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Multi-drug resistance 1 genetic polymorphism and prediction of chemotherapy response in Hodgkin's lymphoma
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نویسنده
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mhaidat n.m. ,alshogran o.y. ,khabour o.f. ,alzoubi k.h. ,matalka i.i. ,haddadin w.j. ,mahasneh i.o. ,aldaher a.n.
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منبع
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journal of experimental and clinical cancer research - 2011 - دوره : 30 - شماره : 1
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چکیده
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Background: the human multi-drug resistance gene (mdr1),which encodes the major trans-membrane transporter p-glycoprotein (p-gp),was found to be associated with susceptibility to cancer and response to chemotherapy. the c3435t polymorphism of mdr1 gene was correlated with expression levels and functions of p-gp. here,we studied the association between mdr1 c3435t polymorphism and susceptibility to hodgkin lymphoma (hl) and patient's response to abvd chemotherapy regimen. methods. a total of 130 paraffin embedded tissue samples collected from hl patients were analyzed to identify the c3435t polymorphism. as a control group,120 healthy subjects were enrolled in the study. the c3435t polymorphism was genotyped by polymerase chain reaction and restriction fragment length polymorphism (pcr-rflp) method. data analysis was carried out using the statistical package spss version 17 to compute all descriptive statistics. chi-square and fisher exact tests were used to evaluate the genotype distribution and allele frequencies of the studied polymorphism. results: these studies revealed that the frequency of t allele was significantly higher in hl patients compared to the controls (p < 0.05). in addition,the frequency of ct and tt genotypes were also significantly higher in hl patients compared to the controls (p < 0.05). no association between c3435t polymorphism and response to abvd was detected among hl patients (p > 0.05). conclusions: these results suggest that mdr1 c3435t polymorphism might play a role in hl occurrence; however this polymorphism is not correlated with the clinical response to abvd. © 2011 mhaidat et al; licensee biomed central ltd.
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کلیدواژه
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C3435T SNP; Lymphoma; MDR-1
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آدرس
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clinical pharmacy department,faculty of pharmacy,jordan university of science and technology,irbid 22110, Jordan, clinical pharmacy department,faculty of pharmacy,jordan university of science and technology,irbid 22110, Jordan, molecular genetics,faculty of applied medical sciences,jordan university of science and technology,irbid 22110, Jordan, clinical pharmacy department,faculty of pharmacy,jordan university of science and technology,irbid 22110, Jordan, pathology department,faculty of medicine,jordan university of science and technology,irbid 22110, Jordan, histology and cytology department,princess iman center for research and laboratory sciences,king hussein medical center,amman 11855, Jordan, hematology and oncology department,jordanian royal medical services,11855 amman, Jordan, clinical pharmacy department,faculty of pharmacy,jordan university of science and technology,irbid 22110, Jordan
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Authors
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