Skip to main content

Recurrent CYP2C19 deletion allele is associated with triple-negative breast cancer



Using a genome-wide approach, we have previously observed an increase in the frequency of rare copy number variants (CNVs) in familial and early-onset breast cancer cases when compared to controls. Moreover, the biological networks of the CNV disrupted genes differed between the two groups. Here, six of the previously observed CNVs were selected for further investigation. Four of these were singletons and disturbed the following genes: DCLRE1C, CASP3, DAB2IP and ITGA9, encoding proteins that are part of the TP53 and β-estradiol centered network. The two others were recurrent alleles and disrupted CDH19 and CYP2C19 genes. Of these, CDH19 encodes a cadherin functioning as a cell-cell adhesion receptor and CYP2C19 a CYP450 enzyme with a major function in estrogen catabolism.


The exact breakpoints of the six previously observed CNV deletion alleles were defined by using qPCR, nested PCR and sequencing. The prevalence of these CNVs was investigated in 842 Northern Finnish breast cancer cases, unselected for family history of cancer and age at disease onset, as well as in 497 healthy female controls by using multiplex PCR. Also the association of the relatively common CDH19 and CYP2C19 deletion alleles with different clinical parameters was studied.


No significant differences in the carrier frequencies between cases and controls were found for any of the studied CNVs. However, the deletion in CYP2C19 showed a significant association with triple-negative breast cancer (p = 0.021).


Our results indicate that inherited changes in CYP2C19 gene participating in estrogen catabolism have an influence on the molecular subtype of breast cancer.

Peer Review reports


Copy number variants (CNVs) are genomic microduplications or microdeletions which can affect gene function and predispose to various diseases [1], including breast cancer. Although no evidence for the association of common CNVs with breast cancer susceptibility has been reported [2], recent genome-wide studies suggest that rare CNVs represent an alternative source of genetic variation influencing hereditary breast cancer risk [3, 4]. In our previous study, we observed a consistent increase in the frequency of rare CNVs in familial and early-onset breast cancer cases when compared to controls. Furthermore, the biological networks of the disrupted genes differed between the two groups: the disrupted genes in breast cancer cases were shown to be closely related to estrogen signalling and TP53 centered tumor suppressor network [4].

Based on their biological functions and recurrence, two of the previously identified deletion alleles disrupting CYP2C19 and CDH19 genes, respectively, were hypothesized to play a role in breast cancer predisposition also in the general population. Of these, CYP2C19 encodes a CYP450 enzyme with a major function in estrogen catabolism: it catalyzes 17 β-hydroxy dehydrogenation and 16 α-hydroxylation of estradiol [5, 6]. CYP2C19 has also been reported to participate in tamoxifen metabolism during breast cancer treatment, as it contributes in tamoxifen 4-hydroxylation [7]. The decreased activity of CYP2C19 through haploinsufficiency might be related to an increase in breast cancer risk, potentially through life-long increased estrogen levels [4]. In contrast, CDH19 encodes a cadherin, which is a cell-cell adhesion receptor establishing and maintaining intercellular connections. Loss of function of cadherins may be connected to cancer formation [8]. In our previous study, the CYP2C19 deletion allele was found twice as frequent in familial breast cancer cases (5.8%) as in controls (2.3%), whereas CDH19 was observed once in both familial (1.0%) and control cohorts (0.8%) [4], implicating the need for a larger dataset for the evaluation of their disease relatedness. Besides the breast cancer risk itself, both changes could also have an effect on tumor biology.

Although a majority of the previously observed CNV alleles, which disrupted genes from the TP53 and β-estradiol centered network, were singletons [4], some could represent founder mutations typical for the Finnish population. Thus, based on their biological functions, four singleton deletion alleles disrupting CASP3, DAB2IP, DCLRE1C and ITGA9 genes, respectively, were included in the study. Of these CASP3 functions in apoptosis, failure of which can lead to cancer [9]. DAB2IP encodes a member of the RAS GTPase-activating gene family and has been reported to act as a tumor suppressor: its inactivation by promoter methylation occurs in several malignancies, including prostate and breast cancer [10]. DCLRE1C operates in the DNA double-strand break repair pathway, defect of which has been strongly associated with breast cancer predisposition [11], and ITGA9 encodes α-integrin, which participates in the control of cell division, differentiation and migration [1214]. The chromosomal region harboring ITGA9 has been reported to be deleted in several epithelial malignancies, including breast carcinoma [15].

