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Table 2 Comparison of Mutations identified in MPE primary cultures and PDX

From: Human lung adenocarcinoma cell cultures derived from malignant pleural effusions as model system to predict patients chemosensitivity

 

KRAS

EGFR

PIK3CA

BRAF

MET

TP53

STK11

Exon19del

T790 M

PE e/10

(p10)

87.9 %

p.Q61H

(c.183 A>C)

    

31.6 %

p. T1010I

(c. 3029 C>T)

  

PE e/10

(PDX)

50.4 %

p.Q61H

(c.183 A>C)

  

49.2 %

p.E545 K

(c.1633 G>A)

   

44.5 %

p.Q37*

(c.109 C>T)

PE b/11

(p3)

    

53.5 %

p.V600E

(c.1799 T>A)

   

PE b/11

(PDX)

 

100 %

p.E746_A750del

(c.2235_2249del15)

15.2 %

p.T790 M

(c.2369 C>T)

   

97.6 %

p.R248Q

(c.743 G>A)

 

PE g/11

(p6)

        

PE g/11

(PDX)

75.5 %

p.Q61H

(c.183 A>C)

  

49.5 %

p.E545 K

(c.1633 G>A)

   

77.7 %

p.Q37*

(c.109 C>T)

PE i/11

(p5)

37.2 %

p.Q61 K

(c.181 C>A)

     

100 %

p.R175H

(c.524 G>A)

 

PE i/11

(PDX)

29.4 %

p.Q61 K

(c.181 C>A)

     

100 %

p.R175H

(c.524 G>A)

 

PE n/11 (p3)

        

PE n/11

(PDX)

27 %

p.Q61 K

(c.181 C>A)

     

100 %

p.R175H

(c.524 G>A)

 

PE s/11

(p3)

 

42 %

p.E746_A750del

(c.2235_2249del15)

15 %

p.T790 M

(c.2369 C>T)

   

14.3 %

p.S241F

(c.722 C>T)

 

PE s/11

(PDX)

 

100 %

p.E746_A750del

(c.2235_2249del15)

15.8 %

p.T790 M

(c.2369 C>T)

   

94.7 %

p.R248Q

(c.743 G>A)

 

PE u/11

(p6)

 

49 %

p.E746_A750del

(c.2235_2249del15)

11.3 %

p.T790 M

(c.2369 C>T)

     

PE u/11

(PDX)

 

92 %

p.E746_A750del

(c.2235_2249del15)

11.8 %

p.T790 M

(c.2369 C>T)

   

100 %

p.R248Q

(c.743 G>A)

 

PE v/11

(p2)

 

57 %

p.E746_A750del

(c.2235_2249del15)

      

PE v/11

(PDX)

 

87.5 %

p.E746_A750del

(c.2235_2249del15)

    

93.5 %

p.R248Q

(c.743 G>A)

 

PE z/11 (p4)

        

PE z/11

(PDX)

 

100 %

p.E746_A750del

(c.2235_2249del15)

14.2 %

p.T790 M

(c.2369 C>T)

   

98.8 %

p.R248Q

(c.743 G>A)

 

PE b/12

(p4)

100 %

p.Q61H

(c.183 A>C)

  

49.1 %

p.E545 K

(c.1633 G>A)

   

100 %

p.Q37*

(c.109 C>T)

PE b/12

(PDX)

65.7 %

p.Q61H

(c.183 A>C)

  

49 %

p.E545 K

(c.1633 G>A)

   

63 %

p.Q37*

(c.109 C>T)

  1. * nonsense mutation