Aberrant microRNAs Expression in CD133+/CD326+ Human Lung Adenocarcinoma Initiating Cells from A549

被引:47
作者
Lin, Sheng [1 ]
Sun, Jian-guo [1 ]
Wu, Jing-bo
Long, Hai-xia [1 ]
Zhu, Cong-hui [1 ]
Xiang, Tong [1 ]
Ma, Hu [1 ]
Zhao, Zhong-quan [1 ]
Yao, Quan [1 ]
Zhang, An-mei [1 ]
Zhu, Bo [1 ]
Chen, Zheng-tang [1 ]
机构
[1] Third Mil Med Univ, Xinqiao Hosp, Inst Canc, Chongqing 400037, Peoples R China
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
A549; microarray; microRNA; paclitaxel; tumor initiating cells; CANCER STEM-CELLS; DOWN-REGULATION; SELF-RENEWAL; IDENTIFICATION; CD133(+); GROWTH; PROLIFERATION; LIVER;
D O I
10.1007/s10059-012-2252-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Increasing evidence demonstrates that miRNAs are involved in the dysregulation of tumor initiating cells (TICs) in various tumors. Due to a lack of definitive markers, cell sorting is not an ideal separation method for lung adenocarcinoma initiating cells. In this study, we combined paclitaxel with serum-free medium cultivation (inverse-induction) to enrich TICs from A549 cells, marked by CD133/CD326, defined features of stemness. We next investigated aberrant microRNAs in this subpopulation compared to normal cells with miRNA microarray and found that 50 miRNAs exhibited a greater than 2-fold change in expression. As further validation, 10 miRNAs were chosen to perform quantitative RT-PCR on the A549 cell line and primary samples. The results suggest that aberrant expression of miRNAs such as miR-29ab, miR-183, miR-175p and miR-127-3P may play an important role in regulating the bio-behavior of TICs.
引用
收藏
页码:277 / 283
页数:7
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