IL-32高表达或下调的细胞系;使用实时测量系统测量它们的侵袭能力,并评估这两种细胞类型中一些参与侵袭的候选下游分子的表达。使用免疫组织化学研究了两种细胞类型的形态变化以及胰腺癌组织中IL-32表达的定位。在IL-32的几种剪接变体中,转染ε亚型的细胞侵袭性增加,而IL-32抑制的细胞侵袭性降低。监测了在两种细胞类型中表达发生变化的几种下游分子。值得注意的是,记录了E-钙黏蛋白、紧密连接蛋白1、CD44、结缔组织生长因子和Wnt的变化。两种细胞类型的形态与原始细胞系不同。免疫组织化学显示,IL-32仅在肿瘤细胞中表达,而在正常胰腺细胞中不表达。总之,发现IL-32通过调节下游分子促进胰腺癌细胞的侵袭性。