Development of drug resistance in the population of colon cancer cells under the effect of multifunctional protein YB-1
The effects of YB-1 gene on the expression level of P-glycoprotein and drug resistance of tumor cells were studied in cultured HCT116 colon cancer cells. Transitory transfection of chimeric YB-1/GFP gene rendered HCT116 cells a selective advantage in a medium with vinblastine, which caused transloca...
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| Published in: | Bulletin of experimental biology and medicine Vol. 143; no. 4; pp. 463 - 466 |
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| Format: | Journal Article |
| Language: | English |
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Springer Nature B.V
01-04-2007
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| Abstract | The effects of YB-1 gene on the expression level of P-glycoprotein and drug resistance of tumor cells were studied in cultured HCT116 colon cancer cells. Transitory transfection of chimeric YB-1/GFP gene rendered HCT116 cells a selective advantage in a medium with vinblastine, which caused translocation of the chimeric protein into cell nuclei. This was paralleled by an increase in the expression of P-glycoprotein (multiple drug resistance protein). |
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| AbstractList | The effects of YB-1 gene on the expression level of P-glycoprotein and drug resistance of tumor cells were studied in cultured HCT116 colon cancer cells. Transitory transfection of chimeric YB-1/GFP gene rendered HCT116 cells a selective advantage in a medium with vinblastine, which caused translocation of the chimeric protein into cell nuclei. This was paralleled by an increase in the expression of P-glycoprotein (multiple drug resistance protein). Issue Title: This issue is a translation of Byulleten' Eksperimental'noi Biologii i Meditsiny (Bulletin of Experimental Biology and Medicine) and Kletochnye Tekhnologii v Biologii i Meditsine (Cell Technologies in Biology and Medicine) The effects of YB-1 gene on the expression level of P-glycoprotein and drug resistance of tumor cells were studied in cultured HCT116 colon cancer cells. Transitory transfection of chimeric YB-1/GFP gene rendered HCT116 cells a selective advantage in a medium with vinblastine, which caused translocation of the chimeric protein into cell nuclei. This was paralleled by an increase in the expression of P-glycoprotein (multiple drug resistance protein). [PUBLICATION ABSTRACT] |
| Author | Vaiman, A V Stavrovskaya, A A Ovchinnikov, L P Sorokin, A V Rybalkina, E Yu Stromskaya, T P |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18214301$$D View this record in MEDLINE/PubMed |
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| Cites_doi | 10.1093/emboj/20.19.5491 10.1038/nm0497-447 10.1093/nar/gkh889 10.1038/sj.onc.1208386 10.1074/jbc.M100311200 10.1002/bies.10300 10.1074/jbc.275.4.2979 10.1074/jbc.273.11.5997 10.1002/(SICI)1097-0215(19991210)83:6<732::AID-IJC6>3.0.CO;2-# 10.1093/nar/25.14.2911 |
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| SubjectTerms | ATP Binding Cassette Transporter, Subfamily B, Member 1 - genetics ATP Binding Cassette Transporter, Subfamily B, Member 1 - metabolism Cell Line, Tumor Cell Nucleus - metabolism Colonic Neoplasms - genetics Colonic Neoplasms - metabolism Colonic Neoplasms - pathology Drug Resistance, Multiple - drug effects Drug Resistance, Multiple - genetics Drug Resistance, Neoplasm - genetics Gene Expression Regulation, Neoplastic - drug effects Green Fluorescent Proteins - genetics Green Fluorescent Proteins - metabolism Humans Microscopy, Fluorescence Protein Transport - drug effects Recombinant Fusion Proteins - genetics Recombinant Fusion Proteins - metabolism Vinblastine - pharmacology Y-Box-Binding Protein 1 - genetics Y-Box-Binding Protein 1 - metabolism Y-Box-Binding Protein 1 - physiology |
| Title | Development of drug resistance in the population of colon cancer cells under the effect of multifunctional protein YB-1 |
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