TTC Logo
     Molecular Pathology of Endometrial Cancer
     About        Contact
Home•  Compounds•  Expert Opinion•  Trial Analysis•  Pathways•  Diseases•  Workspace • TOUR smartlink Bookmark and Share

Welcome to CuraBase® - The Curated and Collaborative Cancer Database

Click Here to Learn More about CuraBase®

signup

 
 

Access to CuraBase® is free-of-charge for users in Academia or Non-Profit Organizations.

Click Here To Register 

 

Region Incidence Overall Incidence Males Incidence Females Deaths Overall Deaths Males Deaths Females
USA 43470 0 43470 7950 0 7950
 
Source: American Cancer Society. Cancer Facts & Figures 2010. Atlanta: American Cancer Society; 2010

Affected Protein Pathway Sub-Type Ethnicity Stage Frequency (%) Gene Amplification Activating Mutation Inactivating Mutation Deletion Promoter Hypermethylation Comment  
FGFR-2 (k-sam) Receptor Tyrosine Kinase Signaling
primary uterine tumor endometrioid subtype 16%
p53 p53 Tumor Suppressor Pathway
high-grade endometrioid adenocarcinomas 17% rare in low-grade endometrioid adenocarcinomas
p53 p53 Tumor Suppressor Pathway
non-endometrioid adenocarcinomas 54 - 85% Immunohistochemical overexpression of p53
Pi3-kinase PI3-Kinase Signaling
endometrial carcinoma 30 - 36% frequent coexistence of PIK3CA and PTEN mutations in endometrial carcinomas
PTEN PI3-Kinase Signaling
endometrial carcinomas 30 - 54% more frequent in endometrioid adenocarcinomas than in non-endometrioid adenocarcinomas
PTEN PI3-Kinase Signaling
endometrial carcinomas 68% absence of protein expression
PTEN PI3-Kinase Signaling
endometrial carcinomas 19%

Click Here For Clinical Trials in in CuraBase®
      CANCER.GOV PDQ® - Standard Treatments for Endometrial Cancer