نتایج جستجو برای: eto

تعداد نتایج: 1205  

Journal: :Cell reports 2016
Amit Mandoli Abhishek A Singh Koen H M Prange Esther Tijchon Marjolein Oerlemans Rene Dirks Menno Ter Huurne Albertus T J Wierenga Eva M Janssen-Megens Kim Berentsen Nilofar Sharifi Bowon Kim Filomena Matarese Luan N Nguyen Nina C Hubner Nagesha A Rao Emile van den Akker Lucia Altucci Edo Vellenga Hendrik G Stunnenberg Joost H A Martens

The t(8;21) acute myeloid leukemia (AML)-associated oncoprotein AML1-ETO disrupts normal hematopoietic differentiation. Here, we have investigated its effects on the transcriptome and epigenome in t(8,21) patient cells. AML1-ETO binding was found at promoter regions of active genes with high levels of histone acetylation but also at distal elements characterized by low acetylation levels and bi...

Journal: :Cell reports 2016
Naidu M Vegi Josef Klappacher Franz Oswald Medhanie A Mulaw Amit Mandoli Verena N Thiel Shiva Bamezai Kristin Feder Joost H A Martens Vijay P S Rawat Tamoghna Mandal Leticia Quintanilla-Martinez Karsten Spiekermann Wolfgang Hiddemann Konstanze Döhner Hartmut Döhner Hendrik G Stunnenberg Michaela Feuring-Buske Christian Buske

Homeobox genes are known to be key factors in leukemogenesis. Although the TALE family homeodomain factor Meis1 has been linked to malignancy, a role for MEIS2 is less clear. Here, we demonstrate that MEIS2 is expressed at high levels in patients with AML1-ETO-positive acute myeloid leukemia and that growth of AML1-ETO-positive leukemia depends on MEIS2 expression. In mice, MEIS2 collaborates w...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1999
S McNeil C Zeng K S Harrington S Hiebert J B Lian J L Stein A J van Wijnen G S Stein

Targeting of gene regulatory factors to specific intranuclear sites may be critical for the accurate control of gene expression. The acute myelogenous leukemia 8;21 (AML1/ETO) fusion protein is encoded by a rearranged gene created by the ETO chromosomal translocation. This protein lacks the nuclear matrix-targeting signal that directs the AML1 protein to appropriate gene regulatory sites within...

Journal: :Carcinogenesis 1986
A Kolman M Näslund C J Calleman

The potential danger of ethylene oxide (EtO*) to human health has been discussed for several years. Although its mutagenic action has been known for a long time (1), it was not until 1967, when cytogenetic studies of workers occupationally exposed to EtO were published that serious attention was paid to its potential cancer risk (2). The toxicological interest in EtO is based, first of all, on ...

Journal: :Development 2005
Jill Wildonger Richard S Mann

The human translocation (t8;21) is associated with approximately 12% of the cases of acute myelogenous leukemia. Two genes, AML1 and ETO, are fused together at the translocation breakpoint, resulting in the expression of a chimeric protein called AML1-ETO. AML1-ETO is thought to interfere with normal AML1 function, although the mechanism by which it does so is unclear. Here, we have used Drosop...

Journal: :Cancer research 2010
Jenny Dunne Duncan M Gascoyne T Andrew Lister Hugh J M Brady Olaf Heidenreich Bryan D Young

A variety of genetic lesions, including chromosomal translocations, internal tandem duplications, and mutations, have been described in acute myeloid leukemia (AML). Expression profiling has shown that chromosomal translocations, in particular, are associated with distinctive patterns of gene expression. AML exhibiting the translocation t(8;21), which fuses the AML1 and ETO genes, has such a ch...

2017
R. E. Yoder Lameck O. Odhiambo Wesley C. Wright L. O. Odhiambo W. C. Wright

Estimated daily reference crop evapotranspiration (ETo) is normally used to determine the water requirement of crops using the crop factor method. Many ETo estimation methods have been developed for different types of climatic data, and the accuracy of these methods varies with climatic conditions. In this study, pair−wise comparisons were made between daily ETo estimated from eight different E...

Journal: :Blood 1998
T Okuda Z Cai S Yang N Lenny C J Lyu J M van Deursen H Harada J R Downing

The t(8;21)-encoded AML1-ETO chimeric product is believed to be causally involved in up to 15% of acute myelogenous leukemias through an as yet unknown mechanism. To directly investigate the role of AML1-ETO in leukemogenesis, we used gene targeting to create an AML1-ETO "knock-in" allele that mimics the t(8;21). Unexpectedly, embryos heterozygous for AML1-ETO (AML1-ETO/+) died around E13.5 fro...

Journal: :Haematologica 2008
Tobias Berg Manfred Fliegauf Jan Burger Martin S Staege Shaohua Liu Natalia Martinez Olaf Heidenreich Stefan Burdach Torsten Haferlach Milton H Werner Michael Lübbert

An inducible model for conditional expression of AML1-ETO in myeloid U-937 cells was generated previously to determine cellular effects of AML1-ETO and to identify target genes. Induction of AML1-ETO expression in U-937 resulted in reduced cell growth, G1 arrest and apoptosis. Microarray analysis showed more genes up-regulated than down-regulated (180 vs. 69). Clustering of AML1-ETO-positive an...

Journal: :Blood 2007
Luke F Peterson Ming Yan Dong-Er Zhang

The 8;21 translocation is a major contributor to acute myeloid leukemia (AML) of the M2 classification occurring in approximately 40% of these cases. Multiple mouse models using this fusion protein demonstrate that AML1-ETO requires secondary mutagenic events to promote leukemogenesis. Here, we show that the negative cell cycle regulator p21(WAF1) gene is up-regulated by AML1-ETO at the protein...

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