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. 2014 Jun;6(6):694–705. doi: 10.3978/j.issn.2072-1439.2014.04.09

Table 3. Correlation between methylation of RUNX3 promoter and clinicopathological characters in NSCLC.

NO. study Characters M+/M– OR (95% CI) I2 (%) P (Egger’ test)
6 Gender Male 73/156 0.80 (0.51-1.26)b 0.8 0.054
Female 57/116
5 Smoking Yes 52/133 0.64 (0.38-1.07)b 25.2 0.438
No 53/102
9 Pathological type ACC/SCC 102/201; 44/180 2.25 (1.48-3.42)b 34.3 0.135
5 ACC/other type 46/124; 18/18 0.49 (0.22-1.10)b 0 0.595
5 SCC/other type 21/106; 18/9 0.10 (0.04-0.29)b 0 0.068
3 Differentiation H/M 40/68 0.39 (0.06-2.36)a 86.4 0.276
P 41/33 0.47 (0.26-0.85)b
6 TNM stage I-II 58/151 0.79 (0.24-2.62)a 78.3 0.953
III-IV 69/105

M+, the number of tissues with methylation; M–, the number of tissues with unmethylation; other type, large-cell carcinoma and adenosquamous cell carcinoma. H/M, highly and moderately differentiated; P, poor differentiation. a, by random effect model (DerSimonian-Laird method); b, by fixed effects model (Mantel-Haenszel). Abbreviations: RUNX3, runt-related transcription factor 3; SCC, squamous cell carcinoma; ACC, adenocarcinoma; NSCLC, non-small cell lung cancer; OR, odds ratio; CI, confidence interval.