VHIO

Growth Factors Group

Joaquín Arribas

Medical Oncologist
César Serrano

Post-Doctoral Fellows
Águeda Martínez Barriocanal, Beatriz Morancho, Josep Lluis Parra-Palau, Kim Pedersen, Mariano F. Zacarías

Graduate Students
Cristina Bernadó, Faiz Bilal, Rocío Vicario

Technicians
Marta Escorihuela, Cristina Ferrer, Mariona Gelabert, Antoni Luque

PhD Student
Junjie Zhang

SUMMARY

Continuing our focus on breast cancer and receptor tyrosine kinases, during 2014 we completed the characterization of the role of the receptor tyrosine kinase HER2 in breast cancer progression and identified PELO as a negative regulator of the signaling pathways initiated by HER2. Importantly, the knock down of PELO increases the metastatic ability of breast cancer cells. In addition, we showed that breast cancer cells that express a fragment of HER2, known as p95HER2, are particularly sensitive to chemotherapy combined with targeted therapies.

We have also been collaborating with other VHIO groups, particularly with the Tumor Biomarkers group led by Josep Villanueva, to characterize how cancer cells remodel the extracellular environment.
We are extremely grateful to the Spanish Association Against Cancer (AECC) and the Breast Cancer Research Foundation (BCRF) for their continued, critical support of our research.
Lastly, but by no means least,

Our group continues to coordinate the Breast Cancer Program within the Red Territorial de Investigación Cooperativa en Cáncer, supported by the Insituto de Salud Carlos III (ISCIII). This network incorporates many of the most active groups working on breast cancer in Spain. We work in close connection to deliver on complex projects that require the input and expertise of multiple groups.

PUBLICATIONS

Total 4.
Impact Factor 32.684
Average I.F. 8.171

  • Parra-Palau, J. Ll., Morancho, B., Peg, P., Scaltriti, M., Vicario, R., Zacarias-Fluck, M., Pedersen, K., Pandiella, A., Nuciforo, P., Serra, V., Cortés, J., Baselga, J., M. Perou, C. M., Prat, A., Isabel Rubio, I & Arribas, J. (2014) Effect of p95HER2/611CTF on the Response to Trastuzumab and Chemotherapy. J Natl Cancer Inst 106, dju291 http://jnci.oxfordjournals.org/content/106/11/dju291.abstract
    Comment in Cancer Discovery http://cancerdiscovery.aacrjournals.org/content/5/1/OF7.full
  • García-Parra, J., Arpí, O., Morancho, B., Dalmases, A., Menendez, S., Zazo, S., Chamizo, C., Eroles, P., Servitja, S., Tusquets, I., Yelamos, J., Lluch, A., Arribas, J., Rojo, F., Rovira, A. and Albanell, J. (2014) Poly (ADP-ribose) polymerase inhibition enhances trastuzumab antitumor activity in HER2 overexpressing breast cancer. Eur J Can 50, 2725-2734. http://www.ncbi.nlm.nih.gov/pubmed/?term=PMID%3A+25128455
  • Gregori, J., Méndez, O., Katsila, T., Pujals, M., Salvans, C., Villarreal, L., Arribas, J., Tabernero, J., Sánchez, A. and Villanueva, J. (2014) Enhancing the Biological Relevance of Secretome-based Proteomics by Linking Tumor Cell Proliferation and Protein Secretion. J Proteom Res 13, 3706–3721. http://pubs.acs.org/doi/abs/10.1021/pr500304g
  • Pedersen, K., Canals, F., Tabernero, J. and Arribas, J. PELO negatively regulates HER-receptor signaling and metastasis (2014). Oncogene 33, 1190-1197. http://www.nature.com/onc/journal/v33/n9/full/onc201335a.html