Shahrzad Siranoush, Bertrand Kelsey, Minhas Kanwal, Coomber Brenda L
Department of Biomedical Sciences, University of Guelph, Guelph, Ontario, Canada.
Epigenetics. 2007 Apr-Jun;2(2):119-25. doi: 10.4161/epi.2.2.4613. Epub 2007 Jun 14.
In cancer, the extensive methylation found in the bulk of chromatin is reduced, while the normally unmethylated CpG islands become hypermethylated. Regions of solid tumors are transiently and/or chronically exposed to ischemia (hypoxia) and reperfusion, conditions known to contribute to cancer progression. We hypothesized that hypoxic microenvironment may influence local epigenetic alterations, leading to inappropriate silencing and re-awakening of genes involved in cancer. We cultured human colorectal and melanoma cancer cell lines under severe hypoxic conditions, and examined their levels of global methylation using HPLC to quantify 5-methylcytosine (5-mC), and found that hypoxia induced losses of global methylation. This was more extensive in normal human fibroblasts than cancer cell lines. Cell lines from metastatic colorectal carcinoma or malignant melanoma were found to be markedly more hypomethylated than cell lines from their respective primary lesions, but they did not show further reduction of 5-mC levels under hypoxic conditions. To explore these epigenetic changes in vivo, we established xenografts of the same cancer cells in immune deficient mice. We used Hypoxyprobe to assess the magnitude of tissue hypoxia, and immunostaining for 5-mC to evaluate DNA methylation status in cells from different regions of tumors. We found an inverse relationship between the presence of extensive tumor hypoxia and the incidence of methylation, and a reduction of 5-mC in xenografts compared to the levels seen in the same cancer cell lines in vitro, verifying that methylation patterns are also modulated by hypoxia in vivo. This suggests that epigenetic events in solid tumors may be modulated by microenvironmental conditions such as hypoxia.
在癌症中,大部分染色质中发现的广泛甲基化减少,而通常未甲基化的CpG岛则发生高甲基化。实体瘤区域会短暂和/或长期暴露于缺血(缺氧)和再灌注状态,已知这些状况会促进癌症进展。我们推测缺氧微环境可能会影响局部表观遗传改变,导致参与癌症的基因发生不适当的沉默和重新激活。我们在严重缺氧条件下培养人结肠直肠癌和黑色素瘤细胞系,并用高效液相色谱法(HPLC)定量5-甲基胞嘧啶(5-mC)来检测其整体甲基化水平,发现缺氧诱导整体甲基化缺失。这种情况在正常人类成纤维细胞中比在癌细胞系中更广泛。发现转移性结肠直肠癌或恶性黑色素瘤的细胞系比其各自原发灶的细胞系甲基化程度明显更低,但在缺氧条件下它们并未显示5-mC水平进一步降低。为了在体内探索这些表观遗传变化,我们在免疫缺陷小鼠中建立了相同癌细胞的异种移植模型。我们使用Hypoxyprobe评估组织缺氧程度,并用5-mC免疫染色评估肿瘤不同区域细胞中的DNA甲基化状态。我们发现广泛的肿瘤缺氧与甲基化发生率之间呈负相关,并且与体外相同癌细胞系中所见水平相比,异种移植模型中5-mC减少,证实甲基化模式在体内也受缺氧调节。这表明实体瘤中的表观遗传事件可能受缺氧等微环境条件的调节。