Comparative gene-expression profiling of CD133+ and CD133- D10 melanoma cells

被引:10
|
作者
Roudi, Raheleh [1 ,2 ]
Ebrahimi, Marzieh [3 ]
Sabet, Mehrdad Nasrollahzadeh [2 ]
Najafi, Ali [4 ]
Nourani, Mohamad Reza [5 ]
Fomeshi, Motahareh Rajabi [3 ]
Samadikuchaksaraei, Ali [6 ,7 ]
Shariftabrizi, Ahmad [8 ]
Madjd, Zahra [1 ,2 ]
机构
[1] Iran Univ Med Sci, Oncopathol Res Ctr, Tehran 1449614530, Iran
[2] Iran Univ Med Sci, Fac Adv Technol Med, Dept Mol Med, Tehran 1449614530, Iran
[3] ACECR, Royan Inst Stem Cell Biol & Technol, Dept Stem Cells & Dev Biol, Cell Sci Res Ctr, Tehran, Iran
[4] Baqiyatallah Univ Med Sci, Mol Biol Res Ctr, Tehran, Iran
[5] Baqiyatallah Univ Med Sci, Syst Biol Inst, Genom Div, Chem Injury Res Ctr, Tehran, Iran
[6] Iran Univ Med Sci, Cellular & Mol Res Ctr, Tehran 1449614530, Iran
[7] Iran Univ Med Sci, Fac Adv Technol Med, Dept Tissue Engn & Regenerat Med, Tehran 1449614530, Iran
[8] SUNY Buffalo, Dept Nucl Med & Mol Imaging, Buffalo, NY 14260 USA
关键词
cancer stem cells; CD133; cDNA microarray; D10 cell line; melanoma; CANCER STEM-CELLS; INITIATING CELLS; IDENTIFICATION; PROMININ-1; APOPTOSIS; FAMILY; GROWTH; TUMORS;
D O I
10.2217/fon.15.174
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims: The present study aimed to compare the gene-expression profiling of CD133(+) and CD133(-) D10 cells. Materials & methods: Cancer stem cell-like properties and gene-expression profiling of CD133(+) D10 cells versus CD133(-) cells were evaluated. Results: The CD133(+) D10 cells showed significantly higher clonogenic and spheroid forming potential, also higher expression of stemness genes NANOG and OCT4A compared with the CD133(-) cells. Gene-expression profiling of CD133(+) versus CD133(-) D10 cells revealed that 130 genes including ABC transporter superfamily (ABCC1, ABCG2 and ABCC6) were upregulated, while 61 genes including apoptosis modifying genes (CASP8 and TNFRSF4) were downregulated. Conclusion: We conclude that many genes involved in drug resistance and tumor aggressiveness are upregulated in CD133(+) D10 cells and targeting them might be an efficient strategy for treatment of melanoma.
引用
收藏
页码:2383 / 2393
页数:11
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