Here we have defined the exact breakpoints of six previously identified deletion alleles disrupting the CYP2C19, CDH19, CASP3, DCLRE1C, DAB2IP and ITGA9 genes, respectively, and evaluated their association with breast cancer risk and disease subtype using a Northern Finnish case–control cohort. As a result, we provide evidence suggestive of the CYP2C19 deletion allele being associated particularly with susceptibility to triple-negative breast cancer.



Patient cohort consisted of 842 Northern Finnish breast cancer cases diagnosed at the Oulu University Hospital between the years 2000 and 2011. All cases were unselected for a family history of the disease and age at disease onset. The median age at diagnosis for cases was 57 years (variation 28–92 years). 497 geographically matched anonymous cancer-free female Northern Finnish Red-Cross blood donors (median age at monitoring was 42 years, variation 18–66 years) were used as controls. Control samples were provided by Finnish Red Cross Blood Service, with the information only about their gender, age and place of blood donation. Controls have given their informed consent to use part of their sample for research purposes at the time of donation. The genomic DNA of cases and controls was extracted from blood samples using either the standard phenol-chloroform method, Puregene D-50 K purification kit (Gentra, Minneapolis, MN, USA), or UltraClean Blood DNA Isolation Kit (MoBio, Carlsbad, CA, USA)

For 551 of the breast cancer cases we had access to the clinical parameters obtained from the pathology reports. These included tumor histology, grade, size, nodal status, distant metastases, estrogen receptor (ER), progesterone receptor (PR), HER2 and Ki-67 status. For ER and PR, positive staining was defined as nuclear immunostaining in 1 to 10% (weak), 10 to 50% (moderate), or >50% (strong) of the tumor cells, whereas negative indicated no staining. HER2 expression was studied by means of immunohistochemistry (positivity defined as weak, moderate or strong levels of staining and negativity completely negative staining) and chromogenic in situ hybridization (CISH). Cut-off values used for Ki-67 were negative (0), weak (1), moderate (2) and strong (3). ER, PR and HER2 status were used as surrogate markers to divide the tumors further into luminalA, luminalB, HER2 type and triple-negative subtypes [16, 17]. LuminalA was defined as positive ER or PR expression and no HER2 overexpression, luminalB had positive ER or PR and HER2 overexpression, HER2 type as negative ER and PR but with HER2 overexpression, and triple-negative as negative for all three markers.

All specimens and clinical information were collected with the informed consent of the patients. This study was approved by the Ethical Board of the Oulu University Hospital Health Care District and the Finnish Ministry of Social Affairs and Health.

Genotyping of the deletion alleles

The exact breakpoints of CYP2C19, CDH19, CASP3, DCLRE1C, DAB2IP and ITGA9 genes disrupting deletion CNVs were defined by performing qPCR (BioRad CFX96, BioRad, Hercules, CA, USA) and nested PCR (GeneAmp High Fidelity PCR System, Applied Biosystems, Foster City, CA, USA) with the primers surrounding the breakpoint coordinates received from Illumina HumanOmni1-Quad BeadChips, analyzed with GenomeStudio Genotyping module (Illumina Inc., San Diego, CA, USA) and Nexus Copy Number Discovery Edition 5.1 software (BioDiscovery Inc. El Segundo, CA, USA) [4]. The breakpoints were verified by direct sequencing (ABI3130xl Genetic Analyzer, Applied Biosystems, Foster City, CA, USA). Nested allele-specific PCR for the detection of the deletion alleles was designed in a multiplex format, containing control primers to monitor PCR success. Deletion CNV containing samples were used as positive controls. Primers to amplify the deletion alleles are presented in Additional file 1: Table S1. The obtained PCR amplicons were analyzed with Bioanalyzer (Agilent Technologies, Waldbronn, Germany). All the observed deletion carrier samples were verified by direct sequencing. The heterozygosity of the CYP2C19 and CDH19 deletion alleles was confirmed by second, wild type allele specific PCR. For CYP2C19, the same forward primer as in multiplex reaction was used, reverse (ACTTGACGATGGAGGGTGAA) resided on genomic region present only in wild type allele. For CDH19, the reverse primer was the same as in multiplex reaction, whereas the forward primer (TCTGAATCTGGTGAGGGAACA) was wild type specific.

