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PAI1 is a Marker of Bad Prognosis in Rectal Cancer but Predicts a Better Response to Treatment with PIM Inhibitor AZD1208

Authors :
Ministerio de Ciencia, Innovación y Universidades (España)
Agencia Estatal de Investigación (España)
European Commission
Centro de Investigación Biomédica en Red Cáncer (España)
Junta de Andalucía
Asociación Española Contra el Cáncer
Fundación Eugenio Rodríguez Pascual
Instituto de Salud Carlos III
Muñoz-Galván, Sandra
Rivero, María
Peinado-Serrano, Javier
Martínez-Pérez, Julia
Fernández-Fernández, María Carmen
Ortiz Gordillo, M. J.
García-Heredia, J. M.
Carnero, Amancio
Ministerio de Ciencia, Innovación y Universidades (España)
Agencia Estatal de Investigación (España)
European Commission
Centro de Investigación Biomédica en Red Cáncer (España)
Junta de Andalucía
Asociación Española Contra el Cáncer
Fundación Eugenio Rodríguez Pascual
Instituto de Salud Carlos III
Muñoz-Galván, Sandra
Rivero, María
Peinado-Serrano, Javier
Martínez-Pérez, Julia
Fernández-Fernández, María Carmen
Ortiz Gordillo, M. J.
García-Heredia, J. M.
Carnero, Amancio
Publication Year :
2020

Abstract

Colorectal cancer (CRC) is the third most common cancer worldwide. The standard treatment in locally advanced rectal cancer is preoperative radiation alone or in combination with chemotherapy, followed by adjuvant chemotherapy. Rectal cancer is highly lethal, with only 20% of patients showing a complete remission (by RECIST) after standard treatment, although they commonly show local or systemic relapse likely due to its late detection and high chemotherapy resistance, among other reasons. Here, we explored the role of PAI1 (Serpin E1) in rectal cancer through the analyses of public patient databases, our own cohort of locally advanced rectal cancer patients and a panel of CRC cell lines. We showed that PAI1 expression is upregulated in rectal tumors, which is associated with decreased overall survival and increased metastasis and invasion in advanced rectal tumors. Accordingly, PAI1 expression is correlated with the expression of (Epithelial-to-Mesenchymal Transition) EMT-associated genes and genes encoding drug targets, including the tyrosine kinases PDGFRb, PDGFRa and FYN, the serine/threonine kinase PIM1 and BRAF. In addition, we demonstrate that cells expressing PAI1 protein are more sensitive to the PIM inhibitor AZD1208, suggesting that PAI1 could be used to predict response to treatment with PIM inhibitors and to complement radiotherapy in rectal tumors.

Details

Database :
OAIster
Publication Type :
Electronic Resource
Accession number :
edsoai.on1286562446
Document Type :
Electronic Resource