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1.
J Clin Invest ; 123(6): 2551-63, 2013 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-23635776

RESUMEN

The PI3K signaling pathway regulates diverse cellular processes, including proliferation, survival, and metabolism, and is aberrantly activated in human cancer. As such, numerous compounds targeting the PI3K pathway are currently being clinically evaluated for the treatment of cancer, and several have shown some early indications of efficacy in breast cancer. However, resistance against these agents, both de novo and acquired, may ultimately limit the efficacy of these compounds. Here, we have taken a systematic functional approach to uncovering potential mechanisms of resistance to PI3K inhibitors and have identified several genes whose expression promotes survival under conditions of PI3K/mammalian target of rapamycin (PI3K/mTOR) blockade, including the ribosomal S6 kinases RPS6KA2 (RSK3) and RPS6KA6 (RSK4). We demonstrate that overexpression of RSK3 or RSK4 supports proliferation upon PI3K inhibition both in vitro and in vivo, in part through the attenuation of the apoptotic response and upregulation of protein translation. Notably, the addition of MEK- or RSK-specific inhibitors can overcome these resistance phenotypes, both in breast cancer cell lines and patient-derived xenograft models with elevated levels of RSK activity. These observations provide a strong rationale for the combined use of RSK and PI3K pathway inhibitors to elicit favorable responses in breast cancer patients with activated RSK.


Asunto(s)
Antineoplásicos/farmacología , Neoplasias de la Mama/enzimología , Imidazoles/farmacología , Fosfatidilinositol 3-Quinasas/metabolismo , Quinolinas/farmacología , Proteínas Quinasas S6 Ribosómicas 90-kDa/metabolismo , Aminopiridinas/farmacología , Animales , Apoptosis/efectos de los fármacos , Neoplasias de la Mama/tratamiento farmacológico , Supervivencia Celular/efectos de los fármacos , Resistencia a Antineoplásicos , Sinergismo Farmacológico , Femenino , Expresión Génica , Regulación Enzimológica de la Expresión Génica/efectos de los fármacos , Regulación Neoplásica de la Expresión Génica/efectos de los fármacos , Compuestos Heterocíclicos con 3 Anillos/farmacología , Humanos , Células MCF-7 , Ratones , Ratones Desnudos , Terapia Molecular Dirigida , Morfolinas/farmacología , Sistemas de Lectura Abierta , Inhibidores de las Quinasa Fosfoinosítidos-3 , Proteínas Quinasas S6 Ribosómicas 90-kDa/antagonistas & inhibidores , Proteínas Quinasas S6 Ribosómicas 90-kDa/genética , Transducción de Señal , Transcriptoma , Carga Tumoral/efectos de los fármacos , Ensayos Antitumor por Modelo de Xenoinjerto
2.
Medisan ; 21(4)abr. 2017.
Artículo en Español | LILACS | ID: biblio-1000051

RESUMEN

La educación en valores constituye un aspecto esencial en la educación contemporánea, dada la necesidad de formar hombres capaces de transformar creadoramente el entorno donde habitan y, al mismo tiempo, ser ejemplo de comportamiento ciudadano y cívico. Se aborda la formación de valores en los predios universitarios. A tales efectos se muestran criterios sobre la naturaleza de los valores y su proceso en el contexto ecuatoriano.


Values education constitutes an essential aspect in contemporary education, due to the necessity of training men able to transform, in a creative way, the environment where they live in and, at the same time, be an example of citizen and civic behaviour. Values training is dealt with in the University grounds. To such effects some criteria about values nature and their process in the Ecuatorian context are shown.


Asunto(s)
Humanos , Masculino , Femenino , Valores Sociales , Educación Profesional , Docentes/educación , Gestión del Conocimiento , Deseabilidad Social , Desarrollo de Personal , Comunicación , Ecuador/etnología
3.
Clin Cancer Res ; 16(9): 2688-95, 2010 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-20406840

RESUMEN

PURPOSE: A subgroup of human epidermal growth factor receptor 2 (HER2)-overexpressing breast tumors coexpresses p95HER2, a truncated HER2 receptor that retains a highly functional HER2 kinase domain but lacks the extracellular domain and results in intrinsic trastuzumab resistance. We hypothesized that lapatinib, a HER2 tyrosine kinase inhibitor, would be active in these tumors. We have studied the correlation between p95HER2 expression and response to lapatinib, both in preclinical models and in the clinical setting. EXPERIMENTAL DESIGN: Two different p95HER2 animal models were used for preclinical studies. Expression of p95HER2 was analyzed in HER2-overexpressing breast primary tumors from a first-line lapatinib monotherapy study (EGF20009) and a second-line lapatinib in combination with capecitabine study (EGF100151). p95HER2 expression was correlated with overall response rate (complete + partial response), clinical benefit rate (complete response + partial response + stable disease > or =24 wk), and progression-free survival using logistic regression and Cox proportional hazard models. RESULTS: Lapatinib inhibited tumor growth and the HER2 downstream signaling of p95HER2-expressing tumors. A total of 68 and 156 tumors from studies EGF20009 and EGF100151 were evaluable, respectively, for p95HER2 detection. The percentage of p95HER2-positive patients was 20.5% in the EGF20009 study and 28.5% in the EGF100151 study. In both studies, there was no statistically significant difference in progression-free survival, clinical benefit rate, and overall response rate between p95HER2-positive and p95HER2-negative tumors. CONCLUSIONS: Lapatinib as a monotherapy or in combination with capecitabine seems to be equally effective in patients with p95HER2-positive and p95HER2-negative HER2-positive breast tumors.


Asunto(s)
Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , Neoplasias de la Mama/tratamiento farmacológico , Receptores ErbB/metabolismo , Quinazolinas/uso terapéutico , Receptor ErbB-2/metabolismo , Células 3T3 , Animales , Neoplasias de la Mama/genética , Neoplasias de la Mama/metabolismo , Capecitabina , Desoxicitidina/administración & dosificación , Desoxicitidina/análogos & derivados , Femenino , Fluorouracilo/administración & dosificación , Fluorouracilo/análogos & derivados , Humanos , Immunoblotting , Hibridación Fluorescente in Situ , Lapatinib , Neoplasias Mamarias Experimentales/tratamiento farmacológico , Ratones , Ratones Endogámicos BALB C , Ratones Desnudos , Inhibidores de Proteínas Quinasas/administración & dosificación , Inhibidores de Proteínas Quinasas/uso terapéutico , Quinazolinas/administración & dosificación , Ensayos Clínicos Controlados Aleatorios como Asunto , Receptor ErbB-2/genética , Análisis de Supervivencia , Resultado del Tratamiento , Ensayos Antitumor por Modelo de Xenoinjerto
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