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Molecular underpinning of extranodal NK/T-cell lymphoma
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Molecular underpinning of extranodal NK/T-cell lymphoma

Yenlin Huang, Laurence De LevalPhilippe Gaulard
Best Practice and Research: Clinical Haematology, 卷.26(1), 頁碼.57-74
03/2013
PMID: 23768641

摘要

Epstein-Barr virus extranodal NK/T-cell lymphoma gene expression profiling natural killer tumor suppressor genes Oncology Clinical Biochemistry
Peripheral NK/T-cell lymphoma (PTCL) is a heterogeneous group of uncommon hematologic malignancies with aggressive clinical course and unfavorable prognosis. Extranodal NK/T-cell lymphoma, nasal type (NKTCL) is the most common extranodal entity worldwide, with heterogeneous geographic distribution, and it is characterized by its association with EBV, a nasal or less often extranasal presentation and aggressive behavior. Recent works using array-based technologies have provided novel insights into the pathogenesis and discovered new biomarkers with diagnostic and therapeutic implications in NKTCL. Gene expression profiling identified that most of the NKTCL are derived from activated natural killer cells with distinctively high expression of granzyme H compared to other PTCLs, which might serve as a new diagnostic biomarker. Frequent deletions and promoter methylations in PRDM1, ATG5, AIM1, FOXO3, HACE1 mapping to 6q21-q25, suggest their roles as potential tumor suppressors. The deregulation of oncogenic pathways (PDGF, JAK-STAT, AKT) provides a rationale for developing targeted therapies in the future. © 2013 Elsevier Ltd. All rights reserved.

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