Analysis of the E-cadherin repressor snail in primary human cancers

被引:115
作者
Becker, K.-F.
Rosivatz, E.
Blechschmidt, K.
Kremmer, E.
Sarbia, M.
Hoefler, H.
机构
[1] Tech Univ Munich, Inst Pathol, DE-81675 Munich, Germany
[2] GSF, Natl Res Ctr Environm & Hlth, Inst Mol Immunol, Munich, Germany
[3] GSF, Natl Res Ctr Environm & Hlth, Inst Pathol, Neuherberg, Germany
关键词
cadherin; adhesion; transcription factor; monoclonal antibody; formalin-fixed tissues;
D O I
10.1159/000101321
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
Epithelial-mesenchymal transition (EMT), a normal developmental process, is known to play a crucial role in tumor progression. Molecules involved in this process, such as the E-cadherin repressor Snail, facilitate migration and invasion of carcinoma cells. A growing number of studies addressing the expression of Snail in clinical samples have been reported and are discussed in this review. A total of 2,112 cases from 9 different tumor types were evaluated. So far, a clear picture has emerged only in some cancer types analyzed with regard to overexpression of Snail and clinical-pathological parameters. Currently, it seems that Snail may play a role in hormone-dependent carcinomas but may be of minor importance in gastrointestinal cancers for tumor dedifferentiation and the maintenance of the invasive phenotype. It should be kept in mind, however, that the threshold for Snail activity does not have to be the same in every tumor type analyzed. The recent introduction of well-characterized novel monoclonal antibodies reacting with the short-lived nuclear Snail protein may help to establish a potential clinical usefulness for this master molecule of EMT, at least for certain types of cancer. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:204 / 212
页数:9
相关论文
共 42 条
  • [1] Glycogen synthase kinase-3 is an endogenous inhibitor of snail transcription: implications for the epithelial-mesenchymal transition
    Bachelder, RE
    Yoon, SO
    Franci, C
    de Herreros, AG
    Mercurio, AM
    [J]. JOURNAL OF CELL BIOLOGY, 2005, 168 (01) : 29 - 33
  • [2] Regulation of Snail transcription during epithelial to mesenchymal transition of tumor cells
    Barberà, MJ
    Puig, I
    Domínguez, D
    Julien-Grille, S
    Guaita-Esteruelas, S
    Peiró, S
    Baulida, J
    Francí, C
    Dedhar, S
    Larue, L
    de Herreros, AG
    [J]. ONCOGENE, 2004, 23 (44) : 7345 - 7354
  • [3] The Snail genes as inducers of cell movement and survival: implications in development and cancer
    Barrallo-Gimeno, A
    Nieto, MA
    [J]. DEVELOPMENT, 2005, 132 (14): : 3151 - 3161
  • [4] The transcription factor Snail is a repressor of E-cadherin gene expression in epithelial tumour cells
    Batlle, E
    Sancho, E
    Franci, C
    Domínguez, D
    Monfar, M
    Baulida, J
    de Herreros, AG
    [J]. NATURE CELL BIOLOGY, 2000, 2 (02) : 84 - 89
  • [5] Clinical proteomics:: New trends for protein microarrays
    Becker, K. -F.
    Metzger, V.
    Hipp, S.
    Hoefler, H.
    [J]. CURRENT MEDICINAL CHEMISTRY, 2006, 13 (15) : 1831 - 1837
  • [6] Correlation of Snail expression with histological grade and lymph node status in breast carcinomas
    Blanco, MJ
    Moreno-Bueno, G
    Sarrio, D
    Locascio, A
    Cano, A
    Palacios, J
    Nieto, MA
    [J]. ONCOGENE, 2002, 21 (20) : 3241 - 3246
  • [7] BLECHSMIDT K, 2006, UNPUB ECADHERIN REPR
  • [8] THE DROSOPHILA DEVELOPMENTAL GENE SNAIL ENCODES A PROTEIN WITH NUCLEIC-ACID BINDING FINGERS
    BOULAY, JL
    DENNEFELD, C
    ALBERGA, A
    [J]. NATURE, 1987, 330 (6146) : 395 - 398
  • [9] The transcription factor Snail controls epithelial-mesenchymal transitions by repressing E-cadherin expression
    Cano, A
    Pérez-Moreno, MA
    Rodrigo, I
    Locascio, A
    Blanco, MJ
    del Barrio, MG
    Portillo, F
    Nieto, MA
    [J]. NATURE CELL BIOLOGY, 2000, 2 (02) : 76 - 83
  • [10] Mechanisms of inactivation of E-cadherin in breast carcinoma: modification of the two-hit hypothesis of tumor suppressor gene
    Cheng, CW
    Wu, PE
    Yu, JC
    Huang, CS
    Yue, CT
    Wu, CW
    Shen, CY
    [J]. ONCOGENE, 2001, 20 (29) : 3814 - 3823