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. 2016 Jun 10;6:26351. doi: 10.1038/srep26351

Table 1. Relationship between PKM2 expression and clinicopathological characteristics of GBC.

Variable No. of cases PKM2-low expression N (%) PKM2-high expression N (%) P-value
Age Mean 65 (range: 39–87)    
 <60 20 9 (45.0) 11 (55.0) 0.574
 ≥60 50 22 (44.0) 28 (56.0)
Sex
 Male 18 5 (27.8) 13 (72.2) 0.086
 Female 52 26 (50) 26 (50)
Histological Grade
 Well-differentiated 6 2 (33.3) 4 (66.7) 0.851
 Moderately differentiated 51 23 (45.1) 28 (54.9)
 Poorly differentiated 13 6 (46.2) 7 (53.8)
Neurovascular Infiltration
 Absent 34 18 (52.9) 16 (47.1) 0.126
 Present 36 13 (36.1) 23 (63.9)
Pathologic T stage
 pT1 13 10 (76.9) 3 (23.1) 0.0003
 pT2 17 10 (58.8) 7 (41.2)
 pT3 20 7 (35.0) 13 (65.0)
 pT4 20 4 (20.0) 16 (80.0)
Lymph node metastasis
 N0 37 20 (54.1) 17 (45.9) 0.041
 N1 24 9 (37.5) 15 (62.5)
 N2 9 2 (22.2) 7 (77.8)
Distant metastasis
 Not present at operation 47 20 (54.1) 21 (44.7) 0.007
 Present at operation 23 9 (37.5) 18 (78.3)
TNM stage
 Stage I 8 7 (87.5) 1 (12.5) 0.003
 Stage II 14 9 (64.3) 5 (35.7)
 Stage III 17 7 (41.2) 10 (58.8)
 Stage IV 31 8 (25.8) 23 (74.2)

Note: The clinicopathological information of 70 GBC patients from Xinhua Hospital who enrolled in the study were used for statistical analysis of the association between PKM2 expression and age, sex, or histological grade.