Features of endometrial precancers
| Prediction | Evidence |
|---|---|
| Precancers differ from normal tissue | Monoclonal precancers12,21,23,25 arise from a polyclonal normal field24 |
| Mutations are acquired in precancers23,38,49–53 | |
| Precancers share some, but not all, features of cancer | Precancer–cancer lineage hierarchy26 |
| May share PTEN,37,38,55 K-ras,52–54,56 MLH151,57 changes | |
| Both are monoclonal21,23,25,58,59 | |
| Precancers increase risk for carcinoma | Increased concurrent cancer rate30 |
| Increased future cancer rate31,32 | |
| Precancers can be diagnosed | Morphometric standard21,22,29,50 |
| Endometrial intraepithelial neoplasia = precancers (table 1) | |
| Hormonal and genetic risks are linked | Hormonal modulation of the PTEN gene,45 frequently inactivated in premalignant disease37,38,41,53 |
| Precancers can be induced by manipulating genetic and/or hormonal variables | 100% of PTEN mutant heterozygote mice get endometrial “hyperplasia” and 21% of these evolve to carcinoma60 |









