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Leukemia & Lymphoma Volume 53, 2012 - Issue 11
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Research Article

WT1 mutations and single nucleotide polymorphism rs16754 analysis of patients with pediatric acute myeloid leukemia in a Chinese population

Xi ChenCenter for Clinical Molecular Medicine, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Pediatrics in Chongqing, Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Children’s Hospital, Chongqing Medical University, Chongqing, China
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Yongchen YangShanghai Children’s Hospital, Shanghai Children’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China
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Yi HuangCenter for Clinical Molecular Medicine, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Pediatrics in Chongqing, Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Children’s Hospital, Chongqing Medical University, Chongqing, China
,
Junjie TanCenter for Clinical Molecular Medicine, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Pediatrics in Chongqing, Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Children’s Hospital, Chongqing Medical University, Chongqing, China
,
Yuanyuan ChenCenter for Clinical Molecular Medicine, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Pediatrics in Chongqing, Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Children’s Hospital, Chongqing Medical University, Chongqing, China
,
Jing YangCenter for Clinical Molecular Medicine, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Pediatrics in Chongqing, Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Children’s Hospital, Chongqing Medical University, Chongqing, China
,
Hu DouCenter for Clinical Molecular Medicine, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Pediatrics in Chongqing, Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Children’s Hospital, Chongqing Medical University, Chongqing, China
,
Lin ZouCenter for Clinical Molecular Medicine, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Pediatrics in Chongqing, Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Children’s Hospital, Chongqing Medical University, Chongqing, China
,
Jie YuDepartments of Hematology, Children’s Hospital of Chongqing Medical University, Chongqing, China
&
Liming BaoCenter for Clinical Molecular Medicine, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Pediatrics in Chongqing, Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Children’s Hospital, Chongqing Medical University, Chongqing, China;Division of Human Genetics, Cincinnati Children’s Hospital Medical Center, and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USACorrespondence[email protected]
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Pages 2195-2204 | Received 05 Feb 2012, Accepted 11 Apr 2012, Published online: 21 May 2012

Citations (9)

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Read on this site (2)

Xi Chen, Hu Dou, Xingjuan Wang, Yi Huang, Ling Lu, Junqing Bin, Yongchun Su, Lin Zou, Jie Yu & Liming Bao. (2018) KIT mutations correlate with adverse survival in children with core-binding factor acute myeloid leukemia. Leukemia & Lymphoma 59:4, pages 829-836.
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Paula Marlton. (2014) The many facets of WT1 in acute myeloid leukemia: clarity remains elusive. Leukemia & Lymphoma 55:2, pages 235-237.
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Articles from other publishers (7)

Xin Yu, Yuan Zhang, Shuang Liu, Yu Mu, Fengjia Shang & Nan Zhang. (2020) Association between the Wilms tumor-1 rs16754 polymorphism and acute myeloid leukemia. Medicine 99:27, pages e20713.
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Zhenzhen Yang, Xingjuan Wang, Xi Chen, Hu Dou, Yi Huang, Ling Lu, Lin Zou, Junqin Bi, Meng Su, Jie Yu & Liming Bao. (2019) GATA2 mutations and overexpression in pediatric acute myeloid leukemia. Pediatric Hematology Oncology Journal 4:2, pages 56-63.
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Xingjuan Wang, Xi Chen, Zhenzhen Yang, Hu Dou, Ling Lu, Junqin Bi, Lin Zou, Jie Yu & Liming Bao. (2018) Correlation of TET2 SNP rs2454206 with improved survival in children with acute myeloid leukemia featuring intermediate-risk cytogenetics . Genes, Chromosomes and Cancer 57:8, pages 379-386.
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J E Megías-Vericat, M J Herrero, L Rojas, P Montesinos, V Bosó, F Moscardó, D Martínez-Cuadrón, J L Poveda, M Á Sanz & S F Aliño. (2015) A systematic review and meta-analysis of the impact of WT1 polymorphism rs16754 in the effectiveness of standard chemotherapy in patients with acute myeloid leukemia. The Pharmacogenomics Journal 16:1, pages 30-40.
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SURASAK SANGKHATHAT, WANWISA MANEECHAY, WELAWEE CHAIYAPAN, SAMORNMAS KANNGERN & TEERANUT BOONPIPATTANAPONG. (2015) Association of Wilms' tumor 1 gene single-nucleotide polymorphism rs16754 with colorectal cancer. Molecular and Clinical Oncology 3:6, pages 1401-1405.
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Dao-Yu Zhang, Han Yan, Shan Cao, Wei Zhang, Xiao-Lin Li, Hui Zeng & Xiao-Ping Chen. (2015) Wilms Tumor 1 rs16754 predicts favorable clinical outcomes for acute myeloid leukemia patients in South Chinese population. Leukemia Research 39:6, pages 568-574.
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Xingru Li, Sihan Wang, Raviprakash T. Sitaram, Charlotta Andersson, Börje Ljungberg & Aihong Li. (2013) Single Nucleotide Polymorphisms in the Wilms’ Tumour Gene 1 in Clear Cell Renal Cell Carcinoma. PLoS ONE 8:3, pages e58396.
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