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Table 1.

Clinicopathological and molecular features of 21 endometrial cancers with mutations in the PTEN or PIK3CA genes

Patient no. Age (years) FIGO stage Grade MSI PTEN mutation PIK3CA mutation p‐AKT expression
1 70 Ib 1 H Ex5; G389T, R130L Ex20; A3140T, H1047L +
2 58 Ib 3 L Ex20; A3140G, H1047R
3 71 Ib 1 H Ex8; G871A, E291K
Ex8; 863 del A, fs (stop at 868) Ex20; A3140T, H1047L +
4 52 Ic 2 H Ex8; 946 ins G, fs (stop at 970)
Ex8; 987 del TAAA, fs (stop at 1024)
5 41 Ic 2 H Ex5; A446G, Q149R
Ex8; 863 del A, fs (stop at 868) ++
6 44 Ia 1 H Ex8; A938G, K313R
Ex8; 963 del A, fs (stop at 1027) ++
7 47 Ib 1 H Ex8; 963 del A, fs (stop at 1027) ±
8 58 Ib 1 H Ex8; 923 ins A, fs (stop at 931)
9 62 Ib 2 MSS Ex20; A3140G, H1047R
10 54 Ib 1 MSS Ex5; C388G, R130G +
11 64 Ic 2 MSS Ex1; A76C, T26P
12 43 Ia 1 H Ex8; A815G, H272R
Ex8; 950 del TACT, fs (stop at 955) +
13 67 Ia 1 MSS Ex5; G389A, R130Q Ex9; C1636G, Q546E ++
14 33 Ia 1 H Ex5; 336 del AAGTG, fs (stop at 340) +
15 68 Ia 1 H Ex8; 956 del CTTT (stop at 1024) +
16 49 Ia 1 MSS Ex5; C388T, R130stop
17 55 Ic 3 L Ex5; C462A, F154L ++
18 59 Ib 1 H Ex20; A3036G, E1002E ++
19 63 Ib 1 MSS Ex5; G389A, R130Q
Ex5; C424T, R142W Ex20; A3062G, Y1021C ±
20 55 Ib 1 ND Ex5; C388T, R130stop ±
21 53 Ic 3 ND Ex5; 493 ins A, fs (stop at 499) +

– negative, +/– weak, + moderate, ++ strong. Some of the data have been reported previously.( 3 , 19 ) EX, exon; FIGO, International Federation of

Gynecology and Obstetrics; H, high‐frequency microsatellite instability; L, low‐frequency microsatellite instability; MSI, microsatellite instability; MSS, microsatellite stable; ND, not done; p‐AKT, phosphorylated AKT.