Multidrug resistance protein 2 genetic polymorphism and colorectal cancer recurrence in patients receiving adjuvant FOLFOX-4 chemotherapy

被引:15
作者
Mirakhorli, Mojgan [1 ]
Rahman, Sabariah Abdul [1 ,2 ]
Abdullah, Syahrilnizam [3 ]
Vakili, Masoud [4 ]
Rozafzon, Reza
Khoshzaban, Ahad [5 ]
机构
[1] Univ Putra Malaysia, Dept Pathol, Fac Med & Hlth Sci, Serdang 43400, Selangor, Malaysia
[2] Univ Teknol MARA, Fac Med, Batu Caves 68100, Selangor, Malaysia
[3] Univ Putra Malaysia, Med Genet Lab, Fac Med & Hlth Sci, UPM Serdang, Serdang 43400, Selangor, Malaysia
[4] Univ Tehran Med Sci, Dept Oncol, Hazrate Rasoul Akram Hosp, Tehran, Iran
[5] Univ Tehran Med Sci, Dept Dent Biomat, Fac Dent, Tehran, Iran
关键词
G1249A; ABCC2/MRP1; colorectal cancer; recurrence; survival; oxaliplatin; STAGE-II; COLON-CANCER; CISPLATIN; CELLS; MRP2; LEUCOVORIN; ABCC2;
D O I
10.3892/mmr.2012.1226
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Multidrug resistance protein 2 (MRP2), encoded by the ATP-binding cassette C2 (ABCC2) gene, is an efflux pump located on the apical membrane of many polarized cells, which transports conjugate compounds by an ATP-dependent mechanism. The correlation of G1249A ABCC2 polymorphism with the development of colorectal cancer (CRC) and poor prognosis was evaluated in patients who were treated with fiuorouracil/leucovorin (FL) plus oxaliplatin (FOLFOX-4). A total of 50 paraffin-embedded tissue samples collected from CRC patients were analyzed to identify the polymorphism. Patients were in stage II/III and received postoperative FOLFOX-4 chemotherapy. As a control group, an equal number of unrelated healthy subjects were enrolled in the study. The polymorphism was genotyped by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method, and results were compared with clinicopathological markers, early relapse and survival rates. During the 12 months of follow-up, local and distant recurrences were observed in 15 (30%) patients. No significant difference in the distribution of wild-type and polymorphic genotypes was observed between the patient and control groups and between the patients who experienced recurrence within 1 year and those who did not (all P>0.05). In conclusion, the G1249A polymorphism is not associated with CRC risk and early recurrence. However, significant correlation was observed between G1249A polymorphism and the overall survival and disease-free survival of the patients.
引用
收藏
页码:613 / 617
页数:5
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