Skip to main content

Table 1 The role of STAT3 in regulating signaling proteins in immnue cells

From: Coordinated regulation of immune contexture: crosstalk between STAT3 and immune cells during breast cancer progression

Immune cells

Proteins

Relathionship with STAT3

References

MDSCs

IDO

MDSCs-activated STAT3 suppressed the T cell expansion and Th1 polarization via the IDO manner

[37]

 

IRF-8

STAT3 downregulted the IRF-8 expression and promoted the MDSCs formation

[44]

 

G-CSF

G-CSF mediated the STAT3/IRF-8 axis functions in MDSCs

[45]

 

IL-6

IL-6 stimulated STAT3 phosphorylation in MDSCs

[48]

 

S100A8/A9

STAT3 stimulated the S100A8/A9-mediated ROS, then suppressed CD4+ T cells accumulation

[59]

Macrophages

CD206/Arg-1/PTGS2

STAT3 inhibition suppressed these markers expression

[64, 73]

 

HA

HA actived the STAT3 cascade

[72]

 

A-FABP

A-FABP stimulated the STAT3 activation by promoting IL-6 production

[67]

 

HIF-1α/TGF-β1

STAT3 upregulated HIF-1α/TGF-β1 expression, and influenced angiogenesis, tumor cells proliferation and metastasis

[82]

 

PD-L1

STAT3 promoted the PD-L1 secretion on macrophages of tumor milieu

[87]

Dendritic Cells

PKCβII/PRKCB2

STAT3 reduce the PKCβII protein and PRKCB2 expression and suppressed DCs generation

[98]

 

HER-2/neu

STAT3 inhibition downregulated the tumor surface HER-2/neu expression

[103]

 

IL-10

IL-10-related signaling plays an important role in STAT3-elicited cDCs immunosuppressive response

[105]

 

FLT3L

FLT3L promoted DCs proliferation via STAT3-dependent manners

[111]

 

Tcf4

STAT3 interacted with Tcf4 promoters and increased the pDCs population

[110]

CD4 + T cells

IL-10

STAT3 increased the IL-10 expression and counteracted CD4 + T cells tumoricidal function

[34]

Tregs

Foxp3

STAT3 directly regulated the expression of Foxp3, and promoted the Tregs generation and immunosuppressive abilities

[138]

 

IDO1

STAT3-mediated IDO1 expression increased the Foxp3+ Tregs in tumor milieu

[150]

CD8 + T cells

INF-α/β

STAT3-blocking induced INF-α/β production and triggered CD8+ T cells responses

[165, 167]

 

GAPDH/HK2

STAT3 activation repressed GAPDH/HK2, which were critical glycolic indicators for T cells

[172, 174]

 

FGFR4

Genetic instability of FGFR4 enhanced the STAT3 activation and possibly suppressed CD8+ T cells infiltration

[137]