Role of co-expression of estrogen receptor beta and Ki67 in prostate adenocarcinoma

• Main Authors: Nornazirah Azizan, Firdaus Hayati, Nur Maya Sabrina Tizen, Wirda Indah Farouk, Noraidah Masir
• Format: Article
• Language: English; English
• Published: Korean Urological Association 2018
• Subjects: RC870-923 Diseases of the genitourinary system. Urology
• Online Access: https://eprints.ums.edu.my/id/eprint/30583/1/Role%20of%20co-expression%20of%20estrogen%20receptor%20beta%20and%20Ki67%20in%20prostate%20adenocarcinoma%20FULL%20TEXT.pdf; https://eprints.ums.edu.my/id/eprint/30583/3/Role%20of%20co-expression%20of%20estrogen%20receptor%20beta%20and%20Ki67%20in%20prostate%20adenocarcinoma%20ABSTRACT.pdf; https://eprints.ums.edu.my/id/eprint/30583/; https://pubmed.ncbi.nlm.nih.gov/29984337/; https://doi.org/10.4111/icu.2018.59.4.232
• Institution: Universiti Malaysia Sabah

Purpose: To evaluate the expression of estrogen receptor (ER)-beta and Ki67 in prostate cancer and study their relationship. Materials and Methods: We analyzed 101 cases of prostate adenocarcinoma diagnosed from January 2011 to June 2015 in 100 patients. Immunohistochemical staining of ER-beta and Ki67 was analyzed according to Gleason score categorized into prognostic groups of 1 to 5. Double-immunofluorescent staining of ER-beta and Ki67 was performed in a total of 20 cases to study the co-expression and the relationship between these markers within the same tumor. Results: A total of 53 of 101 cases (52.5%) were positive for ER-beta expression. There was a positive correlation whereby a high percentage of ER-beta expression was seen in the higher prognostic groups (groups 4 and 5; p=0.007). High Ki67 expression was observed in the higher prognostic group, whereas low Ki67 or negative expression was found in the lower prognostic group (p<0.001). The majority of cases evaluated with double-immunofluorescent staining (14/20) showed co-expression of ER-beta and Ki67 at the individual cell level. Conclusions: ER-beta and Ki67 are independent tumor markers in high prognostic groups. Hence, co-expression of ER-beta and Ki67 indicates a more aggressive tumor with a poorer prognosis.