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. 2020 Sep 29;11:564499. doi: 10.3389/fimmu.2020.564499

Table 1.

Tumor marker ganglioside targets.

Malignancy GD2 GD3 Fucosyl-GM1 GM2 GM3 PolySia (52) Sialyl Lewis X
Neuroblastoma (5355) (55) (56) (57, 58) (59) (60, 61)
Melanoma (55) (55, 62) (63) (64) (65)
Glioma (66) (6769) (52, 70) (7173) (74)
Non-small cell lung cancer (NSCLC) (75) (76) (77, 78) (79, 80) (81, 82)
Small cell lung cancer (SCLC) (83) (83) (75, 83, 84) (83)
Breast carcinoma (85) (8587) (85) (85) (88) (81, 82)
Renal cell cancer (89) (90) (91) (92)
Ovarian cancer (93) (94) (93) (93) (95)
Soft tissue sarcomas (96) (96)
Osteosarcoma (97) (98, 99)
Ewing's sarcoma (100, 101) (99) (102)
Desmoplastic Round Cell (103) (99)
Rhabdomyosarc. (99) (99)
Retinoblastoma (104) (105)
Wilms tumor (91, 106) (107)
Medullary thyroid cancer (108)
Prostate Cancer (109)
Gastric cancer (109) (109) (81)
Endometrial (109) (52, 109)
Pancreatic (109) (109) (81)
Colon Cancer (109) (81, 82)
Esophageal (81)
Head and neck (81, 82)

Select cancers where there is evidence for TMG expression in >50% of all patients in the indicated malignancy. This table is shown to exemplify the prevalence of TMGs. The cells with no entry reflect ≤ 50% prevalence, or that we omitted literature that we deem unreliable for this review because very few biopsies were phenotyped. The list ranges from ~95% (Neuroblastoma), to ~80% (Melanoma), to ~50% (Head and Neck) of patients. When expressed in a patient the TMGs are present homogeneously in tumor nodules and cells. Gold color denotes literature from many laboratories, or evidence confirmed by the authors of this review.