Background: P-glycoprotein (Pgp), encoded by the multidrug resistance 1 (MDR1) gene, is an efflux transporterwhich plays an important role in pharmacokinetics. The current preliminary study was designed to determineassociations between a germ-line polymorphism in the MDR1 gene with differentiated thyroid carcinoma (DTC).Materials and Methods: In the current case-control study, 60 differentiated thyroid cancers (DTC)- 45 papillaryTC (PTC), 9 follicular TC(FTC) and 6 well-differentiated tumors of uncertain malignant potential (WDT-UMP)were examined. Results were compared to a healthy control group (n=58) from the same population. GenomicDNA was extracted from peripheral blood with EDTA and the target gene was genotyped by real-time PCR. Results: Carriers of the variant allele of MDR1 exon 26 polymorphism were at 2.8-fold higher risk of DTC thanthe control group (odds ratio [OR]: 0.3805, 95% confidence interval [Cl]: 0.1597-0.9065 (p> 0.046). Conclusions:Presented results suggest that the MDR1 3435TT genotype might influence risk of development of DTC andthat the CC genotype might be linked to a poor prognosis. Large-scale studies are now needed to validate thisassociation.
(2013). Possible Roles of the Xenobiotic Transporter P-glycoproteins Encoded by the MDR1 3435 C>T Gene Polymorphism in Differentiated Thyroid Cancers. Asian Pacific Journal of Cancer Prevention, 14(5), 3213-3217.
MLA
. "Possible Roles of the Xenobiotic Transporter P-glycoproteins Encoded by the MDR1 3435 C>T Gene Polymorphism in Differentiated Thyroid Cancers". Asian Pacific Journal of Cancer Prevention, 14, 5, 2013, 3213-3217.
HARVARD
(2013). 'Possible Roles of the Xenobiotic Transporter P-glycoproteins Encoded by the MDR1 3435 C>T Gene Polymorphism in Differentiated Thyroid Cancers', Asian Pacific Journal of Cancer Prevention, 14(5), pp. 3213-3217.
VANCOUVER
Possible Roles of the Xenobiotic Transporter P-glycoproteins Encoded by the MDR1 3435 C>T Gene Polymorphism in Differentiated Thyroid Cancers. Asian Pacific Journal of Cancer Prevention, 2013; 14(5): 3213-3217.