Department of Pathology, First Affiliated Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, Liaoning, China.
BMC Cancer. 2013 Aug 2;13:368. doi: 10.1186/1471-2407-13-368.
We previously reported that Axin1 (Axin) is down-regulated in many cases of lung cancer, and X-ray irradiation increased Axin expression and inhibited lung cancer cells. The mechanisms, however, were not clear.
Four lung cancer cell lines were used to detect the methylation status of Axin with or without X-ray treatment. Real-time PCR was used to quantify the expression of Axin, and western blot analysis was applied to measure protein levels of Axin, β-catenin, Cyclin D1, MMP-7, DNMTS, MeCP2 and acetylated histones. Flow cytometric analysis, colony formation assay, transwell assay and xenograft growth experiment were used to study the biological behavior of the cells with hypermethylated or unmethylated Axin gene after X-ray treatment.
Hypermethylated Axin gene was detected in 2 of 4 cell lines, and it correlated inversely with Axin expression. X-ray treatment significantly up-regulated Axin expression in H446 and H157 cells, which possess intrinsic hypermethylation of the Axin gene (P<0.01), but did not show up-regulation in LTE and H460 cells, which have unmethylated Axin gene. 2Gy X-ray significantly reduced colony formation (from 71% to 10.5%) in H157 cells, while the reduction was lower in LTE cells (from 71% to 20%). After X-ray irradiation, xenograft growth was significantly decreased in H157 cells (from 1.15 g to 0.28 g) in comparison with LTE cells (from 1.06 g to 0.65 g). Significantly decreased cell invasiveness and increased apoptosis were also observed in H157 cells treated with X-ray irradiation (P<0.01). Down-regulation of DNMTs and MeCP2 and up-regulation of acetylated histones could be detected in lung cancer cells.
X-ray-induced inhibition of lung cancer cells may be mediated by enhanced expression of Axin via genomic DNA demethylation and histone acetylation. Lung cancer cells with a different methylation status of the Axin gene showed different radiosensitivity, suggesting that the methylation status of the Axin gene may be one important factor to predict radiosensitivity of the tumor.
我们之前报道过,Axin1(Axin)在许多肺癌病例中表达下调,X 射线照射可增加 Axin 的表达并抑制肺癌细胞。然而,其机制尚不清楚。
用或不用 X 射线处理,检测四种肺癌细胞系中 Axin 的甲基化状态。用实时 PCR 定量 Axin 的表达,用 Western blot 分析测量 Axin、β-catenin、Cyclin D1、MMP-7、DNMTS、MeCP2 和乙酰化组蛋白的蛋白水平。流式细胞术分析、集落形成实验、Transwell 实验和异种移植生长实验用于研究 X 射线处理后具有高甲基化或非甲基化 Axin 基因的细胞的生物学行为。
在 4 种细胞系中检测到 2 种细胞系的 Axin 基因呈高甲基化状态,其与 Axin 的表达呈负相关。X 射线处理显著上调 H446 和 H157 细胞中固有高甲基化的 Axin 基因的表达(P<0.01),但在 LTE 和 H460 细胞中未出现上调,这些细胞的 Axin 基因无甲基化。2Gy X 射线显著降低 H157 细胞的集落形成(从 71%降至 10.5%),而 LTE 细胞的降低幅度较低(从 71%降至 20%)。X 射线照射后,与 LTE 细胞(从 1.06 克降至 0.65 克)相比,H157 细胞的异种移植生长显著减少(从 1.15 克降至 0.28 克)。还观察到 X 射线照射后 H157 细胞的细胞侵袭能力显著降低,凋亡增加(P<0.01)。在肺癌细胞中可检测到 DNMTs 和 MeCP2 的下调以及组蛋白乙酰化的上调。
X 射线诱导的肺癌细胞抑制可能是通过基因组 DNA 去甲基化和组蛋白乙酰化增强 Axin 的表达介导的。具有不同 Axin 基因甲基化状态的肺癌细胞表现出不同的放射敏感性,表明 Axin 基因的甲基化状态可能是预测肿瘤放射敏感性的一个重要因素。