Oncotarget

Research Papers:

E-cadherin downregulation sensitizes PTEN-mutant tumors to PI3Kβ silencing

África Millán-Uclés, Susana Zuluaga, Miriam Marqués, Jesus Vallejo-Díaz, Lorena Sanz, Ariel E. Cariaga-Martínez, Francisco X. Real and Ana C. Carrera _

PDF  |  HTML  |  Supplementary Files  |  How to cite  |  Order a Reprint

Oncotarget. 2016; 7:84054-84071. https://doi.org/10.18632/oncotarget.13414

Metrics: PDF 1901 views  |   HTML 2117 views  |   ?  


Abstract

África Millán-Uclés1,*, Susana Zuluaga1,*, Miriam Marqués2, Jesus Vallejo-Díaz1, Lorena Sanz1, Ariel E. Cariaga-Martínez1, Francisco X. Real2,3 and Ana C. Carrera1

1 Department of Immunology and Oncology, Centro Nacional de Biotecnología/CSIC, Universidad Autónoma de Madrid, Cantoblanco, Madrid, Spain

2 Centro Nacional de Investigaciones Oncológicas, Melchor Fernández Almagro 3, Madrid, Spain

3 Departament de Ciències Experimentals i de la Salut, Universitat Pompeu Fabra, Barcelona, Spain

* These authors have contributted equally to this work

Correspondence to:

Ana C. Carrera, email:

Keywords: PI3Kbeta, PTEN, urothelial carcinoma, bladder cancer, siRNA

Received: October 15, 2016 Accepted: October 25, 2016 Published: November 16, 2016

Abstract

Alterations in phosphatidylinositol 3-kinase (PI3K) and in PTEN (phosphatase and tensin homolog), the negative regulator of the PI3K pathway, are found in nearly half of human tumors. As PI3Kβ, the main isoform activated in PTEN-mutant tumors, has kinase-dependent and -independent activities, we compared the effects of depleting vs. drug-inhibiting PI3Kβ kinase activity in a collection of diverse tumor types and in a set of bladder carcinoma cell lines grown as xenografts in mice. PI3Kβ depletion (by intratumor injection of PIK3CB siRNA) induced apoptosis and triggered regression of PTEN-mutant tumors more efficiently than PI3Kβ inhibition. A small proportion of these tumors was resistant to PI3Kβ downregulation; we analyzed what determined resistance in these cases. Using add-back experiments, we show that both PTEN mutation and low E-cadherin expression are necessary for PI3Kβ dependence. In bladder carcinoma, loss of E-cadherin expression coincides with N-cadherin upregulation. We found that PI3Kβ associated with N-cadherin and that PIK3CB depletion selectively disrupted N-cadherin cell adhesions in PTEN-mutant bladder carcinoma. These results support the use of PIK3CB interfering RNA as a therapeutic approach for high-risk bladder cancers that show E-cadherin loss and express mutant PTEN.


Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.
PII: 13414