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Table 4 Association between PDGFRA mutational status and clinicopathological parameters, PDGFRα expression and RAS mutational status

From: Dysregulated PDGFR alpha expression and novel somatic mutations in colorectal cancer: association to RAS wild type status and tumor size

Tissue samples (N = 55 CRC)

PDGFRA intron 17–18

PDGFRA exon 18

PDGFRA intron 18–19

Present

P-value

Present

P-value

Present

P-value

Age (years)

 

0.239

 

0.5

 

0.643

 < 50 years

7 (70%)

4 (40%)

0 (0%)

 ≥ 50 years

21 (51.2%)

19 (46.3%)

2 (4.9%)

Gender

 

0.43

 

0.55

 

0.599

 Male

17 (48.6%)

15 (42.9%)

1 (2.9%)

 Female

11 (55%)

9 (45%)

1 (5%)

Location

 

0.119

 

0.083

 

0.339

 Colon

25 (56.8%)

22 (50%)

1 (2.3%)

 Rectum

3 (30%)

2 (20%)

1 (10%)

Diameter of tumor

 

0.521

 

0.258

 

0.635

 ≤ 5 cm

16 (51.6%)

15 (48.4%)

1 (3.2%)

 > 5 cm

11 (55%)

7 (35%)

1 (5%)

Invasion of tumor

 

0.228

 

0.957

 

0.952

 T2

2 (100%)

1 (50%)

0 (0%)

 T3

16 (55.2%)

13 (44.8%)

1 (3.4%)

 T4

10 (41.7%)

10 (41.7%)

1 (4.2%)

Lymph node metastasis

 

0.077

 

0.924

 

0.125

 N0

14 (70%)

9 (45%)

0 (0%)

 N1

6 (33.3%)

7 (38.9%)

2 (11.1%)

 N2

8 (50%)

7 (43.8%)

0 (0%)

Histological gradation

 

0.283

 

0.871

 

0.035

 Well differentiated

9 (69.2%)

5 (38.5%)

2 (15.4%)

 Moderately differentiated

16 (47.1%)

15 (44.1%)

0 (0%)

 Poorly differentiated

3 (37.5%)

4 (50%)

0 (0%

PDGFRα expression

 

0.089

 

0.024

 

0.103

 Low

16 (43.2%)

4 (22.2%)

2 (11.1%)

 High

12 (66.7%)

20 (54.1%)

0 (0%)

RAS status

 

0.333

 

0.08

 

0.666

 Wild type

15 (46.9%)

17 (53.1%)

1 (3.1%)

 Mutated

13 (56.5%)

7 (30.4%)

1 (4.3%)