Liu Fang, Li Qingbao, Zhang Ping, Chen Fang, Cheng Yufeng
Department of Radiation Oncology, Qilu Hospital of Shandong University, Jinan, Shandong 250012, P.R. China.
Department of Cardiac Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, Shandong 250021, P.R. China.
Mol Med Rep. 2015 May;11(5):3349-53. doi: 10.3892/mmr.2015.3227. Epub 2015 Jan 20.
Non‑small cell lung cancer (NSCLC) remains the leading cause of cancer‑related mortality despite the fact that great advances have been made in therapeutic treatment methods. Therefore, in the present study, the role of adenovirus-mediated retinoblastoma 94 (Ad‑RB94) gene therapy in NSCLC was investigated. Following treatment with Ad‑RB94, the proportion of A549 cells in the G2/M phase was increased. In the mouse xenograft model, the overexpression of RB94 inhibited the tumor growth compared with the control group and the Ad-‑LacZ-treated group. In the transplanted tumors, the overexpression of RB94 induced the apoptosis of tumors as well as an increase in the mRNA levels of cyclinB1. In conclusion, the results of the present study suggested that RB94 may effectively inhibit NSCLC tumor cell growth by inducing G2/M cell cycle arrest and apoptosis, indicating that RB94 may be a promising candidate for adjuvant therapy with radiation or chemotherapy in NSCLC.
尽管在治疗方法上取得了巨大进展,但非小细胞肺癌(NSCLC)仍然是癌症相关死亡的主要原因。因此,在本研究中,研究了腺病毒介导的视网膜母细胞瘤94(Ad-RB94)基因治疗在NSCLC中的作用。用Ad-RB94处理后,G2/M期A549细胞的比例增加。在小鼠异种移植模型中,与对照组和Ad-LacZ处理组相比,RB94的过表达抑制了肿瘤生长。在移植瘤中,RB94的过表达诱导了肿瘤细胞凋亡以及细胞周期蛋白B1 mRNA水平的增加。总之,本研究结果表明,RB94可能通过诱导G2/M细胞周期阻滞和凋亡来有效抑制NSCLC肿瘤细胞生长,这表明RB94可能是NSCLC放疗或化疗辅助治疗的有希望的候选者。