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. 2015 Jan 27;9(4):1927–1933. doi: 10.3892/ol.2015.2910

Table II.

Correlation between IMP3 expression and the clinicopathological features of non-small cell lung cancer.

IMP3 protein expression, n (%)

Variables +/++ χ2 P-value
Age, years 0.458 0.500
 <62 66 (72.5) 25 (27.5)
 ≥62 73 (76.8) 22 (23.2)
Gender 2.624 0.106
 Male 79 (70.5) 33 (29.5)
 Female 60 (81.1) 14 (18.9)
Tumor size, cm 6.214 0.013a
 ≤3 51 (65.4) 27 (34.6)
 >3 88 (81.5) 20 (18.5)
Differentiation 19.170 0.000b
 Well 22 (51.2) 21 (48.8)
 Moderately 67 (77.0) 20 (23.0)
 Poorly 50 (89.3) 6 (10.7)
Pathological subtype 1.018 0.314
 SCC 68 (78.2) 19 (21.8)
 AC 71 (71.7) 28 (28.3)
Clinical stage 20.761 0.000b
 I–II 59 (60.8) 38 (39.2)
 III–IV 80 (89.9) 9 (10.1)
LN metastasis 8.331 0.004b
 Positive 84 (83.2) 17 (16.8)
 Negative 55 (64.7) 30 (35.3)
CEA level 0.037 0.849
 Normal 54 (74.0) 19 (26.0)
 Increased 85 (75.2) 28 (24.8)
Smoking status 0.364 0.547
 Yes 94 (73.4) 34 (26.6)
 No 45 (77.6) 13 (22.4)

Statistical analyses were performed using Pearson χ2 tests.

a

P<0.05 and

b

P<0.01.

IMP3, insulin-like growth factor II mRNA-binding protein 3; SCC, squamous cell carcinoma; AC, adenocarcinoma; CEA, carcinoembryonic antigen.