Highly Altered Protein Expression Profile in the Adriamycin Resistant MCF-7 Cell Line
- 6 December 2003
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Proteome Research
- Vol. 3 (3) , 403-409
- https://doi.org/10.1021/pr0340577
Abstract
The protein expression pattern in the cytosol fraction of the adriamycin resistant MCF-7 cell line (MCF-7/ADR) was compared to that of the parental MCF-7 cell line using two-dimensional gel electrophoresis and mass spectrometry. Twenty proteins with altered abundances were identified and studied in MCF-7/ADR. Both up regulation and down regulation are characterized. The most striking differences were found for proteins that were uniquely expressed in this cell line and not detectable in the parental MCF-7 cell line. These proteins include annexin I, the neuronal ubiquitin carboxyl hydrolase isoenzyme L-1 (also known as PGP9.5), glutathione-S-transferase pi class, nicotinamide N-methyltransferase, and interleukin-18 precursor. On the other hand, catechol-O-methyltransferase was expressed in the parental cell line, but was not detected in the adriamycin resistant cell line. This protein expression pattern was unique to MCF-7/ADR and not observed in MCF-7 cell lines selected for resistant to etoposide, mitoxantrone or melphalan. Keywords: comparative proteomics • adriamycin • MCF-7 • ubiquitin carboxyl hydrolase • glutathione S-transferase • annexins • chemoresistanceKeywords
This publication has 18 references indexed in Scilit:
- Identification of metastasis‐associated proteins by proteomic analysis and functional exploration of interleukin‐18 in metastasisProteomics, 2003
- Annexins: From Structure to FunctionPhysiological Reviews, 2002
- Multidrug resistance in cancer: role of ATP–dependent transportersNature Reviews Cancer, 2002
- Lack of glutathione conjugation to adriamycin in human breast cancer MCF-7/DOX cells: Inhibition of glutathione s-transferase p1–1 by glutathione conjugates from anthracyclinesBiochemical Pharmacology, 2000
- PGP9.5 As a Candidate Tumor Marker for Non-Small-Cell Lung CancerThe American Journal of Pathology, 1999
- P-Glycoprotein Shows Strong Catalytic Cooperativity between the Two Nucleotide SitesBiochemistry, 1998
- The Neuron-Specific Protein PGP 9.5 Is a Ubiquitin Carboxyl-Terminal HydrolaseScience, 1989
- Role of the Glutathione Redox Cycle in Acquired and de Novo Multidrug ResistanceScience, 1988
- Multidrug Resistance1JNCI Journal of the National Cancer Institute, 1988
- Studies on the interaction of cupric isonicotinohydrazide with DNABiochemistry, 1987