Genotyping for other CYP2C19 metabolizer alleles in CYP2C19deletion carriers

The status of the remaining CYP2C19 allele both in carriers with breast cancer and those remaining healthy was investigated by genotyping for the three literature described metabolizer types: CYP2C19*2 (c.681G > A, rs4244285, poor metabolizer), CYP2C19*3 (c.636G > A, rs57081121, poor metabolizer) and CYP2C19*17 (-806C > T, rs12248560, ultra-rapid metabolizer) [1821]. Genotyping was performed with direct sequencing (ABI3130xl Genetic Analyzer) using primers in Additional file 1: Table S2 [2224].

Statistical analysis

Statistical analyses were performed with IBM SPSS Statistics 20 (IBM Corporation, Armonk, NY, USA). P-values for comparisons between cases and controls and for the evaluation of the differences in tumor characteristics were obtained using Pearson’s chi-squared or Fisher’s exact test. Fisher’s exact test was used if any of the crosstab cells had expected count less than 5. P-values were not corrected for multiple testing in order not to eliminate potentially significant findings obtained with small number of CNV carriers. All p-values were two-sided.


The exact coordinates for the deletion alleles corresponded well to that received from microarrays [4], except for DAB2IP, for which the deletion was significantly larger than originally predicted (Additional file 1: Table S3). The sequencing verified genomic coordinates of the deletions and the carrier frequencies in the analyzed cohorts are presented in Table 1. When performing case–control comparisons, no additional CASP3, DCLRE1C or DAB2IP deletion allele carriers were observed, indicating that these alleles are either truly singletons or extremely rare. In contrast, ITGA9 deletion allele carriers were observed once in cases and once in controls, leaving its potential role in breast cancer predisposition uncertain. Of the two recurrent alleles, the CDH19 deletion showed higher frequency in cases (12/842, 1.4%) than in controls (3/497, 0.6%), but because of its rarity the difference remained below the level of statistical significance (p = 0.168). The CYP2C19 deletion carrier frequency was only marginally higher in the breast cancer cases (31/842, 3.7%) when compared to the controls (17/497, 3.4%), being relatively high in both groups (sequence of the CYP2C19 deletion breakpoints and its surrounding area is presented in Additional file 2: Figure S1). All CDH19 and CYP2C19 mutation positive individuals were verified to be heterozygotes.

Table 1 Genomic coordinates, sizes and carrier frequencies of the studied deletion alleles

The case–control comparisons were followed by case-case analysis for the differences in clinical parameters between CNV carriers and non-carriers. The tumor characteristics of CDH19 deletion carriers did not significantly differ from non-carrier cases, although the carrier tumors tended to be more frequently of higher grade (7/12, 58.3%, of the tumors categorized as grade 3) than the non-carrier tumors (197/522, 37.7%) (Additional file 1: Table S4). In contrast, for CYP2C19 the tumors of deletion carriers showed association with negative ER (p = 0.048) and PR status (p = 0.078), the latter, however, remaining slightly below the level of statistical significance. HER2 negativity was at similar level as in wild type tumors (Table 2). When combining all three parameters, CYP2C19 deletion carriers were at significantly higher risk for developing triple-negative (ER/PR/HER2 negative) tumors than non-carriers (p = 0.021, OR 2.83; 95% CI 1.20-6.66). Altogether, these results indicate that the tumor characteristics of CYP2C19 deletion carriers are related to estrogen responsiveness. As the known biological function of CYP2C19 is related to estrogen catabolism, and as the studied deletion allele is expected to be a null allele, we further defined the status of the remaining CYP2C19 allele in relation to literature described metabolizer genotypes both in carriers with breast cancer and those remaining healthy. No CYP2C19*3 poor metabolizers were identified, whereas four CYP2C19*2 poor metabolizers were identified in patients (4/31, 12.9%) and one in controls (1/17, 5.9%). There was no difference in the frequency of CYP2C19*17 ultra-rapid metabolizer genotypes (7/31, 22.6% in patients vs. 3/17, 17.6% in healthy controls), indicating that the disease risk of individual with CYP2C19 deletion was not significantly affected by the metabolizer status of the remaining allele. Furthermore, in a majority (7/10) of the deletion carriers with ER negative cancer the second allele was found to be wild type, whereas one (1/10) had a poor-metabolizer CYP2C19*2 allele and the rest (2/10) an ultra-rapid metabolizer CYP2C19*17 allele.

