癌症研究
细胞周期
胰腺癌
顺铂
细胞周期检查点
癌症
生物
细胞凋亡
癌细胞
医学
内科学
化疗
遗传学
作者
Yunfeng Li,Haili Qian,Xiao Li,Haili Qian,Jing Yu,Yongjun Liu,Xueyan Zhang,Xiao Liang,Ming Fu,Qimin Zhan,Lin Chen
摘要
Abstract Background The extremely poor prognosis of patients with pancreatic ductal adenocarcinoma indicates the need for novel therapeutic approaches. The growth arrest and DNA damage‐inducible (Gadd) gene Gadd45a is a member of a group of genes that are induced by DNA damaging agents and growth arrest signals. Methods We evaluated the biological activity of Gadd45a in pancreatic ductal adenocarcinoma cancer‐derived cell lines and assessed the efficacy of a combined treatment with adenoviral‐mediated expression of Gadd45a (Ad‐G45a) and anticancer drug (Etoposide, cisplatin, 5‐fluorouracil, respectively) for the PANC1 cell line. Results Gadd45a is variously expressed in cell lines derived from pancreatic ductal adenocarcinoma cancer and adenoviral‐mediated expression of Gadd45a (Ad‐G45a) in these cells results in apoptosis via caspase activation and cell‐cycle arrest in the G2/M phase. Gadd45a significantly increased the chemosensitivity of PANC1, which may be due to abundant apoptosis induction and cell cycle arrest. By combinational treatment of Ad‐G45a infection and chemotherapeutics, Gadd45a expression was elevated to a higher extent in cancer cells with wild‐type p53 than in that with knocked‐out p53 status, indicating a higher chemosensitivity to cancer chemotherapy. Conclusions Gadd45a may be a promising candidate for use in cancer gene therapy in combination with chemotherapeutic agents. Copyright © 2008 John Wiley & Sons, Ltd.
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