Okamura Masahiko, Kobayashi Masaki, Suzuki Fumika, Shimada Jun, Sakagami Hiroshi
Division of Oral Maxillofacial Surgery, Meikai University School of Dentistry, Sakado, Saitama 350-0283, Japan.
Anticancer Res. 2007 Sep-Oct;27(5A):3331-7.
The possible apoptosis-inducing activity of several sequential treatments of cisplatin (CDDP) and 5-fluorouracil (5-FU) against the human oral squamous cell carcinoma HSC-2 cell line was investigated. The following three combination treatments (CT) were used: simultaneous treatment with CDDP and 5-FU (for 72 hours) (CT-1), CDDP treatment (24 hours) followed by 5-FU treatment (48 hours) (CT-2) and 5-FU treatment (24 hours) followed by CDDP treatment (48 hours) (CT-3). CT-1 produced the highest cytotoxicity, followed by CT-3 and CT-2. No treatment induced any detectable internucleosomal DNA fragmentation, and caspase-3,-8 and -9 were activated to a much lesser extent than that attained using actinomycin D. High-performance liquid chromatography analysis demonstrated that 5-FU, as well as CT-1 and CT-2, preferentially reduced the intracellular concentration of putrescine. These results suggest that simultaneous treatment with CDDP and 5-FU induces lower level of apoptotic cell death in HSC-2 cells.
研究了顺铂(CDDP)和5-氟尿嘧啶(5-FU)序贯治疗对人口腔鳞状细胞癌HSC-2细胞系可能的凋亡诱导活性。采用了以下三种联合治疗(CT):CDDP和5-FU同时治疗(72小时)(CT-1)、CDDP治疗(24小时)后接5-FU治疗(48小时)(CT-2)以及5-FU治疗(24小时)后接CDDP治疗(48小时)(CT-3)。CT-1产生的细胞毒性最高,其次是CT-3和CT-2。没有任何治疗诱导出可检测到的核小体间DNA片段化,并且半胱天冬酶-3、-8和-9的激活程度远低于使用放线菌素D时达到的程度。高效液相色谱分析表明,5-FU以及CT-1和CT-2优先降低了细胞内腐胺的浓度。这些结果表明,CDDP和5-FU同时治疗在HSC-2细胞中诱导的凋亡性细胞死亡水平较低。