Yu Hong-Gang, Huang Jie-An, Yang Yan-Ning, Luo He-Sheng, Yu Jie-Ping, Meier Juris J, Schrader Henning, Bastian Andreas, Schmidt Wolfgang E, Schmitz Frank
Department of Gastroenterology, Renmin Hosptial of Wuhan University, China.
Regul Pept. 2003 Jul 15;114(2-3):101-7. doi: 10.1016/s0167-0115(03)00084-3.
Acetylsalicylic acid (ASA) has been confirmed to inhibit proliferation and to induce apoptosis in human colorectal cancer cells in vitro. However, the mechanism by which ASA exhibits antiproliferative and proapoptotic effects in cyclooxygenase 2 (COX-2)-negative cells remains to be further elucidated. In the present study, SW480, a COX-2-negative colon cancer cell line, was treated with various concentrations of ASA (0, 2.5, 5, and 10 mM). The antiproliferative and proapoptotic effects of ASA were confirmed by MTT assay, flow cytometry of propidium iodide (PI)-stained cells, and terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick-end labeling (TUNEL) assay. After treatment with ASA, intracellular cyclic AMP (cAMP) levels were increased and the production of prostaglandin E2 (PGE2) was decreased. RT-PCR analysis revealed that treatment of ASA induced a concentration-dependent downregulation of cytosolic phospholipase A2 (cPLA2) mRNA expression in SW480 cells and also in two other colorectal cancer cell lines, Colo320 and HT-29 cells. Intracellular calcium levels were unaffected by ASA treatment. Our results indicate that the ASA-induced downregulation of cytosolic phospholipase A2 mRNA expression might be a novel mechanism for ASA-mediated growth inhibition and apoptosis in colon cancer cells.
乙酰水杨酸(ASA)已被证实在体外可抑制人结肠癌细胞的增殖并诱导其凋亡。然而,ASA在环氧合酶2(COX-2)阴性细胞中发挥抗增殖和促凋亡作用的机制仍有待进一步阐明。在本研究中,用不同浓度的ASA(0、2.5、5和10 mM)处理COX-2阴性结肠癌细胞系SW480。通过MTT法、碘化丙啶(PI)染色细胞的流式细胞术以及末端脱氧核苷酸转移酶介导的脱氧尿苷三磷酸缺口末端标记(TUNEL)法证实了ASA的抗增殖和促凋亡作用。用ASA处理后,细胞内环磷酸腺苷(cAMP)水平升高,前列腺素E2(PGE2)的产生减少。逆转录聚合酶链反应(RT-PCR)分析显示,ASA处理可诱导SW480细胞以及另外两种结肠癌细胞系Colo320和HT-29细胞中胞质磷脂酶A2(cPLA2)mRNA表达呈浓度依赖性下调。细胞内钙水平不受ASA处理的影响。我们的结果表明,ASA诱导的胞质磷脂酶A2 mRNA表达下调可能是ASA介导的结肠癌细胞生长抑制和凋亡的新机制。