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. 2022 Sep;11(9):3108–3127. doi: 10.21037/tcr-22-660

Table 1. ESCRT pathway genes mutation across TCGA project on NIH national cancer institute CDC Data Portal database.

Symbol
CHMP2A CHMP2B CHMP3 CHMP4B CHMP4C CHMP5 CHMP6 CHMP7
Project
   SSM (N=530)
    SSM affected cases 21 26 15 22 14 19 9 36
    SSM affected cases in TCGA % 0.0396 0.0491 0.0283 0.0415 0.0264 0.0358 0.017 0.0679
   CNV (N=510)
    CNV gains 26 11 8 22 14 21 53 3
    CNV gains in TCGA % 0.0510 0.0216 0.0157 0.0431 0.0275 0.0412 0.1039 0.0059
    CNV losses 23 23 9 11 5 5 7 32
    CNV losses in TCGA % 0.0451 0.0451 0.0176 0.0216 0.0098 0.0098 0.0137 0.0627
   All SSM affected cases in UCEC 70 59 32 55 31 45 28 68
   Somatic mutation 22 35 16 24 19 22 9 43
   Somatic mutation in all SSM affected cases in UCEC % 0.3143 0.5932 0.5 0.4364 0.6129 0.4888 0.3214 0.6324
Disease type
   Adenomas and adenocarcinomas 32 31 18 32 21 26 28 40
   Cystic, mucinous and serous neoplasms 38 28 13 23 10 19 0 28
   Epithelial neoplasms 1
Survival
   Dead 13 10 5 10 8 14 16 9
   Alive 57 49 27 45 23 31 51 59
   Survival rate 0.82 0.72 0.81 0.76 0.68 0.65 0.25 0.84
   Interval of last follow-up (Year) 5.095 5.142 5.136 5.106 5.106 5.095 5.008 5.106

ESCRT, endosomal sorting complex required for transport; TCGA, The Cancer Genome Atlas; CNV, copy-number variant; SSM, simple somatic mutation; SNV, single nucleotide variation; UCEC, uterine corpus endometrial carcinoma.