Effect of MDR1 polymorphism on multidrug resistance expression in breast cancer patients

被引:49
|
作者
Taheri, M. [1 ,2 ]
Mahjoubi, F. [1 ]
Omranipour, R. [3 ]
机构
[1] Natl Inst Genet Engn & Biotechnol, Dept Clin Genet, Tehran, Iran
[2] Zahedan Univ Med Sci, Sch Med, Dept Genet, Zahedan, Iran
[3] Univ Tehran Med Sci, Imam Khomeini Hosp, Inst Canc, Tehran, Iran
关键词
Multidrug resistance; MDR1; gene; C3435T polymorphism; Real-time polymerase chain reaction; Breast cancer; P-GLYCOPROTEIN EXPRESSION; C3435T POLYMORPHISM; GENE; TRANSPORTERS; LEUKEMIA;
D O I
10.4238/vol9-1gmr669
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
One of the limitations in the treatment of cancer patients with chemotherapy is the development of multidrug resistance (MDR). A well-known mechanism responsible for drug resistance is over-expression of ABC-transporter genes such as MDR1. This gene encodes p-glycoprotein (P-gp), a transmembrane glycoprotein that transports many hydrophobic substrates and anti-cancer drugs out of the cell. MDR1 gene polymorphisms could alter the expression level of P-gp and consequently result in drug resistance. We investigated a possible association between MDR1 gene C3435T polymorphism and its expression in Iranian breast cancer patients. PCR-RFLP was used for the detection of C3435T single nucleotide polymorphism in 54 breast cancer patients and 50 healthy individuals. The expression level of MDR1 was determined by real-time quantitative PCR. We observed no difference in the frequency of C3435T polymorphism between breast cancer patients and healthy controls. However, there was a significant association between MDR1 expression levels and C3435T polymorphism in the patients. C3435T polymorphism may play a role in inducing drug resistance by altering the expression level of the MDR1 gene.
引用
收藏
页码:34 / 40
页数:7
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