Tsunoo H, Komura S, Ohishi N, Akiyama S, Kasai Y, Ito K, Nakao A, Yagi K
Department of Surgery II Nagoya University School of Medicine, Aichi, Japan.
Anticancer Res. 2001 Sep-Oct;21(5):3301-6.
The possible antiproliferative potency of human recombinant interferon-beta (hIFN-beta) towards ten human esophageal cancer cell lines was examined in comparison with the activity of the factor towards human malignant melanoma cell lines. The cell growth of esophageal cancer cell lines was inhibited by hIFN-beta in a dose- and time- dependent manner. The 50% inhibitory concentrations (IC50) of hIFN-beta on nine cell lines out of ten ranged between 23 to 332 IU/ml of culture medium. The remaining cell line, T.Tn, was less sensitive to the interferon (IC50, 611 IU/ml). Under the same culture conditions, the melanoma cell lines tested differed markedly in their sensitivity to hIFN-beta. When the esophageal cancer cells were treated with 5-fluorouracil (5-FU) in the presence of a low concentration of hIFN-beta, the effectiveness of 5-FU was markedly enhanced. In particular, the rate of growth inhibition of T.Tn cells was more than the added potencies of 5-FU and hIFN-beta indicating that the interferon is an effective biomodulator of 5-FU. All these data suggest that combination therapy with hIFN-beta and the anticancer drug 5-FU would be beneficial for the treatment of carcinoma of the esophagus.
研究了重组人β干扰素(hIFN-β)对10种人食管癌细胞系的抗增殖效力,并与该因子对人恶性黑色素瘤细胞系的活性进行了比较。hIFN-β以剂量和时间依赖性方式抑制食管癌细胞系的细胞生长。hIFN-β对10种细胞系中的9种的50%抑制浓度(IC50)在培养基中为23至332 IU/ml。其余的细胞系T.Tn对干扰素较不敏感(IC50为611 IU/ml)。在相同培养条件下,所测试的黑色素瘤细胞系对hIFN-β的敏感性差异显著。当食管癌细胞在低浓度hIFN-β存在下用5-氟尿嘧啶(5-FU)处理时,5-FU的有效性显著增强。特别是,T.Tn细胞的生长抑制率超过了5-FU和hIFN-β的相加效力,表明干扰素是5-FU的有效生物调节剂。所有这些数据表明,hIFN-β与抗癌药物5-FU联合治疗对食管癌治疗有益。