IndraLab
Statements
sparser
"Analysis of the pooled OR showed thatp16 INK4A andp14 ARF promoter methylation were significantly higher in patients with RCC than in control subjects, suggesting thatp16 INK4A andp14 ARF inactivation via promoter methylation may play an important role in the tumorigenesis of RCC."
sparser
"The pooled OR from seven studies and from three studies suggested thatp16 INK4A andp14 ARF promoter methylation was not significantly correlated with tumor grade in RCC (OR = 1.20, 95% CI = 0.58-2.45, P = 0.625; OR = 2.13, 95% CI = 0.96-4.75, P = 0.063, respectively) (Table xref )."
sparser
"Of these studies, which involvedp16 INK4A andp14 ARF gene promoter methylation, nine studies evaluated the association betweenp16 INK4A promoter methylation and RCC risk, five studies assessed the correlation betweenp14 ARF promoter methylation and RCC risk, ten studies evaluated the relation betweenp16 INK4A promoter methylation and clinicopathological features, and four studies evaluated the relation betweenp14 ARF promoter methylation and clinicopathological features."
sparser
"The prognostic data involving the pooled hazard ratio (HR) were insufficient and not available, as only three studies reporting showed thatp16 INK4A andp14 ARF gene promoter methylation were not significantly correlated with the prognosis of RCC in OS or DFS [ xref , xref , xref ]."