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. 2015 Dec 17;13(2):1551–1557. doi: 10.3892/mmr.2015.4687

Table I.

Association between clinicopathologic features, VEGF and TP expression levels and MVD.

Clinicopathologic featurea Cases n=84 VEGF expression
TP expression
MVD
High
(n=53)
Low
(n=31)
P-value High
(n=55)
Low
(n=29)
P-value High
(n=39)
Low
(n=45)
P-value
Gender 0.27 0.15 0.11
 Male 55 37 18 33 22 29 26
 Female 29 16 13 22 7 10 19
Location 0.77 0.57 0.72
 Colon 47 29 18 32 15 21 26
 Rectum 37 24 13 23 14 18 19
Histological type 0.25 0.21 0.11
 Well 35 24 11 23 12 21 14
 Moderate 43 27 16 30 13 16 27
 Poor/Other 6 2 4 2 4 2 4
Lymph node metastasis 0.13 0.84 0.15
 pN0 36 26 10 24 12 20 16
 pN1–4 48 27 21 31 17 19 29
Lymphatic invasion 0.78 0.81 0.63
 ly0–1 45 29 16 30 15 22 23
 ly2–3 39 24 15 25 14 17 22
Venous invasion 0.57 0.76 0.37
 v0–1 62 38 24 40 22 27 35
 v2–3 22 15 7 15 7 12 10
Budding 0.88 0.41 0.21
 Grade 0–1 47 30 17 29 18 19 28
 Grade 2–3 37 23 14 26 11 20 17
Dukes' stage 0.49 0.58 0.047b
 A 8 6 2 7 1 7 1
 B 26 18 8 16 10 13 13
 C 27 14 13 17 10 12 15
 D 23 15 8 15 8 7 16
a

Clinicopathological feature, according to the TNM classification (3) and the Japanese classification of colorectal carcinoma (7).

b

Statistical significance between stage A and D. VEGF, vascular endothelial growth factor; TP, thymidine phosphorylase; MVD, microvessel density.