Wiebke Eric A, Grieshop Neil A, Loehrer Patrick J, Eckert George J, Sidner Richard A
Department of Surgery, Indiana University School of Medicine and Surgical Service, Roudebush VA Medical Center, Indianapolis, Indiana 46202, USA.
J Surg Res. 2003 May 1;111(1):63-9. doi: 10.1016/s0022-4804(03)00053-2.
The addition of levamisole (Lev) to 5-fluorouracil (5-FU) for the adjuvant treatment of stage III colon cancer has been shown to improve 5-year survival in patients. The mechanism of action of Lev remains unknown. Because we showed little in vitro immunological effect of Lev, we asked whether Lev, alone or in combination with 5-FU, had antitumor activity in vitro.
Proliferation of COLO-205 and HT-29 colon cancer cells incubated for 2 to 3 days in Lev and 5-FU was measured in 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium colorimetric assays. Cell cycle analysis was performed by treating tumor cells for 6, 24, and 48 h with Lev and 5-FU, staining cells with propidium iodide, and measuring DNA content by flow cytometry.
The addition of Lev to 5-FU did not reduce proliferation below that of 5-FU alone. The inhibitory concentration 50% (IC(50)) for 5-FU was 3.2 x 10(-6) M for COLO-205 and 1.3 x 10(-5) M for HT-29. An IC(50) was not reached for Lev, even at millimolar doses. DNA analysis of cells treated for 48 h revealed significant S-phase accumulation of both HT-29 (from 17% in control cells to 36% in treated cells) and COLO-205 (from 35% in control cells to 59% in treated cells) cell lines at micromolar 5-FU concentrations. In contrast, Lev alone did not affect cell cycle distribution for either cell line. The addition of Lev to 5-FU not only did not augment, but inhibited, the effects of 5-FU.
Levamisole has no direct cytotoxic effect and no additive or synergistic cytotoxic effect when combined with 5-FU on two colon cancer cell lines. Either the observed clinical effects of Lev treatment occur through an as yet unknown mechanism, require longer treatment periods in vitro to become evident, or the results of clinical trials showing its effectiveness should be carefully reexamined.
已证明在Ⅲ期结肠癌辅助治疗中,将左旋咪唑(Lev)添加到5-氟尿嘧啶(5-FU)中可提高患者的5年生存率。Lev的作用机制尚不清楚。由于我们发现Lev在体外几乎没有免疫效应,因此我们研究了Lev单独使用或与5-FU联合使用时在体外是否具有抗肿瘤活性。
采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑比色法测定COLO-205和HT-29结肠癌细胞在Lev和5-FU中孵育2至3天的增殖情况。通过用Lev和5-FU处理肿瘤细胞6、24和48小时,用碘化丙啶对细胞进行染色,并通过流式细胞术测量DNA含量来进行细胞周期分析。
将Lev添加到5-FU中并没有使增殖降低到低于单独使用5-FU的水平。5-FU对COLO-205的50%抑制浓度(IC50)为3.2×10⁻⁶ M,对HT-29为1.3×10⁻⁵ M。即使在毫摩尔剂量下,Lev也未达到IC50。对处理48小时的细胞进行DNA分析发现,在微摩尔浓度的5-FU作用下,HT-29(从对照细胞中的17%增加到处理细胞中的36%)和COLO-205(从对照细胞中的35%增加到处理细胞中的59%)细胞系均出现明显的S期积累。相比之下,单独使用Lev对这两种细胞系的细胞周期分布均无影响。将Lev添加到5-FU中不仅没有增强,反而抑制了5-FU的作用。
左旋咪唑对两种结肠癌细胞系没有直接细胞毒性作用,与5-FU联合使用时也没有相加或协同细胞毒性作用。Lev治疗所观察到的临床效果要么是通过一种尚不清楚的机制发生,要么需要在体外更长的治疗时间才能显现,要么应该仔细重新审视显示其有效性的临床试验结果。