Pihlstrøm Nicklas, Jin Yang, Nenseth Zeynep, Kuzu Omer F, Saatcioglu Fahri
Department of Biosciences, University of Oslo, 0315 Oslo, Norway.
Institute for Cancer Genetics and Informatics, Oslo University Hospital, 0188 Oslo, Norway.
Cancers (Basel). 2021 Mar 30;13(7):1579. doi: 10.3390/cancers13071579.
Inflammatory events and dysregulated cytokine expression are implicated in prostate cancer (PCa), but the underlying molecular mechanisms are poorly understood at present. We have previously identified six transmembrane protein of the prostate 2 (STAMP2, also known as STEAP4) as an androgen-regulated gene, as well as a key regulator of PCa growth and survival. STAMP2 is also regulated by, and participates in, inflammatory signaling in other tissues and pathologies. Here, we show that the proinflammatory cytokines interleukin 6 (IL-6) and Interleukin 1 beta (IL-1β) significantly increase and strongly synergize in promoting STAMP2 expression in PCa cells. The two cytokines increase androgen-induced STAMP2 expression, but not expression of other known androgen target genes, suggesting a unique interplay of androgens and cytokines in regulating STAMP2 expression. Interestingly, STAMP2 knockdown significantly increased the ability of IL-6 and IL-1β to inhibit PCa cell growth in vitro. These results suggest that STAMP2 may represent a unique node through which inflammatory events mediate their effects on PCa growth and survival.
炎症事件和细胞因子表达失调与前列腺癌(PCa)有关,但目前对其潜在分子机制了解甚少。我们之前已确定前列腺六次跨膜蛋白2(STAMP2,也称为STEAP4)是一种雄激素调节基因,也是PCa生长和存活的关键调节因子。STAMP2在其他组织和病理状态下也受炎症信号调节并参与其中。在此,我们表明促炎细胞因子白细胞介素6(IL-6)和白细胞介素1β(IL-1β)在促进PCa细胞中STAMP2表达方面显著增加且具有强烈协同作用。这两种细胞因子增加雄激素诱导的STAMP2表达,但不增加其他已知雄激素靶基因的表达,提示雄激素和细胞因子在调节STAMP2表达方面存在独特的相互作用。有趣的是,敲低STAMP2显著增强了IL-6和IL-1β在体外抑制PCa细胞生长的能力。这些结果表明,STAMP2可能代表一个独特的节点,炎症事件通过该节点介导其对PCa生长和存活的影响。