A novel recurrent NPM1-TYK2 gene fusion in cutaneous CD30-positive lymphoproliferative disorders

Author:

Velusamy Thirunavukkarasu1,Kiel Mark J.1,Sahasrabuddhe Anagh A.1,Rolland Delphine1,Dixon Catherine A.1,Bailey Nathanael G.1,Betz Bryan L.1,Brown Noah A.1,Hristov Alexandra C.1,Wilcox Ryan A.2,Miranda Roberto N.3,Medeiros L. Jeffrey3,Jeon Yoon K.4,Inamdar Kedar V.5,Lim Megan S.1,Elenitoba-Johnson Kojo S. J.1

Affiliation:

1. Department of Pathology, University of Michigan Medical School, Ann Arbor, MI;

2. Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI;

3. Department of Hematopathology, University of Texas MD Anderson Cancer Center, Houston TX;

4. Department of Pathology, Seoul National University Hospital, Seoul, South Korea; and

5. Department of Pathology, Henry Ford Health System, Detroit, MI

Abstract

Key Points Whole-transcriptome sequencing reveals NPM1-TYK2 gene fusion in cutaneous CD30-positve lymphoproliferative disorders. NPM1-TYK2 activates STAT signaling and is a therapeutic target in a subset of cutaneous CD30-positive lymphoproliferative disorders.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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