The abnormalities in the p53/p21WAF1 pathway have a significant role in the pathogenesis and progression of gastrointestinal stromal tumors.

To elucidate the prognostic role and relationship of the p53/p21/PCNA path way in gastrointestinal stromal tumors (GISTs), a total of 167 resected gastric and small intestinal CD117-positive stromal tumor specimens were collected from January 1987 to December 2000. Immunohistochemical studies were performed on the paraffin sections with antibodies of p53, p21/WAF1, proliferating cell nuclear antigen (PCNA) and Ki-67. The immunoreactivity of four markers was recorded by labeling index (LI, %) for clinicopathologic and survival correlation. The labeling index was 0-83% for p53, 0-81% for p21/WAF1, 0-33% for Ki-67 and 12-92% for PCNA. Completely negative immunostaining (LI < 1%) was found in 54.5% of p53,25.8% of p21/WAF1 and 44.3% of Ki-67. The LI of four markers strongly correlate with each other (p < 0.05). Furthermore, the LI of all four markers positively correlate to microscopic tumor mitotic counts (p < 0.05). Only the LI of p53 and PCNA positively correlate to tumor sizes. Tumors with non-spindle cell type (versus spindle cell) and high cellular pleomorphism (versus low) exhibited a higher p53, p21/WAF1 and PCNA LI (p < 0.05). Increased NIH risk significantly correlates to increased p53, PCNA and Ki-67 (p < 0.05) LI. Survival analysis indicated that a large tumor size (2:5 cm, p=0.003), increased tumor mitosis (>= 5/50 HPF, p < 0.001), high NIH risk (p < 0.001), non-spindle cell type (p=0.024), high p53 LI (p < 0.001), high p21/WAF1 LI (p=0.007), high Ki-67 LI (p < 0.001) and high PCNA LI (p < 0.001) were prognostic factors for poor disease-free survival. Independent factors are tumor size, NIH risk, p53 and p21/WAF1 LI. We demonstrated the first evidence of the linear relationship and prognostic role of the p53/p21/PCNA pathway in gastrointestinal stromal tumors. Abnormalities of the p53/p21WAF1 pathway lead to increased proliferating states, thereby triggering the progression of GISTs.