Liu Y Q, Li N, Huang H F, Li H X
Department of Pathology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Zhonghua Yi Xue Za Zhi. 2018 Jan 23;98(4):269-273. doi: 10.3760/cma.j.issn.0376-2491.2018.04.006.
To explore the effect of hypoxia inducible factor (HIF)-2α on biological characteristics of breast cancer stem cells (BCSCs). Stem cells were isolated and purified from MCF-7 cells by using the immunomagnetic microbeads. HIF-2α ORF/shRNA lentiviral vectors were transduced into MCF-7 stem cells respectively, and then the stable stem cell lines were detected and gained. Using the method of Cell Counting Kit-8 (CCK-8) and flow cytometry, the effect of HIF-2α on cell vitality and apoptosis of MCF-7 cancer stem cells (CSCs) were tested. Serum-free suspension culture was used on MCF-7 cells to get breast CSCs microspheres. The expression of CD44(+) in different groups were detected by flow cytometry. Tumor-bearing nude mice model was established to compare tumor growth rate and pulmonary metastasis probability of MCF-7 CSC HIF-2α knock up/down . Compared with MCF-7 CSC group, the apoptosis rate of MCF-7 CSCs HIF-2α knockup group decreased obviously and cell proliferation activity increased significantly (all <0.05). However, the MCF-7 CSCs HIF-2α knock down group had the opposite trend. Results of flow cytometry showed that the proportion of CD44(+) cells in HIF-2α knock up group(93.0%)was much higher than MCF-7 group(83.8%)and MCF-7 HIF-2α knock down group(51.6%). The tumor growth rate, quality and lung metastasis rate of MCF-7 CSC HIF-2α knock up group were significantly higher than those in MCF-7 CSCs group and MCF-7 CSCs HIF-2α knock down group (<0.01). In hypoxic microenvironment, up-regulation of HIF-2αpromoted the formation of MCF-7 CSCs. Over-expression of HIF-2α can promote proliferation and inhibit apoptosis of MCF-7 CSCs, and thus increase the risk of tumorigenic ablility and pulmonary metastasis.
探讨缺氧诱导因子(HIF)-2α对乳腺癌干细胞(BCSCs)生物学特性的影响。采用免疫磁珠法从MCF-7细胞中分离纯化干细胞。将HIF-2α ORF/shRNA慢病毒载体分别转导至MCF-7干细胞中,然后检测并获得稳定的干细胞系。采用细胞计数试剂盒-8(CCK-8)法和流式细胞术检测HIF-2α对MCF-7癌干细胞(CSCs)细胞活力和凋亡的影响。对MCF-7细胞进行无血清悬浮培养以获得乳腺CSCs微球。采用流式细胞术检测不同组中CD44(+)的表达。建立荷瘤裸鼠模型,比较MCF-7 CSC HIF-2α敲低/敲高组的肿瘤生长速率和肺转移概率。与MCF-7 CSC组相比,MCF-7 CSCs HIF-2α敲高组的凋亡率明显降低,细胞增殖活性显著增加(均P<0.05)。然而,MCF-7 CSCs HIF-2α敲低组则呈现相反趋势。流式细胞术结果显示,HIF-2α敲高组中CD44(+)细胞的比例(93.0%)远高于MCF-7组(83.8%)和MCF-7 HIF-2α敲低组(51.6%)。MCF-7 CSC HIF-2α敲高组的肿瘤生长速率、质量和肺转移率均显著高于MCF-7 CSCs组和MCF-7 CSCs HIF-2α敲低组(P<0.01)。在缺氧微环境中,HIF-2α的上调促进了MCF-7 CSCs的形成。HIF-2α的过表达可促进MCF-7 CSCs的增殖并抑制其凋亡,从而增加致瘤能力和肺转移风险。