Literature DB >> 19824073

Characterization of a WiT49 cell line derived orthotopic model of Wilms tumor.

Mei-Hong Li1, Harold Yamase, Fernando Ferrer.   

Abstract

Wilms tumor is the most common malignant renal tumor in children. However, to date no Wilms tumor mouse model is available due to the lack of Wilms tumor cell lines. Herein for the first time we report an orthotopic xenograft mouse model utilizing the recently described Wilms tumor cell line WiT49. It has a high tumor occurrence rate (85%) without metastasis. Hematoxylin and eosin staining showed it is subcapsular in location and mainly biphasic with stromal and epithelial components while blastemal component is unappreciable. This model provides the prerequisite for the screening and development of new anti-tumor agents for Wilms tumor. (c) 2009 Wiley-Liss, Inc.

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Year:  2010        PMID: 19824073      PMCID: PMC2834252          DOI: 10.1002/pbc.22205

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  18 in total

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2.  Combination antiangiogenic therapy: increased efficacy in a murine model of Wilms tumor.

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Journal:  J Pediatr Surg       Date:  2001-08       Impact factor: 2.545

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4.  Pregnancy outcome after treatment for Wilms tumor: a report from the National Wilms Tumor Study Group.

Authors:  Daniel M Green; Eve M Peabody; Bin Nan; Susan Peterson; John A Kalapurakal; Norman E Breslow
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5.  Osteopenia in survivors of Wilms tumor.

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Journal:  Int J Oncol       Date:  2002-04       Impact factor: 5.650

Review 6.  One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice.

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7.  Derivation and characterization of a Wilms' tumour cell line, WiT 49.

Authors:  Jennifer Alami; Bryan R Williams; Herman Yeger
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8.  Characterization of ARC-111 as a novel topoisomerase I-targeting anticancer drug.

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9.  Effects of potent VEGF blockade on experimental Wilms tumor and its persisting vasculature.

Authors:  Jason S Frischer; Jianzhong Huang; Anna Serur; Angela Kadenhe-Chiweshe; Kimberly W McCrudden; Kathleen O'Toole; Jocelyn Holash; George D Yancopoulos; Darrell J Yamashiro; Jessica J Kandel
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2.  Monitoring therapy with MEK inhibitor U0126 in a novel Wilms tumor model in Wt1 knockout Igf2 transgenic mice using 18F-FDG PET with dual-contrast enhanced CT and MRI: early metabolic response without inhibition of tumor growth.

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3.  SIX2 Effects on Wilms Tumor Biology.

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4.  Senescence Process in Primary Wilms' Tumor Cell Culture Induced by p53 Independent p21 Expression.

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5.  The Iroquois homeobox proteins IRX3 and IRX5 have distinct roles in Wilms tumour development and human nephrogenesis.

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  5 in total

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