Table 2 Tumor characteristics of CYP2C19 deletion allele carriers compared with the tumors of non-carrier unselected breast cancer cases


Inherited genomic alterations are expected to have an effect on individual’s risk of getting cancer. However, these alterations may affect not only the risk but also the pattern of somatically acquired mutations and thereby tumor biology. Much of the work in this field has been concentrating on single nucleotide polymorphisms (SNPs) whereas the role of CNVs has remained poorly defined, partially because their detection with Sanger or even with sophisticated Next-Generation sequencing is hard or even impossible, and the fast and cost-efficient investigation of CNV alleles requires the characterization of their breakpoints in exact detail. Of the currently studied rare CNV alleles, the breakpoints of five out of six were adequately well described by the used analysis software, indicating that high-resolution microarrays can predict fairly well the genuine genomic coordinates of the aberrations. The singleton CNVs previously identified in familial or early-onset cases [4] were absent from, or remained extremely rare in the unselected breast cancer cases, but the two recurrent alleles were observed at higher frequency. The carrier frequency of the CDH19 deletion was twice as high in unselected breast cancer cases as in controls but remained below statistical significance, indicating the need for larger case–control cohorts to demonstrate its association with breast cancer. The other recurrent CNV allele, CYP2C19 deletion, had surprisingly high prevalence both in the studied cases and controls (>3%), particularly when considering that deletion CNVs have rarely been reported in CYP genes, despite the numerous studies performed. This can be explained by the poor detection of CNV alleles by conventional genotyping methods, but also by the fact that our study was performed with samples from Finnish founder population. Founder populations are known to harbor unique mutations and some of the mutations rare in other populations can also show enrichment in them. In regard to cancer predisposition, the effect of the CYP2C19 deletion was reminiscent to that of a low-penetrance allele. However, it was found to be associated specifically with the triple-negative molecular subtype of the breast cancer.

There are multiple lines of evidence for the profound role of estrogen in breast cancer development: disruptions in estrogen signalling and metabolism have long been considered to affect breast cancer risk. This can result from different reproductive and hormonal factors [25], but could also be due to variations in the enzymatic machinery responsible for estrogen metabolism. Indeed, the currently studied CYP2C19 deletion CNV is expected to result in a null allele of a gene encoding an enzyme involved in estrogen catabolism [5, 6]. All currently identified mutation positive individuals were heterozygous for the CYP2C19 deletion, and the genotype of the remaining allele seemed not to play a role in the observed association with tumor triple-negativity. This could be explained by a genuine haploinsufficient situation, in which single allele is unable to sustain full functionality when compared to the protein levels produced by two wild type alleles. Alternatively, as the CYP2C19 deletion allele extends over 60 kb, starting only 1377 bp from the 3’ end of the adjacent CYP2C18 gene, it could change the genomic landscape of this region in a way that leads to aberrant expression of both genes. It is also possible that large genomic deletions disturb the communication between the homologous alleles required for their full function by deleting regulatory elements required for this process [26].

Another CYP2C19 allele, CYP2C19*17, defining an ultra-rapid metabolizer phenotype, has previously been associated with a decreased risk for breast cancer. This suggests that increased catabolism of estrogens by CYP2C19 may lead to decreased estrogen levels and therefore reduced breast cancer risk [27]. Correspondingly, our initial hypothesis was that CYP2C19 deletion allele effects are mediated through life-long increased estrogen levels. Why this would predispose particularly to ER negative breast cancer is currently, however, puzzling and the mechanism through which the CYP2C19 deletion operates remains unclear. However, any perturbations in estrogen metabolism are still among the possible explanations. Curiously, there are also reports linking obesity with triple-negative breast cancer [28]. Although obesity-related insulin resistance and chronic inflammatory could be possible explanations for this phenomenon, increased body mass index is known to cause changes in the hormonal cycles and result in excessive adipose tissue [29, 30]. This can increase the estrogen production and availability, leading again to the unexpected association with receptor negative breast cancer. Nevertheless, as triple-negative breast cancer is a tumor subtype with unique characteristics not only in its pathological presentation but also in prognosis and response to therapy, identification of additional risk factors specifically associated with this subgroup of breast cancer could help to understand its etiology.


Our results indicate that an inherited defect in the CYP2C19 gene with a role in estrogen catabolism has an influence on the molecular subtype of breast cancer and is significantly associated with triple-negative tumors. The role of the CYP2C19 deletion allele, as well as that of the CDH19 deletion, in breast cancer predisposition warrants further studies and the obtained results should be replicated with larger and independent case–control cohorts.


  1. Weischenfeldt J, Symmons O, Spitz F, Korbel JO: Phenotypic impact of genomic structural variation: insights from and for human disease. Nat Rev Genet. 2013, 14 (2): 125-138. 10.1038/nrg3373.

