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Table 1 Clinical data and mutation status of CTNNB1 in correlation with the expression pattern of FGFR2 in adrenocortical carcinoma samples (n = 26)

From: Subcellular localization of fibroblast growth factor receptor type 2 and correlation with CTNNB1 genotype in adrenocortical carcinoma

Sample number

Sex [F/M]

Age [range in years]

Survival [months]

Ki-67 [%]

Hormonal activity

Nuclear staining

Cytoplasmatic staining

CTNNB1-mutation

1

F

30–40

   

+

+

No mutation

2

F

40–50

> 132

 

Cortisol

0

+

No PCR-amplicon

3

F

20–30

> 9

  

0

+

No mutation

4

M

40–50

   

+

+

p.S45P

5

M

80–90

   

0

+

No mutation

6

F

40–50

   

0

+

No mutation

7

M

60–70

   

0

+

No mutation

8

M

50–60

> 48

30–40

Cortisol, androgen

+

+

No mutation

9

M

30–40

48

 

Cortisol, androgen

+

+

No mutation

10

F

40–50

> 360

  

+

+

No mutation

11

M

20–30

> 30

  

+

+

No mutation

12

F

30–40

> 22

 

Androgen

+

+

p.S33P

13

F

40–50

   

+

+

No mutation

14

M

60–70

   

+

+

No mutation

15

M

40–50

   

+

+

p.T41A

16

F

50–60

99

  

+

+

p.A5V

17

F

30–40

> 151

60

 

+

+

No mutationa

18

M

60–70

   

0

+

No mutation

19

F

60–70

25

  

+

+

No mutation

20

F

40–50

> 89

5–10

Cortisol, androgen

0

+

No mutation

21

M

50–60

> 4

 

Cortisol

+

+

No mutation

22

F

70–80

> 4

 

Cortisol

0

+

p.T41A

23

F

50–60

5

 

Cortisol

0

0

p.L513F

24

F

50–60

> 6

25

Cortisol, androgen

0

0

 

25

M

50–60

 

30–40

 

0

+

No mutation

26

M

70–80

   

+

+

 
  1. aThis tumour specimen harbours a TP53 Cy135Phe mutation; blank field: data not available; survival: > indicates right censored data. Data on age is presented as a range to protect patient’s anonymity