Department of Oral and Maxillofacial Surgery, College of Dentistry, Gangneung-Wonju National University, Gangneung 210-702, Republic of Korea.
Oncol Rep. 2011 Dec;26(6):1527-32. doi: 10.3892/or.2011.1436. Epub 2011 Aug 24.
Cisplatin is a representative anti-cancer drug and 4-hexylresorcinol (4-HR) is known as an antiparasitic and antiseptic agent. The aims of this study were to evaluate the effect of 4-HR on the activation of nuclear factor-κB (NF-κB) in cell cultures, to evaluate the antitumor effect of 4-HR plus cisplatin combination therapy in a xenograft model, and to evaluate transglutaminase-2 (TG-2) and phosphorylated NF-κB (pNF-κB) expression in the xenograft model. To determine the effect of 4-HR on NF-κB phosphorylation, co-immunoprecipitation and Western blot analysis were done in KB cells. To examine the in vivo effect of the cisplatin plus 4-HR combination therapy, KB cells were grafted into nude mice. Drugs were injected into the peritoneal cavity daily. Tumor size, body weight, and duration of survival were checked daily. Specimens from main mass were used in immunohistochemical staining for the analysis of TG-2 and pNF-κB expression. In the in vitro test, as the 4-HR concentrations increased, the fraction of the bound complex NF-κB-inhibitory-κB (IκB) increased. Consequently, the level of free IκB decreased. In the xenograft model, the cisplatin plus 4-HR group exhibited a significantly decreased tumor growth rate than in the saline group (P=0.039). The mean survival time of the cisplatin plus 4-HR group was 51.20±3.96 days and was significantly prolonged compared with the other groups (P<0.05). The body weight of the cisplatin plus 4-HR group had significantly less weight loss than the cisplatin only group (P=0.045). In the immunohistochemical analysis, the cisplatin plus 4-HR group had a significantly lower expression of TG-2 and pNF-κB compared to the saline group (P<0.05). In conclusion, cisplatin plus 4-HR combination therapy had clear advantages over the cisplatin only treatment such as similar tumor growth inhibition compared to the cisplatin only treatment despite the reduced dosage of cisplatin, less body weight loss, and prolonged survival time.
顺铂是一种代表性的抗癌药物,而 4-己基间苯二酚(4-HR)则是一种抗寄生虫和防腐剂。本研究旨在评估 4-HR 对细胞培养物中核因子-κB(NF-κB)激活的影响,评估顺铂联合 4-HR 治疗在异种移植模型中的抗肿瘤作用,并评估异种移植模型中转谷氨酰胺酶-2(TG-2)和磷酸化 NF-κB(pNF-κB)的表达。为了确定 4-HR 对 NF-κB 磷酸化的影响,在 KB 细胞中进行了共免疫沉淀和 Western blot 分析。为了检测顺铂联合 4-HR 组合治疗的体内作用,将 KB 细胞移植到裸鼠体内。每天向腹腔内注射药物。每天检查肿瘤大小、体重和生存时间。使用免疫组织化学染色分析主要肿块中 TG-2 和 pNF-κB 的表达。在体外试验中,随着 4-HR 浓度的增加,结合复合物 NF-κB-抑制-κB(IκB)的分数增加。因此,游离 IκB 的水平下降。在异种移植模型中,与生理盐水组相比,顺铂联合 4-HR 组的肿瘤生长速度明显降低(P=0.039)。顺铂联合 4-HR 组的平均生存时间为 51.20±3.96 天,明显长于其他组(P<0.05)。顺铂联合 4-HR 组的体重减轻明显少于顺铂单药组(P=0.045)。在免疫组织化学分析中,与生理盐水组相比,顺铂联合 4-HR 组的 TG-2 和 pNF-κB 表达明显降低(P<0.05)。总之,与单独使用顺铂相比,顺铂联合 4-HR 联合治疗具有明显的优势,如与单独使用顺铂相比,肿瘤生长抑制相似,但顺铂剂量减少、体重减轻减少、生存时间延长。