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. 2008 May 13;98(10):1690–1695. doi: 10.1038/sj.bjc.6604333

Table 2. Clinicopathological features and results of RUNX3 hypermethylation in pancreatic cancer tissues.

    Hypermethylation
 
Variable No. of cases + P a
Age
 <60 10 5 5 0.325
 ⩾60 22 15 7  
         
Gender
 M 18 13 5 0.198
 F 14 7 7  
         
Tumour size
 TS1 5 2 3 >0.9999
 ⩾TS2 27 18 9  
         
S
 − 18 11 7 0.854
 + 14 9 5  
         
RP
 − 10 6 4 0.844
 + 22 14 8  
         
CH
 − 13 9 4 0.515
 + 19 11 8  
         
DU
 − 21 13 8 0.923
 + 11 7 4  
         
PV
 − 12 8 4 0.706
 + 20 12 8  
         
A
 − 27 16 11 0.379
 + 5 4 1  
         
PL
 − 27 16 11 0.379
 + 5 4 1  
         
DPM
 − 26 15 11 0.242
 + 6 5 1  
         
N
 0 14 8 6 0.581
 1 18 12 6  
         
Differentiation
 Mod 21 12 9 0.241
 Poor 6 5 1  
a

Analysed by Fisher's exact test or χ2 test for independence.

bTumour size according to the Classification of Pancreatic Carcinoma; A=arterial invasion; CH=choledocal invasion; DPM=dissected peripancreatic tissue margin; DU=duodenal invasion; F=female; PL=peripancreatic nerve plexus invasion; M=male; mod=moderately differentiated adenocarcinoma; N=lymph node metastasis; poor=poorly differentiated adenocarcinoma; pTNM=pathological TNM; PV=portal vein invasion; RP=retroperitoneal invasion; S=serosal invasion.

cClassified according to the classification of The General Rules for the Clinical and Pathological Study of Primary Pancreatic Cancer. April 2002, Pancreatic Cancer Study Group of Japan.