Correlation of Immunohistochemical Expression of MDR1, MRP1, Topoisomerase IIalpha with Prognostic Factors and Histoculture Drug Response Assay (HDRA) Result in Breast Carcinoma.
10.4048/jkbcs.2004.7.4.228
- Author:
Hee Joon KANG
1
;
Sung Hee HONG
;
Byung Ho SON
;
Ho Sung YOON
;
Gyung Yub GONG
;
Sei Hyun AHN
Author Information
1. Department of Surgery, Hallym University College of Medicine, Korea.
- Publication Type:In Vitro ; Original Article
- Keywords:
Breast cancer;
Prognostic factor;
Chemoresistance;
Chemosensitivity;
HDRA;
MDR1;
MRP1;
Topoisomerase II alpha
- MeSH:
Breast Neoplasms*;
Breast*;
Cyclophosphamide;
Doxorubicin;
Drug Resistance;
Drug Therapy;
Fluorouracil;
Paclitaxel
- From:Journal of Korean Breast Cancer Society
2004;7(4):228-235
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: Drug resistance plays an important role in the failure of chemotherapy in breast cancer. The purpose of the study was to investigate the chemosensitive and chemoresistance indices of breast carcinomas and see if the in vitro chemosensitivity test correlated with the prognostic indices. METHODS: The immunohistochemical expressions of MDR1, MRP1 and topoisomerase IIalpha(topo IIalpha) were studied and then correlated these with the in vitro chemosensitivities using the histoculture drug response assay (HDRA) and clinicopathological factors in 51 breast carcinomas. RESULTS: In the breast carcinomas examined, the immunohistochemical expressions of MDR1, MRP1 and topo II alpha were strongly observed in 26 (51.0%), 16 (32.0%), 15 (31.3%) carcinomas, respectively. The MRP1 was more frequently expressed in poorly differentiated carcinomas (P= 0.006), and those of MDR1 and topo II alpha were more frequently observed in tumor overexpressing cerbB2 (P=0.038, P=0.036). The expression of MDR1 was related to that of topo II alpha (P=0.015). Comparing these markers with the in vitro chemosensitivities to cyclophosphamide, 5-FU, adriamycin, taxol and taxotere, no correlations were found between the expression of MDR1, MRP1, and topo II alpha but from the chemosensitivity using the HDRA, the growth inhibition rate for cyclophosphamide was higher in MRP1 expressing carcinomas (P=0.009). CONCLUSION: MDR1, MRP1 and topo II alpha were all found to be associated with the poor prognostic indices, but assessment of their immunohistochemical expressions did not allow for prediction of the response to chemotherapy by the in vitro chemosensitivity test in breast carcinomas.
