Division of Thoracic Surgery, Department of Surgery, Taipei Veterans General Hospital, Taipei, 112, Taiwan.
Exp Hematol Oncol. 2012 Jul 20;1(1):18. doi: 10.1186/2162-3619-1-18.
The transcription factor E2F1 has been implicated in cell cycle control and DNA damage response. Paradoxically, E2F1 can promote apoptosis and function as tumor suppressor. In non-small cell lung cancer (NSCLC), there are conflicting data for clinical significance of E2F1 expression. In this study, we investigated the protein expression of E2F1 in patients with stage I-III NSCLC, and its correlation with clinical outcome.
56 paired adjacent non-tumor/tumor matched samples were prospectively obtained from patients undergoing surgery for stage I-III NSCLC at Taipei Veterans General Hospital. The protein expression of E2F1 was determined by Western blot analysis. The levels of E2F1 protein were significantly higher in tumor samples than in non-tumor lung specimens (P = 0.008). Overexpression of E2F1 was defined as a more than 2-fold expression in the tumorous sample compared with the corresponding nontumorous one, and was noted in 21 patients (37.5%). There was no significant difference in overall survival (P = 0.44) or probability of freedom from recurrence (P = 0.378) between patients with E2F1 overexpression vs. non-overexpressors. Additionally, there was no significant association between E2F1 overexpression and any clinicopathologic parameter such as histological type, stage, or angiolymphatic invasion of tumor.
E2F1 protein is frequently overexpressed in NSCLC. There is no correlation between E2F1 protein expression and clinical outcome such as survival and freedom from progression.
转录因子 E2F1 参与细胞周期控制和 DNA 损伤反应。矛盾的是,E2F1 可以促进细胞凋亡并作为肿瘤抑制因子发挥作用。在非小细胞肺癌(NSCLC)中,E2F1 表达的临床意义存在相互矛盾的数据。在这项研究中,我们调查了 E2F1 在 I-III 期 NSCLC 患者中的蛋白表达及其与临床结局的相关性。
从台北荣民总医院接受 I-III 期 NSCLC 手术的患者中前瞻性地获得了 56 对相邻的非肿瘤/肿瘤配对样本。通过 Western blot 分析确定 E2F1 的蛋白表达。肿瘤样本中 E2F1 蛋白的水平明显高于非肿瘤肺标本(P = 0.008)。E2F1 蛋白的过表达定义为肿瘤样本中与相应非肿瘤样本相比表达增加 2 倍以上,在 21 例患者(37.5%)中观察到。E2F1 过表达患者的总生存率(P = 0.44)或无复发生存率(P = 0.378)与非过表达患者无显著差异。此外,E2F1 过表达与任何临床病理参数(如组织学类型、分期或肿瘤的血管淋巴管侵犯)之间均无显著相关性。
E2F1 蛋白在 NSCLC 中经常过表达。E2F1 蛋白表达与生存和无进展等临床结局之间无相关性。