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. 2023 Feb 27;13:1104659. doi: 10.3389/fonc.2023.1104659

Table 2.

Most altered genes among representative cancers in our cohort (number of patients, along with genetic alterations and frequency).

Cancer type Genes Nb Freq. (%) Cancer type Genes Nb Freq. (%)
Glioma (n=33) TP53 8 24 Prostate (n=10) TP53 6 60
TERT 8 24 AR 4 40
PTEN 7 21 Pancreatic (n=8) CTNNB1 2 25
NF1 6 18 KRAS 2 25
EGFR 5 15 SMAD4 2 25
Lung (n=27) TP53 14 52 TP53 2 25
KRAS 4 15 Ovarian (n=7) TP53 6 86
Breast (n=25) PIK3CA 9 36 PIK3R1 2 29
ESR1 7 28 Head & Neck (n=6) TP53 3 50
C11orf30 (EMSY) 6 24 CCND1 2 33
TP53 6 24 CDKN2A/B 2 33
CCND1 5 20 DNMT3A 2 33
FGF19 5 20 FGF19 2 33
FGF3 5 20 FGF3 2 33
FGF4 5 20 TERT 2 33
FGFR1 5 20 Gastric (n=5) TP53 3 60
ZNF703 5 20 ARID1A 2 40
CDH1 4 16 ATM 2 40
NSD3 (WHSC1L1) 4 16 CDKN2A/B 2 40
Colorectal (n=10) TP53 8 80 PIK3CA 2 40
APC 6 60
KRAS 3 30
SMAD4 3 30

Cancers for which more than five patients had available sequencing results were analyzed. Genes with class 4-5 variants in at least four patients with the most represented cancers (glioma, lung, and breast cancers), and those with class 4-5 variants in at least two patients with the least frequent cancers (colorectal, prostate, pancreatic, ovarian, head and neck, and gastric cancers), were selected for the global cohort. Abbreviations: Nb., number of patients with genetic alterations; Freq., frequency (in %).