Association Between Cytochrome 1B1*3 Polymorphism and the Breast Cancer in a Group of Iranian Women


Faezeh Kholousi Adab 1 , Zahra Tahmasebi Fard ORCID 2 , * , Mohammad Esmaeil Akbari 2

1 Department of Molecular and Cellular Sciences, Faculty of Advanced Sciences & Technology, Pharmaceutical Sciences Branch, Islamic Azad University, Tehran, Iran

2 Cancer Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran

How to Cite: Kholousi Adab F, Tahmasebi Fard Z, Esmaeil Akbari M. Association Between Cytochrome 1B1*3 Polymorphism and the Breast Cancer in a Group of Iranian Women, Int J Cancer Manag. 2017 ; 10(1):e6428. doi: 10.17795/ijcp-6428.


Iranian Journal of Cancer Prevention: 10 (1); e6428
Published Online: January 24, 2017
Article Type: Research Article
Received: April 17, 2016
Revised: March 24, 2016
Accepted: January 14, 2017


Background: As a hormone-dependent cancer, estrogen is involved in the development of breast cancer. CYP1B1 belongs to the P450 superfamily of enzymes and is involved in the metabolism of estrogen. The present study investigates the relationship between CYP1B1*3 rs1056836 polymorphism and breast cancer in Iranian women.

Methods: The present case-control study was conducted on 79 women with breast cancer and 79 healthy women admitted to Shohadaye Tajrish hospital in Tehran. Blood samples were taken from all the participants and their leukocyte DNA was extracted. The PCR-RFLP method was used for genotyping the participants based on the size of the pieces on the gel. Based on Hardy-Weinberg equilibrium model, the frequency of alleles was calculated.

Results: The mean age of participants was 48 ± 8 years old in the cancer group and 43±6 years old in the control group. After counting the genotypes, their percentages were calculated as 30.38% for the GG genotype, 37.97% for the GC/CG and 31.65% for the CC in the cancer group and as 32.91% for the GG genotype, 53.16% for the GC/CG and 13.93% for the CC in the control group. Based on Hardy-Weinberg equilibrium model, the frequency of the G allele and C allele was 49.37% and 50.63 in the cancer group, and about 59.49% and 40.51% in the control group. A statistically significant difference was observed between the two groups in terms of the CC homozygotes (P = 0.008).

Conclusions: The results obtained showed possibility of a significant relationship between CYP1B1 rs1056836 polymorphism and the risk of developing breast cancer, and the polymorphism can, therefore, be said to be involved in the development of this condition.

1. Background

Breast cancer is one of the most common cancers in women (1). Recent studies suggest that the rising trend of breast cancer has turned the condition into one of the most common malignancies among Iranian women with a prevalence of 120 per every 100,000 women. It is therefore essential to investigate the etiology of breast cancer among Iranian women (2, 3). Breast cancer is a hormone-dependent cancer and the interaction between estrogen and progesterone is involved in its development (4, 5). CYP1B1 belongs to the cytochrome P450 superfamily of enzymes that has been reported to have a strong role in initiating malignancy in organs responding to estrogen, such as the breast, as well as in causing hormone-dependent cancers (6). CYP1B1 is overexpressed in breast tumors and other tumor tissues such as the lungs, the skin, the ovaries and the testicles (7-9).

Cytochrome P450 enzymes have an active presence in all living creatures, from Eukaryotes to Eubacteria and Archaebacteria. These enzymes catalyze a variety of reactions and are part of the electron transfer system in the complex network of endoplasmic detoxification (10). They are also responsible for the catalysis of many reactions, including steroid and other lipid reactions. These hemoproteins (10) are a combination of mono-oxygenases composed of about 500 amino acids and one iron group at their active site. These enzymes catalyze the oxidation of potentially hazardous waste substances by dissolving them in water and use iron for the oxidation of some other compounds (11).

