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. 2021 Jan 5;34(2):654–666. doi: 10.1007/s13577-020-00473-0

Table 3.

Correlation between miR-675-3p expression and clinicopathological features

Variables Total (N = 230) miR-675-3p expression p value
High (N = 115) Low (N = 115)
Age (year)
 < 65 120 (52.2%) 61 (53.0%) 59 (51.3%) 0.792
 ≥ 65 110 (47.8%) 54 (47.0%) 56 (48.7%)
Gender
 Male 144 (62.6%) 68 (59.1%) 76 (66.1%) 0.276
 Female 86 (37.4%) 47 (40.9%) 39 (33.9%)
Family history of cancer
 No 133 (57.8%) 66 (57.4%) 67 (58.3%) 0.713
 Yes 67 (29.1%) 32 (27.8%) 35 (30.4%)
Unknown 30 (13.0%) 17 (14.8%) 13 (11.3%)
TNM stage
 I 57 (24.8%) 31 (27.0%) 26 (22.6%) 0.531
 II 78 (33.9%) 35 (30.4%) 43 (37.4%)
 III 89 (38.7%) 47 (40.9%) 42 (36.5%)
 IV 6 (2.6%) 2 (1.7%) 4 (3.5%)
Histologic grade
 G1–G2 155 (67.4%) 70 (60.9%) 85 (73.9%) 0.035*
 G3–G4 75 (32.6%) 45 (39.1%) 30 (26.1%)
Pathologic_M
 M0 224 (97.4%) 113 (98.3%) 111 (96.5%) 0.408
 M1 6 (2.6%) 2 (1.7%) 4 (3.5%)
Clark's level
 I–III 47 (20.4%) 17 (14.8%) 30 (26.1%) 0.034*
 IV–V 183 (79.6%) 98 (85.2%) 85 (73.9%)
Pathologic_N
 N0–N1 135 (75.2%) 69 (60.0%) 66 (57.4%) 0.688
 N2–N4 95 (24.8%) 46 (40.0%) 49 (42.6%)
Pathologic_T
 T1–T2 82 (35.7%) 45 (39.1%) 37 (32.2%) 0.271
 T3–T4 148 (64.3%) 70 (60.9%) 78 (67.8%)

*indicates statistically significant. The high expression of miR-675-3p was correlated with tumor histologic grade and Clark’s level