Establishment of Initiated Cell Line Derived From NIH3T3 Fibroblasts

IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
IUBMB Life Pub Date : 2025-07-17 DOI:10.1002/iub.70039
Myeong-Han Ro, Taehyun Park, SungHee Hwang, Hye-Gyo Kim, Michael Lee, Misu Lee
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引用次数: 0

Abstract

Autophagy plays contrasting roles depending on the stage of cellular transformation. However, although advanced tumor cell models are abundant, cell lines at the initiation stage of transformation are very limited. Therefore, the development of initiated cell lines—cells that have acquired early genetic alterations but not yet completed the multistep transformation process —is crucial for the development of anticancer drugs targeting autophagy. In this study, we successfully established a new initiated cell line (Foci #3) from foci formed in the in vitro two-stage cell transformation assay with NIH3T3 fibroblast cells. Foci #3 cells retained typical features of epithelial morphology, similar to its parental untransformed NIH3T3 cells. However, unlike NIH3T3 cells, where many dead cells were found during the long-term culture of 40 days, few dead cells were observed in Foci #3 cells. Particularly, the sensitivity of Foci #3 cells to the autophagy inhibitor CQ was higher than that of NIH3T3 cells and similar to that of Bhas 42 cells, the most commonly used initiated cell line. Moreover, Foci #3 cells maintained a higher level of autophagic flux than NIH3T3 cells throughout the extended culture period, indicating acquisition of the characteristic of dependence on autophagy for survival, which is typical of transformed cells. Importantly, qPCR analysis of epithelial–mesenchymal transition gene expression revealed that the Foci #3 cell line exhibited characteristics of both non-tumorigenic and tumorigenic states. Whole-genome sequencing analysis revealed that among the 17 genes with exon mutations in the Foci #3 cells, four were tumor suppressors and eight were involved in oncogenesis. Additionally, the Foci #3 cell line exhibited the loss of copy number variations in several tumor suppressors. Together, our results suggest that the newly developed Foci #3 cell line may be an efficient tool for elucidating the role of autophagy in the early stages of transformation.

NIH3T3成纤维细胞起始细胞系的建立
根据细胞转化的不同阶段,自噬起着不同的作用。然而,虽然晚期肿瘤细胞模型丰富,但处于转化起始阶段的细胞系非常有限。因此,启动细胞系(即获得早期遗传改变但尚未完成多步转化过程的细胞)的发展对于开发靶向自噬的抗癌药物至关重要。在这项研究中,我们成功地从NIH3T3成纤维细胞在体外两阶段细胞转化实验中形成的灶中建立了一个新的启动细胞系(Foci #3)。Foci #3细胞保留了典型的上皮形态特征,与其亲代未转化的NIH3T3细胞相似。然而,与NIH3T3细胞在40天的长期培养过程中发现许多死细胞不同,Foci #3细胞很少观察到死细胞。特别是Foci #3细胞对自噬抑制剂CQ的敏感性高于NIH3T3细胞,与最常用的起始细胞系Bhas 42细胞相似。此外,在延长的培养期间,Foci #3细胞比NIH3T3细胞保持了更高水平的自噬通量,表明获得了依赖自噬生存的特征,这是转化细胞的典型特征。重要的是,对上皮-间质转化基因表达的qPCR分析显示,Foci #3细胞系具有非致瘤性和致瘤性两种状态。全基因组测序分析显示,在Foci #3细胞的17个外显子突变基因中,有4个是肿瘤抑制基因,8个与肿瘤发生有关。此外,Foci #3细胞系在几种肿瘤抑制因子中表现出拷贝数变化的缺失。总之,我们的研究结果表明,新开发的Foci #3细胞系可能是阐明自噬在转化早期阶段的作用的有效工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
IUBMB Life
IUBMB Life 生物-生化与分子生物学
CiteScore
10.60
自引率
0.00%
发文量
109
审稿时长
4-8 weeks
期刊介绍: IUBMB Life is the flagship journal of the International Union of Biochemistry and Molecular Biology and is devoted to the rapid publication of the most novel and significant original research articles, reviews, and hypotheses in the broadly defined fields of biochemistry, molecular biology, cell biology, and molecular medicine.
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