Okamura Masahiko, Shimada Jun, Sakagami Hiroshi
Division of Oral Maxillofacial Surgery, Department of Diagnostic and Therapeutic Sciences, Meikai University School of Dentistry, Sakado, Saitama 350-0283, Japan.
Anticancer Res. 2008 Jan-Feb;28(1A):253-9.
We established the optimal conditions for the induction of cell death by cisplatin (CDDP) and 5-fluorouracil (5-FU) in human oral squamous cell carcinoma (HSC-2, HSC-3, HSC-4) and human hepatocellular carcinoma (HepG2) cell lines. HSC-3 cells were the most sensitive to 48 hours' continuous treatment with CDDP, followed by HepG2, HSC-2 and HSC-4 cells. On the other hand, HSC-4 cells were the most sensitive to 48-hour continuous treatment with 5-FU, followed by HSC-2, HSC-3 and HepG2 cells. CDDP induced internucleosomal DNA fragmentation in HSC-2 and HSC-3 cells, but not in HSC-4 cells, while 5-FU failed to induce internucleosomal DNA fragmentation in all of these cells. The treatment of HSC-2, HSC-3 and HSC-4cells with CDDP for 12 hours (followed by incubation for 36 hours without CDDP) showed comparable magnitude of cytotoxicity and caspase-3 activation with that attained by continuous 48-hour CDDP treatment. On the other hand, the cytotoxicity of 5-FU depended both on the dose and the exposure time. The present study demonstrate that the most effective treatment time is 12 hours for CDDP and much longer for 5-FU in all studied cell lines, underlining the importance of optimizing the treatment time for each chemotherapeutic agent.
我们确定了顺铂(CDDP)和5-氟尿嘧啶(5-FU)诱导人口腔鳞状细胞癌(HSC-2、HSC-3、HSC-4)和人肝癌(HepG2)细胞系细胞死亡的最佳条件。HSC-3细胞对CDDP连续处理48小时最为敏感,其次是HepG2、HSC-2和HSC-4细胞。另一方面,HSC-4细胞对5-FU连续处理48小时最为敏感,其次是HSC-2、HSC-3和HepG2细胞。CDDP在HSC-2和HSC-3细胞中诱导了核小体间DNA片段化,但在HSC-4细胞中未诱导,而5-FU在所有这些细胞中均未能诱导核小体间DNA片段化。用CDDP处理HSC-2、HSC-3和HSC-4细胞12小时(随后在无CDDP的情况下孵育36小时)显示出与CDDP连续处理48小时相当的细胞毒性和半胱天冬酶-3激活程度。另一方面,5-FU的细胞毒性取决于剂量和暴露时间。本研究表明,在所有研究的细胞系中,CDDP最有效的处理时间为12小时,5-FU则需要更长时间,这突出了优化每种化疗药物处理时间的重要性。