Zhang Shimin, Tsai Shien, Lo Shyh-Ching
Department of Environmental & Infectious Disease Sciences, Armed Forces Institute of Pathology, Washington, DC 20306-6000, USA.
BMC Cancer. 2006 May 4;6:116. doi: 10.1186/1471-2407-6-116.
Mycoplasmas are the smallest microorganisms capable of self-replication. Our previous studies show that some mycoplasmas are able to induce malignant transformation of host mammalian cells. This malignant transformation is a multistage process with the early infection, reversible and irreversible stages, and similar to human tumor development in nature. The purpose of this study is to explore mechanisms for this malignant transformation.
To better understand mechanisms for this unique process, we examined gene expression profiles of C3H cells at different stages of the mycoplasma-induced transformation using cDNA microarray technology. A total of 1185 genes involved in oncogenesis, apoptosis, cell growth, cell-cycle regulation, DNA repair, etc. were examined. Differences in the expression of these genes were compared and analyzed using the computer software AtlasImage.
Among 1185 genes screened, 135 had aberrant expression at the early infection stage, 252 at the reversible stage and 184 at the irreversible stage. At the early infection stage, genes with increased expression (92 genes) were twice more than those with decreased expression (42 genes). The global gene expression at the reversible stage appeared to be more volatile than that at any other stages but still resembled the profile at the early infection stage. The expression profile at the irreversible stage shows a unique pattern of a wide range of expression levels and an increased number of expressing genes, especially the cancer-related genes. Oncogenes and tumor suppressors are a group of molecules that showed significant changes in expression during the transformation. The majority of these changes occurred in the reversible and irreversible stages. A prolonged infection by mycoplasmas lead to the expression of more cancer related genes at the irreversible stage.
The results indicate that the expression profiles correspond with the phenotypic features of the cells in the mycoplasma induced transformation process. The early mycoplasma infection stage shares a common phenomenon with many other acute infections, genes with increased expression significantly outnumbering those with decreased expression. The reversible stage is a transition stage between benignancy and malignancy at the molecular level. Aberrant expression of oncogenes and tumor repressors plays a key role in mycoplasma-induced malignant transformation.
支原体是能够自我复制的最小微生物。我们之前的研究表明,一些支原体能够诱导宿主哺乳动物细胞发生恶性转化。这种恶性转化是一个多阶段过程,包括早期感染、可逆阶段和不可逆阶段,本质上类似于人类肿瘤的发展。本研究的目的是探索这种恶性转化的机制。
为了更好地理解这一独特过程的机制,我们使用cDNA微阵列技术检测了支原体诱导转化不同阶段的C3H细胞的基因表达谱。共检测了1185个参与肿瘤发生、细胞凋亡、细胞生长、细胞周期调控、DNA修复等的基因。使用计算机软件AtlasImage对这些基因表达的差异进行比较和分析。
在筛选的1185个基因中,135个在早期感染阶段表达异常,252个在可逆阶段表达异常,184个在不可逆阶段表达异常。在早期感染阶段,表达增加的基因(92个)是表达减少的基因(42个)的两倍。可逆阶段的整体基因表达似乎比其他任何阶段都更不稳定,但仍与早期感染阶段的图谱相似。不可逆阶段的表达图谱显示出一种独特的模式,即表达水平范围广泛且表达基因数量增加,尤其是与癌症相关的基因。癌基因和肿瘤抑制基因是一组在转化过程中表达发生显著变化的分子。这些变化大多发生在可逆和不可逆阶段。支原体的长期感染导致在不可逆阶段更多与癌症相关的基因表达。
结果表明,表达谱与支原体诱导转化过程中细胞的表型特征相对应。支原体早期感染阶段与许多其他急性感染有共同现象,表达增加的基因明显多于表达减少的基因。可逆阶段是分子水平上良性和恶性之间的过渡阶段。癌基因和肿瘤抑制基因的异常表达在支原体诱导的恶性转化中起关键作用。