Abstract:【Abstract】Objective To compare the expression of ECadherin, βCatenin, PTEN, PI3K110α, pAktSer 473 and P53 proteins in low grade serous carcinoma (LGSC), high grade serous carcinoma (HGSC), early clear cell carcinoma (ECCC) and advanced clear cell carcinoma (ACCC), explore the dualistic mechanism of ovarian cancer (OC) and provide the basis for diagnosis and treatment of prognosis. Methods The ovarian serous carcinoma (OSC) was graded using a twolevel histological grade system at M.D.Anderson cancer center. The OC stage was staged using the international union of obstetrics and gynecology (FIGO) staging system. The expression of ECadherin, βCatenin, PTEN, PI3K110α, pAktSer473 and P53 protein in 22 LGSC,38 HGSC,20 ECCC, and 20 ACCC tissues was examined by immunohistochemical method and statistically analyzed in combination with clinicopathological features. Results The expression of ECadherin, βCatenin protein was statistically significant between LGSC and HGSC between ECCC and ACCC (P<005). The expression of PTEN, PI3K110α, pAktSer 473 and P53 protein was statistically significant between LGSC and HGSC between ECCC and ACCC(Pp<005). In LGSC, the expression of ECadherin and βCatenin protein was negatively correlated (P<005). In HGSC, PTEN was negatively correlated with the expression of PI3K110α, pAktSer 473 and P53 protein (P<005), and in ECCC, PTEN was negatively correlated with the expression of PI3K110α, pAktSer 473(P<005). The difference between LGSC and HGSC between ECCC and ACCC between age≤50 and>50 was statistically significant (P<005). The difference between LGSC and HGSC between ECCC and ACCC between G1~2 and G3 was statistically significant (P<005). The difference between clinical stage ⅠⅡ and ⅢⅣ was statistically significant between LGSC and HGSC between ECCC and ACCC (P<005).Conclusion The deletion of ECadherin protein expression and the excessive activation of βCatenin protein may be involved in the occurrence and development of LGSC and ECCC. The deletion of PTEN protein expression and the excessive activation of PI3K110α, and pAktSer 473 protein may participate in the occurrence and development of HGSC and ECCC. The excessive activation of p53 protein is involved in the development of HGSC and ACCC, which provides a basis for exploring the dualistic pathogenesis, clinical diagnosis and treatment of OC.