Potter Ekaterina A, Dolgova Evgenia V, Proskurina Anastasia S, Efremov Yaroslav R, Minkevich Alexandra M, Rozanov Aleksey S, Peltek Sergey E, Nikolin Valeriy P, Popova Nelly A, Seledtsov Igor A, Molodtsov Vladimir V, Zavyalov Evgeniy L, Taranov Oleg S, Baiborodin Sergey I, Ostanin Alexander A, Chernykh Elena R, Kolchanov Nikolay A, Bogachev Sergey S
Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia.
Novosibirsk State University, Novosibirsk 630090, Russia.
Oncotarget. 2017 Feb 7;8(6):9425-9441. doi: 10.18632/oncotarget.14116.
Using the ability of poorly differentiated cells to natively internalize fragments of extracellular double-stranded DNA as a marker, we isolated a tumorigenic subpopulation present in Krebs-2 ascites that demonstrated the features of tumor-inducing cancer stem cells. Having combined TAMRA-labeled DNA probe and the power of RNA-seq technology, we identified a set of 168 genes specifically expressed in TAMRA-positive cells (tumor-initiating stem cells), these genes remaining silent in TAMRA-negative cancer cells. TAMRA+ cells displayed gene expression signatures characteristic of both stem cells and cancer cells. The observed expression differences between TAMRA+ and TAMRA- cells were validated by Real Time PCR. The results obtained corroborated the biological data that TAMRA+ murine Krebs-2 tumor cells are tumor-initiating stem cells. The approach developed can be applied to profile any poorly differentiated cell types that are capable of immanent internalization of double-stranded DNA.
利用低分化细胞天然内化细胞外双链DNA片段的能力作为标记,我们从克雷布斯-2腹水瘤中分离出一个致瘤亚群,该亚群表现出肿瘤诱导癌干细胞的特征。结合TAMRA标记的DNA探针和RNA测序技术的强大功能,我们鉴定出一组168个在TAMRA阳性细胞(肿瘤起始干细胞)中特异性表达的基因,这些基因在TAMRA阴性癌细胞中保持沉默。TAMRA +细胞显示出干细胞和癌细胞特有的基因表达特征。通过实时PCR验证了TAMRA +和TAMRA-细胞之间观察到的表达差异。获得的结果证实了生物学数据,即TAMRA +小鼠克雷布斯-2肿瘤细胞是肿瘤起始干细胞。所开发的方法可应用于分析任何能够内在化双链DNA的低分化细胞类型。