نتایج جستجو برای: ژن wt1

تعداد نتایج: 17804  

2015
Namhee Kim In-Suk Kim Chulhun L. Chang Jeong-Eun Kang Eun Yup Lee Ho-Jin Shin

The genetic variant rs16754 of Wilms tumor gene 1 (WT1) has recently been described as an independent prognostic factor in AML patients. It is of great interest to test whether WT1 single nucleotide polymorphism can be used as a molecular marker in other types of cancer, to improve risk and treatment stratification. We performed sequencing analysis of exons 7 and 9 of WT1, which are known mutat...

Journal: :Journal of the Chinese Medical Association : JCMA 2004
Be-Fong Chen Chin-yuen Tzen Der-Cherng Liang Hsi-Che Liu Yu-Wen Huang Chi-Chen Fan

BACKGROUND Approximately 10% of nephroblastomas (Wilms' tumors) carry mutations in the Wilms' tumor 1 (WT1) gene. Recently, a WT1 antibody raised against N-terminal 1-181 amino acids of human WT1 became commercially available for immunohistochemical use on paraffin-embedded tissue. The aim of this study was to investigate the diagnostic and prognostic value of WT1 N-terminal antibody in nephrob...

Journal: :The Journal of biological chemistry 2007
Ho-Shik Kim Myoung Shin Kim Anne L Hancock James C P Harper Jik Young Park George Poy Alan O Perantoni Margaret Cam Karim Malik Sean Bong Lee

The Wilms' tumor suppressor gene (WT1) encodes a zinc finger transcription factor that is vital during development of several organs including metanephric kidneys. Despite the critical regulatory role of WT1, the pathways and mechanisms by which WT1 orchestrates development remain elusive. To identify WT1 target genes, we performed a genome-wide expression profiling analysis in cells expressing...

Journal: :Physiological genomics 2001
T H Lee J Pelletier

The Wilms' tumor suppressor gene, wt1, encodes a zinc finger transcription factor that can regulate gene expression. It plays an essential role in tumorigenesis, kidney differentiation, and urogenital development. To identify WT1 downstream targets, gene expression profiling was conducted using a cDNA array hybridization approach. We confirm herein that the human vitamin D receptor (VDR), a lig...

Journal: :Blood 2002
Olga A Elisseeva Yoshihiro Oka Akihiro Tsuboi Kiyoyuki Ogata Fei Wu Eui Ho Kim Toshihiro Soma Hiroya Tamaki Manabu Kawakami Yusuke Oji Naoki Hosen Takeshi Kubota Masashi Nakagawa Tamotsu Yamagami Akira Hiraoka Machiko Tsukaguchi Keiko Udaka Hiroyasu Ogawa Tadamitsu Kishimoto Taisei Nomura Haruo Sugiyama

Wilms tumor gene WT1 is expressed at high levels in hematopoietic malignancies, such as leukemias and myelodysplastic syndromes (MDS), and in various kinds of solid tumors, including lung cancer, and it exerts an oncogenic function in these malignancies. IgM and IgG WT1 antibodies were measured by means of dot blot assay in 73 patients with hematopoietic malignancies (16 acute myeloid leukemia ...

2013
Caihua Xu Chen Wu Yang Xia Zhaopeng Zhong Xiang Liu Jing Xu Fei Cui Bin Chen Oluf Dimitri Røe Aihong Li Yijiang Chen

The Wilms' tumor suppressor gene (WT1) has been identified as an oncogene in many malignant diseases such as leukaemia, breast cancer, mesothelioma and lung cancer. However, the role of WT1 in non-small-cell lung cancer (NSCLC) carcinogenesis remains unclear. In this study, we compared WT1 mRNA levels in NSCLC tissues with paired corresponding adjacent tissues and identified significantly highe...

2014
Jayasha Shandilya Eneda Toska Derek J Richard Kathryn F Medler Stefan GE Roberts

Tumour suppressors safeguard the fidelity of the mitotic checkpoint by transcriptional regulation of genes that encode components of the mitotic checkpoint complex (MCC). Here we report a new role for the tumour suppressor and transcription factor, WT1, in the mitotic checkpoint. We show that WT1 regulates the MCC by directly interacting with the spindle assembly checkpoint protein, MAD2. WT1 c...

Journal: :Biochemical Society transactions 2004
K J Wagner S G E Roberts

Wilms' tumour is a paediatric malignancy of the kidneys and is the most common solid tumour found in children. The Wilms' tumour suppressor protein WT1 is mutated in approximately 15% of Wilms' tumours, and is aberrantly expressed in many others. WT1 can manifest both tumour suppressor and oncogenic activities, but the reasons for this are not yet clear. The Wilms' tumour suppressor protein WT1...

Journal: :Nucleic acids research 1999
T H Lee P Moffett J Pelletier

We have studied the ability of the wt1 tumor suppressor gene product to repress different classes of activation domains previously shown to stimulate the initiation and elongation steps of RNA polymerase II transcription in vivo. Repression assays revealed that WT1 represses all three classes of activation domains: Sp1 and CTF, which stimulate initiation (type I), human immunodeficiency virus t...

Journal: :American journal of physiology. Renal physiology 2008
Avril A Morrison Rebecca L Viney Moin A Saleem Michael R Ladomery

The Wilms tumor suppressor gene WT1 is essential for early urogenital development: homozygous mutations in WT1 result in embryonic lethality due to a failure in the development of kidneys and gonads. In the adult kidney, WT1 expression is limited to the glomerular podocytes. Several human nephrotic diseases arise from mutations of the WT1 gene, including mutations that affect its zinc-fingers a...

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