Oncogenic MITF dysregulation in clear cell sarcoma: Defining the MiT family of human cancers

被引:161
作者
Davis, Ian J.
Kim, Jessica J.
Ozsolak, Fatih
Widlund, Hans R.
Rozenblatt-Rosen, Orit
Granter, Scott R.
Du, Jinyan
Fletcher, Jonathan A.
Denny, Christopher T.
Lessnick, Stephen L.
Linehan, W. Marston
Kung, Andrew L.
Fisher, David E. [1 ]
机构
[1] Dana Farber Canc Inst, Melanoma Program Med Oncol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[4] Childrens Hosp, Dept Med, Div Hematol Oncol, Boston, MA 02115 USA
[5] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[6] Univ Calif Los Angeles, Gwynne Hazen Cherry Mem Labs, Div Hematol Oncol, Dept Pediat, Los Angeles, CA 90095 USA
[7] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
[8] NCI, Urol Oncol Branch, Bethesda, MD 20892 USA
关键词
D O I
10.1016/j.ccr.2006.04.021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Clear cell sarcoma (CCS) harbors a pathognomonic chromosomal translocation fusing the Ewing's sarcoma gene (EWS) to the CREB family transcription factor ATF1 and exhibits melanocytic features. We show that EWS-ATF1 occupies the MITF promoter, mimicking melanocyte-stimulating hormone (MSH) signaling to induce expression of MITF, the melanocytic master transcription factor and an amplified oncogene in melanoma. Knockdown/rescue studies revealed that MITF mediates the requirement of EWS-ATF1 for CCS survival in vitro and in vivo as well as for melanocytic differentiation. Moreover, MITF and TFE3 reciprocally rescue one another in lines derived from CCS or pediatric renal carcinoma. Seemingly unrelated tumors thus employ distinct strategies to oncogenically dysregulate the MiT family, collectively broadening the definition of MiT-associated human cancers.
引用
收藏
页码:473 / 484
页数:12
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