Made up of three exons and two introns, CYP1B1 is located at 2p21-22. Open reading framework (ORF) begins with the second exon and encodes an enzyme with 543 amino acids (12-14); that is, only two exons are encoded from this gene (15). The different polymorphisms of this gene have been reported as m1 (CYP1B1*1), m2 (CYP1B1*2), m3 (CYP1B1*3), m4 (CYP1B1*4), m5 (CYP1B1*5), m6 (CYP1B1*6) and m7 (CYP1B1*7) (16-18), which vary widely across different races and populations.

Various genotypes have been reported for the rs1056836 polymorphism in Asian and European populations (19, 20). The different genotypes of this polymorphism have been examined and their frequency reported in countries such as Poland, China, Sweden, the US, India, and Ethiopia and in Caucasian populations. In Asian and African-American countries, Guanine (G) is normally located at the nucleotide 4326 locus of CYP1B1, which encodes Valine in the protein chain (19), whereas in European countries, Cytosine (C) is located at the same locus of the gene, encoding Leucine (Leu) in the protein chain (21). The wild-type nucleotide located at the 4326 locus of CYP1B1 has been reported to take different positions in different populations.

2. Objectives

The present study is the first to examine the CYP1B1 polymorphism Leu432Val (m3) in relation to the risk of breast cancer development in Iranian women.

3. Methods

The present case-control study was conducted on 79 women with breast cancer whose diagnosis was confirmed through medical examinations and clinical tests performed in Shohadaye Tajrish hospital and 79 women who were confirmed to not have special diseases such as diabetes and hypertension and a history of diseases such as breast cancer, particularly among their first degree relatives.

DNA was extracted from the blood samples using the saturated salt method (22) and the extracted DNA concentration was examined in all the samples. Specific primers complementary to the target area and previously used were selected to perform the polymerase chain reaction (23) in the following order:



The optimal annealing temperature for the primers was determined as 64°C. The thermocycler was scheduled for one cycle of 5 minutes at 95°C, followed by 37 cycles of one minute at 95°C, 30 seconds at 64°C, 40 seconds at 75°C and finally one cycle of 7 minutes at 72°C for completing the synthesis of DNA strands. The PCR products were loaded on the gel and a 294 bp band was seen according to the marker size.

The PCR restriction fragment length polymorphism (PCR-RFLP) method was used for the genotyping. Five units of the Eco571 enzyme were added to the PCR products and the mixture was then incubated at 37°C for 20 - 24 hours. The fragmented pieces were then loaded on agarose 3% for visualization under UV light. Observing three pieces 294 bp, 187 bp and 107 bp in length indicated a GC or heterozygous genotype. Observing two pieces 107 bp and 187 bp in length indicated a CC or mutant homozygous genotype, indicating changes at the target locus. Observing one unchanged piece 294 bp in length indicated a normal homozygous genotype (the absence of polymorphisms at the target locus) (Figure 1).

First well is GC genotype, Wells 2, 3 and 4 CC genotype and 5 well is GG genotype.

First well is GC genotype, Wells 2, 3 and 4 CC genotype and 5 well is GG genotype.

Figure 1. show Result of Digest Samples

4. Results

Both groups were at the age range of 32 to 70 years old; the mean age of the participants was 49.68 years old in the cancer group and 47.34 years old in the control group. The mean weight of the participants was 68 ± 8 kg in the cancer group and 61 ± 2 in the control group.

According to their medical records, estrogen receptor expression was observed in 58% and progesterone receptor expression in 42% of the cancer patients.

Among the cancer patients, 26 (32.91%) had Invasive Lobular Carcinoma (ILC), 45 (56.96%) had invasive ductal carcinoma (IDC), 5 (6.33%) had Ductal Carcinoma in Situ (DCIS) and 3 (3.80%) had Lobular Carcinoma in Situ (LCIS). In 38 of the patients, the tumor had metastasized while 16 had grade III tumors, 13 grade II/III and 12 grade II. According to their medical records, estrogen receptor expression was observed in 69.62% and progesterone receptor expression in 41.77% of the cancer patients. Characteristics of patients group are summarized in Table 1.

