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U87MG 胶质母细胞瘤细胞系在体外连续传代过程中的致瘤性降低。

The Tumorgenicity of Glioblastoma Cell Line U87MG Decreased During Serial In Vitro Passage.

机构信息

Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, Guangdong, People's Republic of China.

Department of Neurosurgery, The Fifth Affiliated Hospital, Sun Yat-Sen University, Zhuhai, 519000, Guangdong, People's Republic of China.

出版信息

Cell Mol Neurobiol. 2018 Aug;38(6):1245-1252. doi: 10.1007/s10571-018-0592-7. Epub 2018 Jun 8.

DOI:10.1007/s10571-018-0592-7
PMID:29948550
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11481925/
Abstract

Established cancer cell lines are routinely used to study cancer. Several factors such as serial passage may affect the reproducibility of experiments with cancer cell lines, but few researches focused on these changes. In the present study, different morphology and decreased tumorigenicity were observed in late passage U87MG cells. In vitro experiments further revealed that late passage U87MG cells possessed lower invasion properties than early passage, whereas no significant differences of proliferation and migration were found between early and late passage U87MG cells. In particular, we confirmed that late passage U87MG cells exhibited more epithelial phenotype with decreased PI3K/Akt pathway and TGF-β pathway expressions at protein level. In summary, our results focused on the changes of U87MG cells during serial in vitro passage, suggested that passage-induced changes may lead to notable changes of biological characteristics and several molecular transitions in cancer cell lines, indicating the necessity to shorten experiment-span and accomplish experiments with the same or similar passage cancer cell strains.

摘要

已建立的癌细胞系通常用于癌症研究。细胞系传代等几个因素可能会影响癌症细胞系实验的可重复性,但很少有研究关注这些变化。在本研究中,我们观察到 U87MG 细胞在晚期传代时出现了不同的形态和降低的致瘤性。体外实验进一步表明,晚期传代的 U87MG 细胞具有比早期传代更低的侵袭性,而早期和晚期传代的 U87MG 细胞在增殖和迁移方面没有明显差异。特别地,我们证实晚期传代的 U87MG 细胞表现出更多的上皮表型,其 PI3K/Akt 通路和 TGF-β 通路表达水平降低。综上所述,我们的研究结果集中在 U87MG 细胞在体外连续传代过程中的变化,表明传代诱导的变化可能导致癌细胞系的生物学特性和几个分子转变发生显著变化,这表明有必要缩短实验周期,并使用相同或相似传代数的癌细胞株完成实验。

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本文引用的文献

1
EMT in cancer.肿瘤中的 EMT。
Nat Rev Cancer. 2018 Feb;18(2):128-134. doi: 10.1038/nrc.2017.118. Epub 2018 Jan 12.
2
Epithelial-to-mesenchymal transition, circulating tumor cells and cancer metastasis: Mechanisms and clinical applications.上皮-间质转化、循环肿瘤细胞与癌症转移:机制及临床应用
Oncotarget. 2017 May 26;8(46):81558-81571. doi: 10.18632/oncotarget.18277. eCollection 2017 Oct 6.
3
PAK signalling drives acquired drug resistance to MAPK inhibitors in BRAF-mutant melanomas.PAK信号传导驱动BRAF突变型黑色素瘤对MAPK抑制剂产生获得性耐药。
Nature. 2017 Oct 5;550(7674):133-136. doi: 10.1038/nature24040. Epub 2017 Sep 27.
4
SMARCB1 is required for widespread BAF complex-mediated activation of enhancers and bivalent promoters.广泛的BAF复合物介导的增强子和二价启动子激活需要SMARCB1。
Nat Genet. 2017 Nov;49(11):1613-1623. doi: 10.1038/ng.3958. Epub 2017 Sep 25.
5
The N-methyladenosine (mA)-forming enzyme METTL3 controls myeloid differentiation of normal hematopoietic and leukemia cells.形成N-甲基腺苷(mA)的酶METTL3控制正常造血细胞和白血病细胞的髓系分化。
Nat Med. 2017 Nov;23(11):1369-1376. doi: 10.1038/nm.4416. Epub 2017 Sep 18.
6
Detection of dysregulated protein-association networks by high-throughput proteomics predicts cancer vulnerabilities.通过高通量蛋白质组学检测失调的蛋白质关联网络可预测癌症易感性。
Nat Biotechnol. 2017 Oct;35(10):983-989. doi: 10.1038/nbt.3955. Epub 2017 Sep 11.
7
Mutations in ACTRT1 and its enhancer RNA elements lead to aberrant activation of Hedgehog signaling in inherited and sporadic basal cell carcinomas.ACTRT1 及其增强子 RNA 元件的突变导致遗传性和散发性基底细胞癌中 Hedgehog 信号的异常激活。
Nat Med. 2017 Oct;23(10):1226-1233. doi: 10.1038/nm.4368. Epub 2017 Sep 4.
8
A computational modelling framework to quantify the effects of passaging cell lines.一种用于量化传代细胞系影响的计算建模框架。
PLoS One. 2017 Jul 27;12(7):e0181941. doi: 10.1371/journal.pone.0181941. eCollection 2017.
9
MicroRNA-199b-5p attenuates TGF-β1-induced epithelial-mesenchymal transition in hepatocellular carcinoma.微小RNA-199b-5p减弱转化生长因子-β1诱导的肝细胞癌上皮-间质转化
Br J Cancer. 2017 Jul 11;117(2):233-244. doi: 10.1038/bjc.2017.164. Epub 2017 Jun 6.
10
EMT- and MET-related processes in nonepithelial tumors: importance for disease progression, prognosis, and therapeutic opportunities.非上皮性肿瘤中与上皮-间质转化和间质-上皮转化相关的过程:对疾病进展、预后及治疗机会的重要性
Mol Oncol. 2017 Jul;11(7):860-877. doi: 10.1002/1878-0261.12085. Epub 2017 Jun 19.