Sawada Seiji, Mese Hiroshi, Sasaki Akira, Yoshioka Norie, Matsumura Tomohiro
Department of Oral and Maxillofacial Surgery, Biopathological Science, Graduate School of Medicine and Dentistry, Okayama University Graduate Schools, 2-5-1 Shikata-Cho, 700-8525, Okayama, Japan.
Cancer Chemother Pharmacol. 2003 Jun;51(6):505-11. doi: 10.1007/s00280-003-0614-z. Epub 2003 Apr 23.
Paclitaxel (Taxol, TXL) is an antimicrotubule agent that stabilizes microtubules, arrests the cell cycle at the G(2)/M phase and induces apoptosis. In vitro drug sensitivity assays have shown that the combination of TXL and CDDP is more effective in CDDP-resistant ovarian carcinoma cell lines, with different cytotoxicities depending on the sequence of drug exposure. CDDP also shows poor results in human epidermoid carcinoma particularly of the head and neck region.
We investigated the effects and the molecular mechanisms of combination chemotherapy with TXL and CDDP in the CDDP-resistant cell line A431/CDDP2, and in its parental human epidermoid cell line A431/P. Drug sensitivity was determined using the MTS assay and cell cycle perturbation was analyzed using flow cytometry. DNA fragmentation was then analyzed and the protein levels of caspase-3 and Bcl-2, and phosphorylated of Bcl-2 were determined by Western blotting.
In the drug sensitivity assay, exposure to CDDP prior to TXL was more effective than exposure TXL prior to CDDP in A431/P cells. In A431/CDDP2 cells, exposure to TXL prior to CDDP was more effective than exposure to CDDP prior to TXL. Exposure to TXL arrested the cells in the G(2)/M phase in both cell lines. In A431/CDDP2 cells, exposure to TXL prior to CDDP arrested the cells in the G(2)/M phase, an effect caused by either CDDP or TXL. Analysis of DNA fragmentation showed similar results to the drug sensitivity assay. Expression of caspase-3 protein active form was detected following exposure to TXL only and to the TXL/CDDP combination in both A431/P and A431/CDDP2 cells, but phosphorylation of Bcl-2 protein was detected only following exposure to TXL and only in A431/CDDP2 cells.
These results indicate that exposure to TXL prior to CDDP plays a key role in circumventing CDDP resistance by phosphorylating Bcl-2 protein in the human epidermoid carcinoma cell line A431/CDDP2.
紫杉醇(泰素,TXL)是一种抗微管药物,可使微管稳定,将细胞周期阻滞在G(2)/M期并诱导细胞凋亡。体外药敏试验表明,TXL与顺铂(CDDP)联合应用对耐CDDP的卵巢癌细胞系更有效,其细胞毒性因药物暴露顺序而异。CDDP在人类表皮样癌尤其是头颈部区域的治疗效果也不佳。
我们研究了TXL与CDDP联合化疗对耐CDDP细胞系A431/CDDP2及其亲本人类表皮样细胞系A431/P的影响及分子机制。采用MTS法测定药物敏感性,用流式细胞术分析细胞周期扰动。然后分析DNA片段化情况,通过蛋白质印迹法测定半胱天冬酶-3和Bcl-2的蛋白水平以及Bcl-2的磷酸化水平。
在药敏试验中,在A431/P细胞中,先给予CDDP再给予TXL比先给予TXL再给予CDDP更有效。在A431/CDDP2细胞中,先给予TXL再给予CDDP比先给予CDDP再给予TXL更有效。给予TXL可使两种细胞系的细胞阻滞在G(2)/M期。在A431/CDDP2细胞中,先给予TXL再给予CDDP可使细胞阻滞在G(2)/M期,这一作用可由CDDP或TXL单独引起。DNA片段化分析结果与药敏试验相似。仅在A431/P和A431/CDDP2细胞中,给予TXL以及TXL/CDDP联合用药后可检测到活性形式的半胱天冬酶-3蛋白表达,但仅在A431/CDDP2细胞中给予TXL后可检测到Bcl-2蛋白的磷酸化。
这些结果表明,在人类表皮样癌细胞系A431/CDDP2中,先给予TXL再给予CDDP通过使Bcl-2蛋白磷酸化在克服CDDP耐药中起关键作用。