Weerasinghe Priya, Garcia Gabriela E, Zhu Qiqing, Yuan Ping, Feng Lili, Mao Li, Jing Naijie
Department of Medicine, Baylor College of Medicine, Houston, TX 77030, USA.
Int J Oncol. 2007 Jul;31(1):129-36.
Lung cancer is the leading cause of cancer mortality in the United States. Despite advances made over the past decades, the overall survival of patients with lung cancer remains dismal. Here we report novel G-quartet oligodeoxynucleotides (GQ-ODN) that were designed to selectively target signal transducer and activator of transcription 3 (Stat3), in the treatment of human non-small cell lung cancer (NSCLC). The objective of this study was to evaluate the effects of two novel GQ-ODN STAT3 inhibitors, T40214 and T40231, on NSCLC bearing nude mice. NSCLC bearing nude mice were assigned to 5 groups, which were treated by vehicle, control ODN, T40214, T40231, and Paclitaxel, respectively. Tumors were measured, isolated and analyzed using Western blotting, immuno-histochemistry, RPA and TUNEL. Results show that GQ-ODN T40214 and T40231 significantly suppress the growth of NSCLC tumors in nude mice by selectively inhibiting the activation of Stat3 and its downstream proteins Bcl-2, Bcl-xL, Mcl-1, survivin, VEGF, Cyclin D1 and c-myc; thereby, promoting apoptosis and reducing angiogenesis and cell proliferation. These findings validate Stat3 as an important molecular target for NSCLC therapy and demonstrate the efficacy of GQ-ODN in inhibiting Stat3 phosphorylation.
肺癌是美国癌症死亡的主要原因。尽管在过去几十年里取得了进展,但肺癌患者的总体生存率仍然很低。在此,我们报告了一种新型的G-四链体寡脱氧核苷酸(GQ-ODN),其设计用于选择性靶向信号转导和转录激活因子3(Stat3),用于治疗人类非小细胞肺癌(NSCLC)。本研究的目的是评估两种新型GQ-ODN Stat3抑制剂T40214和T40231对荷瘤裸鼠非小细胞肺癌的影响。将荷瘤裸鼠分为5组,分别用赋形剂、对照ODN、T40214、T40231和紫杉醇进行治疗。使用蛋白质免疫印迹法、免疫组织化学、RNA酶保护分析和末端脱氧核苷酸转移酶介导的缺口末端标记法对肿瘤进行测量、分离和分析。结果表明,GQ-ODN T40214和T40231通过选择性抑制Stat3及其下游蛋白Bcl-2、Bcl-xL、Mcl-1、生存素、血管内皮生长因子、细胞周期蛋白D1和c-myc的激活,显著抑制荷瘤裸鼠非小细胞肺癌肿瘤的生长;从而促进细胞凋亡,减少血管生成和细胞增殖。这些发现证实Stat3是NSCLC治疗的一个重要分子靶点,并证明了GQ-ODN在抑制Stat3磷酸化方面的疗效。