Source:http://linkedlifedata.com/resource/pubmed/id/18480994
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2008-5-15
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pubmed:abstractText |
In order to evaluate the effect of mitofusin-2 gene (mfn2) on proliferation and chemotherapy sensitivity of human breast carcinoma cell line MCF-7 in vitro, pEGFPmfn2 plasmid carrying full length of mitofusin-2 gene was transfected, by using sofast, into MCF-7 cells. Mitofusin-2 gene expression in MCF-7 cells transfected by sofast after 48 h was detected by PCR and Western blotting, and the stable expression of GFP protein in MCF-7 cells by Western blot analysis. The proliferation of MCF-7 cells was assayed by MTT and cell counting. By using PI method, the effects of mfn2 on the cell cycle distribution of MCF-7 were measured. Annexin-V/PI double labeling method was employed to detect the changes in apoptosis induced by chemotherapeutics before and after transfection. The results showed that the MCF-7 cells transfected with mfn2 gene could stably and highly express GFP protein. MTT assay revealed that after transfection of mfn2 cDNA, the proliferation of MCF-7 cells was significantly inhibited. DNA histogram showed that cells arrested in S phase, and the percentage of S phase cells was 42.7, 17.2 and 19.6 in mfn2 cDNA transfection group, blank plasmid transfection group and blank control group, respectively (P<0.05). The apoptosis ratio of the cells transfected with mfn2 gene was increased from 3.56% to 15.95%, that of the cells treated with camptothecin (CAMP) followed by mfn2 gene transfection was 69.6%, and that in blank plasmid transfection group and blank control group was 31.0% and 23.4% respectively (P<0.05). It was suggested that transfection of mfn2 gene could significantly inhibit the proliferation of MCF-7 cells and promote their sensitivity to CAMP with a synergic effect.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents, Phytogenic,
http://linkedlifedata.com/resource/pubmed/chemical/Camptothecin,
http://linkedlifedata.com/resource/pubmed/chemical/Green Fluorescent Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/MFN2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Mitochondrial Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1672-0733
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
28
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
185-9
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pubmed:meshHeading |
pubmed-meshheading:18480994-Antineoplastic Agents, Phytogenic,
pubmed-meshheading:18480994-Apoptosis,
pubmed-meshheading:18480994-Camptothecin,
pubmed-meshheading:18480994-Cell Cycle,
pubmed-meshheading:18480994-Cell Line, Tumor,
pubmed-meshheading:18480994-Cell Proliferation,
pubmed-meshheading:18480994-Drug Screening Assays, Antitumor,
pubmed-meshheading:18480994-Flow Cytometry,
pubmed-meshheading:18480994-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:18480994-Green Fluorescent Proteins,
pubmed-meshheading:18480994-Humans,
pubmed-meshheading:18480994-Membrane Proteins,
pubmed-meshheading:18480994-Mitochondrial Proteins,
pubmed-meshheading:18480994-Transfection
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pubmed:year |
2008
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pubmed:articleTitle |
Effects of mitofusin-2 gene on cell proliferation and chemotherapy sensitivity of MCF-7.
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pubmed:affiliation |
Department of General Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China. xiayun7373@126.com
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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