*Ρ < 0.01 compared with the HCT-8/VCR and HCT-8/VCR-sh-mock cells. Knocking down GCS positively related with caspase-3 protein

level in HCT-8/VCR cells #Q-VD-Oph nmr randurls[1|1|,|CHEM1|]# The downregulation of Bcl-2 or other antiapoptotic proteins could either induce apoptosis in cancer cells or sensitize these cells to chemotherapy [10, 11]. Moreover, functional P-gp inhibits the activation of caspase-3 by some apoptotic stimuli [14, 15]. We measured the protein levels of caspase-3 in HCT-8, HCT-8/VCR, HCT-8/VCR-sh-mock and HCT-8/VCR-sh-GCS cells. As shown in Figure 4 the relative expression levels of caspase-3 were respectively 34.2 ± 0.6%, 93.0 ± 0.7%, 109.09 ± 0.7%, 42.7 ± 1.3%. Figure 4 Knocking down GCS affects Caspase-3 protein level. The Caspase-3 protein level decreased when transfected with shGCS plasmids. HCT-8/VCR cells apoptosis decreased in GCS knockdown HCT-8/VCR cells The mechanisms mediating drug resistance include defective apoptotic signaling that regulate apoptotic cell death playing an important role in determining the sensitivity of tumor cells to chemotherapy [7]. We measured the apoptosis rates of cells by flow www.selleckchem.com/products/DMXAA(ASA404).html cytometry. The rates were shown in Figure 5, it demonstrated that the rates were 8.77 ± 0.14%, 12.75 ± 0.54%, 15.39 ± 0.41% and 8.49 ± 0.23%. By further analysis, there were differences

in HCT-8, and HCT-8/VCR compared to HCT-8/VCR-sh-mock and HCT-8/VCR-sh-GCS(Ρ < 0.01). There were differences between HCT-8/VCR-sh -mock and HCT-8/VCR-sh-GCS (Ρ < 0.01). Figure 5 Knocking down GCS affects HCT-8/VCR cells apoptosis. why The apoptosis of HCT-8, HCT-8/VCR, HCT-8/VCR sh-mock or sh-GCS stably transfected cells were measured with flow cytometry (A, HCT-8, B, HCT-8/VCR, C, HCT-8/VCR-sh-mock and D, HCT-8/VCR-sh-GCS). Discussion Multidrug resistance is one of the main obstacles to the successful treatment in patients with colon cancer, and the underlying mechanisms are complex [1]. It is known that

P-glycoprotein (P-gp), the drug efflux protein, and inhibitors of apoptosis proteins (IAPs) are involved in the MDR of leukemic cells [16]. Recently research has indicated that overexpression of P-gp and cIAP may enhance the infiltration of leukemic cells [16]. Lavie et al. revealed that chemotherapy resistant MCF-7-AdrR breast cancer cells accumulate GC compared to wild-type MCF-7 cells [17]. Furthermore, GCS has been found to confer MDR in many other cancers [18–20]. The level of protein P-gp in MCF-7-AdrR is higher than that in MCF-7. The GCS expression in these two cell lines has the same pattern. These phenomena give us the clue that these two proteins are closely related. The high expression of GCS in the same cell lines shows us that there may be some relation between P-gp and GCS. Our results indicated that the mRNA level of GCS in HCT-8/VCR was higher than that in HCT-8, and its level decreased when the HCT-8/VCR were transfected with UGCG shRNA Plasmid.