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. 2013 Aug 13;109(5):1137–1146. doi: 10.1038/bjc.2013.463

Table 1. Crosstabulated of RSK4 immunostaining vs clinicalpathological features of all RCC cases.

 
RSK4
 
Clinicalpathological features (n) + P-value
Gender
 
 
0.34
Male (75) 44 (58.7%) 31 (41.3%)  
Female (26)
18 (69.2%)
8 (30.8%)
 
Age (years)
 
 
0.677
⩾55 (57) 36 (63.2%) 21 (36.8%)  
<55 (44)
26 (59.1%)
18 (40.9%)
 
Tumour size (cm)
 
 
0.776
>6.7 (38) 24 (63.1%) 14 (36.9%)  
<6.7 (63)
38 (60.3%)
25 (39.7%)
 
Histological type
 
 
0.021a
ccRCC (47) 29 (61.7%) 18 (38.3%)  
PRCC (42) 20 (47.6%) 22 (52.4%)  
CRCC (6) 1 (16.7%) 5 (83.3%)  
CDC and medullary carcinoma (6)
5 (83.3%)
1 (16.7%)
 
pT stage
 
 
<0.001b
pT1-pT2 (61) 21 (34.4%) 40 (65.6%)  
pT3-pT4 (40)
32 (80%)
8 (20%)
 
Fuhrman grade
 
 
<0.001b
1–2 (45) 13 (28.9%) 32 (71.1%)  
3–4 (56)
40 (71.4%)
16 (28.6%)
 
Lymph node involved
 
 
<0.001b
Yes (22) 20 (90.9%) 2 (9.1%)  
No (79)
42 (53.2%)
37 (46.8%)
 
Distant metastasis
 
 
0.039b
Yes (8) 7 (87.5%) 1 (12.5%)  
No (93) 46 (49.5%) 47 (50.5%)  

Abbreviations: CDC=collecting duct carcinoma; ccRCC=clear cell RCC; CRCC=chromophobe; PRCC=papillary RCC; RCC; RCC=renal cell carcinoma; RSK4=ribosomal s6 protein kinase 4.

P<0.05 is considered significant.

a

The expression of RSK4 varied in different RCC subtypes.

b

RSK4 expression was positively correlated with higher pT stage, higher Fuhrman grade, and presence of lymphnode and distant matastasis.