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1.
Arch. argent. pediatr ; 117(1): 41-46, feb. 2019. ilus
Article in Spanish | LILACS, BINACIS | ID: biblio-983778

ABSTRACT

Los tumores neuroectodérmicos primitivos a nivel extraóseo son una neoplasia muy rara, con pocas publicaciones en la literatura. Se reporta un caso de una paciente de nueve años quien se presentó con signos de compresión medular. Se estableció un grupo de diagnósticos diferenciales en el abordaje, entre los que debió incluirse la patología oncológica. En la paciente, se observó la presencia de una masa en la columna dorsal con compromiso del cordón medular, que requirió cirugía descompresiva de urgencia y, posteriormente, se diagnosticó sarcoma de Ewing. Cabe resaltar la importancia del caso debido a la baja incidencia del origen extraóseo en esta neoplasia y su rara localización en la columna dorsal, y destacar la presencia de la compresión medular como forma de presentación del cáncer en pediatría, además de la poca información que, hasta el momento, se posee referida al mejor abordaje terapéutico en esta patología, en esta localización.


Extraosseous primitive neuroectodermal tumors are very rare neoplasms. Only a few cases have been published in the literature. This report is about a 9-year-old female patient whose clinical manifestations showed spinal cord compression, so different diagnosis should be considered, including oncology disease. The patient showed a mass of the dorsal spine with spinal cord compression. She was diagnosed with Ewing Sarcoma after surgical intervention and pathology study. It is necessary to highlight the importance of the present case due to the low incidence of the extraosseous Ewing Sarcoma, and its infrequent location at the dorsal spine and the spinal cord compression as initial presentation of pediatric cancer, as well as the poor information related to the best therapeutic strategy to treat this disease at this location.


Subject(s)
Humans , Female , Child , Sarcoma, Ewing , Spine , Child , Neuroectodermal Tumors , Neoplasms
2.
Arch Argent Pediatr ; 117(1): e41-e46, 2019 02 01.
Article in Spanish | MEDLINE | ID: mdl-30652454

ABSTRACT

Extraosseous primitive neuroectodermal tumors are very rare neoplasms. Only a few cases have been published in the literature. This report is about a 9-year-old female patient whose clinical manifestations showed spinal cord compression, so different diagnosis should be considered, including oncology disease. The patient showed a mass of the dorsal spine with spinal cord compression. She was diagnosed with Ewing Sarcoma after surgical intervention and pathology study. It is necessary to highlight the importance of the present case due to the low incidence of the extraosseous Ewing Sarcoma, and its infrequent location at the dorsal spine and the spinal cord compression as initial presentation of pediatric cancer, as well as the poor information related to the best therapeutic strategy to treat this disease at this location.


Los tumores neuroectodérmicos primitivos a nivel extraóseo son una neoplasia muy rara, con pocas publicaciones en la literatura. Se reporta un caso de una paciente de nueve años quien se presentó con signos de compresión medular. Se estableció un grupo de diagnósticos diferenciales en el abordaje, entre los que debió incluirse la patología oncológica. En la paciente, se observó la presencia de una masa en la columna dorsal con compromiso del cordón medular, que requirió cirugía descompresiva de urgencia y, posteriormente, se diagnosticó sarcoma de Ewing. Cabe resaltar la importancia del caso debido a la baja incidencia del origen extraóseo en esta neoplasia y su rara localización en la columna dorsal, y destacar la presencia de la compresión medular como forma de presentación del cáncer en pediatría, además de la poca información que, hasta el momento, se posee referida al mejor abordaje terapéutico en esta patología, en esta localización.


Subject(s)
Sarcoma, Ewing/complications , Spinal Cord Compression/etiology , Spinal Neoplasms/complications , Thoracic Vertebrae , Child , Female , Humans
3.
Front Aging Neurosci ; 6: 243, 2014.
Article in English | MEDLINE | ID: mdl-25309427

ABSTRACT

CDK5 is a member of the cyclin-dependent kinase family with diverse functions in both the developing and mature nervous system. The inappropriate activation of CDK5 due to the proteolytic release of the activator fragment p25 from the membrane contributes to the formation of neurofibrillary tangles and chronic neurodegeneration. At 18 months of age 3xTg-AD mice were sacrificed after 1 year (long term) or 3 weeks (short term) of CDK5 knockdown. In long-term animals CDK5 knockdown prevented insoluble Tau formation in the hippocampi and prevented spatial memory impairment. In short-term animals, CDK5 knockdown showed reduction of CDK5, reversed Tau aggregation, and improved spatial memory compared to scrambled treated old 3xTg-AD mice. Neither long-term nor short-term CDK5 knock-down had an effect on old littermates. These findings further validate CDK5 as a target for Alzheimer's disease both as a preventive measure and after the onset of symptoms.

4.
Front Aging Neurosci ; 6: 232, 2014.
Article in English | MEDLINE | ID: mdl-25225483

ABSTRACT

Alzheimer's disease (AD) is the most common cause of dementia worldwide. One of the main pathological changes that occurs in AD is the intracellular accumulation of hyperphosphorylated Tau protein in neurons. Cyclin-dependent kinase 5 (CDK5) is one of the major kinases involved in Tau phosphorylation, directly phosphorylating various residues and simultaneously regulating various substrates such as kinases and phosphatases that influence Tau phosphorylation in a synergistic and antagonistic way. It remains unknown how the interaction between CDK5 and its substrates promotes Tau phosphorylation, and systemic approaches are needed that allow an analysis of all the proteins involved. In this review, the role of the CDK5 signaling pathway in Tau hyperphosphorylation is described, an in silico model of the CDK5 signaling pathway is presented. The relationship among these theoretical and computational models shows that the regulation of Tau phosphorylation by PP2A and glycogen synthase kinase 3ß (GSK3ß) is essential under basal conditions and also describes the leading role of CDK5 under excitotoxic conditions, where silencing of CDK5 can generate changes in these enzymes to reverse a pathological condition that simulates AD.

5.
Neuroreport ; 24(17): 976-81, 2013 Dec 04.
Article in English | MEDLINE | ID: mdl-24089016

ABSTRACT

Histone acetyltransferase activity by transcriptional cofactors such as CREB-binding protein (CBP) and post-translational modifications by small ubiquitin-like modifier-1 (SUMO-1) have shown to be relevant for synaptic and neuronal activity. Here, we investigate whether SUMOylation of CBP plays a role in spatial learning. We assessed protein levels of CBP/p300, SUMO-1, and CBP SUMOylation in the hippocampi of rats trained on the Morris water maze task. Furthermore, we evaluated the post-translational modifications at Zif268, BDNF, and Arc/Arg3.1 promoters using chromatin immunoprecipitation with anti-Acetyl-Histone H3-Lys14 (H3K14Ac) and SUMO-1. We found that CBP/p300 protein expression is unchanged in animals trained for 7 days. However, H3K14Ac-specific histone acetyltransferase activity showed specific hyperacetylation at promoters of Zif268 and BDNF-pI but not of Arc/Arg3.1 and BDNF-pIV. In naive animals, CBP is selectively SUMOylated and the Arc/Arg3.1 promoter is differentially occupied by SUMO-1, although SUMO-1 levels are unchanged. These results suggest a specific negative regulation by SUMO-1 on CBP function and its effect on epigenetic changes triggered by spatial learning and memory processes.


Subject(s)
CREB-Binding Protein/metabolism , Epigenesis, Genetic , Hippocampus/metabolism , Maze Learning/physiology , SUMO-1 Protein/metabolism , Sumoylation/genetics , Animals , Histone Acetyltransferases/metabolism , Male , Rats , Rats, Wistar
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