نتایج جستجو برای: wilms tumor gene 1

تعداد نتایج: 3825016  

2002
Brett Delahunt Margaret E. Lewis Kevin C. Pringle Esko J. Wiltshire Michael J. Crooke

A right-sided renal mass in an 11-month-old girl was diagnosed by percutaneous needle biopsy as Wilms tumor, which on histologic examination was found to be predominantly rhabdomyomatous. As part of the examination, serum creatine kinase (CK) and CK-MB levels were measured and were significantly elevated at 994 U/L (reference range, 42-180 U/L) and 40 U/L (reference range, 0-3 U/L), respectivel...

Journal: :Cancer research 1992
M J Coppes G J Liefers M Higuchi A B Zinn J W Balfe B R Williams

Patients with the Denys-Drash syndrome (Wilms' tumor, genital anomalies, and nephropathy) have been demonstrated to carry de novo constitutional mutations in WT1, the Wilms' tumor gene at chromosome 11p13. We report three new cases, two carrying a previously described WT1 exon 9 mutation and one with a novel WT1 exon 8 mutation. However, unlike patients in previous reports, one of our three pat...

Journal: :Cancer research 1995
N Bardeesy J B Beckwith J Pelletier

The p53 gene product is required for activation of an apoptotic pathway triggered by oncogenes and cytotoxic agents. Wilms' tumor, a pediatric renal malignancy, provides a paradigm for evaluating genetic events involved in tumor progression. This malignancy is generally not associated with p53 mutations, and even in advanced disease states is quite responsive to current treatment regimens. The ...

2014
Linda Li Jennifer Light Michael Marchick Robyn Hoelle

Wilms tumor is found in 1 in 10,000 children and most commonly presents in asymptomatic toddlers whose care givers notice a nontender abdominal mass in the right upper quadrant. This case of Wilms tumor presented as a critically ill eleven-year old with significant tachypnea, dyspnea, vague abdominal pain, intermittent emesis, new onset seizure, metabolic acidosis, and hypoxemia. This is the fi...

2010
Gowreeson Thevendran Hugo A. Farne Amir V. Kaisary

UNLABELLED Wilms tumor is rare in adults. Though the approach to diagnosis and treatment of adult Wilms tumor (AWT) is closely modeled on recommendations for childhood Wilms tumor, views differ on how aggressive the treatment should be. We report a case of a 37-year-old with Stage III favorable histology AWT. A radical nephrectomy was performed and the patient was due for chemotherapy. Recent a...

Journal: :Journal of Immunotherapy and Precision Oncology 2020

Journal: :The Journal of clinical endocrinology and metabolism 1997
G Dong R Rajah T Vu A R Hoffman R G Rosenfeld C T Roberts D M Peehl P Cohen

Benign prostatic hyperplasia (BPH) is a common proliferative disorder of unknown etiology. We have previously documented that the insulin-like growth factor (IGF) axis is critical for prostate cell growth and is abnormal in BPH. The type 1 IGF receptor (IGF-1R) is constitutively expressed by most body tissues and plays a significant role in regulating cell proliferation, consistent with the rol...

Journal: :Cancer research 2006
Yu Rong Long Cheng Hongxiu Ning Jizhen Zou Yuanjiang Zhang Fang Xu Li Liu Zhijie Chang Xin-Yuan Fu

Transcription factor Wilms' tumor 1 (WT1) was originally identified as a tumor suppressor for Wilms' tumor, but it is also overexpressed in a variety of cancer cells, suggesting a potential oncogenic function of WT1. It is important to understand molecular mechanisms underlying these dual functions of WT1 in tumorigenesis. In the current study, we report a synergistic role for signal transducer...

Journal: :Cancer research 1994
C Walker F Rutten X Yuan H Pass D M Mew J Everitt

Induction of mesothelioma in the rat is an important animal model for assessing the carcinogenic potential of fibers and for understanding the molecular basis underlying the development of these tumors. Mesotheliomas and nephroblastoma (Wilms' tumor) have many developmental, biochemical, and histological similarities; however, the expression of the Wilms' tumor suppressor gene, WT-1, has not be...

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