CYP1B1 gene polymorphisms have higher risk for endometrial cancer, and positive correlations with estrogen receptor α and estrogen receptor β expressions

• Published in: Cancer research (Chicago, Ill.) Ill.), 2003-07, Vol.63 (14), p.3913-3918
• Main Authors: SASAKI, Masahiro, TANAKA, Yuichiro, KANEUCHI, Masanori, SAKURAGI, Noriaki, DAHIYA, Rajvir
• Format: Article
• Language: English
• Subjects: Adult; Aged; Aryl Hydrocarbon Hydroxylases - genetics; Biological and medical sciences; Cytochrome P-450 CYP1B1; Endometrial Neoplasms - enzymology; Endometrial Neoplasms - genetics; Endometrial Neoplasms - metabolism; Estrogen Receptor alpha; Estrogen Receptor beta; Female; Female genital diseases; Genetic Predisposition to Disease; Gynecology. Andrology. Obstetrics; Humans; Medical sciences; Middle Aged; Polymorphism, Genetic; Receptors, Androgen - biosynthesis; Receptors, Estrogen - biosynthesis; Receptors, Progesterone - biosynthesis; Tumors
• ISSN: 0008-5472; 1538-7445

The estradiol metabolites by CYP1B1 received particular attention because of their causative role in malignant transformation of endometrium. We hypothesize that polymorphisms of CYP1B1 gene can predict higher incidence of endometrial cancer. To test this hypothesis, the genetic distributions of six different CYP1B1 gene polymorphisms were investigated, by sequence-specific PCR and direct DNA sequencing, in 113 Japanese endometrial cancer patients and 202 healthy controls. We also investigated whether the expression of estrogen receptors (ERalpha and ERbeta), progesterone receptor, and androgen receptor genes are influenced by the CYP1B1 genotypes in endometrial cancer. The results of our study demonstrated that the distributions of CYP1B1 genotypes at codons 119 and 432 were significantly different between endometrial cancer patients and healthy normal controls. The relative risks of 119T/T and 432G/G in endometrial cancer were calculated as 3.32 and 2.49 compared with wild-types. The 119T/T showed significant correlation for positivities of ERalpha and ERbeta. The 432G/G also showed weak correlations for ERalpha positivity. Other loci, intron 1, codon 48, and codon 449 were not different between endometrial cancer patients and healthy normal control. This is the first report that demonstrates that the rare polymorphisms at codons 119 and 432 of CYP1B1 gene have higher risk for endometrial cancer, and positive correlations with ERalpha and ERbeta expressions in endometrial cancer.