نتایج جستجو برای: EVI1

تعداد نتایج: 316  

Journal: :Blood 2003
Sahar Barjesteh van Waalwijk van Doorn-Khosrovani Claudia Erpelinck Wim L J van Putten Peter J M Valk Sonja van der Poel-van de Luytgaarde Ronald Hack Rosalyn Slater Elisabeth M E Smit H Berna Beverloo Gregor Verhoef Leo F Verdonck Gert J Ossenkoppele Pieter Sonneveld Georgine E de Greef Bob Löwenberg Ruud Delwel

The proto-oncogene EVI1 encodes a DNA binding protein and is located on chromosome 3q26. The gene is aberrantly expressed in acute myeloid leukemia (AML) patients carrying 3q26 abnormalities. Two mRNAs are transcribed from this locus: EVI1 and a fusion of EVI1 with MDS1 (MDS1-EVI1), a gene located 5' of EVI1. The purpose of this study was to investigate which of the 2 gene products is involved ...

2011
Anjan Kumar Pradhan Alok Das Mohapatra Kasturi Bala Nayak Soumen Chakraborty

EVI1 (Ecotropic Viral Integration site I), which was originally identified as a myeloid transforming gene by means of retroviral insertional mutagenesis in mouse leukemia, encodes a nuclear DNA binding zinc finger protein. The presence of zinc fingers that are able to bind to specific sequences of DNA suggests that EVI1 is a transcriptional regulator; however, except a few, target genes of EVI1...

2013
Daniel J. White Richard D. Unwin Eric Bindels Andrew Pierce Hsiang-Ying Teng Joanne Muter Brigit Greystoke Tim D. Somerville John Griffiths Simon Lovell Tim C. P. Somervaille Ruud Delwel Anthony D. Whetton Stefan Meyer

The EVI1 (ecotropic viral integration site 1) gene at 3q26 codes for a transcriptional regulator with an essential role in haematopoiesis. Overexpression of EVI1 in acute myeloid leukaemia (AML) is frequently associated with 3q26 rearrangements and confers extremely poor prognosis. EVI1 mediates transcriptional regulation, signalling, and epigenetic modifications by interacting with DNA, protei...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2013
Emilie A Bard-Chapeau Jayantha Gunaratne Pankaj Kumar Belinda Q Chua Julius Muller Frederic A Bard Walter Blackstock Neal G Copeland Nancy A Jenkins

Ecotropic viral integration site-1 (EVI1) is an oncogenic zinc finger transcription factor whose expression is frequently up-regulated in myeloid leukemia and epithelial cancers. To better understand the mechanisms underlying EVI1-associated disease, we sought to define the EVI1 interactome in cancer cells. By using stable isotope labeling by amino acids in cell culture (SILAC)-based quantitati...

2012
Norio Yamakawa Kazuko Kaneda Yusuke Saito Emi Ichihara Kazuhiro Morishita

Ecotropic viral integration site-1 (EVI1) is one of the candidate oncogenes for human acute myeloid leukemia (AML) with chromosomal alterations at 3q26. High EVI1 expression (EVI1(high)) is a risk factor for AML with poor outcome. Using DNA microarray analysis, we previously identified that integrin α6 (ITGA6) was upregulated over 10-fold in EVI1(high) leukemia cells. In this study, we determin...

Journal: :Haematologica 2003
Giovanni Martinelli Emanuela Ottaviani Silvia Buonamici Alessandro Isidori Gabriela Borsaru Giuseppe Visani Pier Paolo Piccaluga Michele Malagola Nicoletta Testoni Michela Rondoni Giuseppina Nucifora Sante Tura Michele Baccarani

BACKGROUND AND OBJECTIVES Patients with acute myeloblastic leukemia (AML) with features of myelodysplastic syndrome and abnormalities of megakaryocytopoiesis often have cytogenetic aberrations of 3q21 and 3q26 bands involving the paracentric inversion [inv(3) (q21q26)] or a reciprocal translocation [t(3;3) (q21;q26)]. These abnormalities frequently cause inappropriate expression of the EVI1 gen...

2015
Gerwin Heller Anna Rommer Katarina Steinleitner Julia Etzler Hubert Hackl Petra Heffeter Erwin Tomasich Martin Filipits Birgit Steinmetz Thais Topakian Simone Klingenbrunner Barbara Ziegler Andreas Spittler Sabine Zöchbauer-Müller Walter Berger Rotraud Wieser

BACKGROUND The transcription factor Ecotropic Virus Integration site 1 (EVI1) regulates cellular proliferation, differentiation, and apoptosis, and its overexpression contributes to an aggressive course of disease in myeloid leukemias and other malignancies. Notwithstanding, knowledge about the target genes mediating its biological and pathological functions remains limited. We therefore aimed ...

2014
Emilie A. Bard-Chapeau Dorota Szumska Bindya Jacob Belinda Q. L. Chua Gouri C. Chatterjee Yi Zhang Jerrold M. Ward Fatma Urun Emi Kinameri Stéphane D. Vincent Sayadi Ahmed Shoumo Bhattacharya Motomi Osato Archibald S. Perkins Adrian W. Moore Nancy A. Jenkins Neal G. Copeland

The ecotropic viral integration site 1 (Evi1) oncogenic transcription factor is one of a number of alternative transcripts encoded by the Mds1 and Evi1 complex locus (Mecom). Overexpression of Evi1 has been observed in a number of myeloid disorders and is associated with poor patient survival. It is also amplified and/or overexpressed in many epithelial cancers including nasopharyngeal carcinom...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2012
Emilie A Bard-Chapeau Justin Jeyakani Chung H Kok Julius Muller Belinda Q Chua Jayantha Gunaratne Arsen Batagov Piroon Jenjaroenpun Vladimir A Kuznetsov Chia-Lin Wei Richard J D'Andrea Guillaume Bourque Nancy A Jenkins Neal G Copeland

Ecotropic viral integration site 1 (EVI1) is an oncogenic dual domain zinc finger transcription factor that plays an essential role in the regulation of hematopoietic stem cell renewal, and its overexpression in myeloid leukemia and epithelial cancers is associated with poor patient survival. Despite the discovery of EVI1 in 1988 and its emerging role as a dominant oncogene in various types of ...

Journal: :Blood 1995
J H Ohyashiki K Ohyashiki T Shimamoto K Kawakubo T Fujimura S Nakazawa K Toyama

We investigated expression of the human ecotropic virus integration site-1 (EVI1) gene in patients with leukemia and myelodysplastic syndrome (MDS) using the reverse transcriptase-polymerase chain reaction (RT-PCR) method. The EVI1 transcripts were detected in 5 (10.0%) of 50 patients with de novo acute myeloid leukemia (AML), including two AML patients with trilineage myelodysplasia, and in 8 ...

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