Table 3.
Multivariate linear regression of SMO, GLI‐1, p53 and p16 correlated with multiple parameters
SMO | GLI‐1 | p53 | p16 | |||||
---|---|---|---|---|---|---|---|---|
t‐value | P‐value | t‐value | P‐value | t‐value | P‐value | t‐value | P‐value | |
pT | −0.376 | 0.708 | −1.970 | 0.053 | −0.301 | 0.765 | 0.701 | 0.486 |
pN | 0.795 | 0.430 | 1.249 | 0.216 | −0.420 | 0.676 | 0.328 | 0.744 |
Grading | −0.391 | 0.697 | 1.024 | 0.309 | 2.969 | 0.004 | −0.536 | 0.594 |
SMO | NA | NA | 2.810 | 0.007 | 1.084 | 0.282 | −1.798 | 0.077 |
GLI‐1 | 2.810 | 0.007 | NA | NA | −0.494 | 0.623 | 1.316 | 0.193 |
p53 | 1.084 | 0.282 | −0.494 | 0.623 | NA | NA | 0.304 | 0.762 |
p16 | −1.798 | 0.077 | 1.316 | 0.193 | 0.304 | 0.762 | NA | NA |
Significant associations are depicted in bold type. pT, tumour–node–metastasis (TNM) classification of malignant tumours T stage; pN, TNM classification of malignant tumours N stage; GLI‐1, GLI family zinc finger 1; SMO, smoothened, frizzled class receptor; p53, tumour protein p53; NA, not applicable; P16, cyclin‐dependent kinase inhibitor 2A, multiple tumour suppressor 1.