Table 1. Characteristic of Patients Group
Characteristic of Patients GroupNo. (%)
Invasive lobular carcinoma (ILC)26 (32.92)
Invasive ductal carcinoma (IDC)45 (56.96)
Ductal carcinoma in situ (DCIS)5 (6.33)
Lobular carcinoma in Situ (LCIS)3 (3.79)
Metastasis38 (48.10)
Grade III16 (20.26)
Grade II/III13 (16.45)
Grade II12 (15.19)

4.1. Data Analysis

The direct counting method was used for finding the frequency of the different alleles and genotypes in the two groups. The data obtained were then analyzed in SPSS-21 using the Chi-square test at a significance level of P < 0.05. The frequency of the alleles was then calculated in both groups using the Hardy-Weinberg equilibrium model and the frequency of the genotypes was then compared between the groups using the Chi-square test.

According to the genotype counting, the homozygous GG genotype was present in 24 (30.38%) of the patients in the cancer group and 26 (32.91%) in the control group (P = 0.732). The CC genotype was present in 25 (31.65%) of the patients in the cancer group and 11 (13.93%) in the control group (P = 0.008). The GC/CG genotype was present in 30 (37.97%) of the patients in the cancer group and 42 (53.16%) in the control group (P = 0.055).

According to the Hardy-Weinberg principle, the frequency of the G allele was 49.37% in the cancer group and 59.49% in the control group. The frequency of the C allele was 50.63% in the cancer group and 40.51% in the control group. According to the results, the C allele had the highest prevalence among the cancer patients with a frequency of 50.63% compared to the G allele with a frequency of 49.37%. The opposite was true for the control group, as the G allele was more prevalent with a frequency of 59.49% compared to the C allele with a frequency of 40.51%, which showed the lowest prevalence in this group.

The odds ratio of the CC genotype was calculated as 2.862 (CI 95%: 1.294 - 6.332 and P = 0.008), showing the significant effect of this genotype in causing the disease. In contrast, the odds ratio of the GG genotype was calculated as 0.89 (CI 95%: 0.455 - 1.740 and P = 0.732), showing that this genotype has no role in causing the disease. Finally, the odds ratio of the CG genotype was calculated as 0.539 (CI 95%: 0.286 - 1.017 and P = 0.055); (Table 2).

Table 2. The Odds Ratio and Genotype Frequency in the Cancer Group and the Control Group
GenotypeCancer GroupControl GroupP ValueOdds RatioCI (95%)
CC25 (31.65)11 (13.93)0.0082.862(6.332 - 1.294)
GG24 (30.38)26 (32.91)0.7320.89(1.740 - 0.455)
GC30 (37.97)42 (53.16)0.0550.539(1.017 - 0.286)

In the cancer group, positive estrogen receptor expression was observed in 16 of the 24 patients with a GG genotype, 21 of the 25 with a CC genotype and 18 of the 30 with a CG/GC genotype. Positive progesterone receptor expression was observed in 13 of the 24 patients with a GG genotype, 11 of the 25 with a CC genotype and 9 of the 30 with a CG/GC genotype.

Data on other factors such as age, weight, disease grade, estrogen receptor (ER) and progesterone receptor (PR) were extracted from the patients’ records so as to analyze the relationship between the genotypes and each of the factors. The results obtained showed that a significant relationship existed only between the CC genotype and disease grade (P = 0.046).

5. Discussion

The prevalence of breast cancer is increasing in many countries; however, mortality rates have remained constant or have insignificantly dropping in some cases. In Iran, the mean age of developing breast cancer is 48.8, with the highest rate of malignancy occurring in the 40 - 49 age group (31.8%) and the lowest in the below-40 age group (23%) (24).

