National Cancer Institute-Designated Cancer Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA.
Moores Cancer Center, University of California, San Diego, La Jolla, CA.
J Exp Med. 2020 Sep 7;217(9). doi: 10.1084/jem.20200388.
Tumor cells rely on glutamine to fulfill their metabolic demands and sustain proliferation. The elevated consumption of glutamine can lead to intratumoral nutrient depletion, causing metabolic stress that has the potential to impact tumor progression. Here, we show that nutrient stress caused by glutamine deprivation leads to the induction of epithelial-mesenchymal transition (EMT) in pancreatic ductal adenocarcinoma (PDAC) cells. Mechanistically, we demonstrate that glutamine deficiency regulates EMT through the up-regulation of the EMT master regulator Slug, a process that is dependent on both MEK/ERK signaling and ATF4. We find that Slug is required in PDAC cells for glutamine deprivation-induced EMT, cell motility, and nutrient stress survival. Importantly, we decipher that Slug is associated with nutrient stress in PDAC tumors and is required for metastasis. These results delineate a novel role for Slug in the nutrient stress response and provide insight into how nutrient depletion might influence PDAC progression.
肿瘤细胞依赖于谷氨酰胺来满足其代谢需求并维持增殖。谷氨酰胺的消耗增加会导致肿瘤内营养物质枯竭,从而导致代谢应激,有可能影响肿瘤的进展。在这里,我们表明,谷氨酰胺剥夺引起的营养应激导致胰腺导管腺癌 (PDAC) 细胞中上皮-间充质转化 (EMT) 的诱导。在机制上,我们证明谷氨酰胺缺乏通过 EMT 主调控因子 Slug 的上调来调节 EMT,这一过程依赖于 MEK/ERK 信号和 ATF4。我们发现 Slug 在 PDAC 细胞中是谷氨酰胺剥夺诱导的 EMT、细胞迁移和营养应激存活所必需的。重要的是,我们揭示 Slug 与 PDAC 肿瘤中的营养应激有关,并且是转移所必需的。这些结果描绘了 Slug 在营养应激反应中的新作用,并深入了解营养物质耗竭如何影响 PDAC 的进展。