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. 2012 Mar 6;104(8):599–613. doi: 10.1093/jnci/djs033

Table 2.

Spectrum of current and potential therapeutic cancer vaccine targets*

Target type Examples Selected references
Oncoprotein point mutated: ras, B-raf, frame shift mutations, undefined unique tumor mutations; HER2/neu, MUC-1 C-terminus, p53 (1,7,8,48,49)
Oncofetal antigen CEA, MUC-1 (24,19,26)
Cancer–testes MAGE-A3, BAGE, SEREX-defined, NY-ESO (10,5052)
Tissue lineage PAP, PSA, gp100, tyrosinase, glioma antigen (5,6,24,25,27,41,44,53)
Stem cell/EMT Brachyury, SOX-2, OCT-4, TERT, CD44high/CD24lo, CD133+ (5462)
Viral HPV, HCV (63,64)
Glycopeptides STn-KLH (15,16)
Antiangiogenic VEGF-R (65,66,67)
B-cell lymphoma Anti-id (1114)
*

BAGE = B melanoma antigen; CEA = carcinoembryonic antigen; EMT = epithelial–mesenchymal transition; gp100 = glycoprotein 100; HCV = hepatitis C virus; HPV = human papillomavirus; MAGE-A3 = melanoma-associated antigen-A3; MUC-1 = mucin 1; NY-ESO = New York esophageal carcinoma antigen 1; OCT-4 = octamer-binding transcription factor 4; PAP = prostatic acid phosphatase; PSA = prostate-specific antigen; SOX-2 = (sex determining region Y)-box-2; STn-KLH = sialyl-Tn–keyhole limpet hemocyanin; TERT = telomerase reverse transcriptase; VEGF-R = vascular endothelial growth factor receptor.