Table 2.
Ref.
|
TME changes in a high-risk group
|
Therapeutic significance
|
Experimental validation
|
Mechanism
|
Yang et al[9] | CD8+ T cells, T cells, B cells, plasmacytoid dendritic cells, immature dendritic cells, and cytotoxic cells | Higher sensitivity to cisplatin and paclitaxel in the high-risk group | qPCR: MRNA expression | None |
Ren et al[10] | CD8+ T cells, CD4+ T cells, and endothelial cells; Macrophages and fibroblasts | Higher sensitivity to paclitaxel, erlotinib, and cisplatin in the high-risk group; No significant difference in TMB, PD1, PD-L1, CTLA4 and IPS score | None | None |
Huang et al[11] | None | KRAS mutations are more frequent in the hypoxic subtype | qPCR: MRNA expression | None |
Li et al[12] | T cell exclusion scores | Lower PD1 expression in the high-risk subgroup | None | None |
Ren et al[13] | CD8+ T cells, B cells, macrophage, eosinophil, and monocyte; Immune activation score | Higher sensitivity to paclitaxel and erlotinib in the high-risk group; No significant difference in TMB, MSI, and IPS score | None | None |
Zhou et al[14] | CD8+ T cells, activated CD4+ memory T cells, naïve B cells, and plasma cells; M0 macrophages; Scores in CD4+ T cell recruiting, Th17 cell recruiting, dendritic cell recruiting, macrophage recruiting, and killing of cancer cells | None | qPCR: MRNA expression; Wound-healing assay: Migration; Transwell assay: Invasion | ChIP assay: BHLHE40/TLR3 axis |
Sun et al[15] | CD8+ T cells and B cells | None | qPCR: MRNA expression; MTT assay: Proliferation; Transwell assay: Invasion | ChIP assay and luciferase reporter assay: HIF-1α/ TSPOAP1-AS1 axis |
Tian et al[16] | CD8+ T cells and regulatory T cell | Lower PD1 and CTLA4 expression in a high-risk group | qPCR: MRNA expression | None |
Zhang et al[17] | T cells; M0 macrophages | Higher LDHA methylation in pancreatic cancer tissues | None | None |
Chen et al[18] | CD8+ T cells, follicular helper T cells, memory B cells, monocytes, M1 macrophages, M2 macrophages, resting mast cells, and eosinophils; Immune score and stromal score | Higher TMB in the high-risk groups | None | None |
Ding et al[19] | CD8+ T cells, plasma cells, and naïve B cells; M2 macrophages, resting memory CD4+ T cells, and resting natural killer cells | None | None | None |
BHLHE40: Basic helix-loop-helix family member e40; ChIP: Chromatin immunoprecipitation; CTLA4: Cytotoxic T-lymphocyte-associated protein 4; HIF-1α: Hypoxia-inducible factor 1α; IPS: Immunophenoscore; KRAS: Kirsten rat sarcoma viral oncogene homologue; LDHA: Lactate dehydrogenase A; MSI: Microsatellite instability; MTT: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; PD1: Programmed cell death protein 1; PD-L1: Programmed death ligand 1; qPCR: Quantitative real-time PCR; TMB: Tumor mutation burden; TSPOAP1-AS1: TSPO-associated protein 1 antisense RNA 1; TLR3: Toll-like receptor 3.