CYP1B1 located in the endoplasmic reticulum plays a major role in activating several environmental carcinogens such as polycyclic aromatic hydrocarbons (PAHs) (25) and aromatic amines (AAs) (26) and in metabolizing 17β estradiol (25). This cytochrome can catalyze 17β estradiol (E2) into catechol metabolites of estrogen, including 2-OH-E2 and 4-OH-E2, which play a major role in breast carcinogenesis. The active metabolites produced by CYP1B1 are able to harm DNA. CYP1B1 may therefore have a significant role in tumorigenesis. The role of CYP1B1 in fetal development has recently been uncovered. The gene of this protein is also expressed in several extrahepatic tissues such as the breast, uterus, kidney, prostate and lungs (26).

Studies suggest that four CYP1B1 polymorphisms at codons, including (CYP1B1*1) Arg48Gly, (CYP1B1*2) Ala119Ser, (CYP1B1*3) Leu432Val and (CYP1B1*4) Asn453Ser, increase hydroxylation activity more than the normal varieties (27, 28). Polymorphisms at codons including (CYP1B1*2) Ala119Ser and (CYP1B1*3) Leu432Val have also been found to increase enzyme activity by two to four times the normal varieties (27). Studies have shown that both the homozygous and heterozygous genotypes of the Leu432Val polymorphism are associated with an increase in the risk of breast cancer to the same amount as ovarian cancer (29-32). Some studies have shown that replacing a G allele with a C allele can be associated with an increased risk of various cancers such as lung (15, 33), prostate (34), breast (20, 35-37) cancer and bone abnormalities (37).

Studies have examined the relationship between CYP1B1 polymorphisms and breast cancer among Chinese, Japanese and Turkish women. The risk of breast cancer increases dramatically in women with CYP1B1 432Val polymorphisms through an exposure to tobacco smoke and a prolonged use of hormones (hormone replacement therapy) (27-30, 37).

Martinez-Ramirez et al. (2013) (38) showed that polymorphisms including CYP1B1 rs1056836, CYP1A1 rs1048943, COMT rs4680, GSTP1 rs1695, GSTT1 null and GSTM1 null in the estrogen metabolic pathway are related to an increased risk of breast cancer in Mexican women. Haiyan Jiao et al. (2010) (39) found a relationship between the polymorphisms in exon 2 of CYP1B1 (codon 119 (G→T)) and exon 3 of this gene (Codon 432, G→C) and an increased risk of breast cancer among the Chinese. Zimarina TC et al. (40) found three polymorphisms of CYP1B1, including Arg48Gly, Val432Leu and Ala119Ser, to be associated with an increased risk of breast cancer and endometriosis; however, De Vivo et al. (2002) (6) found no significant relationships between polymorphisms including Val432Leu (m1) or Ala453Ser (m2) and the risk of breast cancer in Caucasian women. But other studies confirmed the association between rs1056836 and hepatocellular carcinoma risk (41) and laryngeal cancer (42).

The present study found a significant relationship between the rs1056836 polymorphism and breast cancer, but no significant relationships between the cancer group (30.38%) and the control group (32.91%) in terms of the homozygous genotype GG; (P = 0.732). Nevertheless, a significant relationship was found in terms of the CC genotype between the cancer group (31.65%) and the control group (13.93%) (P = 0.008). As for the GC/CG genotype, no significant relationships were observed between the two groups (P = 0.06). The high frequency of the C allele in the cancer group (50.63%) compared to in the control group (40.51%) and the odds ratio of CC genotype shows the significant effect of this genotype in causing the disease. A significant relationship was also found between the CC genotype and the disease grade (P = 0.046).

Given that breast cancer is a complex disease with various factors joining to cause its incidence, no single factor can be said to be solely responsible for its development. Nevertheless, identifying the different factors contributing to its incidence can help improve its prognosis and facilitate its early diagnosis. The results of the present study suggest that CYP1B1 rs1056836 polymorphism may be associated with the susceptibility of breast cancer. Further studies are recommended to be conducted with larger sample sizes in order to assess the accuracy of these findings.




