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. Author manuscript; available in PMC: 2017 Apr 1.
Published in final edited form as: Gynecol Oncol. 2016 Apr;141(1):65–71. doi: 10.1016/j.ygyno.2016.01.003

Table 1.

Proportion of molecular aberrations in the PI3K pathway by tumor type UNK, unknown

Molecular
Aberration
Endometrial Ovarian Cervical
Endometrioid Non-
endometrioid
High
Grade
Serous
Low
Grade
Serous
Clear
Cell
Endometrioid Mucinous Squamous Adenocarcinoma
PTEN
protein
loss
80 5 45 rare 24 rare 13 3.6
PTEN
mutation
43 0–11 rare <1 3–
20
5–33 2 6 rare
PI3KCA
mutation
30–40 20 rare 2 20–
34
20 13 14–48 14–25
PI3KCA
amplification
2–4 46 68 20 20 20 UNK UNK UNK
AKT
mutation
2–3 0 rare rare UN
K
UNK UNK UNK UNK
PI3KR1
mutation
43 12 UNK UNK UN
K
UNK UNK UNK UNK
ARID1A
mutation
34 0 UNK UNK 29 32 UNK UNK UNK
IGF-IR
over-
expression
75 rare 25 75 UN
K
UNK UNK UNK UNK