Multivariable analysis indicated that multiple tumor nodules, poorer TNM staging, and high UBE2T expression were independent risk factors for TTR (all P < 0.05, Table 2) and that higher CA199, lower ALB, larger tumor size, multiple tumor nodules, presence of MVI, poorer TNM staging, and high UBE2T expression were significant risk factors for OS (all P < 0.05, Table 3). This evidence concerns the gene TTR and neoplasm.