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Comparative proteome profiling of MCF10A and 184A1 human breast epithelial cells emphasized involvement of CDK4 and cyclin D3 in cell proliferation
被引:5
作者:
Bhaskaran, Nimesh
[1
]
Lin, Kah Wai
[1
]
Gautier, Aude
[1
,2
]
Woksepp, Hanna
[1
,2
]
Hellman, Ulf
[2
]
Souchelnytskyi, Serhiy
[1
]
机构:
[1] Karolinska Univ Hosp, Karolinska Biom Ctr, Dept Oncol Pathol, Karolinska Inst, SE-17176 Stockholm, Sweden
[2] Uppsala Univ, Ludwig Inst Canc Res, Uppsala, Sweden
基金:
瑞典研究理事会;
关键词:
Breast epithelial cells;
CDK4;
Cyclin D3;
Proliferation;
Proteome profiling;
CANCER CELLS;
MASS-SPECTROMETRY;
EXPRESSION;
PHOSPHORYLATION;
ELECTROPHORESIS;
TRANSCRIPTION;
MODELS;
LINES;
BETA;
D O I:
10.1002/prca.200800045
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Acquiring high proliferation rate is crucial for carcinogenic transformation of cells. We report here proteome profiling of human breast epithelial cells with low (184A1) and high (MCF10A) proliferation rates. We identified 183 proteins in 184A1 and 318 proteins in MCF10A cells. These datasets provide the most comprehensive proteome annotations of 184A1 and MCF10A cells. Proteins were taken for identification from 2-D gels in a systematic and unbiased way. Functional clustering of the identified proteins showed similarities in distribution of proteins to the same functional domains, indicating similarities in proteomes of 184A1 and MCF10A cells. Among observed differences in protein expression, we validated correlation of expression of endogenous cyclin-dependent kinase 4 (CDK4), cyclin D3, cdc25B, and p38 gamma with cell proliferation. Furthermore, down-regulation of CDK4 and cyclin D3 with specific siRNA inhibited cell proliferation, which emphasized the role of CDK4 and cyclin D3 in enhancement of cell proliferation rate of human breast epithelial cells.
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页码:68 / 77
页数:10
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