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. Author manuscript; available in PMC: 2016 Sep 9.
Published in final edited form as: Gastroenterology. 2016 Jun 11;151(3):440–447.e1. doi: 10.1053/j.gastro.2016.06.004

Table 3.

Molecular features in The Cancer Genome Atlas colorectal and endometrial cancer cases by MSI subgroup.

Somatic gene mutationa All cases Double somatic Lynch syndrome MLH1 Methyl Microsatellite stable p-valueb
All cases (n=291) n=291 n=8 n=8 n=73 n=202
PIK3CA 135 (46%) 8 (100%) 4 (50%) 37 (51%) 86 (43%) 0.007
BRAF 15 (5%) 0 0 13 (18%) 2 (1%) <0.0001
KRAS 79 (27%) 2 (25%) 4 (50%) 24 (33%) 79 (39%) 0.22
NRAS 10 (3%) 0 0 3 (4%) 7 (3%) 0.85
PTEN 147 (51%) 8 (100%) 4 (50%) 56 (77%) 79 (39%) <0.0001
Colorectal cancer (n=113) n=113 n=2 n=4 n=17 n=90
PIK3CA 34 (30%) 2 (100%) 1 (25%) 7 (41%) 24 (27%) 0.09
BRAF 14 (12%) 0 0 12 (71%) 2 (2%) <0.0001
KRAS 43 (38%) 1 (50%) 3 (75%) 3 (18%) 36 (40%) 0.08
NRAS 6 (5%) 0 0 0 6 (7%) 0.70
PTEN 12 (11%) 2 (100%) 1 (25%) 3 (18%) 6 (7%) 0.004
Endometrial cancer (n=178) n=178 n=6 n=4 n=56 n=112
PIK3CA 101 (57%) 6 (100%) 3 (75%) 30 (54%) 62 (55%) 0.13
BRAF 1 (1%) 0 0 1 (2%) 0 0.37
KRAS 36 (20%) 1 (17%) 1 (25%) 21 (38%) 13 (12%) 0.0009
NRAS 4 (2%) 0 0 3 (5%) 1 (1%) 0.29
PTEN 135 (76%) 6 (100%) 3 (75%) 53 (95%) 73 (65%) <0.0001

MLH1 methyl = MLH1 hypermethylation

a

Only activating mutations in BRAF, KRAS, and NRAS are included in these analyses.

b

p-value from Fisher’s exact test