| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2513557 | Biochemical Pharmacology | 2010 | 13 Pages |
NO-donating aspirin (NO-ASA, para isomer) has been reported to exhibit strong growth inhibitory effect in Jurkat T-acute lymphoblastic leukemia (T-ALL) cells mediated in part by β-catenin degradation and caspase activation, but the mechanism(s) still remains unclear. In this study, DNA oligoarrays with 263 genes were used to examine the gene expression profiles relating to stress and drug metabolism, and characterize the stress responses at IC50 and subIC50 concentrations of p-NO-ASA (20 and 10 μM, respectively) in Jurkat T cells. A total of 22 genes related to heat shock response, apoptosis signaling, detoxifiers and Phase II enzymes, and regulators of cell growth were altered in expression by array analysis based on the expression fold change criteria of ≥1.5-fold or ≤0.65-fold. Real time quantitative RT-PCR confirmed that 20 μM p-NO-ASA strongly upregulated the mRNA levels of two heat shock genes HSPA1A (41.5 ± 7.01-fold) and HSPA6 (100.4 ± 8.11-fold), and FOS (16.2 ± 3.2-fold), moderately upregulated HSPH1 (1.71 ± 0.43-fold), FMO4 (4.5 ± 1.67-fold), CASP9 (1.77 ± 0.03-fold), DDIT3 (5.6 ± 0.51-fold), and downregulated NF-κB1 (0.54 ± 0.01-fold) and CCND1 (0.69 ± 0.06-fold). Protein levels of Hsp70, the product of HSPA1A, and fos were increased in p-NO-ASA-treated Jurkat T and HT-29 colon cancer cells in a dose-dependent manner. Silencing of Hsp70 enhanced the growth inhibitory effect of p-NO-ASA at low concentrations. The altered gene expression patterns by NO-ASA in Jurkat T cells suggest mechanisms for carcinogen metabolism, anti-proliferative activity and possible chemoprotective activity in T-ALL.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slide
