From: Distinct genetic alterations in small cell carcinoma from different anatomic sites
Location | Genes | Small cell carcinoma | Non-small cell carcinoma | Notes |
---|---|---|---|---|
Lung | TP53 mutation | 80–90% [5] | 40-60% |  |
RB1 mutation | 60–90% [71] | 15-30% |  | |
PTEN mutation | 60-90% of cases [8] | 40% | Â | |
PARP1 high expression | 2.6 fold higher than non-Small cell carcinoma [10] | Â | PARP-1 inhibitors as anti-cancers | |
Urinary bladder | TERT promoter mutation | 100% | 60-70% | Not see in SmCC from prostate, lung, ovary, or esophagus [10] |
TP53 | overexpression 54% p53 negative staining 46% [72] | TP53 mutations 14% 30% | Â | |
Prostate | ERG gene rearrangements | 40-60% [63] | True prostate cancer specific biomarkers: PCA3 and TMPRSS2:ERG gene fusion [73] | |
(TMPRSS2–ERG gene fusions) | ||||
RB1 loss | 90% [68] | 34% of primary 74% of met [14] | Loss of RB1 function late in prostate cancer, early in other common cancers | |
RAS/RAF | No report | 43% of primary, 90% of met [14] | Â | |
PTEN | 63%[68] | 4% of primary, 58% of met [14] | Â | |
SCCOHT | SMARCA4 mutations | Characteristic mutation in SCCOHT | ||
Merkel cell carcinoma | MCV clonally integrated | Characteristic integration in MCC |