- Author:
Jian-Hui YUAN
1
;
Jin-Quan CHENG
;
Long-Yuan JIANG
;
Wei-Dong JI
;
Liang-Feng GUO
;
Jian-Jun LIU
;
Xing-Yun XU
;
Jing-Song HE
;
Xian-Ming WANG
;
Zhi-Xiong ZHUANG
Author Information
- Publication Type:Journal Article
- MeSH: ATP Binding Cassette Transporter, Sub-Family G, Member 2; ATP-Binding Cassette Transporters; metabolism; Adult; Antimetabolites, Antineoplastic; pharmacology; Chromatography, High Pressure Liquid; Drug Resistance, Neoplasm; Female; Fluorouracil; pharmacology; Humans; Immunohistochemistry; Middle Aged; Neoplasm Proteins; metabolism; Reverse Transcriptase Polymerase Chain Reaction
- From: Biomedical and Environmental Sciences 2008;21(4):290-295
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo filtrate breast cancer resistance protein (BCRP)-mediated resistant agents and to investigate clinical relationship between BCRP expression and drug resistance.
METHODSMTT assay was performed to filtrate BCRP-mediated resistant agents with BCRP expression cell model and to detect chemosensitivity of breast cancer tissue specimens to these agents. A high performance liquid chromatography (HPLC) assay was established, and was used to measure the relative dose of intracellular retention resistant agents. RT-PCR and immunohistochemistry (IHC) were employed to investigate the BCRP expression in breast cancer tissue specimens.
RESULTSMTT assay showed that the expression of BCRP increased with the increasing resistance of 5-fluorouracil (5-Fu) (P<0.05, n=3) in the cell model, while HPLC assay indicated that the intracellular retention dose of 5-Fu was significantly correlated with the expression of BCRP (r=-0.897, P<0.05, n=3). A total of 140 breast cancer tissue specimens were collected. BCRP-positive expression was detected in forty-seven specimens by both RT-PCR and IHC. As shown by MTT assay subsequently, the resistance index (RI) of 47 BCRP-positive breast cancer tissue specimens to 5-Fu was 7-12 times as high as that of adjacent normal tissue samples. BCRP expression was related to 5-Fu resistance (R2=0.8124, P<0.01).
CONCLUSIONResistance to 5-Fu can be mediated by BCRP. Clinical chemotherapy for breast cancer patients can be optimized based on BCRP-positive expression.