American Journal of Epidemiology Advance Access published online on November 16, 2006
American Journal of Epidemiology, doi:10.1093/aje/kwk015
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1 Department of Epidemiology and Biostatistics, Memorial Sloan-Kettering Cancer Center, New York, NY
* To whom correspondence should be addressed. Variants in genes involved in estrogen biosynthesis are likely to be important in the etiology of endometrial cancer. This review summarizes data on variants in seven genes in the estrogen biosynthesis pathway and their relation to circulating levels of sex steroid hormones in women and to risk of endometrial cancer. Little or no association was found between genotypes of the cytochrome P-450 genes CYP11A1 (-528[TTTTA]n) or CYP17A1 (-34T/C) or the 17
Received March 10, 2006
Accepted July 5, 2006
HUMAN GENOME EPIDEMIOLOGY (HuGE) REVIEW
Variants in Estrogen Biosynthesis Genes, Sex Steroid Hormone Levels, and Endometrial Cancer: A HuGE Review
Sara H. Olson 1 *, Elisa V. Bandera 2, and Irene Orlow 1
2 Cancer Prevention and Control Program, Cancer Institute of New Jersey, New Brunswick, NJ
Sara H. Olson, E-mail: olsons{at}mskcc.org
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Abstract
-hydroxysteroid dehydrogenase 1 gene HSD17B1 (Ser312Gly) and levels of progesterone, androgens, or estrogens. The position -34T/C variant in CYP17A1 appears to be associated with reduced risk of endometrial cancer, with those homozygous for the variant allele having about half the risk of those homozygous for the wild type. Linked variants in CYP19A1 (intron 4 [TTTA]n, intron 4 [TCT] insertion/deletion, exon 10 C/T) are related to some hormone levels and, based on two studies, to risk of endometrial cancer. For other genes (HSD3B1, HSD3B2, HSD17B2), no information is available on these associations. Results indicate the need to study other variants and haplotypes in these genes, particularly CYP17A1 and CYP19A1, as well as variants in other genes involved in hormone biosynthesis and metabolism pathways. Larger studies or combined studies that allow for investigation of gene-gene and gene-environment interactions are warranted.![]()
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