Global protein shotgun expression profiling of proliferating MCF-7 breast cancer cells

被引:28
作者
Sandhu, C
Connor, M
Kislinger, T
Slingerland, J
Emili, A
机构
[1] Univ Toronto, Banting & Best Dept Med Res, Program Proteom & Bioinformat, Toronto, ON, Canada
[2] Sunnybrook Hlth Sci Ctr, Div Canc Biol Res, Toronto, ON M4N 3M5, Canada
[3] Univ Miami, Sylvester Comprehens Canc Ctr, Braman Breast Canc Inst, Miami, FL 33152 USA
关键词
mass spectrometry; protein expression profiling; proteomics; breast cancer; cell cycle; proliferation;
D O I
10.1021/pr0498842
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Protein expression becomes altered in breast epithelium during malignant transformation. Knowledge of these perturbations should provide insight into the molecular basis of breast cancer, as well as reveal possible new therapeutic targets. To this end, we have performed an extensive comparative proteomic survey of global protein expression patterns in proliferating MCF-7 breast cancer cells and normal human mammary epithelial cells using gel-free shotgun tandem mass spectrometry. Pathophysiological alterations associated with the malignant breast cancer phenotype were detected, including differences in the apparent levels of key regulators of the cell cycle, signal transduction, apoptosis, transcriptional regulation, and cell metabolism.
引用
收藏
页码:674 / 689
页数:16
相关论文
共 171 条
  • [1] Comprehensive proteomic analysis of breast cancer cell membranes reveals unique proteins with potential roles in clinical cancer
    Adam, PJ
    Boyd, R
    Tyson, KL
    Fletcher, GC
    Stamps, A
    Hudson, L
    Poyser, HR
    Redpath, N
    Griffiths, M
    Steers, G
    Harris, AL
    Patel, S
    Berry, J
    Loader, JA
    Townsend, RR
    Daviet, L
    Legrain, P
    Parekh, R
    Terrett, JA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) : 6482 - 6489
  • [2] INSULIN-DEGRADING ENZYME - STABLE EXPRESSION OF THE HUMAN COMPLEMENTARY-DNA, CHARACTERIZATION OF ITS PROTEIN PRODUCT, AND CHROMOSOMAL MAPPING OF THE HUMAN AND MOUSE GENES
    AFFHOLTER, JA
    HSIEH, CL
    FRANCKE, U
    ROTH, RA
    [J]. MOLECULAR ENDOCRINOLOGY, 1990, 4 (08) : 1125 - 1135
  • [3] AKAO Y, 1995, CANCER RES, V55, P3444
  • [4] Gene Ontology: tool for the unification of biology
    Ashburner, M
    Ball, CA
    Blake, JA
    Botstein, D
    Butler, H
    Cherry, JM
    Davis, AP
    Dolinski, K
    Dwight, SS
    Eppig, JT
    Harris, MA
    Hill, DP
    Issel-Tarver, L
    Kasarskis, A
    Lewis, S
    Matese, JC
    Richardson, JE
    Ringwald, M
    Rubin, GM
    Sherlock, G
    [J]. NATURE GENETICS, 2000, 25 (01) : 25 - 29
  • [5] It's All in the Timing Linking S Phase to Chromatin Structure and Chromosome Dynamics
    Bailis, Julie M.
    Forsburg, Susan L.
    [J]. CELL CYCLE, 2003, 2 (04) : 303 - 306
  • [6] Genes commonly upregulated by hypoxia in human breast cancer cells MCF-7 and MDA-MB-231
    Bando, H
    Toi, M
    Kitada, K
    Koike, M
    [J]. BIOMEDICINE & PHARMACOTHERAPY, 2003, 57 (08) : 333 - 340
  • [7] The death effector domain protein family
    Barnhart, BC
    Lee, JC
    Alappat, EC
    Peter, ME
    [J]. ONCOGENE, 2003, 22 (53) : 8634 - 8644
  • [8] Batistatou A, 2004, IN VIVO, V18, P661
  • [9] DNA repair/pro-apoptotic dual-role proteins in five major DNA repair pathways: fail-safe protection against carcinogenesis
    Bernstein, C
    Bernstein, H
    Payne, CM
    Garewal, H
    [J]. MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2002, 511 (02) : 145 - 178
  • [10] A review of human papillomavirus vaccines: From basic science to clinical trials
    Berry, JM
    Palefsky, JM
    [J]. FRONTIERS IN BIOSCIENCE, 2003, 8 : S333 - S345