Format

Send to

Choose Destination
Oncologist. 2014 May;19(5):536-44. doi: 10.1634/theoncologist.2013-0407. Epub 2014 Apr 4.

STAT3 inhibitors: finding a home in lymphoma and leukemia.

Author information

1
Hematology-Oncology, Banner, MD Anderson Cancer Center, Gilbert, Arizona, USA; Hematology-Oncology, Louisiana State University Health Sciences Center, New Orleans, Louisiana, USA; Departments of Investigational Cancer Therapeutics (Phase I Clinical Trials Program) and Immunology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

Abstract

The Janus kinase (JAK) and signal transducer and activator of transcription (STAT) pathway is an active mediator of cytokine signaling in the pathogenesis of solid and hematologic malignancies. The seven-member STAT family is composed of latent cytoplasmic transcription factors that are activated by phosphorylation intertwined in a network with activation that ultimately leads to cell proliferation. An activated kinase enzyme phosphorylates one STAT factor or more, which shuttle to the nucleus to regulate gene expression, promoting cell survival. Somatic STAT3 mutations have been recently reported in large granular lymphocytic leukemia, aplastic anemia, and myelodysplastic syndrome. Furthermore, the relationship between BCL6 and STAT3 in diffuse large B-cell lymphomas, particularly on the activated B-cell subtype, needs to be further explored. The search for therapeutic STAT3 inhibitors that abrogate the JAK/STAT pathway is currently under way. Targeting the STAT pathway, which seems to be critical in tumorigenesis, is promising for multiple malignancies including lymphoma and leukemia. In this paper, we review mechanisms of action, failures, and successes of STAT3 inhibitors.

KEYWORDS:

IL6; JAK; Leukemia; Lymphoma; Phase I; STAT

PMID:
24705981
PMCID:
PMC4012967
DOI:
10.1634/theoncologist.2013-0407
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for HighWire Icon for PubMed Central
Loading ...
Support Center