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. 2016 Jan 3;7(8):8823–8838. doi: 10.18632/oncotarget.6815

Table 1. Correlation between the mRNA expressions of COL3A1 and clinicopathological variables in patients with colorectal cancer revealed by data-mining of Oncomine gene array datasets.

Dataseta Clinicopathological parameters Total cases COL3A1b χ2 p
< M ≥ M
Bittner Colon (373) T stage Tis-T1 52 35 17 10.073 0.018
T2 103 47 56
T3 85 35 50
T4 88 47 41
Dukes stage A 49 33 16 7.607 0.022
B 101 49 52
C-D 88 38 50
Smoke Never smoker 179 100 79 4.523 0.033
Smoker 194 87 107
Smith Colorectal (177) Stage I 24 19 5 10.468 0.015
II 57 27 30
III 57 23 34
IV 39 20 19
Recurrence No recurrence 109 62 47 7.502 0.006
Recurrence 36 11 25
Survival Alive 104 64 40 12.78 0
Dead 73 25 48
Jorissen Colorectal 3 (154) Dukes stage A 24 4 20 22.850 0.000
B 54 24 30
C 43 30 13
D 33 19 14
Recurrence No recurrence 27 20 7 6.641 0.008
Recurrence 92 40 52
Age 20-49 years 16 12 4 9.491 0.050
50 - 59 years 29 17 12
60 - 69 years 43 20 23
70 - 79 years 46 21 25
80+ years 24 7 17
Lin Colon 2 (149) Sex Male 70 26 44 8.224 0.004
Female 79 49 30
Vilar Colorectal 2 (104) Age 40-59 years 22 16 6 10.650 0.014
60 - 69 years 42 26 16
70 - 79 years 73 29 44
80+ years 39 17 22
a

The analysis was performed using datasets from the Oncomine cancer gene expression microarray DB (https://www.oncomine.org/resource/login.html). The numbers in the blankets represent the total cases.

b

COL3A1 mRNA expression was dichotomized into lower-than-median (< M) and higher-than-median (≥ M) groups.