A tumor-suppressor function for NFATc3 in T-cell lymphomagenesis by murine leukemia virus

被引:39
作者
Glud, SZ
Sorensen, AB
Andrulis, M
Wang, B
Kondo, E
Jessen, R
Krenacs, L
Stelkovics, E
Wabl, M
Serfling, E
Palmetshofer, A
Pedersen, FS
机构
[1] Aarhus Univ, Dept Mol Biol, DK-8000 Aarhus, Denmark
[2] Univ Wurzburg, Dept Mol Pathol, Inst Pathol, D-97070 Wurzburg, Germany
[3] Picobella, Burlingame, CA USA
[4] Okayama Univ, Grad Sch Med & Dent, Dept Pathol, Okayama, Japan
[5] Bay Zoltan Fdn Appl Res, Lab Tumor Pathol & Mol Diagnost, Inst Biotechnol, Szeged, Hungary
[6] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[7] Univ Aarhus, Dept Med Microbiol & Immunol, Aarhus, Denmark
关键词
D O I
10.1182/blood-2005-02-0493
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nuclear factor of activated T cell (NFAT) transcription factors play a central role in differentiation, activation, and elimination of lymphocytes. We here report on the finding of provirus integration into the NFatc3 locus in T-cell lymphomas induced by the murine lymphomagenic retrovirus SL3-3 and show that NFATc3 expression is repressed in these lymphomas. The provirus insertions are positioned close to the Nfatc3 promoter or a putative polyadenylated RNA (polyA) region. Furthermore, we demonstrate that NFATc3-deficient mice infected with SL3-3 develop T-cell lymphomas faster and with higher frequencies than wild-type mice or NFATc2-deficient mice. These results identify NFATc3 as a tumor suppressor for the development of murine T-cell lymphomas induced by the retrovirus SL3-3.
引用
收藏
页码:3546 / 3552
页数:7
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