Du Hailei, Chen Ling, Luo Fangxiu, Chen Xueyu, Li Yong, Cheng Qijian
Department of Thoracic Surgery, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, P.R. China.
Department of Respiratory and Critical Care Medicine, Ruijin Hospital North, Shanghai Jiaotong University School of Medicine, Shanghai 201821, P.R. China.
Oncol Lett. 2020 Oct;20(4):9. doi: 10.3892/ol.2020.11870. Epub 2020 Jul 15.
Beclin-1 and Bcl-2 expression abnormalities have been confirmed in different types of cancer. As important regulators of autophagy and apoptosis, respectively, these molecules serve a complex role in tumorigenesis. However, limited information is currently available regarding the association between Beclin-1 and Bcl-2 in (NSCLC). In the present study, the expression levels of Beclin-1 and Bcl-2 were detected in lung cancer tissues, and their prognostic significance was analyzed for NSCLC. A total of 120 patients with lung cancer who underwent surgical resection were included in the present study. Beclin-1 and Bcl-2 expression was assessed using immunohistochemistry and their associations with the overall survival (OS) in patients with NSCLC was examined. The expression rate of Beclin-1 was significantly lower in NSCLC tissues compared with that in adjacent tissues, whereas the expression rate of Bcl-2 was significantly higher in lung cancer tissues compared with that in adjacent tissues. Additionally, Beclin-1 and Bcl-2 protein expression was strongly associated (P<0.05) in NSCLC. Patients with NSCLC with low Beclin-1 expression were in more advanced stages, with more lymph node metastasis and more poorly differentiated tumors. Similarly, patients with NSCLC with high Bcl-2 expression were also in a more advanced stage and had more lymph node metastasis. Cox regression analysis revealed that the association between Bcl-2 expression and survival was not significant, while a multivariate analysis revealed that Beclin-1 expression was significantly associated with OS. Notably, Beclin-1 expression was significantly associated with OS only in patients with high Bcl-2 expression. In conclusion, the present data indicated that the autophagy activity is decreased in NSCLC. Beclin-1 expression was downregulated, while Bcl-2 expression was upregulated in NSCLC tissues compared with that in adjacent tissues. Additionally, these two proteins were associated with the occurrence and progression of NSCLC. Beclin-1 may be a promising prognostic marker for patients with NSCLC with high Bcl-2 expression. The present findings provided a more accurate prognostic assessment for patients with NSCLC. Furthermore, they may be used to actively follow-up and promptly treat patients with a poor prognosis, which may benefit a greater number of patients with NSCLC.
在不同类型的癌症中,已证实存在Beclin-1和Bcl-2表达异常。作为自噬和凋亡的重要调节因子,这些分子在肿瘤发生过程中发挥着复杂的作用。然而,目前关于非小细胞肺癌(NSCLC)中Beclin-1和Bcl-2之间关联的信息有限。在本研究中,检测了肺癌组织中Beclin-1和Bcl-2的表达水平,并分析了它们对NSCLC的预后意义。本研究共纳入120例行手术切除的肺癌患者。采用免疫组织化学法评估Beclin-1和Bcl-2的表达,并检测它们与NSCLC患者总生存期(OS)的相关性。与癌旁组织相比,NSCLC组织中Beclin-1的表达率显著降低,而肺癌组织中Bcl-2的表达率显著高于癌旁组织。此外,在NSCLC中,Beclin-1和Bcl-2蛋白表达呈强相关(P<0.05)。Beclin-1低表达的NSCLC患者处于更晚期,有更多的淋巴结转移且肿瘤分化更差。同样,Bcl-2高表达的NSCLC患者也处于更晚期且有更多的淋巴结转移。Cox回归分析显示,Bcl-2表达与生存之间的关联不显著,而多因素分析显示,Beclin-1表达与OS显著相关。值得注意的是,Beclin-1表达仅在Bcl-2高表达的患者中与OS显著相关。总之,目前的数据表明NSCLC中的自噬活性降低。与癌旁组织相比,NSCLC组织中Beclin-1表达下调,而Bcl-2表达上调。此外,这两种蛋白与NSCLC的发生和进展相关。对于Bcl-2高表达的NSCLC患者,Beclin-1可能是一个有前景的预后标志物。本研究结果为NSCLC患者提供了更准确的预后评估。此外,它们可用于对预后不良的患者进行积极随访和及时治疗,这可能使更多NSCLC患者受益。