This Article Full Text Full Text (PDF) Supplementary Data Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Lui, W.-O. Articles by Kroll, T. G. Search for Related Content PubMed PubMed Citation Articles by Lui, W.-O. Articles by Kroll, T. G.

CREB3L2-PPAR Fusion Mutation Identifies a Thyroid Signaling Pathway Regulated by Intramembrane Proteolysis

Departments of ¹ Pathology and ² Surgery, University of Chicago Medical Center, Chicago, Illinois; Departments of ³ Molecular Medicine and Surgery and ⁴ Oncology-Pathology, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden; and ⁵ Department of Pathology, Emory University School of Medicine, Atlanta, Georgia

Requests for reprints: Todd G. Kroll, Department of Pathology, University of Chicago Medical Center, 5841 South Maryland Avenue, AMB P323 (MC1089), Chicago, IL 60637. Phone: 773-702-3017; Fax: 773-834-5251; E-mail: tkroll{at}bsd.uchicago.edu.

Key Words: CREB3L2 • PPAR • thyroid cancer • regulated intramembrane proteolysis • fusion mutation

The discovery of gene fusion mutations, particularly in leukemia, has consistently identified new cancer pathways and led to molecular diagnostic assays and molecular-targeted chemotherapies for cancer patients. Here, we report our discovery of a novel CREB3L2-PPAR fusion mutation in thyroid carcinoma with t(3;7)(p25;q34), showing that a family of somatic PPAR fusion mutations exist in thyroid cancer. The CREB3L2-PPAR fusion encodes a CREB3L2-PPAR fusion protein that is composed of the transactivation domain of CREB3L2 and all functional domains of PPAR1. CREB3L2-PPAR was detected in <3% of thyroid follicular carcinomas. Engineered overexpression of CREB3L2-PPAR induced proliferation by 40% to 45% in primary human thyroid cells, consistent with a dominant oncogenic mechanism. Wild-type CREB3L2 was expressed in the thyroid as a bZIP transcription factor with a transmembrane domain that has flanking S1P and S2P proteolytic cleavage sites. Native CREB3L2 was cleaved to nuclear CREB3L2 by regulated intramembrane proteolysis in normal thyroid cells that expressed the S1P and S2P proteases. Nuclear CREB3L2 stimulated transcription 8-fold from the EVX1 cyclic AMP (cAMP) response element in the absence of cAMP, whereas CREB3L2-PPAR inhibited transcription 6-fold from EVX1 in the same experiments. CREB3L2-PPAR also inhibited 4-fold the expression of thyroglobulin, a native cAMP-responsive gene, in primary thyroid cells treated with thyroid-stimulating hormone. Our findings identify a novel CREB3L2-PPAR gene fusion mutation in thyroid carcinoma and reveal a thyroid signaling pathway that is regulated by intramembrane proteolysis and disrupted in cancer. [Cancer Res 2008;68(17):7156–64]

This article has been cited by other articles:

				H Zhang and A M Oliveira Fusion genes in epithelial neoplasia J. Clin. Pathol., January 1, 2010; 63(1): 4 - 11. [Abstract] [Full Text] [PDF]

				E. Diallo-Krou, J. Yu, L. A. Colby, K. Inoki, J. E. Wilkinson, D. G. Thomas, T. J. Giordano, and R. J. Koenig Paired Box Gene 8-Peroxisome Proliferator-Activated Receptor-{gamma} Fusion Protein and Loss of Phosphatase and Tensin Homolog Synergistically Cause Thyroid Hyperplasia in Transgenic Mice Endocrinology, November 1, 2009; 150(11): 5181 - 5190. [Abstract] [Full Text] [PDF]