Sun J C, He F, Yi W, Wan M H, Li R, Wei X, Wu R, Niu D L
Department of Radiation Oncology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Genet Mol Res. 2015 Dec 22;14(4):18110-20. doi: 10.4238/2015.December.22.37.
Hypoxia-inducible factor-2 alpha (HIF-2α) has been shown to regulate cell stemness, although the expression and effects of HIF-2α in lung cancer stem cells remained unclear. This study investigated HIF-2α expression in lung cancer stem cells, as well as the relationship between HIF-2α expression and radioresistance in lung cancer cells. Stem-like cells (CD133(+)) in the non-small-cell lung cancer cell line A549 were enriched by serum-free culture conditions, and CD133(+) cells were sorted via fluorescence-activated cell sorting. A549 cells were treated with middle-infrared radiation, and the level of HIF-2α expression was determined by a quantitative polymerase chain reaction assay and western blot analysis. The level of HIF-2α expression in tissue sections from 50 cases of clinically confirmed non-small-cell lung cancer was determined via immunohistochemical analysis, and its correlation with prognosis after radiotherapy was analyzed. HIF-2α levels in CD133(+) cells were significantly higher than those in CD133(-) cells (P = 0.032). However, after radiation treatment, these levels were significantly upregulated in both CD133(+) and CD133(-) cells (P = 0.031 and P = 0.023, respectively). After irradiation, the proportions of apoptotic, dead, and autophagic CD133(+) A549 cells were considerably lower than those of CD133(-) A549 cells (P < 0.05). Furthermore, the recovery of carcinoembryonic antigen to pre-radiation levels was more rapid in lung cancer patients with high levels of HIF-2α expression, and these patients had shorter survival times (P = 0.018). HIF-2α is highly expressed in lung cancer stem cells, which may lead to radioresistance. In conclusion, HIF-2α is a potential prognostic marker for lung cancer.
缺氧诱导因子-2α(HIF-2α)已被证明可调节细胞干性,尽管HIF-2α在肺癌干细胞中的表达及作用仍不清楚。本研究调查了肺癌干细胞中HIF-2α的表达情况,以及HIF-2α表达与肺癌细胞放射抗性之间的关系。通过无血清培养条件富集非小细胞肺癌细胞系A549中的干细胞样细胞(CD133(+)),并通过荧光激活细胞分选对CD133(+)细胞进行分选。用中红外辐射处理A549细胞,通过定量聚合酶链反应分析和蛋白质印迹分析测定HIF-2α的表达水平。通过免疫组织化学分析确定50例临床确诊的非小细胞肺癌组织切片中HIF-2α的表达水平,并分析其与放疗后预后的相关性。CD133(+)细胞中的HIF-2α水平显著高于CD133(-)细胞(P = 0.032)。然而,放射治疗后,CD133(+)和CD133(-)细胞中的这些水平均显著上调(分别为P = 0.031和P = 0.023)。照射后,凋亡、死亡和自噬的CD133(+) A549细胞比例明显低于CD133(-) A549细胞(P < 0.05)。此外,HIF-2α表达水平高的肺癌患者癌胚抗原恢复到放疗前水平的速度更快,且这些患者的生存时间更短(P = 0.018)。HIF-2α在肺癌干细胞中高表达,这可能导致放射抗性。总之,HIF-2α是肺癌潜在的预后标志物。