Li Wei, Li Xiaoqing, Li Xiaoping, Li Mingjiang, Yang Pan, Wang Xuhui, Li Lei, Yang Bo
Department of Thoracic Surgery, Tianjin First Central Hospital, Tianjin 300192, People's Republic of China.
Phase I Clinical Trial Department, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin's Clinical Research Centre for Cancer, Tianjin 300052, People's Republic of China.
Onco Targets Ther. 2020 Apr 15;13:3129-3139. doi: 10.2147/OTT.S229997. eCollection 2020.
This study aims to investigate the biological effect and molecular mechanism of Lamin B1(LMNB1) in lung cancer cells and its significance for the prognosis of lung adenocarcinoma(LUAD) patients.
In this study, Bioinformatics was performed to analyze the expression at mRNA level and prognosis effect of LMNB1 in LUAD from TCGA dataset. The immunohistochemistry(IHC) assay was conducted to analyzed the expression of LMNB1 at the protein level in LUAD tissues. The correlation between the expression of LMNB1 and the clinical factors in patients with LUAD was analyzed. Next, LMNB1 transfected into LUAD cell lines (A549 and PC-9) which was proved by Western blot. CCK8 assay, cloning formation assay, and xenograft assay were conducted to explore the effect and mechanism of LMNB1 on the proliferation of LUAD cell lines in vitro and in vivo.
The results of the present study demonstrated that LMNB1 was highly expressed in LUAD tissues and related to tumor stage. High LMNB1 expression was related with more advanced clinicopathological factors such as low degree of differentiation (P=0.02), large tumor size (P<0.01), lymph node metastasis (P<0.01) and higher tumor stage (P<0.01). After knocking down LMNB1, the cell growth rate (P<0.01) and the number of colonies (P<0.01) were significantly reduced, and the level of the proliferating marker Ki67 (P<0.01) was significantly decreased. At the same time, in vivo experiments showed that the tumor volume and tumor of the mice were significantly reduced (P<0.01). Moreover, we found that knockdown LMNB1 can inhibit the proliferation of lung cancer cells by inhibiting AKT phosphorylation by Western blot.
In summary, LMNB1 play an of vital roles in the growth of LUAD cells, highlighting its potential as a therapeutic target for the treatment of LUAD patients.
本研究旨在探讨核纤层蛋白B1(LMNB1)在肺癌细胞中的生物学效应和分子机制及其对肺腺癌(LUAD)患者预后的意义。
本研究利用生物信息学分析来自TCGA数据集的LUAD中LMNB1的mRNA水平表达及预后影响。采用免疫组织化学(IHC)检测分析LUAD组织中LMNB1的蛋白水平表达。分析LMNB1表达与LUAD患者临床因素之间的相关性。接下来,将LMNB1转染到LUAD细胞系(A549和PC-9)中,通过蛋白质印迹法进行验证。进行CCK8检测、克隆形成检测和异种移植检测,以探讨LMNB1在体外和体内对LUAD细胞系增殖的影响及机制。
本研究结果表明,LMNB1在LUAD组织中高表达且与肿瘤分期相关。LMNB1高表达与更多进展期临床病理因素相关,如低分化程度(P=0.02)、肿瘤体积大(P<0.01)、淋巴结转移(P<0.01)及更高肿瘤分期(P<0.01)。敲低LMNB1后,细胞生长速率(P<0.01)和集落数量(P<0.01)显著降低,增殖标志物Ki67水平(P<0.01)显著下降。同时,体内实验表明小鼠的肿瘤体积和肿瘤重量显著减小(P<0.01)。此外,通过蛋白质印迹法我们发现敲低LMNB1可通过抑制AKT磷酸化来抑制肺癌细胞增殖。
综上所述,LMNB1在LUAD细胞生长中起着至关重要的作用,凸显了其作为LUAD患者治疗靶点的潜力。