Expression of cross-tolerance to a wide range of conditions in a human lung cancer cell line after adaptation to nitric oxide

Abstract

Previously, we have shown that A549, a human lung adenocarcinoma, can be adapted to nitric oxide (NO). NO is a nitrogen-based free radical that is synthesized by a family of enzymes known as nitric oxide synthases. NO has been shown to be overexpressed in patient populations of different cancers. In addition, it has been observed that patients who express high levels of nitric oxide synthases tend to have poorer clinical outcomes than those with low levels of expression. The original cell line A549 (parent) and the adapted A549-HNO (high nitric oxide) cell line serve as a useful model system to investigate the role of NO in tumor progression and prognosis. We have previously shown that the A549-HNO-adapted cells grow aggressively when compared to A549-parent cells. Furthermore, we have shown that the A549-HNO-adapted cells exhibit a higher percentage of cell viability when exposed to ultraviolet and X-ray radiation than the A549-parent cells. Cancer patients who develop resistance to one treatment often become resistant to other previously unencountered forms of treatment. This phenomenon is known as cross-tolerance. To determine whether NO is a potential cross-tolerance causing agent, we have expanded our research by conducting parallel studies to a variety of other agents and conditions beyond radiation and ultraviolet exposure. We exposed both cell lines to varying levels of chemotherapeutic drugs (taxol and doxorubicin), temperature, pH, calcium chloride, cadmium chloride, copper chloride, sodium chloride, ferrous chloride, and sodium-R-lipoic acid. Our results show that the A549-HNO cells exhibit greater viability than the A549-parent cells when exposed to each of the various conditions. Therefore, NO is one potential driving force that can make tumor cells exhibit cross-tolerance.

DNA Methylation in Human Breast Cancer Cell Lines Adapted to High Nitric Oxide

“…However, to our knowledge, the epigenetic effects of NO in terms of DNA methylation of promoters have never been investigated in breast cancer. To fully understand the influence of NO on DNA methylation in breast cancer, we utilized a model cell line system which was previously designed by our laboratory utilizing some of the breast cancer cell lines that were adapted to NO (16)(17)(18)(19)(20)(21)(22)(23). These cells were progressively adapted to high concentrations of NO over a period of 2 months (4).…”