Harada Koji, Ferdous Tarannum, Ueyama Yoshiya
Department of Oral and Maxillofacial Surgery Yamaguchi University Graduate School of Medicine, Ube, Japan
Department of Oral and Maxillofacial Surgery Yamaguchi University Graduate School of Medicine, Ube, Japan.
Anticancer Res. 2016 Nov;36(11):5923-5930. doi: 10.21873/anticanres.11179.
BACKGROUND/AIM: Gimeracil or 5-chloro-2, 4-dihydroxypyridine (CDHP) has been reported to exert radiosensitization effects in cancer cells by suppressing DNA repair pathways. Here, we investigated the antitumor effect of gimeracil and radiation combination therapy against oral squamous cell carcinoma (OSCC).
The antitumor activity of gimeracil and/or radiation was investigated in HSC2 and/or SAS cells by growth inhibition assays and clonogenic survival assay. The expression of DNA double-strand break repair proteins were assessed by western blotting and immunohistochemistry, also fluorescent measurements of intracellular reactive oxygen/nitrogen species (ROS/RNS) were carried out in gimeracil and/or radiation-treated HSC2 cells/tumors.
Gimeracil and radiation combination treatment significantly inhibited OSCC cell/tumor growth and colony formation. Down-regulated expressions of DNA double-strand break repair proteins were observed in gimeracil and/or radiation treated cells/tumors. Additionally, the growth inhibitory effect of this combination treatment was associated with reactive oxygen species/reactive nitrogen species (ROS/RNS) generation.
Gimeracil might exert radiosensitizing effects on OSCC cells.
背景/目的:据报道,吉美嘧啶或5-氯-2,4-二羟基吡啶(CDHP)可通过抑制DNA修复途径在癌细胞中发挥放射增敏作用。在此,我们研究了吉美嘧啶与放疗联合治疗对口腔鳞状细胞癌(OSCC)的抗肿瘤作用。
通过生长抑制试验和克隆形成存活试验,在HSC2和/或SAS细胞中研究吉美嘧啶和/或放疗的抗肿瘤活性。通过蛋白质印迹法和免疫组织化学评估DNA双链断裂修复蛋白的表达,同时在经吉美嘧啶和/或放疗处理的HSC2细胞/肿瘤中进行细胞内活性氧/氮物种(ROS/RNS)的荧光测量。
吉美嘧啶与放疗联合治疗显著抑制OSCC细胞/肿瘤生长和集落形成。在经吉美嘧啶和/或放疗处理的细胞/肿瘤中观察到DNA双链断裂修复蛋白表达下调。此外,这种联合治疗的生长抑制作用与活性氧/活性氮物种(ROS/RNS)的产生有关。
吉美嘧啶可能对OSCC细胞发挥放射增敏作用。