  • 1.

    Safaei Keshtgar M, Rob S. Breast cancer [in Persian]. 1388; : 138 -684

  • 2.

    Mousavi SM, Montazeri A, Mohagheghi MA, Jarrahi AM, Harirchi I, Najafi M, et al. Breast cancer in Iran: an epidemiological review. Breast J. 2007; 13(4) : 383 -91 [DOI][PubMed]

  • 3.

    Yavari P, Mosavizadeh M, Sadrol-Hefazi B, Mehrabi Y. Reproductive characteristics and the risk of breast cancer--a case-control study in Iran. Asian Pac J Cancer Prev. 2005; 6(3) : 370 -5 [PubMed]

  • 4.

    Tonini G, Schiavon G, Fratto ME, Vincenzi B, Santini D. Hormono-biological therapy in metastatic breast cancer: preclinical evidence, clinical studies and future directions. Expert Opin Biol Ther. 2008; 8(2) : 221 -34 [DOI][PubMed]

  • 5.

    Massarweh S, Schiff R. Resistance to endocrine therapy in breast cancer: exploiting estrogen receptor/growth factor signaling crosstalk. Endocr Relat Cancer. 2006; 13 Suppl 1 : 15 -24 [DOI][PubMed]

  • 6.

    De Vivo I, Hankinson SE, Li L, Colditz GA, Hunter DJ. Association of CYP1B1 polymorphisms and breast cancer risk. Cancer Epidemiol Biomarkers Prev. 2002; 11(5) : 489 -92 [PubMed]

  • 7.

    McFadyen MC, Breeman S, Payne S, Stirk C, Miller ID, Melvin WT, et al. Immunohistochemical localization of cytochrome P450 CYP1B1 in breast cancer with monoclonal antibodies specific for CYP1B1. J Histochem Cytochem. 1999; 47(11) : 1457 -64 [DOI][PubMed]

  • 8.

    Murray GI, Taylor MC, McFadyen MC, McKay JA, Greenlee WF, Burke MD, et al. Tumor-specific expression of cytochrome P450 CYP1B1. Cancer Res. 1997; 57(14) : 3026 -31 [PubMed]

  • 9.

    Murray GI, Melvin WT, Greenlee WF, Burke MD. Regulation, function, and tissue-specific expression of cytochrome P450 CYP1B1. Annu Rev Pharmacol Toxicol. 2001; 41 : 297 -316 [DOI][PubMed]

  • 10.

    Shoun H, Tanimoto T. Denitrification by the fungus Fusarium oxysporum and involvement of cytochrome P-450 in the respiratory nitrite reduction. J Biol Chem. 1991; 266(17) : 11078 -82 [PubMed]

  • 11.

    Nelson D. Bacterial P450 Links, Estimate 90 Bacteria P450 Genes 2004;

  • 12.

    Hayes CL, Spink DC, Spink BC, Cao JQ, Walker NJ, Sutter TR. 17 beta-estradiol hydroxylation catalyzed by human cytochrome P450 1B1. Proc Natl Acad Sci U S A. 1996; 93(18) : 9776 -81 [DOI][PubMed]

  • 13.

    Shimada T, Fujii-Kuriyama Y. Metabolic activation of polycyclic aromatic hydrocarbons to carcinogens by cytochromes P450 1A1 and 1B1. Cancer Sci. 2004; 95(1) : 1 -6 [DOI][PubMed]

  • 14.

    Shimada T, Hayes CL, Yamazaki H, Amin S, Hecht SS, Guengerich FP, et al. Activation of chemically diverse procarcinogens by human cytochrome P-450 1B1. Cancer Res. 1996; 56(13) : 2979 -84 [PubMed]

  • 15.

    Xu W, Zhou Y, Hang X, Shen D. Current evidence on the relationship between CYP1B1 polymorphisms and lung cancer risk: a meta-analysis. Mol Biol Rep. 2012; 39(3) : 2821 -9 [DOI][PubMed]

  • 16.

