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. 2020 May 25;52(4):1162–1177. doi: 10.4143/crt.2020.138

Table 1.

Association analysis of the FGFR4 Gly388Arg polymorphism and clinicopathological parameters in gastric cancer patients

Variable Total (n=102) GG (n=45) GA+AA (n=57) Pearson’s χ2 value p-value
Age (yr)
 < 60 52 23 29 0.001 > 0.99
 ≥ 60 50 22 28
Sex
 Male 74 35 39 1.105 0.373
 Female 28 10 18
Tumor size (cm)
 < 4 67 30 37 0.004 > 0.99
 ≥ 4 34 15 19
Differentiation
 G1+G2 44 16 28 1.887 0.227
 G3+G4 58 29 29
T category
 T1+T2 43 24 19 4.125 0.047
 T3+T4 59 21 38
N category
 N0 47 29 28 0.607 0.436
 N1+N2+N3 54 26 28
M category
 M0 95 41 51 2.713 0.130
 M1 7 1 6
Borrmann type
 Local type (early GC+Ⅰ+Ⅱ) 50 15 35 3.494 0.071
 Infiltrating type (Ⅲ+Ⅳ) 52 25 27
Lauren type
 Intestinal type 45 17 28 0.070 0.840
 Diffuse infiltration type 57 23 34
WHO type
 Tubular adenocarcinoma 42 17 25 3.264 0.515
 Papillary adenocarcinoma 3 0 3
 Mucous adenocarcinoma 3 2 1
 Signet ring cell carcinoma 18 8 10
 Poorly differentiated adenocarcinoma 36 13 23
FGFR4 status
 Low expression 33 17 16 1.083 0.394
 High expression 69 28 41
STAT3 status
 Negative 37 14 23 0.929 0.408
 Positive 65 31 34
p-STAT3 status
 Negative 46 27 19 7.222 0.009
 Positive 56 18 38
Vimentin status
 Negative 41 24 17 5.781 0.025
 Positive 61 21 40
E-cadherin status
 Negative 35 12 23 2.089 0.208
 Positive 67 33 34

FGFR4, fibroblast growth factor receptor 4; GC, gastric cancer; WHO, World Health Organization.