Immunohistochemical staining properties of PCNA, Ki-67, p53, beta-hCG and HPL in trophoblastic disease

Objective:In this study proliferating markers PCNA (proliferating cell nucl ear antigen) Ki-67 and mutation of. supressor gene p53 were investigated in gestational trophoblastic disease (GTL). These markers were tested by usin g immunostaining with beta subunits of human chorionic gonadotropin (hCG) a nd human placental lactogen (HPL). Material and Methods: Twenty curetting samples, 20 spontaneous abortions, 16 hydatidifor m moles and two choriocarcinomas were studied and compared. Hydatidiform mo les were subdivided into 10 complete and six partial moles by using flow cy tometry analysis. All slides were stained with PCNA, Ki-67, p53, hCG, and H PL immunohistochemically. PCNA and Ki-67 stained slides were studied quanti tatively to determine the PCNA and Ki-67 index. Other slides that were stai ned with p53, hCG, HPL were evaluated according to staining percentage and intensity. Staining properties of all groups were compared with each other. Variance analysis and the Mann Whitney U test were used for statistical an alysis. Choriocarcinomas were not included in the statistical analysis. Ki- 67 and the PCNA index in two choriocarcinoma cases found 81.4% and 41%, and 44% and 64%, respectively. One case was stained in 70% with (++) intensity by p53. While both were stained in 80% with (++) intensity by hCG, one was stained in 30% field (+) intensity by HPL. Results: The four groups of complete and incomplete diagnosed hydatiform mo les, spontaneous abortions and retention curettage were matched in pairs an d evaluated according to the PCNA index. This index showed significant diff erences among the groups. The differences among the Ki-67 index, p53, hCG a nd HPL staining properties were not statistically significant. Conclusion Our findings showed that PCNA is a significant and useful marker for trophoblastic diseases and can be used as a prognostic factor.