Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic.
Department of Cell Biology, Faculty of Science, Charles University, Prague, Czech Republic.
Apoptosis. 2023 Feb;28(1-2):186-198. doi: 10.1007/s10495-022-01775-4. Epub 2022 Oct 25.
LACTB was recently identified as a mitochondrial tumour suppressor that negatively affects cancer cell proliferation by inducing cell death and/or differentiation, depending on the cell type and tissue. However, the detailed mechanism underlying the LACTB-induced cancer cell death is largely unknown.
We used cell-based, either in 2D or 3D conditions, and in vivo experiments to understand the LACTB mechanisms. In this regard, protein array followed by an enrichment analysis, cell proliferation assays using different compounds, western blot analysis, flow cytometry and immunofluorescence were performed. Differences between quantitative variables following normal distribution were valuated using Student t test for paired or no-paired samples according to the experiment. For in vivo experiments differences in tumour growth were analyzed by 2-way ANOVA.
We show, that LACTB expression leads to cell cycle arrest in G1 phase and increase of DNA oxidation that leads to activation of intrinsic caspase-independent cell death pathway. This is achieved by an increase of mitochondrial reactive oxygen species since early time points of LACTB induction.
Our work provides a deeper mechanistic insight into LACTB-mediated cancer-cell death and shows the dynamics of the cellular responses a particular tumor suppressive stimulus might evoke under different genetic landscapes.
最近发现 LACTB 是一种线粒体肿瘤抑制因子,它通过诱导细胞死亡和/或分化来影响癌细胞的增殖,具体取决于细胞类型和组织。然而,LACTB 诱导癌细胞死亡的详细机制在很大程度上尚不清楚。
我们使用基于细胞的 2D 或 3D 条件和体内实验来了解 LACTB 的机制。在这方面,进行了蛋白质阵列分析和富集分析、使用不同化合物的细胞增殖测定、western blot 分析、流式细胞术和免疫荧光。根据实验,使用配对或非配对样本的学生 t 检验评估正态分布后定量变量之间的差异。对于体内实验,通过 2 路方差分析分析肿瘤生长的差异。
我们表明,LACTB 表达导致细胞周期在 G1 期停滞,并增加 DNA 氧化,从而激活内在 caspase 非依赖性细胞死亡途径。这是通过增加线粒体活性氧来实现的,因为 LACTB 诱导的早期时间点就出现了这种情况。
我们的工作提供了对 LACTB 介导的癌细胞死亡的更深入的机制见解,并显示了特定肿瘤抑制刺激在不同遗传背景下可能引发的细胞反应的动态。