Man

Antonio . Garcia de Herreros Madueno

Senior Scientist and Full Professor

Hospital del Mar

Barcelona, España

Líneas de Investigación


Characterization of the mechanisms controlling E-cadherin gene expression in tumor cells. The factors repressing E-cadherin transcription in invasive cells. Analysis of the elements involved in thetranscription of mesenchymal genes during EMT.

Educación

  •  PhD in Biochemistry, Universidad Autonoma de Madrid. España, 1985
  •  Licenciatura en Ciencias Quimicas, UNIVERSIDAD COMPLUTENSE DE MADRID. España, 1980

Formación de Capital Humano


Ph.D Thesis Director

Number of thesis accomplished: 20; A. Skoudy (1995), E. Batlle (1999), M. M. Llosas (2000), S. Roura (2001), J. A. Piedra (2003), D. Domínguez (2003), S. Miravet (2003), I. Puig (2005), S. Guaita (2005), J. Castaño ( 2005); B. Montserrat (2006); M. Escrivà (2008); A. Virgós (2008); P. Villagrasa (2010), M. Beltran (2010), N. Herranz (2011), R. Batlle (2011), R. Viñas (2013), A. Millanes (2014), E. Aparicio (2014).



 

Article (22)

Multivesicular GSK3 sequestration upon Wnt signaling is controlled by p120-catenin/cadherin interaction with LRP5/6.
Nuclear ubiquitination by FBXL5 modulates Snail1 DNA binding and stability.
Snail1 expression is required for sarcomagenesis
Snail1 controls TGF- responsiveness and differentiation of Mesenchymal Stem Cells.
Akt2 interacts with Snail1 in E-cadherin promoter
Cooperation, amplification, and feed-back in epithelial-mesenchymal
Rac1 activation upon Wnt stimulation requires Rac1 and Vav2 binding to p120-catenin.
A coordinated action of CK1 isoforms in Wnt signaling.
Functional cooperation between Snail1 and Twist in the regulation of Zeb1 expression during epithelial-to-mesenchymal transition.
Wnt controls Kaiso transcriptional factor activity through CK1- dependent phosphorylation of p120-catenin.
A p120-catenin/CK1 complex regulates Wnt signalling
Snail family regulation and epithelial mesenchymal transitions in breast cancer progression.
A natural antisense transcript regulates Zeb2/Sip1 gene expression during Snail1-induced epithelial-mesenchymal transition
Polycomb complex 2 is required for E-cadherin repression by the Snail1 transcription factor
Expression of Snail protein in tumor-stroma interface.
Regulation of Snail transcription during epithelial to mesenchymal-transition of tumor cells.
) p120-catenin-associated Fer and Fyn tyrosine kinases regulate -catenin Tyr-142 phosphorylation and -catenin--catenin interaction
Phosphorylation regulates nuclear export and activity of Snail transcriptional repressor
Snail induction of epithelial-to-mesenchymal transition in tumor cells is accompanied by MUC-1 repression and ZEB1 expression
Regulation of -catenin structure and function by tyrosine phosphorylation
The transcription factor Snail is a repressor of E-cadherin gene expression in epithelial tumour cells.
Regulation of E-cadherin/catenin association by tyrosine phosphorylation
22
Antonio Garcia de Herreros

Senior Scientist and Full Professor

Parc de Recerca Biomèdica de Barcelona

Hospital del Mar

Barcelona, España