“…Not only FDG but also other radiomarkers prove useful in various cancer types [9]. Below, a number of metabolic pathways together with their radiomarkers are mentioned, important for oncology and detectable through PET [10]:-
11 C-thymidine, 18 F-thymidine (FLT) – replication of DNA, cellular proliferation,
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11 C-methionine (MET), 18 F-ethyl-tyrosine (FET), 18 F-methyl-tyrosine (FMT), 18 F-dihydroxy-phenylalanine (F-DOPA) – protein synthesis, amino acid transport,
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18 F-acetate, 11 C-choline, 18 F-choline (FCH) – membrane lipid synthesis,
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18 F-misonidazole (FMISO), 64 Cu-copper-ATSM – hypoxia,
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18 F-annexin V – apoptosis,
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18 F-galacto-RGD – angiogenesis,
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18 F-deoxy-arabinofuranosyl-nucleosides (FEAU, FIAU, FMAU) – reporter genes,
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18 F-uracil (FU) – tumor therapy control,
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18 F-oestradiol (FES) – receptor binding (estrogen),
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68 Ga-DOTATOC/DOTANOC – receptor binding (somatostatin).
…”