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. 2021 Sep 3;31(6):495–503. doi: 10.1097/CMR.0000000000000777

Table 2.

The main differences of the CNVs in cyclin-dependent kinase 4 pathway between cutaneous melanoma a and mucosal melanomab

Gene Cutaneous melanoma (TCGA database) (n = 367) Mucosal melanoma (n = 65)
Gain Loss Total number Total frequency Gain Loss Total number Total frequency
CDKN2A 1 112 113 30.8% 0 14 14 21.5%
CCND1 23 1 24 6.5% 11 2 13 20.0%
CDK4 14 0 14 3.8% 33 1 34 52.3%
RB1 1 3 4 1.1% 4 2 6 9.2%
KIT 10 0 10 2.7% 16 0 16 24.6%
EGFR 2 1 3 0.8% 10 3 13 20.0%
MET 6 0 6 1.6% 12 1 13 20.0%
PTEN 0 28 28 7.6% 2 8 10 15.4%
BRAF 15 1 16 4.4% 15 1 16 24.6%
TP53 0 3 3 0.8% 0 4 4 6.2%
NF1 2 0 2 0.5% 1 7 8 12.3%
NRAS 11 0 11 3.0% 2 4 6 9.2%
KRAS 5 0 5 1.4% 10 3 13 20.0%
HRAS 1 0 1 0.3% 0 5 5 7.7%

BRAF, V-raf murine sarcoma viral oncogene homolog B1; CCND, cyclin D; EGFR, epidermal growth factor receptor; HRAS, v-Ha-ras Harvey rat sarcoma viral oncogene homolog; KIT, v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog; KRAS, v-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog; MET, cellular-mesenchymal to epithelial transition factor; NRAS, neuroblastoma RAS viral (v-ras) oncogene homolog; PTEN, phosphatase and tensin homolog deleted on chromosome ten.

a

Genomic data of cutaneous melanomas was downloaded from the TCGA database using the cBioPortal (http://www.cbioportal.org) with available mutation and CNV data.

b

Genomic data of mucosal melanomas derived from our previous study [2].