Gonzalez-Torres Carolina, Gaytan-Cervantes Javier, Vazquez-Santillan Karla, Mandujano-Tinoco Edna Ayerim, Ceballos-Cancino Gisela, Garcia-Venzor Alfredo, Zampedri Cecilia, Sanchez-Maldonado Paulina, Mojica-Espinosa Raul, Jimenez-Hernandez Luis Enrique, Maldonado Vilma
Laboratorio de Epigenética del Cáncer.
Laboratorio de genómica funcional del cáncer.
Arch Med Res. 2017 May;48(4):343-351. doi: 10.1016/j.arcmed.2017.08.001. Epub 2017 Sep 5.
NF-κB is a transcription factor involved in cancer stem cells maintenance of many tumors. Little is known about the specific stem-associated upstream regulators of this pathway in ovarian cancer. The Aim of the study was to analyze the role of the canonical and non-canonical NF-κB pathways in stem cells of ovarian cancer cell lines.
Stem cells were isolated using sorting cytometry. Western blot and RT-PCR were used to quantify protein and messenger RNA levels. Loss and gain of function assays were performed using siRNAs and dominant-negative proteins, respectively. NF-κB binding activity was measured with a reporter gene assay. The stem phenotype was estimated with clonogenic assays using soft agar, colony formation, ovospheres formation and in vivo tumorigenicity assays.
The CD44+ subpopulation of SKOV3 ovarian cancer cell line presented higher mRNA levels of key stemness genes, an increased tumorigenic capacity and higher expression of the RelA, RelB and IKKα. When the canonical pathway was inhibited by means of a dominant-negative version of IkBα, the stem cell population was reduced, as shown by a reduced CD44+ subpopulation, a decrease in the expression of the stemness genes and a reduction of the stem phenotype. In addition, IKKα, the main upstream non-canonical kinase, was highly expressed in the CSC population. Accordingly, when IKKα was inhibited using shRNAs, the expression of the stemness genes was reduced.
This report is the first to show the importance of several elements of both NF-κB pathway in maintaining the ovarian cancer stem cell population.
核因子-κB(NF-κB)是一种参与多种肿瘤干细胞维持的转录因子。关于卵巢癌中该信号通路特定的与干细胞相关的上游调节因子,我们所知甚少。本研究的目的是分析经典和非经典NF-κB信号通路在卵巢癌细胞系干细胞中的作用。
使用流式细胞术分选分离干细胞。采用蛋白质印迹法和逆转录-聚合酶链反应(RT-PCR)定量蛋白质和信使核糖核酸(mRNA)水平。分别使用小干扰RNA(siRNAs)和显性负性蛋白进行功能缺失和功能获得实验。通过报告基因实验检测NF-κB结合活性。使用软琼脂克隆形成实验、集落形成实验、卵球体形成实验和体内致瘤性实验评估干细胞表型。
SKOV3卵巢癌细胞系的CD44+亚群呈现关键干性基因的mRNA水平较高、致瘤能力增强以及RelA、RelB和IKKα的表达较高。当通过IkBα的显性负性形式抑制经典信号通路时,干细胞群体减少,表现为CD44+亚群减少、干性基因表达降低以及干细胞表型减弱。此外,主要的上游非经典激酶IKKα在癌症干细胞(CSC)群体中高表达。因此,当使用短发夹RNA(shRNAs)抑制IKKα时,干性基因的表达降低。
本报告首次表明NF-κB信号通路的多个元件在维持卵巢癌干细胞群体中的重要性。