Vimentin and epithelial-mesenchymal transition in human breast cancer - Observations in vitro and in vivo

被引:323
作者
Kokkinos, Maria I.
Wafai, Razan
Wong, Meng Kang
Newgreen, Donald F.
Thompson, Erik W.
Waltham, Mark
机构
[1] Univ Melbourne, St Vincents Hosp, Dept Surg, Melbourne, Vic, Australia
[2] Royal Childrens Hosp, Embryol Lab, Murdoch Childrens Res Inst, Melbourne, Vic, Australia
[3] St Vincents Inst Med Res, Invas & Metastasis Unit, Victorian Breast Canc Res Consortium, Melbourne, Vic, Australia
关键词
breast cancer; epithelial-mesenchymal transition; PMC42; prognosis; vimentin; xenograft;
D O I
10.1159/000101320
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Breast cancer is a highly prevalent disease among women worldwide. While the expression of certain proteins within these tumours is used for prognosis and selection of therapies, there is a continuing need for additional markers to be identified. A considerable amount of current literature, based predominantly on cell culture systems, suggests that a major mechanism responsible for the progression of breast cancer is due to tumour cells losing their epithelial features and gaining mesenchymal properties. These events are proposed to be very similar to the epithelial-mesenchymal transition (EMT) process that has been well characterised in embryonic development. For the developmental and putative cancer EMT, the cell intermediate filament status changes from a keratin-rich network which connects to adherens junctions and hemidesmosomes, to a vimentin-rich network connecting to focal adhesions. This review summarises observations of vimentin expression in breast cancer model systems, and discusses the potential role of EMT in human breast cancer progression, and the prognostic usefulness of vimentin expression. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:191 / 203
页数:13
相关论文
共 68 条
[1]   Epidermal growth factor-induced epithelio-mesenchymal transition in human breast carcinoma cells [J].
Ackland, ML ;
Newgreen, DF ;
Fridman, M ;
Waltham, MC ;
Arvanitis, A ;
Minichiello, J ;
Price, JT ;
Thompson, EW .
LABORATORY INVESTIGATION, 2003, 83 (03) :435-448
[2]   PULMONARY BLASTOMA, CARCINOSARCOMA AND SPINDLE-CELL CARCINOMA - AN IMMUNOHISTOCHEMICAL STUDY OF KERATIN INTERMEDIATE FILAMENTS [J].
ADDIS, BJ ;
CORRIN, B .
JOURNAL OF PATHOLOGY, 1985, 147 (04) :291-301
[3]  
Badwaik NK, 1998, J REPROD FERTIL, V114, P307
[4]   Phosphatidylinositol 3-kinase function is required for transforming growth factor β-mediated epithelial to mesenchymal transition and cell migration [J].
Bakin, AV ;
Tomlinson, AK ;
Bhowmick, NA ;
Moses, HL ;
Arteaga, CL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (47) :36803-36810
[5]   OVEREXPRESSION OF THE VIMENTIN GENE IN TRANSGENIC MICE INHIBITS NORMAL LENS CELL-DIFFERENTIATION [J].
CAPETANAKI, Y ;
SMITH, S ;
HEATH, JP .
JOURNAL OF CELL BIOLOGY, 1989, 109 (04) :1653-1664
[6]   Vimentin antibodies: A non-HLA antibody as a potential risk factor in renal transplantation [J].
Carter, V ;
Shenton, BK ;
Jaques, B ;
Turner, D ;
Talbot, D ;
Gupta, A ;
Chapman, CE ;
Matthews, CJ ;
Cavanagh, G .
TRANSPLANTATION PROCEEDINGS, 2005, 37 (02) :654-657
[7]   Intravital imaging of cell movement in tumours [J].
Condeelis, J ;
Segall, JE .
NATURE REVIEWS CANCER, 2003, 3 (12) :921-930
[8]   Alterations in the immunohistochemical localization patterns of α-smooth muscle actin (SMA) and vimentin in the postnatally developing bovine cryptorchid testis [J].
Devkota, Bhuminand ;
Sasaki, Motoki ;
Matsui, Motozumi ;
Montoya, Carlos Amaya ;
Miyake, Yoh-Ichi .
JOURNAL OF REPRODUCTION AND DEVELOPMENT, 2006, 52 (03) :329-334
[9]  
Duband JL, 1995, ACTA ANAT, V154, P63
[10]   Understanding breast cancer risk - where do we stand in 2005? [J].
Dumitrescu, RG ;
Cotarla, I .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2005, 9 (01) :208-221