Abstract
Endometrial carcinoma (EC) is the most common malignant tumors in female derived from the endometrial epithelium. Several previous studies have described estrogen receptors (ER), progesterone Receptor (PR) and phosphatase and tensin homolog (PTEN) are associated with clinicopathological factors and prognosis in EC patients. However, during EC patients follow-up, we found that some EC patients with down-regulation of PTEN, but up-regulation of ER or PR , and some EC patients with down-regulation of ER or PR, but up-regulation of PTEN also had a poor prognosis. Therefore, to reveal the prognosis of EC patients with different phenotypes based on PTEN, ER and PR expression, 120 cases formalin-fixed paraffin-embedded EC tissues and 543 cases uterine corpus endometrial carcinoma (UCEC) patients from the cancer genome atlas (TCGA) UCEC datasets were analyzed. Results showed that EC tissues can be classified to PTEN(L)ER(L)PR(L), PTEN(H)ER(L)PR(L), PTEN(H)ER(H)PR(H), PTEN(L)ER(H)PR(H), PTEN(H)ER(H)PR(L), PTEN(H)ER(L)PR(H), and PTEN(L)ER(H)PR(L) phenotypes basing on IHC analysis. Additionally, EC patients with PTEN(L)ER(L)PR(L) showed high malignancy, while patients with PTEN(H)ER(H)PR(H) showed low malignancy. Therefore, combined detection of PTEN, ER, PR may help identify a small subset of EC with more aggressive behavior and may aid in risk stratification.