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Table 2 The relationship between PGC mRNA expression and the clinicopathological characteristics of breast cancer

From: The relationship between pepsinogen C and gastric carcinogenesis: a transgene and population study

Clinicopathological features

Variable

Low expression

High expression

P

Age, n (%)

≦60

292 (27%)

309 (28.5%)

0.345

 > 60

249 (23%)

233 (21.5%)

 

T stage, n (%)

T1

137 (12.7%)

140 (13%)

0.537

T2

321 (29.7%)

308 (28.5%)

 

T3

62 (5.7%)

77 (7.1%)

 

T4

19 (1.8%)

16 (1.5%)

 

N stage, n (%)

N0

259 (24.3%)

255 (24%)

0.136

N1

177 (16.6%)

181 (17%)

 

N2

64 (6%)

52 (4.9%)

 

N3

29 (2.7%)

47 (4.4%)

 

M stage, n (%)

M0

456 (49.5%)

446 (48.4%)

0.111

M1

6 (0.7%)

14 (1.5%)

 

Pathologic stage, n (%)

Stage I

91 (8.6%)

90 (8.5%)

0.304

Stage II

311 (29.3%)

308 (29.1%)

 

Stage III

118 (11.1%)

124 (11.7%)

 

Stage IV

5 (0.5%)

13 (1.2%)

 

Histological type, n (%)

IDC

417 (42.7%)

355 (36.3%)

 < 0.001

ILC

71 (7.3%)

134 (13.7%)

 

PR status, n (%)

Negative

200 (19.3%)

142 (13.7%)

 < 0.001

Indeterminate

2 (0.2%)

2 (0.2%)

 

Positive

313 (30.3%)

375 (36.3%)

 

ER status, n (%)

Negative

146 (14.1%)

94 (9.1%)

 < 0.001

Indeterminate

2 (0.2%)

0 (0%)

 

Positive

367 (35.5%)

426 (41.2%)

 

HER2 status, n (%)

Negative

286 (39.3%)

272 (37.4%)

0.843

Indeterminate

7 (1%)

5 (0.7%)

 

Positive

83 (11.4%)

74 (10.2%)

 

PAM50, n (%)

Normal

16 (1.5%)

24 (2.2%)

 < 0.001

Luminal A

244 (22.5%)

318 (29.4%)

 

Luminal B

108 (10%)

96 (8.9%)

 

Her2 + 

32 (3%)

50 (4.6%)

 

Basal

141 (13%)

54 (5%)

 
  1. ILC Invasive lobular carcinoma, IDC Invasive ductal carcinoma, ER Estrogen receptor, PR Progesterone receptor