GATA-3 expression identifies a high-risk subset of PTCL, NOS with distinct molecular and clinical features

Author:

Wang Tianjiao1,Feldman Andrew L.2,Wada David A.3,Lu Ye1,Polk Avery1,Briski Robert1,Ristow Kay4,Habermann Thomas M.4,Thomas Dafydd5,Ziesmer Steven C.4,Wellik Linda E.4,Lanigan Thomas M.6,Witzig Thomas E.4,Pittelkow Mark R.7,Bailey Nathanael G.5,Hristov Alexandra C.5,Lim Megan S.5,Ansell Stephen M.4,Wilcox Ryan A.1

Affiliation:

1. Division of Hematology and Oncology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI;

2. Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN;

3. Department of Dermatology, University of Utah, Salt Lake City, UT;

4. Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, MN;

5. Department of Pathology, and

6. Division of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI; and

7. Department of Dermatology, Mayo Clinic, Rochester, MN

Abstract

Key Points Alternatively polarized macrophages are abundant constituents of the tumor microenvironment in T-cell lymphoproliferative disorders. GATA-3 expression identifies a subset of PTCL, NOS with a distinct cytokine profile and inferior survival.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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