Pharmacology Department, Universidade Federal de São Paulo, São Paulo, Brazil.
Epigenetics. 2011 Apr;6(4):450-64. doi: 10.4161/epi.6.4.14917. Epub 2011 Apr 1.
Melanoma progression requires deregulation of gene expression by currently uncharacterized epigenetic mechanisms. A mouse model based on changes in cell microenvironment was developed by our group to study melanocyte malignant transformation. Melanoma cell lines (4C11- and 4C11+) were obtained as result of 5 sequential anchorage blockades of non-tumorigenic melan-a melanocytes. Melan-a cells submitted to 4 de-adhesion cycles were also established (4C), are non-tumorigenic and represent an intermediary phase of tumor progression. The aim of this work was to identify factors contributing to epigenetic modifications in early and later phases of malignant transformation induced by anchorage impediment. Epigenetic alterations occur early in tumorigenesis; 4C cell line shows changes in global and gene-specific DNA methylation and histone marks. Many histone modifications differ between melan-a, 4C, 4C11- (non-metastatic melanoma cell line) and 4C11+ (metastatic melanoma cell line) which could be associated with changes in gene and microRNA expression. These epigenetic alterations seem to play a key role in malignant transformation since melanocytes treated with 5-Aza-2'-deoxycytidine before each anchorage blockade do not transform. Some epigenetic changes seem to be also responsible for the maintenance of malignant phenotype, since melanoma cell lines (4C11- and 4C11+) treated in vitro with 5-Aza-2'-deoxycytidine or Trichostatin A showed reduction of tumor growth in vivo. Changes in gene expression reflecting cell adaptation to new environment were also observed. We propose a model in which sustained microenvironmental stress in melanocytes results in epigenetic reprogramming. Thus, after adaptation, cells may acquire epigenetic marks that could contribute to the establishment of a malignant phenotype.
黑色素瘤的发生发展需要通过目前尚未明确的表观遗传机制来调节基因表达。本课题组构建了一个基于细胞微环境改变的小鼠模型,用于研究黑素细胞的恶性转化。通过对非致瘤性黑素-a 黑素细胞进行 5 次连续的锚定阻断,获得了黑色素瘤细胞系(4C11-和 4C11+)。我们还建立了经历 4 次去黏附循环的黑素-a 细胞(4C),它们是非致瘤性的,代表了肿瘤进展的中间阶段。本研究的目的是鉴定导致锚定障碍诱导的恶性转化早期和晚期表观遗传改变的因素。表观遗传改变发生在肿瘤发生的早期;4C 细胞系表现出全基因组和基因特异性 DNA 甲基化和组蛋白标记的改变。许多组蛋白修饰在黑素-a、4C、4C11-(非转移性黑色素瘤细胞系)和 4C11+(转移性黑色素瘤细胞系)之间存在差异,这可能与基因和 microRNA 表达的变化有关。这些表观遗传改变似乎在恶性转化中起着关键作用,因为在每次锚定阻断前用 5-Aza-2'-脱氧胞苷处理的黑素细胞不会发生转化。一些表观遗传变化似乎也与维持恶性表型有关,因为在体外用 5-Aza-2'-脱氧胞苷或 Trichostatin A 处理的黑色素瘤细胞系(4C11-和 4C11+)在体内显示出肿瘤生长的减少。还观察到反映细胞适应新环境的基因表达变化。我们提出了一个模型,即在黑素细胞中持续的微环境应激导致表观遗传重编程。因此,在适应后,细胞可能获得表观遗传标记,这些标记可能有助于建立恶性表型。