نتایج جستجو برای: evi1

تعداد نتایج: 316  

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2011
Björn Koos Sebastian Bender Hendrik Witt Sonja Mertsch Jörg Felsberg Rudi Beschorner Andrey Korshunov Barbara Riesmeier Stefan Pfister Werner Paulus Martin Hasselblatt

PURPOSE Ependymomas are glial tumors of presumably radial glial origin that share morphologic similarities with ependymal cells. The molecular genetics of ependymomas of supratentorial, infratentorial, and spinal location is heterogeneous. We aimed at identifying pathways operative in the development of infratentorial ependymomas. EXPERIMENTAL DESIGN To do so, gene expression profiles of tumo...

2013
Carolyn Glass Charles Wuertzer Xiaohui Cui Yingtao Bi Ramana Davuluri Ying-Yi Xiao Michael Wilson Kristina Owens Yi Zhang Archibald Perkins

The ecotropic virus integration site 1 (EVI1) transcription factor is associated with human myeloid malignancy of poor prognosis and is overexpressed in 8-10% of adult AML and strikingly up to 27% of pediatric MLL-rearranged leukemias. For the first time, we report comprehensive genomewide EVI1 binding and whole transcriptome gene deregulation in leukemic cells using a combination of ChIP-Seq a...

2011
Sebastian Bender Hendrik Witt Sonja Mertsch Rudi Beschorner Andrey Korshunov Barbara Riesmeier Stefan Pfister Werner Paulus Martin Hasselblatt

Purpose: Ependymomas are glial tumors of presumably radial glial origin that share morphologic similarities with ependymal cells. The molecular genetics of ependymomas of supratentorial, infratentorial, and spinal location is heterogeneous. We aimed at identifying pathways operative in the development of infratentorial ependymomas. Experimental Design: To do so, gene expression profiles of tumo...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

2008
Rubens Jovanovik Vesna Janevska Lidija Cevreska Zlate Stojanoski Milka Zdravkovska Gordana Petrushevska

Material and methods. We isolated DNA from 35 bone marrow biopsies, and measured the blood telomerase activity (RTA) in 21 of the patients. We performed immunostainigs for Ki-67, Bcl-2 and p53 on the biopsy samples in order to test the correlations to the RTA and MDS/EVI1 presence. MDS/EVI1 fusion was detected with touch-down-direct PCR, and RTA was measured using the “TeloTAGGG-PCRELISA-plus k...

Journal: :Blood 2007
Guang Jin Yukari Yamazaki Miki Takuwa Tomoko Takahara Keiko Kaneko Takeshi Kuwata Satoshi Miyata Takuro Nakamura

Cooperative activation of Meis1 and Hoxa9 perturbs myeloid differentiation and eventually leads myeloid progenitors to leukemia, yet it remains to be clarified what kinds of subsequent molecular processes are required for development of overt leukemia. To understand the molecular pathway in Hoxa9/Meis1-induced leukemogenesis, retroviral insertional mutagenesis was applied using retrovirus-media...

Journal: :Blood 2009
Carlos M Santamaría María C Chillón Ramón García-Sanz Cristina Pérez María D Caballero Fernando Ramos Alfonso García de Coca José M Alonso Pilar Giraldo Teresa Bernal José A Queizán Juan N Rodriguez Pascual Fernández-Abellán Abelardo Bárez María J Peñarrubia Ana Balanzategui María B Vidriales María E Sarasquete Miguel Alcoceba Joaquín Díaz-Mediavilla Jesús F San Miguel Marcos Gonzalez

We have evaluated 9 new molecular markers (ERG, EVI1, MLL-PTD, MN1, PRAME, RHAMM, and WT1 gene-expression levels plus FLT3 and NPM1 mutations) in 121 de novo cytogenetically normal acute myeloblastic leukemias. In the multivariate analysis, high ERG or EVI1 and low PRAME expressions were associated with a shorter relapse-free survival (RFS) and overall survival (OS). A 0 to 3 score was given by...

Journal: :Blood 1994
K Suzukawa E Parganas A Gajjar T Abe S Takahashi K Tani S Asano H Asou N Kamada J Yokota

Structural alterations occur in the long arm of chromosome 3 in approximately 2% of patients with acute myelogenous leukemia (AML) or myelodysplastic syndrome (MDS). The major alterations are inv(3)(q21q26) and t(3:3)(q21;q26) and are often classified as the 3q21q26 syndrome. We previously reported that the EVI1 gene is transcriptionally activated in AMLs with t(3;3)(q21;q26) and inv(3)(q21q26)...

Journal: :Blood 2015
Vincent-Philippe Lavallée Patrick Gendron Sébastien Lemieux Giovanni D'Angelo Josée Hébert Guy Sauvageau

The genetic and transcriptional signature of EVI1 (ecotropic viral integration site 1)-rearranged (EVI1-r) acute myeloid leukemias (AMLs) remains poorly defined. We performed RNA sequencing of 12 EVI1-r AMLs and compared the results with those of other AML subtypes (n = 139) and normal CD34(+) cells (n = 17). Results confirm high frequencies of RAS and other activated signaling mutations (10/12...

Journal: :Cell 2014
Stefan Gröschel Mathijs A. Sanders Remco Hoogenboezem Elzo de Wit Britta A.M. Bouwman Claudia Erpelinck Vincent H.J. van der Velden Marije Havermans Roberto Avellino Kirsten van Lom Elwin J. Rombouts Mark van Duin Konstanze Döhner H. Berna Beverloo James E. Bradner Hartmut Döhner Bob Löwenberg Peter J.M. Valk Eric M.J. Bindels Wouter de Laat Ruud Delwel

Chromosomal rearrangements without gene fusions have been implicated in leukemogenesis by causing deregulation of proto-oncogenes via relocation of cryptic regulatory DNA elements. AML with inv(3)/t(3;3) is associated with aberrant expression of the stem-cell regulator EVI1. Applying functional genomics and genome-engineering, we demonstrate that both 3q rearrangements reposition a distal GATA2...

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