STAT3 as a possible therapeutic target in human malignancies: lessons from acute myeloid leukemia

被引:34
作者
Bruserud, Oystein [1 ,2 ,3 ]
Nepstad, Ina [2 ]
Hauge, Michelle [2 ]
Hatfield, Kimberley Joanne [2 ]
Reikvam, Hakon [1 ,2 ]
机构
[1] Haukeland Hosp, Dept Med, N-5021 Bergen, Norway
[2] Univ Bergen, Fac Med & Dent, Dept Clin Sci, Bergen, Norway
[3] Univ Bergen, Haukeland Univ Hosp, Inst Clin Sci, Sect Hematol,Dept Med, N-5021 Bergen, Norway
关键词
acute myeloid leukemia; clinical studies; mitochondria; phosphorylation; prognosis; STAT3; therapy; transcription; ACUTE MYELOGENOUS LEUKEMIA; GENE-EXPRESSION PROFILES; PYRUVATE-KINASE M2; ACTIVATES TRANSCRIPTION; INCREASE PROLIFERATION; SIGNAL TRANSDUCERS; NUCLEAR IMPORT; AML CELLS; KAPPA-B; G-CSF;
D O I
10.1586/17474086.2015.971005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
STAT3 is important for transcriptional regulation in human acute myeloid leukemia (AML). STAT3 has thousands of potential DNA binding sites but usually shows cell type specific binding preferences to a limited number of these. Furthermore, AML is a very heterogeneous disease, and studies of the prognostic impact of STAT3 in human AML have also given conflicting results. A more detailed characterization of STAT3 functions and the expression of various isoforms in human AML will therefore be required before it is possible to design clinical studies of STAT3 inhibitors in this disease, and it will be especially important to investigate whether the functions of STAT3 differ between patients. Several other malignancies also show extensive biological heterogeneity, and the present discussion and the suggested scientific approaches may thus be relevant for other cancer patients.
引用
收藏
页码:29 / 41
页数:13
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