Water extract of Hedyotis Diffusa Willd suppresses proliferation of human HepG2 cells and potentiates the anticancer efficacy of low-dose 5-fluorouracil by inhibiting the CDK2-E2F1 pathway

被引:62
作者
Chen, Xu-Zheng [1 ]
Cao, Zhi-Yun [1 ]
Chen, Tuan-Sheng [2 ,3 ]
Zhang, You-Quan [4 ]
Liu, Zhi-Zhen [1 ]
Su, Yin-Tao [5 ]
Liao, Lian-Ming [1 ]
Du, Jian [1 ]
机构
[1] Fujian Univ Tradit Chinese Med, Acad Integrat Med, Fuzhou 350108, Peoples R China
[2] Fujian Agr & Forestry Univ, Agr Prod Qual Inst, Fuzhou 350002, Peoples R China
[3] Hosp Fujian Agr & Forestry Univ, Fuzhou 350002, Peoples R China
[4] Fujian Univ Tradit Chinese Med, Affiliated Hosp 2, Fuzhou 350003, Peoples R China
[5] Chinese Acad Sci, Fujian Inst Res Struct Matter, Fuzhou 350002, Peoples R China
基金
中国国家自然科学基金;
关键词
Hedyotis Diffusa Willd; hepatocellular carcinoma; 5-fluorouracil; CDK2; E2F1; ADVANCED HEPATOCELLULAR-CARCINOMA; ARTERIAL INFUSION CHEMOTHERAPY; METASTATIC BREAST-CANCER; TRANSCRIPTION FACTOR; CISPLATIN; EXPRESSION; CYCLE; CYCLOPHOSPHAMIDE; INTRAARTERIAL; FLUOROURACIL;
D O I
10.3892/or.2012.1834
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hedyotis Diffusa Willd (HDW), a Chinese herbal medicine, has been widely used as an adjuvant therapy against various cancers, including hepatocellular carcinoma (HCC). However, the underlying anticancer mechanisms are yet to be elucidated. In the present study, the anticancer effects of HDW were evaluated and the efficacy and safety of HDW combined with low-dose 5-fluorouracil (5-FU) were investigated. HepG2 cells were cultured in vitro and nude mouse xenografts were established in vivo. The proliferation of HepG2 cells was measured using the MTT method and flow cytometry. The mRNA and protein expression levels of cyclin-dependent kinase 2 (CDK2), cyclin E and E2F1 were examined using relative quantitative real-time PCR and western blot analysis, respectively. The results showed that water extract of HDW remarkably inhibited HepG2 cell proliferation in a dose-dependent manner via arrest of HepG2 cells at the G0/G1 phase and induction of S phase delay. This suppression was accompanied by a great decrease of E2F1 and CDK2 mRNA expression. In addition, HDW remarkably potentiated the anti-cancer effect of low-dose 5-FU in the absence of overt toxicity by downregulating the mRNA and protein levels of CDK2, cyclin E and E2F1. Our findings support the use of HDW as adjuvant therapy of chemotherapy and suggest that HDW may potentiate the efficiency of low-dose 5-FU in treating HCC.
引用
收藏
页码:742 / 748
页数:7
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