Abstract:
:Myeloid immune cells, such as dendritic cells, monocytes, and macrophages, play a central role in the generation of immune responses and thus are often either disabled or even hijacked by tumors. These new tolerogenic activities of tumor-associated myeloid cells are controlled by an oncogenic transcription factor, signal transducer and activator of transcription 3 (STAT3). STAT3 multitasks to ensure tumors escape immune detection by impairing antigen presentation and reducing production of immunostimulatory molecules while augmenting the release of tolerogenic mediators, thereby reducing innate and adaptive antitumor immunity. Tumor-associated myeloid cells and STAT3 signaling in this compartment are now commonly recognized as an attractive cellular target for improving efficacy of standard therapies and immunotherapies. Hereby, we review the importance and functional complexity of STAT3 signaling in this immune cell compartment as well as potential strategies for cancer therapy.
journal_name
Int J Mol Scijournal_title
International journal of molecular sciencesauthors
Su YL,Banerjee S,White SV,Kortylewski Mdoi
10.3390/ijms19061803subject
Has Abstractpub_date
2018-06-19 00:00:00issue
6issn
1422-0067pii
ijms19061803journal_volume
19pub_type
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journal_title:International journal of molecular sciences
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journal_title:International journal of molecular sciences
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