Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30‐year SIOP‐RTSG experience
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DOI: 10.1002/cncr.33304
Abstract: WAGR syndrome (Wilms tumor, aniridia, genitourinary anomalies, and range of developmental delays) is a rare contiguous gene deletion syndrome with a 45% to 60% risk of developing Wilms tumor (WT). Currently, surveillance and treatment recommendations… read more here.
Keywords: syndrome wilms; characteristics outcomes; clinical characteristics; wilms tumor ... See more keywords
Incidence and management of pleural effusions in patients with Wilms tumor: A Pediatric Surgical Oncology Research Collaborative study
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DOI: 10.1002/ijc.34188
Abstract: Wilms tumor (WT) is the most common renal malignancy in children. Children with favorable histology WT achieve survival rates of over 90%. Twelve percent of patients present with metastatic disease, most commonly to the lungs.… read more here.
Keywords: oncology; pleural effusion; wilms tumor; pleural effusions ... See more keywords
The correlation between LIN28B gene potentially functional variants and Wilms tumor susceptibility in Chinese children
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DOI: 10.1002/jcla.22200
Abstract: Wilms tumor (WT) is the most common urologic cancer in children. However, genetic bases underlying WT remain largely unknown. Previous studies indicated that Lin28 homolog B (LIN28B) level is significantly elevated in some WTs. Enforced… read more here.
Keywords: wilms tumor; lin28b gene; susceptibility;
ALKBH5 gene polymorphisms and Wilms tumor risk in Chinese children: A five‐center case‐control study
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DOI: 10.1002/jcla.23251
Abstract: Wilms tumor is a frequently diagnosed renal cancer among children with unclear genetic causes. N6‐methyladenosine (m6A) modification genes play critical roles in tumorigenesis. However, whether genetic variations of m6A modification genes predispose to Wilms tumor… read more here.
Keywords: m6a modification; gene polymorphisms; alkbh5 gene; wilms tumor ... See more keywords
Non-coding RNAs in Wilms' tumor: biological function, mechanism, and clinical implications.
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DOI: 10.1007/s00109-021-02075-1
Abstract: Non-coding RNAs are involved with maintenance and regulation of physiological mechanisms and are involved in pathological processes, such as cancer. Among the small ncRNAs, miRNAs are the most explored in tumorigenesis, metastasis development, and resistance… read more here.
Keywords: tumor biological; coding rnas; biological function; non coding ... See more keywords
Botryoid Wilms tumor: a non-existent “entity” causing diagnostic and staging difficulties
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DOI: 10.1007/s00428-018-2500-4
Abstract: Wilms tumors growing in a botryoid fashion into the renal pelvis have been reported since the 1960s as a rare tumor type usually associated with stromal histology and a good prognosis. However, the true frequency,… read more here.
Keywords: botryoid wilms; wilms tumor; stage; botryoid growth ... See more keywords
Promotion of Wilms' tumor cells migration and invasion by mono-2-ethyhexyl phthalate (MEHP) via activation of NF-κB signals.
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DOI: 10.1016/j.cbi.2017.04.004
Abstract: Wilms tumor is a pediatric kidney cancer associated with inactivation of the WT1 tumor-suppressor gene in 5-10% of cases. There is an urgent need to illustrate risk factors which can trigger the motility of Wilms… read more here.
Keywords: mmp mmp; mmp; mehp; wilms tumor ... See more keywords
Extensive synchronous bilateral Wilms tumor treated with nephron sparing surgery
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DOI: 10.1016/j.eucr.2018.02.008
Abstract: Wilms tumor presents with 650 cases annually in the U.S. alone; 5% of these cases present as simultaneous bilateral Wilms tumor while an additional 2e3% present with contralateral metachronous disease.1 Bilateral Wilms tumor (BWT) in… read more here.
Keywords: extensive synchronous; tumor treated; bilateral wilms; wilms tumor ... See more keywords
Pedunculated and obstructive Wilms' tumor: A rare presentation in a 2 year-old male
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DOI: 10.1016/j.eucr.2018.06.004
Abstract: Wilms' tumor manifesting as an obstructing ureteral mass is extremely rare. Herein, we report an unusual case in which a child presented with a clinical picture concerning for and suggestive of ureteropelvic junction obstruction (UPJO),… read more here.
Keywords: tumor; tumor rare; rare presentation; wilms tumor ... See more keywords
The contribution of WTAP gene variants to Wilms tumor susceptibility.
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DOI: 10.1016/j.gene.2020.144839
Abstract: Wilms tumor is the most frequently occurring pediatric renal malignancy. Wilms tumor suppressor-1-associated protein (WTAP) is a vital component of N6-methyltransferase complex involved in tumorigenesis. However, the roles of WTAP gene single nucleotide polymorphisms (SNPs)… read more here.
Keywords: wtap gene; tumor risk; wilms tumor; tumor ... See more keywords
Wilms' tumor of the ovary
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DOI: 10.1016/j.gore.2016.12.004
Abstract: Extrarenal Wilms' tumor of the ovary is a very rare tumor likely derived from embryonic mesonephros. We present the first reported case of a teratoid extrarenal Wilms' tumor of the ovary with a short review… read more here.
Keywords: wilms tumor; oncology; tumor ovary;