Gene mutations, epigenetic dysregulation, and personalized therapy in myeloid neoplasia: are we there yet?

Abstract:

:Myeloid neoplasms are characterized by acquired somatic mutations and epigenetic alterations in genes that are crucial for hematopoietic differentiation and cellular proliferation and survival pathways. The heterogeneity and genetic complexity of these disorders is daunting, but the improvement in our knowledge of the pathogenetic mechanisms underlying myeloid transformation, coupled with the increasing availability of agents that target these pathways, offers unique opportunities for improved therapy. This review will focus on common mutations that are of therapeutic or prognostic importance in acute myeloid leukemia (AML) and the classic Philadelphia chromosome-negative myeloproliferative neoplasms (Ph(-) MPNs), in the context of discussing the potential for risk-adapted and targeted therapeutic approaches for these diseases.

journal_name

Semin Oncol

journal_title

Seminars in oncology

authors

Odenike O,Thirman MJ,Artz AS,Godley LA,Larson RA,Stock W

doi

10.1053/j.seminoncol.2011.01.010

subject

Has Abstract

pub_date

2011-04-01 00:00:00

pages

196-214

issue

2

eissn

0093-7754

issn

1532-8708

pii

S0093-7754(11)00020-0

journal_volume

38

pub_type

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