FBXW7 mutation in adult T-cell and B-cell acute lymphocytic leukemias

被引:34
|
作者
Song, Jee Hoon [1 ]
Schnittke, Nikolai [1 ]
Zaat, April [1 ]
Walsh, Christine S. [2 ]
Miller, Carl W. [1 ]
机构
[1] UCLA Cedars Sinai Res Inst, Dept Med, Los Angeles, CA 90034 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Samuel Oschin Comprehens Canc Inst,Dept Obstetr &, Cedars Sinai Womens Canc Res Inst,Div Gynecol Onc, Los Angeles, CA 90095 USA
关键词
FBXW7; mutation; lymphocytic leukemia;
D O I
10.1016/j.leukres.2008.03.040
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The FBXW7 (also known as AGO, hCDC4, FBW7 and SEL-10) gene encodes a subunit of an ubiquitin protein ligase which regulates levels of cyclin E, NOTCH and other proteins. Engineered FBXW7 null cells display cell cycle and chromosome stability defects. Mutations of FBXW7 have been found in human colorectal, ovarian, endometrial tumors and T-cell acute lymphocytic leukemia, B-cell acute lymphocytic leukemia and adult T-cell leukemia DNA for mutations of the FBXW7 gene. Mutations were detected by PCR-SSCP of all coding exons of the three isoforms of FBXW7, shifted bands were direct sequenced. As expected, mutations were found in T-cell acute lymphotic leukemias. However mutations of FBXW7 were also found in four of 118 B-cell acute lymphocytic leukemias and one of 24 adult T-cell leukemia samples. The nucleotide changes consisted of an insertion, resulting in a frameshift mutation, and missense mutations of highly conserved redidues. All mutations affected the FBXW7 target interacting domain. These observations suggest that disruption of FBXW7 has a role in several forms of lymphocytic leukemias and not exclusively T-cell acute lymphocytic leukemia. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1751 / 1755
页数:5
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