    Stoilov I, Akarsu AN, Alozie I, Child A, Barsoum-Homsy M, Turacli ME, et al. Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1. Am J Hum Genet. 1998; 62(3) : 573 -84 [DOI][PubMed]

  • 17.

    McLellan RA, Oscarson M, Hidestrand M, Leidvik B, Jonsson E, Otter C, et al. Characterization and functional analysis of two common human cytochrome P450 1B1 variants. Arch Biochem Biophys. 2000; 378(1) : 175 -81 [DOI][PubMed]

  • 18.

    Aklillu E, Oscarson M, Hidestrand M, Leidvik B, Otter C, Ingelman-Sundberg M. Functional analysis of six different polymorphic CYP1B1 enzyme variants found in an Ethiopian population. Mol Pharmacol. 2002; 61(3) : 586 -94 [PubMed]

  • 19.

    Ahangar N, Masoumi S. Frequency Evaluation of Val432Leu (G4326C) Polymorphism of CYP1B1 Gene in a Healthy Population from Mazandaran Province, Iran. J Mazand Univ Med Sci. 2013; 23(106) : 20 -8

  • 20.

    Bailey LR, Roodi N, Dupont WD, Parl FF. Association of cytochrome P450 1B1 (CYP1B1) polymorphism with steroid receptor status in breast cancer. Cancer Res. 1998; 58(22) : 5038 -41 [PubMed]

  • 21.

    Pia S. Polymorphic low penetrance genes and breast cancer. 2007;

  • 22.

    Noguera NI, Tallano CE, Bragos IM, Milani AC. Modified salting-out method for DNA isolation from newborn cord blood nucleated cells. J Clin Lab Anal. 2000; 14(6) : 280 -3 [PubMed]

  • 23.

    Wen W. Cytochrome P4501B1 and Catechol-O-ethyltransferase Genetic Polymorphisms and Breast Cancer Risk in Chinese Women: Results from the Shanghai Breast Cancer Study and a Meta-analysis. J Cancer Epidemiol Biomarkers Prev. 2014; : 329 -35

  • 24.

    Zangiabadi M, Moatari M, Tabatabaei H. Comparing the Effect of Teaching Breast Self-Examination by Peers and Health Care Personnel on Students Knowledge and Attitude [in Persian]. Iran J Med Edu. 2009; 2 : 195 -203

  • 25.

    Smith G, Stubbins MJ, Harries LW, Wolf CR. Molecular genetics of the human cytochrome P450 monooxygenase superfamily. Xenobiotica. 1998; 28(12) : 1129 -65 [DOI][PubMed]

  • 26.

    Lewis DF, Lake BG, George SG, Dickins M, Eddershaw PJ, Tarbit MH, et al. Molecular modelling of CYP1 family enzymes CYP1A1, CYP1A2, CYP1A6 and CYP1B1 based on sequence homology with CYP102. Toxicology. 1999; 139(1-2) : 53 -79 [PubMed]

  • 27.

    Sasaki M, Tanaka Y, Kaneuchi M, Sakuragi N, Dahiya R. CYP1B1 gene polymorphisms have higher risk for endometrial cancer, and positive correlations with estrogen receptor alpha and estrogen receptor beta expressions. Cancer Res. 2003; 63(14) : 3913 -8 [PubMed]

  • 28.

    Sharma M, Shubert DE, Sharma M, Lewis J, McGarrigle BP, Bofinger DP, et al. Biotransformation of tamoxifen in a human endometrial explant culture model. Chem Biol Interact. 2003; 146(3) : 237 -49 [DOI][PubMed]

  • 29.

    Goodman MT, McDuffie K, Kolonel LN, Terada K, Donlon TA, Wilkens LR, et al. Case-control study of ovarian cancer and polymorphisms in genes involved in catecholestrogen formation and metabolism. Cancer Epidemiol Biomarkers Prev. 2001; 10(3) : 209 -16 [PubMed]

  • 30.

