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. 2018 Apr 24;15(6):9978–9986. doi: 10.3892/ol.2018.8561

Table II.

Associations between BRAFV600E mutation/phospho-MAPK/Mps1 and clinicopathological parameters in thyroid carcinomas.

B-RAFV600E mutation (n=161) Phospho-MAPK in tumor (n=60) MpS1 in tumor (n=60)



Clinicopathological feature + P-value + P-value + P-value
No. (%) 54 (34%) 107 (67%) 2 (3%) 58 (97%) 47 (78%) 13 (22%)
Sex 0.514 >0.999 >0.999
  Male 13 21 1 29 10 3
  Female 41 86 1 29 37 10
Age, years 0.025 0.472 >0.999
  >35 42 97 2 28 38 11
  ≤35 12 10 0 30 9 2
Smoking status 0.727 0.472 >0.999
  Yes 4 5 0 30 2 1
  No 50 102 2 28 45 12
Drinking status 0.190 0.472 >0.999
  Yes 4 2 0 30 2 0
  No 50 105 2 28 45 13
Familial history 0.211 0.472
  Yes 2 0 0 30 0 0
  No 52 107 2 28 47 13
Tumor grade 0.367 0.472
  Papillocarcinoma 54 103 2 28 47 13
  Non-papillocarcinoma 0 4 0 30 0 0
Pathological T stage 0.018 0.472 0.629
  T1-T2 50 83 2 28 41 10
  T3-T4 4 24 0 30 6 3
Pathological N stage 0.004 0.472 0.898
  N0 30 34 0 30 28 8
  N1 24 73 2 28 19 5
Clinical M 0.472
  M0 54 107 2 28 47 13
  M1 0 0 0 30 0 0
Pathological stage 0.585 0.472 >0.999
  I–II 34 72 0 30 33 9
  III–IV 20 35 2 28 14 4

BRAF, B-Raf proto-oncogene serine/threonine kinase; phospho-MAPK, phospho-mitogen-activated protein kinases; T, tumor; N, lymph node; M, metastasis.