Biological Hallmarks and Emerging Strategies to Target STAT3 Signaling in Multiple Myeloma

被引:11
|
作者
Zhou, Jianbiao [1 ,2 ]
Chng, Wee-Joo [1 ,2 ,3 ]
机构
[1] Natl Univ Singapore, Canc Sci Inst Singapore, 14 Med Dr, Singapore 117599, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Med, Singapore 117597, Singapore
[3] Natl Univ Hlth Syst NUHS, Natl Univ Canc Inst Singapore NCIS, Dept Hematol Oncol, 1E Kent Ridge Rd, Singapore 119228, Singapore
基金
新加坡国家研究基金会;
关键词
multiple myeloma; signal transducer and activator of transcription 3 (STAT3); hallmarks of cancer; targeted therapy; JAK inhibitor; BONE-MARROW MICROENVIRONMENT; SUPER-ANTAGONIST SANT7; KINASE INHIBITOR; DENDRITIC CELLS; TRANSCRIPTION; PHASE-I; APOPTOSIS; PRL-3; COMBINATION; PHOSPHATASE;
D O I
10.3390/cells11060941
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Multiple myeloma (MM) is the second most common hematological malignancy, characterized by an abnormal accumulation of plasma cells in the bone marrow. Signal transducer and activator of transcription 3 (STAT3) is a cytoplasmic transcription factor that modulates the transcription of multiple genes to regulate various principal biological functions, for example, cell proliferation and survival, stemness, inflammation and immune responses. Aberrant STAT3 activation has been identified as a key driver of tumorigenesis in many types of cancers, including MM. Herein, we summarize the current evidence for the role of STAT3 in affecting cancer hallmark traits by: (1) sustaining MM cell survival and proliferation, (2) regulating tumor microenvironment, (3) inducing immunosuppression. We also provide an update of different strategies for targeting STAT3 in MM with special emphasis on JAK inhibitors that are currently undergoing clinical trials. Finally, we discuss the challenges and future direction of understanding STAT3 signaling in MM biology and the clinical development of STAT3 inhibitors.
引用
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页数:10
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