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. 2012 Sep 25;7(9):e45357. doi: 10.1371/journal.pone.0045357

Table 5. Clinical, pathological and molecular features of patients according to the LINE-1 methylation levels.

Clinical, pathological or molecular features LINE-1≥65% (n = 23) LINE-1<65% (n = 92) p-value
Sex, n (%)
Male 9 (39.1) 45 (48.9) 0.4
Female 14 (60.9) 47 (51.1)
Mean age (standard deviation)* 37.65 (8.3) 37.36 (8.3) 0.8
Family history of CRC1, n (%)
Yes 4 (17.4) 12 (13) 0.736
No 19 (82.6) 80 (87)
Tumor location, n (%)
Rectum 7 (30.4) 40 (43.5) 0.209
Distal to splenic flexure 6 (26.1) 29 (31.5)
Proximal to splenic flexure 10 (43.5) 23 (25)
Synchronous or metachronous CRC, n (%)
Yes 3 (13) 2 (2.2) 0.054
No 20 (87) 90 (97.)8
TNM tumor stage, n (%)
I–II 9 (39.5) 31 (33.7) 0.625
III–IV 14 (60.9) 61 (66.3)
Tumor differentiation, n (%)
Well or moderate 18 (81.8) 79 (87.8 0.489
Poor 4 (18.2) 11 (12.2)
Mucinous component, n (%)
>50% 14 (60.9) 25 (27.5) 0.003
<50% 9 (39.1) 66 (72.5)
Medullary growth pattern, n (%)
Yes 2 (8.7) 9 (9.9) 1
No 21 (91.3) 82 (90.1)
Crohńs reaction, n (%)
Yes 5 (21.7) 7 (8) 0.124
No 18 (78.3) 80 (92)
Tumor infiltrating lymphocytes, n (%)
Yes 5 (21.7) 21 (23.9) 0.83
No 18 (78.3) 67 (76.1)
Microsatellite instability, n (%)
MSI 6 (26.1) 19 (20.7) 0.572
MSS 17 (73.9) 73 (79.3)
Mismatch repair deficiency2, n (%)
Yes 7 (30.4) 20 (21.7) 0.379
No 16 (69.6) 72 (78.3)
*

P value was calculated by t-test.

1

Including first and second degree relatives.

2

MSI-H and/or loss of expression of MMR proteins by immunohistochemistry.