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. 2018 Sep 3;4(3):156–163. doi: 10.1016/j.cdtm.2018.07.001

Table 1.

Potential biomarkers for gastric cancer prognosis.

Marker Reference Source Elevated amount predicts
TAM infiltration (CD163+) 35 Tumor tissue Poor prognosis
TAM density in solid tumors 36,40 Tumor tissue Poor prognosis
Macrophage M2 infiltration 40 Tumor tissue Poor prognosis
Macrophage M1 infiltration 40 Tumor tissue Improved prognosis
TP 26, 27, 28 Tumor stroma Poor prognosis
Diametrically polarized tumor-associated macrophages (protumoral M2 macrophages) 38 Tumor tissue Poor prognosis
Tumor infiltrating antigen CD11+ 37 Tumor tissue Poor prognosis
Serum macrophage MIF + CEA 41, 42, 43 Serum/tumor tissue Poor prognosis
OPN 29 Tumor stroma Poor prognosis
KRS 34 Tumor tissue/tumor-associated inflammatory cells Poor prognosis
MR 31 Tumor tissue Poor prognosis
CCL5/RANTES 32, 33 Tumor cells, macrophages, T cells Increased tumor invasion
Increased incidence of lymph node metastasis
NF-κB
CCL2/CCR2 chemokines
44 Gene allele rs230510 and CCL2 rs4586 A allele of rs230510 associated with improved OS; T allele of rs4586 associated with poor OS
Gastric adenoma, CD204 positive TAMs 39 Tissue stroma Risk-factor for developing gastric adenocarcinoma
Tim-3 30 Macrophages Increased tumor invasion; increased
incidence of lymph node metastasis & advanced clinical stage

TAM: tumor-associated macrophage; CD: cluster of differentiation; TP: thymidine phosphorylase; MIF: macrophage migration-inhibitory factor; CEA: carcinoembryonic antigen; OPN: osteopontin; KRS: lysyl-tRNA synthetase; MR: mannose receptor; CCL: chemokine (C—C motif) ligand; RANTES: regulated upon activation, normal T-cell expressed and presumably secreted; NF-κB: nuclear factor-kappa B; CCR: C–C chemokine receptor; OS: overall survival; Tim-3: T-cell immunoglobulin and mucin domain-containing molecule-3.