Objective: To discuss the significance of DOG1, CD117 and PDGFRA in the diagnosis of gastrointestinalstromal tumors (GISTs), and analyze their correlations with clinicopathological features and risk ranking. Method: DOG1, CD117 and PDGFRA were detected with IHC Envision ldpe-g-nvp in 63 GISTs and 43 cases ofnon-GISTs, and analyzed for relations with clinicopathological factors (gender, age, location, tumor size, mitoticphase, histology) and risk degree. Results: The positive expression rate of DOG1, CD117 and PDGFRA in GISTswas 84.1% (53/63), 90.5% (57/63), 53.2% (33/63), respectively. Among the 6 CD117 negative cases, all were DOG1positive and 5 were PDGFRA positive. Rates in patients with non-GISTs was 11.6%, 16.3%, 6.98%, respectively.Expression of DOG1 and PDGFRA demonstrated no significant variation with gender, age, position, tumor size,mitotic phase, histology, and risk rank. However, CD117 was related with position and histology (P=0.008 andP=0.045), those in the mesentery having a higher positive rate than those derived from stomach, small intestine,colon and rectum (50.0% vs 94.7%, P=0.008). Furthermore CD117 was also highly expressed in spindle andepithele types. Conclusions: DOG1 had a good sensitivity and specificity as a kind of newly discovered marker,especially for KIT negative GISTs. However, DOG1, CD117 and PDGFRA cannot be used for assessing the rishof patients.
(2012). Expression of DOG1, CD117 and PDGFRA in Gastrointestinal Stromal Tumors and Correlations with Clinicopathology. Asian Pacific Journal of Cancer Prevention, 13(4), 1389-1393.
MLA
. "Expression of DOG1, CD117 and PDGFRA in Gastrointestinal Stromal Tumors and Correlations with Clinicopathology". Asian Pacific Journal of Cancer Prevention, 13, 4, 2012, 1389-1393.
HARVARD
(2012). 'Expression of DOG1, CD117 and PDGFRA in Gastrointestinal Stromal Tumors and Correlations with Clinicopathology', Asian Pacific Journal of Cancer Prevention, 13(4), pp. 1389-1393.
VANCOUVER
Expression of DOG1, CD117 and PDGFRA in Gastrointestinal Stromal Tumors and Correlations with Clinicopathology. Asian Pacific Journal of Cancer Prevention, 2012; 13(4): 1389-1393.