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Prostate cancer resistance
Aytes’s Lab

DESCRIPTION

Dr. Aytes´s laboratory aims at uncovering new mechanisms driving prostate cancer progression and therapeutic resistance. We utilize genetically-engineered mice to recapitulate the progression pathways observed in patients.

At The Aytes Lab we aim at identifying mechanisms of cancer progression and therapy resistance by developing a unique series of genetically-engineered mice (GEM) models, which are a key resource for the research lines currently undergoing in my group at IDIBELL. 

A strong research focus since the inception of my group in 2016 has been to understand how changes in the transcriptional networks of cancer cells determine the cell identity and impinge on treatment response. To this end, we initially defined the regulatory networks of metastatic and non-metastatic CRPC and identified a set of epigenetic chromatin remodelers, including Nsd2, strongly associated metastatic progression and survival. This study was the groundwork upon which we build an extensive program to identify epigenetic targets and vulnerabilities to be translated to preclinical stages. 

In parallel, our group has a strong interest in identifying resistance mechanisms to standard of care treatments in prostate cancer, mainly antiandrogens. Mutations in the Androgen Receptor (AR) are known to affect the molecular structure and are the most frequent alteration in prostate cancer. Yet, the structure-function relationship and how disease associated mutations affect the AR function in cancer is unclear. We have recently characterized some of these AR mutations and showed how they define the response to antiandrogenic treatmetns. 

At the crossroads of targeted therapies and conventional chemotherapy lies the use of PARP inhibitors. We are trying to understand the genomic determinants of response to PARP inhibition to expand the therapeutic landscape beyond DNA damage repair deficiency. This is particularly relevant for prostate cancer to expand PARP inhibitors beyond classical synthetic lethality involving HR mutant carriers.

The above-mentioned fundamental and translational research endeavors have been instrumental in consolidating the interdisciplinary Prostate Cancer research Group at IDIBELL, Hospital de Bellvitge (HUB), the Catalan Institute of Oncology (ICO) and University of Barcelona (UB). 

Group members

Alvaro Aytes

Group leaders

Group Leader

Ana Sofia Semiao Correaia de Rocha

Researchers

Research Associate

Rana El Bizri

Researchers

Postdoc

Lidia Franco Luzon

Researchers

Postdoc

Adrian Martinez Tebar

Researchers

Postdoc

Javier Sigüenza Andrade

Researchers

PhD candidate

Pilar Salamanca Jimenez

Researchers

PhD candidate

Nadia Garcia Lozano

Support staff

Research technician

Publications

ETV4 promotes metastasis in response to activation of PI3-kinase and Ras signaling in a mouse model of advanced prostate cancer

7 de August de 2013/in Aytes's Lab/by miguel

Proc Natl Acad Sci U S A. 2013 Sep 10;110(37):E3506-15. doi: 10.1073/pnas.1303558110. Epub 2013 Aug 5. ABSTRACT Combinatorial activation of PI3-kinase and RAS signaling occurs frequently in advanced prostate cancer and is associated with adverse patient outcome. We now report that the oncogenic Ets variant 4 (Etv4) promotes prostate cancer metastasis in response to coactivation […]

https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg 0 0 miguel https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg miguel2013-08-07 10:00:002013-08-07 10:00:00ETV4 promotes metastasis in response to activation of PI3-kinase and Ras signaling in a mouse model of advanced prostate cancer

B-Raf activation cooperates with PTEN loss to drive c-Myc expression in advanced prostate cancer

28 de July de 2012/in Aytes's Lab/by miguel

Cancer Res. 2012 Sep 15;72(18):4765-76. doi: 10.1158/0008-5472.CAN-12-0820. Epub 2012 Jul 25. ABSTRACT Both the PI3K → Akt → mTOR and mitogen-activated protein kinase (MAPK) signaling pathways are often deregulated in prostate tumors with poor prognosis. Here we describe a new genetically engineered mouse model of prostate cancer in which PI3K-Akt-mTOR signaling is activated by inducible […]

https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg 0 0 miguel https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg miguel2012-07-28 10:00:002012-07-28 10:00:00B-Raf activation cooperates with PTEN loss to drive c-Myc expression in advanced prostate cancer

Dual targeting of the Akt/mTOR signaling pathway inhibits castration-resistant prostate cancer in a genetically engineered mouse model

21 de July de 2012/in Aytes's Lab/by miguel

Cancer Res. 2012 Sep 1;72(17):4483-93. doi: 10.1158/0008-5472.CAN-12-0283. Epub 2012 Jul 19. ABSTRACT Although the prognosis for clinically localized prostate cancer is now favorable, there are still no curative treatments for castration-resistant prostate cancer (CRPC) and, therefore, it remains fatal. In this study, we investigate a new therapeutic approach for treatment of CRPC, which involves dual […]

https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg 0 0 miguel https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg miguel2012-07-21 10:00:002012-07-21 10:00:00Dual targeting of the Akt/mTOR signaling pathway inhibits castration-resistant prostate cancer in a genetically engineered mouse model

Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer

24 de November de 2011/in Aytes's Lab/by miguel

PLoS Biol. 2011 Nov;9(11):e1001199. doi: 10.1371/journal.pbio.1001199. Epub 2011 Nov 15. ABSTRACT Differentiated mammary epithelium shows apicobasal polarity, and loss of tissue organization is an early hallmark of breast carcinogenesis. In BRCA1 mutation carriers, accumulation of stem and progenitor cells in normal breast tissue and increased risk of developing tumors of basal-like type suggest that BRCA1 […]

https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg 0 0 miguel https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg miguel2011-11-24 11:00:002011-11-24 11:00:00Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer
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Research group photo. Aytes's Lab
Program Against Cancer Therapeutic Resistance

CONTACT US

Campus IDIBELL
(L’Hospitalet del Llobregat)
Hospital Duran i Reynals, Gran Via 199,
L’Hospitalet del Llobregat,
Barcelona 08908
Tel. +34 93 260 7952

Campus IGTP-IJC
(Badalona)
Campus Can Ruti – IGTP – Building Muntanya,
Rd. Can Ruti, Camí de les escoles s/n,
Badalona, Barcelona 08916
Tel. +34 93 554 3069

Campus IDIBGI
(Girona)
Parc Hospitalari Martí i Julià de Salt, Dr. Castany s/n,
Salt, Girona 17190
Tel. +34 872 987 087

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