P-Cadherin Linking Breast Cancer Stem Cells and Invasion: A Promising Marker to Identify an "Intermediate/Metastable" EMT State.

作者: Ana Sofia Ribeiro , Joana Paredes

DOI: 10.3389/FONC.2014.00371

关键词:

摘要: Epithelial–mesenchymal transition (also known as EMT) is a fundamental mechanism occurring during embryonic development and tissue differentiation, being also crucial for cancer progression. Actually, the EMT program contributes to dissemination of cells from solid tumors formation micro-metastasis that subsequently develop into clinically detectable metastases. Besides process defined by progressive loss epithelial cell characteristics acquisition mesenchymal features, has been implicated in therapy resistance, immune escape, maintenance stem properties, such self-renewal capacity. However, majority studies usually neglect alterations intermediate states, which imply range phenotypic cellular heterogeneity can potentially generate more metastable plastic tumor cells. In fact, few have tried identify these transitory partly due current lack detailed understanding EMT, well reliable readouts its Herein, brief review evidences presented, showing P-cadherin expression, already identified breast marker invasive promoter, probably able an state associated with phenotype. This hypothesis based on our own work, results described others, suggest use promising marker, clearly functioning important clinical prognostic factor putative therapeutic target carcinogenesis.

参考文章(64)
Rozany Dufloth, André Albergaria, Nair Lopes, Fernanda Milanezi, Bárbara Sousa, Joana Paredes, José Luis Costa, Fernando Schmitt, Daniella Vieira, Sílvia Carvalho, Vitor Carneiro, Luiz Veronese, Diana Martins, Luiz Zeferino, P-cadherin, Vimentin and CK14 for identification of basal-like phenotype in breast carcinomas: an immunohistochemical study Histology and Histopathology. ,vol. 25, pp. 963- 974 ,(2010) , 10.14670/HH-25.963
Siew Ping Han, Alpha S. Yap, The Cytoskeleton and Classical Cadherin Adhesions Subcellular Biochemistry. ,vol. 60, pp. 111- 135 ,(2012) , 10.1007/978-94-007-4186-7_6
L Biddlestone, N Shepherd, Janusz Jankowski, H Barr, P Warner, T Bailey, Altered cadherin and catenin complexes in the Barrett's esophagus-dysplasia-adenocarcinoma sequence. Correlation with disease progression and dedifferentiation American Journal of Pathology. ,vol. 152, pp. 135- 144 ,(1998)
Michael W. Klymkowsky, Pierre Savagner, Epithelial-Mesenchymal Transition The American Journal of Pathology. ,vol. 174, pp. 1588- 1593 ,(2009) , 10.2353/AJPATH.2009.080545
Ana Sofia Ribeiro, Bárbara Sousa, Laura Carreto, Nuno Mendes, Ana Rita Nobre, Sara Ricardo, André Albergaria, Jorge F Cameselle-Teijeiro, Rene Gerhard, Ola Söderberg, Raquel Seruca, Manuel A Santos, Fernando Schmitt, Joana Paredes, P-cadherin functional role is dependent on E-cadherin cellular context : a proof of concept using the breast cancer model The Journal of Pathology. ,vol. 229, pp. 705- 718 ,(2013) , 10.1002/PATH.4143
Jean Paul Thiery, Hervé Acloque, Ruby Y.J. Huang, M. Angela Nieto, Epithelial-Mesenchymal Transitions in Development and Disease Cell. ,vol. 139, pp. 871- 890 ,(2009) , 10.1016/J.CELL.2009.11.007
A Jeanes, C J Gottardi, A S Yap, Cadherins and cancer: how does cadherin dysfunction promote tumor progression? Oncogene. ,vol. 27, pp. 6920- 6929 ,(2008) , 10.1038/ONC.2008.343
Mayssa Nassour, Ysia Idoux-Gillet, Abdelkader Selmi, Christophe Côme, Maria-Luisa M. Faraldo, Marie-Ange Deugnier, Pierre Savagner, Slug Controls Stem/Progenitor Cell Growth Dynamics during Mammary Gland Morphogenesis PLoS ONE. ,vol. 7, pp. e53498- ,(2012) , 10.1371/JOURNAL.PONE.0053498
Carlos Gamallo, Gema Moreno-Bueno, David Sarrió, Francisco Calero, David Hardisson, José Palacios, The Prognostic Significance of P-Cadherin in Infiltrating Ductal Breast Carcinoma Modern Pathology. ,vol. 14, pp. 650- 654 ,(2001) , 10.1038/MODPATHOL.3880367
Ila S. Patel, Pavneesh Madan, Spiro Getsios, Monique A. Bertrand, Colin D. MacCalman, Cadherin switching in ovarian cancer progression International Journal of Cancer. ,vol. 106, pp. 172- 177 ,(2003) , 10.1002/IJC.11086