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1.
Am J Transplant ; 18(10): 2559-2565, 2018 10.
Artículo en Inglés | MEDLINE | ID: mdl-29758123

RESUMEN

Waitlist time for kidney transplantation is long but may be shortened with the utilization of hepatitis C positive allografts. We retrospectively reviewed the course of 36 hepatitis C positive patients awaiting kidney transplantation at 2 large centers within the same health system, with near-identical care delivery models with the exception of timing of hepatitis C treatment, to determine the impact of timing of hepatitis C treatment on access to transplant, waitlist time, and treatment efficacy and tolerability. The majority of patients had hepatitis C genotype 1a or 1b, and all received direct acting antiviral therapy with 100% treatment response. One patient underwent transplantation in the pretransplant treatment group. The 1-year transplantation rate was 12.5% vs 67.9% (P = .0013) in those treated posttransplantation. The median waitlist time in the posttransplant group was 122 (interquartile range [IQR] 21.5, 531.0) days, which was significantly shorter than the center's regional and national wait time. Pathologic review revealed no difference in allograft quality. Overall treatment related adverse events were not different between the 2 groups. A strategy of posttransplant hepatitis C treatment increased access to transplant and reduced waitlist time. Delaying treatment until after transplant did not appear to adversely affect recipients' kidney allograft or overall survival.


Asunto(s)
Supervivencia de Injerto , Hepatitis C/diagnóstico , Fallo Renal Crónico/mortalidad , Trasplante de Riñón/mortalidad , Obtención de Tejidos y Órganos/estadística & datos numéricos , Listas de Espera/mortalidad , Toma de Decisiones , Femenino , Estudios de Seguimiento , Hepacivirus/genética , Hepacivirus/aislamiento & purificación , Hepatitis C/transmisión , Hepatitis C/virología , Humanos , Riñón/virología , Fallo Renal Crónico/cirugía , Masculino , Persona de Mediana Edad , Pronóstico , Tasa de Supervivencia , Factores de Tiempo , Donantes de Tejidos/provisión & distribución
2.
Oncogene ; 34(35): 4591-600, 2015 Aug 27.
Artículo en Inglés | MEDLINE | ID: mdl-25435365

RESUMEN

Relapse after clinical remission remains a leading cause of cancer-associated death. Although the mechanisms of tumor relapse are complex, the ability of cancer cells to survive physiological stress is a prerequisite for recurrence. Ewing sarcoma (ES) and neuroblastoma (NB) are aggressive cancers that frequently relapse after initial remission. In addition, both tumors overexpress the polycomb group (PcG) proteins BMI-1 and EZH2, which contribute to tumorigenicity. We have discovered that ES and NB resist hypoxic stress-induced death and that survival depends on PcG function. Epigenetic repression of developmental programs is the most well-established cancer-associated function of PcG proteins. However, we noted that voltage-gated potassium (Kv) channel genes are also targets of PcG regulation in stem cells. Given the role of potassium in regulating apoptosis, we reasoned that repression of Kv channel genes might have a role in cancer cell survival. Here we describe our novel finding that PcG-dependent repression of the Kv1.5 channel gene KCNA5 contributes to cancer cell survival under conditions of stress. We show that survival of cancer cells in stress is dependent upon suppression of Kv1.5 channel function. The KCNA5 promoter is marked in cancer cells with PcG-dependent chromatin repressive modifications that increase in hypoxia. Genetic and pharmacological inhibition of BMI-1 and EZH2, respectively, restore KCNA5 expression, which sensitizes cells to stress-induced death. In addition, ectopic expression of the Kv1.5 channel induces apoptotic cell death under conditions of hypoxia. These findings identify a novel role for PcG proteins in promoting cancer cell survival via repression of KCNA5.


Asunto(s)
Supervivencia Celular , Regulación Neoplásica de la Expresión Génica , Canal de Potasio Kv1.5/genética , Proteínas del Grupo Polycomb/fisiología , Apoptosis , Hipoxia de la Célula , Línea Celular Tumoral , Células Madre Embrionarias/fisiología , Silenciador del Gen , Células Endoteliales de la Vena Umbilical Humana/fisiología , Humanos , Canal de Potasio Kv1.5/biosíntesis , Estrés Fisiológico
3.
J Med Eng Technol ; 34(2): 124-33, 2010 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-20017713

RESUMEN

Current methods of treatment for retinopathy of prematurity, using laser photocoagulation, require surgeons to assume awkward standing positions, which can result in occupational injury. A new infant surgical table was designed for improving this surgical procedure. To quantify its benefits, an ergonomic comparison of the standard and modified procedures was carried out, using specialized checklists, Nordic Musculoskeletal Questionnaires, and analysis of videotaped procedures using an Ovako Working Posture Analysing System method. Analysis of the typical laser photocoagulation procedure revealed a high risk for cumulative trauma disorders. The majority of the risk factors were lowered considerably with use of the new table. Improvement was largely due to the new table allowing seated postures during surgery, relieving muscular stress on the back, shoulders and legs. This study demonstrates risk reduction through engineering design of new medical devices, and illustrates how combining different assessment approaches can help evaluate ergonomic impact of medical technologies.


Asunto(s)
Cirugía General/instrumentación , Coagulación con Láser/instrumentación , Diseño de Equipo , Humanos , Lactante , Recién Nacido , Quirófanos , Equipo Quirúrgico
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