Department of Physiology, University of Valencia, Valencia, Spain.
Faculty of Experimental Sciences, San Vicente Martir Catholic University, Valencia, Spain.
PLoS One. 2014 May 6;9(5):e96466. doi: 10.1371/journal.pone.0096466. eCollection 2014.
We previously reported an interorgan system in which stress-related hormones (corticosterone and noradrenaline), interleukin-6, and glutathione (GSH) coordinately regulate metastatic growth of highly aggressive B16-F10 melanoma cells. Corticosterone, at levels measured in tumor-bearing mice, also induces apoptotic cell death in metastatic cells with low GSH content. In the present study we explored the potential role of glucocorticoids in the regulation of metastatic cell death/survival during the early stages of organ invasion. Glucocorticoid receptor (GCR) knockdown decreased the expression and activity of γ-glutamylcysteine synthetase (γ-GCS), the rate-limiting step in GSH synthesis, in metastatic cells in vivo independent of the tumor location (liver, lung, or subcutaneous). The decrease in γ-GCS activity was associated with lower intracellular GSH levels. Nrf2- and p53-dependent down-regulation of γ-GCS was associated with a decrease in the activities of superoxide dismutase 1 and 2, catalase, glutathione peroxidase, and glutathione reductase, but not of the O2--generating NADPH oxidase. The GCR knockdown-induced decrease in antioxidant protection caused a drastic decrease in the survival of metastatic cells during their interaction with endothelial cells, both in vitro and in vivo; only 10% of cancer cells attached to the endothelium survived compared to 90% survival observed in the controls. This very low rate of metastatic cell survival was partially increased (up to 52%) in vivo by inoculating B16-F10 cells preloaded with GSH ester, which enters the cell and delivers free GSH. Taken together, our results indicate that glucocorticoid signaling influences the survival of metastatic cells during their interaction with the vascular endothelium.
我们之前报道了一个器官间系统,其中应激相关激素(皮质酮和去甲肾上腺素)、白细胞介素-6 和谷胱甘肽(GSH)协同调节高度侵袭性 B16-F10 黑色素瘤细胞的转移生长。在荷瘤小鼠中测量的皮质酮水平也会诱导具有低 GSH 含量的转移性细胞发生凋亡性细胞死亡。在本研究中,我们探讨了糖皮质激素在器官侵袭早期调节转移性细胞死亡/存活中的潜在作用。糖皮质激素受体(GCR)敲低降低了体内转移性细胞中γ-谷氨酰半胱氨酸合成酶(γ-GCS)的表达和活性,γ-GCS 是 GSH 合成的限速步骤,而与肿瘤位置(肝、肺或皮下)无关。γ-GCS 活性的降低与细胞内 GSH 水平降低有关。Nrf2 和 p53 依赖性下调 γ-GCS 与超氧化物歧化酶 1 和 2、过氧化氢酶、谷胱甘肽过氧化物酶和谷胱甘肽还原酶的活性降低有关,但与生成 O2-的 NADPH 氧化酶无关。GCR 敲低诱导的抗氧化保护降低导致转移性细胞在与内皮细胞相互作用过程中的存活率急剧下降,无论是在体外还是体内;与对照组观察到的 90%存活率相比,只有 10%的癌细胞附着在内皮细胞上存活。通过接种预先加载 GSH 酯的 B16-F10 细胞,体内转移性细胞的这种极低存活率部分增加(高达 52%),GSH 酯进入细胞并提供游离 GSH。总之,我们的结果表明,糖皮质激素信号影响转移性细胞在与血管内皮相互作用过程中的存活。