miRNAs expressed differently in cancer stem cells and cancer cells of human gastric cancer cell line MKN-45

被引:61
作者
Golestaneh, Azadeh Fahim [2 ,5 ]
Atashi, Amir [1 ,2 ]
Langroudi, Lida [3 ,4 ]
Shafiee, Abbas [2 ]
Ghaemi, Nasser [5 ]
Soleimani, Masoud [1 ]
机构
[1] Tarbiat Modares Univ, Dept Hematol, Fac Med Sci, Tehran, Iran
[2] Stem Cell Technol Res Ctr, Stem Cell Biol Dept, Tehran, Iran
[3] Tarbiat Modares Univ, Dept Med Biotechnol, Fac Med Sci, Tehran 14115111, Iran
[4] Stem Cell Technol Res Ctr, Dept Mol Biol & Genet Engn, Tehran, Iran
[5] Univ Tehran, Coll Sci, Dept Biotechnol, Tehran, Iran
关键词
cancer stem cell; gastric cancer; miRNA; signalling; gene expression regulation; COLON-CARCINOMA CELLS; TUMOR-SUPPRESSOR; FRAGILE SITES; REGULATES EXPRESSION; INITIATING CELLS; DOWN-REGULATION; SOLID TUMORS; IN-VITRO; MICRORNAS; METASTASIS;
D O I
10.1002/cbf.2815
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
Recent studies show that cancers may originate from special cells named cancer stem cells (CSCs). As miRNAs have a prominent role in regulating cell activities, a question arise, that is, if there is any difference in miRNA expression level between CSC and other cancer cells of human gastric cancer cell line MKN-45. In this study, CSCs were isolated by fluorescence-activated cell sorter based on the expression level of cell surface marker CD44. CSC characteristics were checked using spheroid formation assay and soft agar assay. Using reverse transcriptase polymerase chain reaction (RT-PCR), the expression level of some stemness genes was studied. Real-time q-PCR was used for analysis of the expression level of miRNAs. CSCs were able to make spheroids and colonies, whereas other cancer cells failed to show aforementioned features. In addition, RT-PCR resulted in a difference in the expression levels of Nanog, Sox2, Lin28 and Oct-4 between these two kinds of cells. Real-time RT-PCR analysis demonstrated an increase in mir-21 and mir-302 expression level in CSCs, relative to cancer cells, whereas let-7a expression level was decreased in CSC in comparison with cancer cells, which may be due to their different differentiation level. On the other hand, mir-372, mir-373 and mir-520c-5p were markedly increased in cancer cells in comparison with CSCs. This study shows that there is a difference in miRNA expression level between CSCs and other cancer cells, which reflects dissimilar molecular pathways in these cells. These miRNAs may be promising objects for targeting CSCs specifically and efficiently. Copyright (C) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:411 / 418
页数:8
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