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Estrogen receptor alpha gene polymorphism and endometrial cancer risk : a case-control study

Wedrén, Sara (author)
Karolinska Institutet
Lovmar, Lovisa (author)
Uppsala universitet,Molekylär medicin
Humphreys, Keith (author)
Karolinska Institutet
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Magnusson, Cecilia (author)
Karolinska Institutet
Melhus, Håkan (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Clinical pharmacogenetics and osteoporosis
Syvänen, Ann-Christine (author)
Uppsala universitet,Molekylär medicin
Kindmark, Andreas (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Metabolic Bone Diseases
Landegren, Ulf (author)
Uppsala universitet,Molekylära verktyg
Fermér, Maria Lagerström (author)
Stiger, Fredrik (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Clinical pharmacogenetics and osteoporosis
Persson, Ingemar (author)
Baron, John A. (author)
Weiderpass, Elisabete (author)
Karolinska Institutet
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 (creator_code:org_t)
2008-11-06
2008
English.
In: BMC Cancer. - : Springer Science and Business Media LLC. - 1471-2407. ; 8, s. 322-
  • Journal article (peer-reviewed)
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  • BACKGROUND: Estrogen is an established endometrial carcinogen. One of the most important mediators of estrogenic action is the estrogen receptor alpha. We have investigated whether polymorphic variation in the estrogen receptor alpha gene (ESR1) is associated with endometrial cancer risk. METHODS: In 702 cases with invasive endometrial cancer and 1563 controls, we genotyped five markers in ESR1 and used logistic regression models to estimate odds ratios (OR) and 95 percent confidence intervals (CI). RESULTS: We found an association between rs2234670, rs2234693, as well as rs9340799, markers in strong linkage disequilibrium (LD), and endometrial cancer risk. The association with rs9340799 was the strongest, OR 0.75 (CI 0.60-0.93) for heterozygous and OR 0.53 (CI 0.37-0.77) for homozygous rare compared to those homozygous for the most common allele. Haplotype models did not fit better to the data than single marker models. CONCLUSION: We found that intronic variation in ESR1 was associated with endometrial cancer risk.

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