Aspirin antagonizes the cytotoxic effect of methotrexate in lung cancer cells

KUN-HUANG YAN, LIANG-MING LEE, MAO-CHIH HSIEH, MING-DE YAN, CHIH-JUNG YAO, PEY-YI CHANG, TSUNG-LI CHEN, HWAN-YOU CHANG, ANN-LII CHENG, GI-MING LAI, SHUANG-EN CHUANG
2013 Oncology Reports  
Methotrexate (MTX) has been widely used for the treatment of cancer and rheumatoid arthritis (RA). Aspirin (ASA) is a non-selective cyclooxygenase (COX) inhibitor that contributes to the treatment of inflammatory conditions such as RA. It has been observed that the antitumor effect of ASA can be attributed to inhibition of cell cycle progression, induction of apoptosis and inhibition of angiogenesis. In the present study, we revealed that the treatment with a combination of MTX and ASA resulted
more » ... in antagonism of the cytotoxic effect as demonstrated by SRB and colony formation assays. ASA alleviated the MTX-mediated S phase accumulation and recovered the G1 phase. MTX-mediated accumulation of the S phase marker cyclin A was also alleviated by ASA. Notably, FAS protein levels were upregulated by MTX in A549 cells. The antagonism of MTX efficacy caused by ASA was accompanied by altered expression of caspase-3, Bcl-2 and FAS but not dihydrofolate reductase (DHFR). This suggests that the alteration of caspase-3, Bcl-2 and FAS was involved in the antagonism between ASA and MTX. Exogenously added folic acid reversed the MTX-mediated DHFR inhibition following either MTX or MTX + ASA treatments. Most importantly, we demonstrated for the first time that the commonly used non-steroidal anti-inflammatory drug for headache ASA and possibly other COX-1/2 inhibitors can produce a strong antagonistic effect on the growth inhibition of lung cancer cells when administered in combination with MTX. The clinical implication of our finding is obvious, i.e., the clinical efficacy of MTX therapy can be compromised by ASA and their concomitant use should be avoided. Abbreviations: ASA, aspirin; NSAIDs, nonsteroidal antiinflammatory drugs; MTX, methotrexate; DHFR, dihydrofolate reductase
doi:10.3892/or.2013.2561 pmid:23799623 fatcat:7q5bstxrwfc6zdvsysavqyt6dy