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. 2015 Sep 30;10(2):195–212. doi: 10.1016/j.molonc.2015.09.008

Table Table 4.

Clinical correlation of 5‐HT5 gene expression in HCC.

Clinicopathological features Frequency (%) Receptor 5‐HT5 P value
Mean ± SD/number of patients
Overexpression
+
Age (year) 0.658
<53 15 (45.5) 14 1
≥53 18 (54.5) 16 2
Sex 0.238
Male 29 (87.9) 27 2
Female 4 (12.1) 3 1
Non‐tumorous liver histology 0.767
Non‐cirrhotic 2 (6.1) 2 0
Chronic hepatitis 16 (48.5) 14 2
Cirrhotic 15 (45.5) 14 1
Tumour size (cm) a 0.266
<5 9 (27.3) 9 0
≥5 24 (72.7) 21 3
Tumour recurrence 0.170
Absence 12 (36.4) 12 0
Presence 21 (63.6) 18 3
Venous infiltration b 0.658
Absence 15 (45.5) 14 1
Presence 18 (54.5) 16 2
Number of tumour nodules 0.072
1 25 (75.8) 24 1
≥2 8 (24.2) 6 2
Cellular differentiation c, d 0.254
Well differentiated 11 (33.3) 11 0
Moderately differentiated 14 (42.4) 12 2
Poorly differentiated 7 (21.2) 7 0
AJCC stage 0.097
I and II 15 (45.5) 15 0
III and IV 18 (54.5) 15 3

*P < 0.05.

Tumour size was defined as the length of the largest tumour nodule.

Venous infiltration was defined based on findings by microscopic and major pathologic examination.

Well differentiated (Edmonson grade 0–2); moderately differentiated (Edmonson grade 3); poorly differentiated (Edmonson grade 4).

Partial data is not available and statistics were based on available data of 32 patients.