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. 2020 May 6;157:104866. doi: 10.1016/j.phrs.2020.104866

Table 2.

CML gene expression profiling.

GENE ID function output on ref
inflammation/
immune resp
ANXA4 high in Sjogren anti infl [87]
ARG1 immunosuppressive pro immun [97]
BTK sustains GVHD anti infl [38]
C3AR1 neutrophils chemotaxis antagonist pro immun [98]
CAMP increased in inflammation anti infl [126]
CASP10 increased in Chron anti infl [88]
CDC20 increased in the adiposity inflamm model anti infl [127]
CEACAM1 inhibits T lynf pro immun [99]
CEACAM8 high in arthritis anti infl [89]
CLEC5A high in neurogen shock anti infl [92]
COL17A1 induce IL7 that sustains T & B lynf anti immun [128]
CTSG high in rheumatic arthritis anti infl [90]
CXCL2 high in Alzheimer anti infl [70]
CXCL3 sustain adipogenesis anti infl [129]
CYBB increased in inflammation anti infl [130]
DAGLB sustains production of arachidonic acid anti infl [131]
ELANE high in LPS inflammation anti infl [132]
EPX high in asthma anti infl [133]
FGFR1 high in prostatic inflammation anti infl [134]
FUT4 increased in bacterial infections anti infl [135]
GENE ID function output on ref
inflammation
GRN high in dementhia anti [94]
GSN increases NK apoptosis pro immun [100]
IL18 high in arthritis anti [91]
ITGAM high in psoriasis anti [95]
LTA4H high after trauma anti [113]
MAP2K1 high in sinusitis anti [114]
MMP8 high in intra-amniotic infections anti [115]
MMP9 high in skin healing anti [116]
MPO high in neutrophils anti [117]
NECTIN1 high in Chlamidial infection pro imm [101]
OLR1 NFkB activator anti [118]
PGLYRP1 high in gengivitis anti [96]
PLAU high after thrombosis anti [119]
PRG2 eosinophils basic protein anti [120]
PTX3 increased by IL6 anti [121]
RNASE2 high in inflamm, anti-viral anti anti-imm [125]
RNASE3 anti viral anti imm [125]
SPTBN1 reduces TGFb pro [122]
TM7SF3 reduces nitric oxid pro [123]
TNFAIP8 high in inflamm anti [124]
GENE ID function output on
ref
inflammation
CCL5 activates NK pro immun [138]
CCR4 high in asthma pro [137]
CCR5 activates NK pro immun [136]
CD28 inactivated by PD1 pro immun [139]
CD74 increases MCHII expression pro immun [140]
CX3CR1 high in antifungal resp pro immun [141]
CXCL16 high in anti-viral resp pro-immun [105]
CXCR3 high in T effector pro immun [142]
FYN high in inflamm/sustains NK pro pro imm [143]
HAVCR2 high in anti-viral resp pro-immun [106]
IFNG antiviral pro immun [107]
JAK3 shift from M1 to M2 resp anti [102]
NFATC2 increases T memory pro immun [144]
PDE4A low in sepsis anti [145]
SERPINB9 activates CD8 pro immun [146]
SOCS3 low in arthritis anti [103]
STAT5A high in colon inflamm pro [147]
TLR3 anti-viral/anti-inflamm anti pro imm [104]

Table represents all genes that resulted Up- (in red) and down- (in green) regulated after 6 months of treatment with Imatinib, as listed in Table 1. Table 2 in addition for each gene reports the respective physiological function (with correspondent literature references) and the final effect resulting from mRNA de-regulation made by 6 months of Imatinib, with focus on the inflammation and on the immunological infection control.