Using Differential Display, we found 122 genes whose expression was altered by DEHP treatment. The concentrations stu died were in the range of concentrations that induced a morphological transfor mation of SHE cells, i. e. concentrations up to 77 uM for Mikalsen et al. and in the range Paclitaxel microtubule 25 uM 150 uM for Cruciani et al. We measured the mRNA level of genes involved in the regulation of the Inhibitors,Modulators,Libraries cytoskeleton using qPCR. This focus is justified by the fact that the modifications of cytoskeleton organization are early events in cell neo plastic process and can be recorded in SHE cells after 7 days of exposure to carcinogenic agents in cell transformation assays. Morphological transformation affects a few percentage of the mixed population of SHE cells and all cell types.
From the present work, Inhibitors,Modulators,Libraries we can assume that the differentially expressed genes mea sured in the first 24 hrs of exposure reflect the first tar gets of DEHP in the entire SHE cell population. The transcriptomic changes which were recorded correspond to the integrated mean of the cell responses significantly different in the exposed populations, without consideration of cell specificity and sensitivity to DEHP. These significant expression changes in genes involved in cytoskeleton regulation, can be Inhibitors,Modulators,Libraries seen as early indica tors of disturbances that will lead to cell transformation further in a few percentage of the most susceptible cells of the SHE population. The role of the cytoskeleton has been extensively studied in relation to invasion and metastasis, but little is known of its implication in the first stages of carcinogenesis.
The identification of geno mic changes associated with the triggering of cell trans formation is useful from a mechanistic point of view and may be valuable in screening. Effects on cytoskeleton related genes DEHP was shown to affect several functions related to the cytoskeleton. The Inhibitors,Modulators,Libraries genes involved in cytoskeleton regulation and identified by Differential Display Inhibitors,Modulators,Libraries are listed in table 2. To summarize, DEHP affects actin polymerisation and stabilization, as well as cell to cell and cell to matrix adhesion processes. The expression of genes involved in organelle transport, in cytoskeleton remodelling, or adhesion in response to external factors was also modified by DEHP. These results are in line with the recent findings of Posnack et al.
who iden tified disturbances in mechanical adhesion function and protein trafficking in rats cardiomyocytes exposed to DEHP. Actin polymerization and stabilization To summarize the basic process, actin polymerization requires the Arp2 3 complex that needs to be stabilized by Enable Homolog and is regulated by coronins. Enah is involved in the dynamic reorganization of the actin selleckchem cytoskeleton, and stimulates nucleation and poly merization.