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Logo of bmccancBioMed Centralsearchsubmit a manuscriptregisterthis articleBMC Cancer
BMC Cancer. 2012; 12: 257.
Published online Jun 18, 2012. doi:  10.1186/1471-2407-12-257
PMCID: PMC3388009
SULT1A1 rs9282861 polymorphism-a potential modifier of efficacy of the systemic adjuvant therapy in breast cancer?
Maria Tengström,corresponding author1,2,3 Arto Mannermaa,3,4 Veli-Matti Kosma,3,4 Ari Hirvonen,5 and Vesa Kataja1,2,3
1Cancer Center, Kuopio University Hospital, P.O.BOX 1777, 70211 Kuopio, Finland
2Department of Oncology, Vaasa Central Hospital, Hietalahdenkatu 2-4, 65130 Vaasa, Finland
3Institute of Clinical Medicine, Pathology; Biocenter Kuopio; Cancer Center of Eastern Finland, University of Eastern Finland, Yliopistonranta 1C, 70210 Kuopio, Finland
4Imaging Center, Pathology, Kuopio University Hospital, P.O.BOX 1777, 70211 Kuopio, Finland
5Finnish Institute of Occupational Health, Topeliuksenkatu 41 a A, 00250 Helsinki, Finland
corresponding authorCorresponding author.
Maria Tengström: maria.tengstrom/at/; Arto Mannermaa: arto.mannermaa/at/; Veli-Matti Kosma: veli-matti.kosma/at/; Ari Hirvonen: ari.hirvonen/at/; Vesa Kataja: vesa.kataja/at/
Received July 25, 2011; Accepted June 18, 2012.
Sulfotransferase 1A1 (SULT1A1) participates in the elimination of 4-hydroxy-tamoxifen (4-OH-TAM), which is one of the major active metabolites of tamoxifen (TAM). Homozygous SULT1A1 variant allele genotype has been associated with lower catalytic activity and thermostability of the enzyme. Previous clinical studies suggest that the SULT1A1 rs9282861 polymorphism may influence the survival of breast cancer patients treated with TAM in the adjuvant setting. We investigated the effect of rs9282861 genotypes on the survival of Finnish breast cancer patients treated with adjuvant chemotherapy or TAM.
The rs9282861 genotypes of 412 Finnish breast cancer patients with early breast cancer were identified by using PCR-RFLP method. Seventy six patients were treated with adjuvant cyclophosphamide based chemotherapy only, 65 patients received adjuvant TAM, and four patients were treated with both adjuvant chemotherapy and TAM. Overall long-term survival (OS), breast cancer specific survival (BCSS), and relapse-free survival (RFS) by rs9282861 genotypes were evaluated by the Kaplan-Meier method and Cox regression analysis.
The multivariate analysis of 145 patients receiving either adjuvant TAM or chemotherapy showed a statistically significantly improved OS in patients with the rs9282861 homozygous variant AA genotype (hazard ratio [HR] = 0.50, 95% confidence interval [CI] = 0.29-0.88, P = 0.015). In the separate analyses of patients receiving only chemotherapy or adjuvant TAM, there were no statistically significant differences in survival.
In this prospective study, we observed a previously unreported association between the SULT1A1 rs9282861 genotype and OS of breast cancer patients treated with adjuvant chemotherapy or TAM. This novel finding suggests that the rs9282861 polymorphism modifies the long-term clinical outcome of patients receiving adjuvant TAM or chemotherapy.
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