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吉美嘧啶增强顺铂对口腔鳞状细胞癌细胞的抗肿瘤作用。

Gimeracil enhances the antitumor effect of cisplatin in oral squamous cell carcinoma cells and .

作者信息

Harada Koji, Ferdous Tarannum, Harada Toyoko, Takenawa Takanori, Ueyama Yoshiya

机构信息

Department of Oral and Maxillofacial Surgery, Yamaguchi University Graduate School of Medicine, Ube, Yamaguchi 755-8505, Japan.

出版信息

Oncol Lett. 2017 Sep;14(3):3349-3356. doi: 10.3892/ol.2017.6602. Epub 2017 Jul 18.

Abstract

Gimeracil or 5-chloro-2,4-dihydroxypyridine (CDHP) enhances the antitumor effects of 5-fluorouracil (5-FU) by inhibiting dihydropyrimidine dehydrogenase (DPD), which is involved in the degradation of 5-FU. CDHP, as part of a combination therapy, was also reported to exert a radiosensitizing effect. Therefore, CDHP may have underlying mechanisms of action other than DPD inhibition. The focus of the present study was to investigate the antitumor effects of CDHP and cisplatin (CDDP) combination treatment and against oral squamous cell carcinoma (OSCC) tumors. The inhibitory growth effects of CDHP and/or CDDP treatment on SAS and HSC2 cells were examined using an MTT assay. The expression levels of DNA double strand break repair proteins, including Ku70, DNA-dependent-protein kinase catalytic subunit (DNA-PKcs), Rad50 and Rad51 in CDHP and/or CDDP-treated cells were detected using western blotting. Nude mice with SAS or HSC2 tumors were treated with CDHP (administered orally 7 times/week) and/or CDDP (administered by intraperitoneal injection once/week) for 2 weeks. Combined treatment of CDHP and CDDP significantly suppressed the growth of SAS and HSC2 cells and that of tumors compared with the effects caused by single drug only or control treatments. Western blotting demonstrated that the expression levels of Ku70, DNA-PKcs, Rad50 and Rad51 were downregulated in cells treated with CDHP and CDDP combination treatment. Immunohistochemistry also identified that the expression of DNA double strand break repair proteins was downregulated in tumors treated with CDHP and CDDP combination treatment compared with that of tumors treated with CDDP alone or control. The results of the current study suggest that CDHP may be responsible for enhancing the antitumor effects of CDDP by suppressing the DNA double strand break repair system. Therefore, the combination of CDHP and CDDP may be a potential effective option for OSCC treatment.

摘要

吉美嘧啶或5-氯-2,4-二羟基吡啶(CDHP)通过抑制参与5-氟尿嘧啶(5-FU)降解的二氢嘧啶脱氢酶(DPD)来增强5-氟尿嘧啶的抗肿瘤作用。据报道,作为联合治疗的一部分,CDHP还具有放射增敏作用。因此,CDHP可能具有除抑制DPD以外的潜在作用机制。本研究的重点是研究CDHP与顺铂(CDDP)联合治疗对口腔鳞状细胞癌(OSCC)肿瘤的抗肿瘤作用。使用MTT法检测CDHP和/或CDDP处理对SAS和HSC2细胞的生长抑制作用。使用蛋白质免疫印迹法检测CDHP和/或CDDP处理的细胞中DNA双链断裂修复蛋白的表达水平,包括Ku70、DNA依赖性蛋白激酶催化亚基(DNA-PKcs)、Rad50和Rad51。用CDHP(每周口服7次)和/或CDDP(每周腹腔注射1次)治疗患有SAS或HSC2肿瘤的裸鼠2周。与仅使用单一药物或对照治疗相比,CDHP和CDDP联合治疗显著抑制了SAS和HSC2细胞以及肿瘤的生长。蛋白质免疫印迹法表明,在CDHP和CDDP联合治疗的细胞中,Ku70、DNA-PKcs、Rad50和Rad51的表达水平下调。免疫组织化学也证实,与单独使用CDDP治疗或对照治疗的肿瘤相比,CDHP和CDDP联合治疗的肿瘤中DNA双链断裂修复蛋白的表达下调。本研究结果表明,CDHP可能通过抑制DNA双链断裂修复系统来增强CDDP的抗肿瘤作用。因此,CDHP和CDDP联合使用可能是OSCC治疗的一种潜在有效选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fa4/5587992/726d053200d8/ol-14-03-3349-g00.jpg

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