Setty Bhuvana A, Pillay Smiley Natasha, Pool Caitlyn M, Jin Yi, Liu Yusen, Nelin Leif D
Pulmonary Hypertension Group, Center for Perinatal Research The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Department of Pediatrics, The Ohio State University, Columbus, Ohio.
Physiol Rep. 2017 Mar;5(6). doi: 10.14814/phy2.13175.
Solid tumors can often be hypoxic in regions, and cancer cells can respond to hypoxia with an increase in proliferation and a decrease in apoptosis, leading to a net increase in viable cell numbers. We have recently found that in an osteosarcoma cell line, hypoxia-induced proliferation depends on arginase II induction. Epidermal growth factor receptor (EGFR) has been shown to mediate the hypoxia-induced cellular proliferation in some cancer cell lines. We hypothesized that hypoxia-induced proliferation of HeLa cells would depend on arginase II induction and that this induction of arginase II would occur through EGFR activation. Exposure of HeLa cells to hypoxia resulted in an upregulation of arginase II mRNA and protein levels, with no effect on arginase I expression. Hypoxia also resulted in significantly greater viable cell numbers than did normoxia. The hypoxia-induced increase in viable cell numbers was prevented by either a small molecule inhibitor of arginase or siRNA targeting arginase II Overexpression of arginase II resulted in an increase in viable cell numbers both in normoxia and hypoxia. Hypoxia caused a substantial induction of both epidermal growth factor (EGF) and EGFR Preventing hypoxia-induced EGFR expression using siRNA abolished hypoxia-induced arginase II expression and the increase in viable cell numbers. Treatment with EGF in normoxia not only induced arginase II expression but also resulted in an increase in viable cell numbers. Blocking EGF interactions with EGFR using either an EGF neutralizing antibody or an EGFR antibody prevented the hypoxia-induced increase in viable cell numbers. These results demonstrate an EGF/EGFR/arginase II pathway that is necessary for hypoxic proliferation in HeLa cells.
实体瘤在某些区域常常会出现缺氧情况,癌细胞对缺氧的反应是增殖增加而凋亡减少,从而导致活细胞数量净增加。我们最近发现,在一种骨肉瘤细胞系中,缺氧诱导的增殖依赖于精氨酸酶II的诱导。表皮生长因子受体(EGFR)已被证明在某些癌细胞系中介导缺氧诱导的细胞增殖。我们假设,缺氧诱导的HeLa细胞增殖将依赖于精氨酸酶II的诱导,并且这种精氨酸酶II的诱导将通过EGFR激活而发生。将HeLa细胞暴露于缺氧环境中会导致精氨酸酶II的mRNA和蛋白质水平上调,而对精氨酸酶I的表达没有影响。与常氧相比,缺氧也导致活细胞数量显著增加。精氨酸酶的小分子抑制剂或靶向精氨酸酶II的siRNA均可阻止缺氧诱导的活细胞数量增加。精氨酸酶II的过表达导致常氧和缺氧条件下活细胞数量均增加。缺氧导致表皮生长因子(EGF)和EGFR大量诱导。使用siRNA阻止缺氧诱导的EGFR表达可消除缺氧诱导的精氨酸酶II表达以及活细胞数量的增加。在常氧条件下用EGF处理不仅诱导了精氨酸酶II的表达,还导致活细胞数量增加。使用EGF中和抗体或EGFR抗体阻断EGF与EGFR的相互作用可阻止缺氧诱导的活细胞数量增加。这些结果证明了一条EGF/EGFR/精氨酸酶II途径,该途径对于HeLa细胞的缺氧增殖是必需的。