نتایج جستجو برای: ژن wt1

تعداد نتایج: 17804  

Journal: :BMC complementary and alternative medicine 2016
Methee Rungrojsakul Trinnakorn Katekunlaphan Aroonchai Saiai Chadarat Ampasavate Siriporn Okonogi Colleen A Sweeney Songyot Anuchapreeda

BACKGROUND Wilms' tumor 1 (WT1) is a biological marker for predicting leukemia progression. In this study, mammea E/BB, an active compound from Saraphi (Mammea siamensis) seed extract was examined for its effect on down-regulatory mechanism of WT1 gene expression, WT1 protein and mRNA stability, and cell proliferation in K562 cell line. METHODS M. siamensis seeds were obtained from the region...

Journal: :Developmental biology 2011
Alexander von Gise Bin Zhou Leah B Honor Qing Ma Anna Petryk William T Pu

An epithelial sheet, the epicardium, lines the surface of the heart. In the developing embryo, the epicardium expresses the transcriptional regulator Wilm's Tumor Gene 1 (Wt1). Through incompletely understood mechanisms, Wt1 inactivation derails normal heart development. We investigated mechanisms by which Wt1 regulates heart development and epicardial epithelial to mesenchymal transition (EMT)...

2015
Naoya Tatsumi Nozomi Hojo Hiroyuki Sakamoto Rena Inaba Nahoko Moriguchi Keiko Matsuno Mari Fukuda Akihide Matsumura Seiji Hayashi Soyoko Morimoto Jun Nakata Fumihiro Fujiki Sumiyuki Nishida Hiroko Nakajima Akihiro Tsuboi Yoshihiro Oka Naoki Hosen Haruo Sugiyama Yusuke Oji Keith William Brown

The Wilms' tumor gene WT1 consists of 10 exons and encodes a zinc finger transcription factor. There are four major WT1 isoforms resulting from alternative splicing at two sites, exon 5 (17AA) and exon 9 (KTS). All major WT1 isoforms are overexpressed in leukemia and solid tumors and play oncogenic roles such as inhibition of apoptosis, and promotion of cell proliferation, migration and invasio...

Journal: :Haematologica 2011
Heiko Becker Kati Maharry Michael D Radmacher Krzysztof Mrózek Klaus H Metzeler Susan P Whitman Sebastian Schwind Jessica Kohlschmidt Yue-Zhong Wu Bayard L Powell Thomas H Carter Jonathan E Kolitz Meir Wetzler Andrew J Carroll Maria R Baer Joseph O Moore Michael A Caligiuri Richard A Larson Guido Marcucci Clara D Bloomfield

BACKGROUND The alleles of the Wilms tumor 1 (WT1) polymorphism rs16754 harbor adenine (A) or guanine (G). Recently, rs16754 has been reported to affect the outcome of patients with cytogenetically normal acute myeloid leukemia. To validate this finding, we investigated pretreatment features and outcome associated with rs16754 in a large cohort of patients with cytogenetically normal acute myelo...

Journal: :Cell reports 2014
Raajit Rampal Altuna Alkalin Jozef Madzo Aparna Vasanthakumar Elodie Pronier Jay Patel Yushan Li Jihae Ahn Omar Abdel-Wahab Alan Shih Chao Lu Patrick S Ward Jennifer J Tsai Todd Hricik Valeria Tosello Jacob E Tallman Xinyang Zhao Danette Daniels Qing Dai Luisa Ciminio Iannis Aifantis Chuan He Francois Fuks Martin S Tallman Adolfo Ferrando Stephen Nimer Elisabeth Paietta Craig B Thompson Jonathan D Licht Christopher E Mason Lucy A Godley Ari Melnick Maria E Figueroa Ross L Levine

Somatic mutations in IDH1/IDH2 and TET2 result in impaired TET2-mediated conversion of 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC). The observation that WT1 inactivating mutations anticorrelate with TET2/IDH1/IDH2 mutations in acute myeloid leukemia (AML) led us to hypothesize that WT1 mutations may impact TET2 function. WT1 mutant AML patients have reduced 5hmC levels similar to T...

2014
Varalakshmi Katuri Stephanie Gerber Xiaofei Qiu Gregory McCarty Seth D. Goldstein Hans Hammers Elizabeth Montgomery Allen R. Chen David M. Loeb

Angiogenesis is required for tumor growth. WT1, a protein that affects both mRNA transcription and splicing, has recently been shown to regulate expression of vascular endothelial growth factor (VEGF), one of the major mediators of angiogenesis. In the present study, we tested the hypothesis that WT1 is a key regulator of tumor angiogenesis in Ewing sarcoma. We expressed exogenous WT1 in the WT...

Journal: :Blood 1996
T Yamagami H Sugiyama K Inoue H Ogawa T Tatekawa M Hirata T Kudoh T Akiyama A Murakami T Maekawa

We have previously reported expression of WT1 in acute leukemia. To elucidate its biological significance, we examined the effect of the suppression of the WT1 expression by WT1 antisense oligomers on the growth of the leukemic cells expressing WT1. When 20 different WT1 antisense (AS) oligomers covering from the 5' cap sites of the WT1 gene to the 3' end were examined for the inhibitory effect...

Journal: :Blood 2000
A Gaiger V Reese M L Disis M A Cheever

The Wilms' tumor (WT1) gene participates in leukemogenesis and is overexpressed in most types of leukemia in humans. WT1 is also detectable in many types of lung, thyroid, breast, testicular, and ovarian cancers and melanoma in humans. Initial studies evaluated whether immune responses to murine WT1 can be elicited in mice. Murine and human WT1 are similar. Thus, mouse models might lead to reso...

2014
Charlotta Andersson Yusuke Oji Nina Ohlson Sihan Wang Xingru Li Ulrika Ottander Eva Lundin Haruo Sugiyama Aihong Li

Ovarian carcinoma (OC) has a poor prognosis and lack early effective screening markers. Wilm's tumor gene 1 (WT1) is overexpressed in OCs. Therefore, it is of great interest to investigate whether WT1-specific antibody (Ab) measurements in plasma can serve as a biomarker of anti-OC response, and is of importance in relation to patient prognosis. Peripheral blood samples were obtained from a tot...

Journal: :Journal of molecular endocrinology 2007
Birgit Köhler Anne-Lise Delezoide Brigitte Boizet-Bonhoure Michael J McPhaul Charles Sultan Serge Lumbroso

The Wilms' tumor suppressor 1 (WT1) is one of the key regulators of early male genital development. The androgen receptor (AR) is the major local factor responsible for the development of the male genitalia. As a subset of patients, with WT1 mutations and virilization defects, were found to present normal testosterone producing testes after birth, which suggests androgen resistance, we hypothes...

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