Endometrial cancer with a POLE mutation progresses frequently through the type I pathway despite its high-grade endometrioid morphology: a cohort study at a single institution in Japan.
Mahina MonsurMunekage YamaguchiHironori TashiroKumiko YoshinobuFumitaka SaitoChimeddulam ErdenebaatarChenyan LiYutaka IwagoiTakashi OhbaKen-Ichi IyamaHidetaka KatabuchiPublished in: Medical molecular morphology (2021)
POLE-mutated endometrial cancer (EC) frequently shows high-grade endometrioid histology, which represents heterogeneity in the dualistic classification of EC. This study aimed to assess the clinicopathology and pathogenesis of POLE-mutated EC due to the scarcity of related information for Asian women. POLE variants were sequenced in tissues of Japanese women with EC. The tumor mutation burden (TMB) was assessed in tissues with a POLE variant of unknown significance. In the POLE-mutated EC tissues, the immunostaining expression of CD8, hormonal receptors, and p53 was evaluated, and the POLE variants in cancer and atypical endometrial hyperplasia (AEH) lesions were assessed by laser-capture microdissection. POLE variants were identified in five patients (3.9%) with high-grade endometrioid carcinoma among 127 patients with EC (S459F in two tissues and P441P in three tissues with a high TMB). The five cancer tissues coexisted with normal endometrium and/or AEH. Both AEH and cancer cells showed hormonal receptor positivity and harbored the same POLE mutation. Two patients showed a subclonal overexpression pattern of p53 in cancer and AEH lesions. In conclusion, POLE-mutated EC progresses through the type I pathway, even though it frequently shows high-grade endometrioid morphology. The common POLE mutation sites in EC might vary among races.
Keyphrases
- endometrial cancer
- high grade
- gene expression
- low grade
- end stage renal disease
- chronic kidney disease
- metabolic syndrome
- healthcare
- deep learning
- poor prognosis
- single cell
- mass spectrometry
- young adults
- skeletal muscle
- high resolution
- insulin resistance
- patient reported outcomes
- clear cell
- binding protein
- pregnancy outcomes