    Kumar V, Singh S, Ahmed RS, Banerjee BD, Ahmed T, Pasha ST. Frequency of common CYP1B1 polymorphic variations in Delhi population of Northern India. Environ Toxicol Pharmacol. 2009; 28(3) : 392 -6 [DOI][PubMed]

  • 31.

    Listgarten J, Damaraju S, Poulin B, Cook L, Dufour J, Driga A, et al. Predictive models for breast cancer susceptibility from multiple single nucleotide polymorphisms. Clin Cancer Res. 2004; 10(8) : 2725 -37 [DOI][PubMed]

  • 32.

    Zheng W, Xie DW, Jin F, Cheng JR, Dai Q, Wen WQ, et al. Genetic polymorphism of cytochrome P450-1B1 and risk of breast cancer. Cancer Epidemiol Biomarkers Prev. 2000; 9(2) : 147 -50 [PubMed]

  • 33.

    Chen B, Qiu LX, Li Y, Xu W, Wang XL, Zhao WH, et al. The CYP1B1 Leu432Val polymorphism contributes to lung cancer risk: evidence from 6501 subjects. Lung Cancer. 2010; 70(3) : 247 -52 [DOI][PubMed]

  • 34.

    Pastina I, Giovannetti E, Chioni A, Sissung TM, Crea F, Orlandini C, et al. Cytochrome 450 1B1 (CYP1B1) polymorphisms associated with response to docetaxel in Castration-Resistant Prostate Cancer (CRPC) patients. BMC Cancer. 2010; 10 : 511 [DOI][PubMed]

  • 35.

    Bandi P. American Cancer Society 2009-2010;

  • 36.

    Napoli N, Rini GB, Serber D, Giri T, Yarramaneni J, Bucchieri S, et al. The Val432Leu polymorphism of the CYP1B1 gene is associated with differences in estrogen metabolism and bone density. Bone. 2009; 44(3) : 442 -8 [DOI][PubMed]

  • 37.

    Rylander-Rudqvist T, Wedren S, Granath F, Humphreys K, Ahlberg S, Weiderpass E, et al. Cytochrome P450 1B1 gene polymorphisms and postmenopausal breast cancer risk. Carcinogenesis. 2003; 24(9) : 1533 -9 [DOI][PubMed]

  • 38.

    Martinez-Ramirez OC, Perez-Morales R, Castro C, Flores-Diaz A, Soto-Cruz KE, Astorga-Ramos A, et al. Polymorphisms of catechol estrogens metabolism pathway genes and breast cancer risk in Mexican women. Breast. 2013; 22(3) : 335 -43 [DOI][PubMed]

  • 39.

    Jiao H, Liu C, Guo W, Peng L, Chen Y, Martin FL. Association of CYP1B1 Polymorphisms with Breast Cancer: A Case-Control Study in the Han Population in Ningxia Hui Autonomous Region, P. R. China. Biomark Insights. 2010; 5 : 21 -7 [PubMed]

  • 40.

    Zimarina TC, Kristensen VN, Imianitov EN, Bershtein LM. [Polymorphisms of CYP1B1 and COMT in breast and endometrial cancer]. Mol Biol (Mosk). 2004; 38(3) : 386 -93 [DOI][PubMed]

  • 41.

    Liu F, Luo LM, Wei YG, Li B, Wang WT, Wen TF, et al. Polymorphisms of the CYP1B1 gene and hepatocellular carcinoma risk in a Chinese population. Gene. 2015; 564(1) : 14 -20 [DOI][PubMed]

  • 42.

    Yu PJ, Chen WG, Feng QL, Chen W, Jiang MJ, Li ZQ. Association between CYP1B1 gene polymorphisms and risk factors and susceptibility to laryngeal cancer. Med Sci Monit. 2015; 21 : 239 -45 [DOI][PubMed]

  • Copyright © 2017, Iranian Journal of Cancer Prevention. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License ( which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.