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. 2021 Aug 19;9(8):1048. doi: 10.3390/biomedicines9081048

Table 1.

An overview illustrating TME characteristics of a selection of simple and complex genome sarcoma types.

Sarcoma Type DNA Alterations Immune Infiltration 1 PD-L1
Expression 2
Genomic/TME Heterogeneity 1 General TME Composition
Simple genome
Alveolar soft-part
sarcoma
TFE3-ASPCR1 29.7–100% −/− CD8 T cells; TAMs [25,26,27]
Chondrosarcoma (low-grade) IDH, COL2A1 0% −/± CD4 and CD8 T cells; TAMs [28,29,30]
Well-differentiated
liposarcoma
MDM2, CDK4, CNA −/± 0–50% −/− CD4 Th and CD8 T cells; B cells, DCs; TAMs [31,32,33,34]
Ewing sarcoma EWSR1-ETS 0% −/− M2-like TAMs; CD4 and CD8 T cells [34,35,36,37]
Synovial sarcoma SS18-SSX 0% −/± TAMs; CD4 FOXP3 Tregs and CD8 T cells [34,35,38]
Complex genome
Chondrosarcoma
(dedifferentiated)
IDH, COL2A1, CNA ± 41–52% +/± CD4 and CD8 T cells; TAMs [29,30]
Chordoma CDKN2A, PBRM1, SMARCB1, CNA + 0–68.5% ±/± CD4 FOXP3 Tregs and CD8 T cells; M1-like and M2-like TAMs [39,40,41,42]
Dedifferentiated liposarcoma MDM2, CDK4, CNA + 10–67% +/+ CD4 Th and CD8 T cells; B cells, DCs; TAMs [24,31,32,33,34]
Myxofibrosarcoma CIN + 16–20% +/+ CD4 Th, CD4 Treg and CD8 T cells; B cells; DCs; M1-like and M2-like TAMs [34,39,43,44,45]
Osteosarcoma CIN ± 0–25% +/+ CD4 and CD8 T cells; M1-like and M2-like TAMs, NK cells; DCs [36,46,47,48]
Soft tissue leiomyosarcoma CNA ± 34–59% +/+ M2-like TAMs, CD4 T cells [32,39,43,49]
Undifferentiated soft tissue sarcoma CIN, SNV + 0–33% +/+ CD4 Th, CD4 Treg and CD8 T cells; B cells; DCs; M2-like TAMs [24,34,39,43,45,50,51]
Uterine leiomyosarcoma CNA ± 0–70% +/+ M2-like TAMs; CD4 T cells; NK cells [39,43,49,52,53]

1 Amount of immune infiltration, genomic heterogeneity, and TME heterogeneity: −, low; ±, moderate; +, high. 2 Percentage of tumors expressing PD-L1 in tumor cells. Abbreviations: CIN, chromosomal instability; CNA, copy number alteration; DCs, dendritic cells; MDSCs, myeloid-derived suppressor cells; PD-L1, programmed death-ligand 1; SNV, single nucleotide variant; TAMs, tumor-associated macrophages; Th, T helper cells; TME, tumor microenvironment; Tregs, regulatory T cells.