    Article  CAS  PubMed  Google Scholar 

  2. Wellcome Trust Case Control Consortium: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature. 2007, 447 (7145): 661-678. 10.1038/nature05911.

    Article  Google Scholar 

  3. Krepischi AC, Achatz MI, Santos EM, Costa SS, Lisboa BC, Brentani H, Santos TM, Goncalves A, Nobrega AF, Pearson PL, Vianna-Morgante AM, Carraro DM, Brentani RR, Rosenberg C: Germline DNA copy number variation in familial and early-onset breast cancer. Breast Cancer Res. 2012, 14 (1): R24-10.1186/bcr3109.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Pylkäs K, Vuorela M, Otsukka M, Kallioniemi A, Jukkola-Vuorinen A, Winqvist R: Rare copy number variants observed in hereditary breast cancer cases disrupt genes in estrogen signaling and TP53 tumor suppression network. PLoS Genet. 2012, 8 (6): e1002734-10.1371/journal.pgen.1002734.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Cheng ZN, Shu Y, Liu ZQ, Wang LS, Ou-Yang DS, Zhou HH: Role of cytochrome P450 in estradiol metabolism in vitro. Acta Pharmacol Sin. 2001, 22 (2): 148-154.

    CAS  PubMed  Google Scholar 

  6. Cribb AE, Knight MJ, Dryer D, Guernsey J, Hender K, Tesch M, Saleh TM: Role of polymorphic human cytochrome P450 enzymes in estrone oxidation. Cancer Epidemiol Biomarkers Prev. 2006, 15 (3): 551-558. 10.1158/1055-9965.EPI-05-0801.

    Article  CAS  PubMed  Google Scholar 

  7. Crewe HK, Notley LM, Wunsch RM, Lennard MS, Gillam EM: Metabolism of tamoxifen by recombinant human cytochrome P450 enzymes: formation of the 4-hydroxy, 4'-hydroxy and N-desmethyl metabolites and isomerization of trans-4-hydroxytamoxifen. Drug Metab Dispos. 2002, 30 (8): 869-874. 10.1124/dmd.30.8.869.

    Article  CAS  PubMed  Google Scholar 

  8. Kremmidiotis G, Baker E, Crawford J, Eyre HJ, Nahmias J, Callen DF: Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity. Genomics. 1998, 49 (3): 467-471. 10.1006/geno.1998.5281.

    Article  CAS  PubMed  Google Scholar 

  9. Hengartner MO: The biochemistry of apoptosis. Nature. 2000, 407 (6805): 770-776. 10.1038/35037710.

    Article  CAS  PubMed  Google Scholar 

  10. Dote H, Toyooka S, Tsukuda K, Yano M, Ouchida M, Doihara H, Suzuki M, Chen H, Hsieh JT, Gazdar AF, Shimizu N: Aberrant promoter methylation in human DAB2 interactive protein (hDAB2IP) gene in breast cancer. Clin Cancer Res. 2004, 10 (6): 2082-2089. 10.1158/1078-0432.CCR-03-0236.

    Article  CAS  PubMed  Google Scholar 

  11. Stratton MR, Rahman N: The emerging landscape of breast cancer susceptibility. Nat Genet. 2008, 40 (1): 17-22. 10.1038/ng.2007.53.

    Article  CAS  PubMed  Google Scholar 

  12. Singh P, Chen C, Pal-Ghosh S, Stepp MA, Sheppard D, Van De Water L: Loss of integrin alpha9beta1 results in defects in proliferation, causing poor re-epithelialization during cutaneous wound healing. J Invest Dermatol. 2009, 129 (1): 217-228. 10.1038/jid.2008.201.

    Article  CAS  PubMed  Google Scholar 

  13. Grassinger J, Haylock DN, Storan MJ, Haines GO, Williams B, Whitty GA, Vinson AR, Be CL, Li S, Sorensen ES, Tam PP, Denhardt DT, Sheppard D, Choong PF, Nilsson SK: Thrombin-cleaved osteopontin regulates hemopoietic stem and progenitor cell functions through interactions with alpha9beta1 and alpha4beta1 integrins. Blood. 2009, 114 (1): 49-59. 10.1182/blood-2009-01-197988.

    Article  CAS  PubMed  Google Scholar 

  14. Young BA, Taooka Y, Liu S, Askins KJ, Yokosaki Y, Thomas SM, Sheppard D: The cytoplasmic domain of the integrin alpha9 subunit requires the adaptor protein paxillin to inhibit cell spreading but promotes cell migration in a paxillin-independent manner. Mol Biol Cell. 2001, 12 (10): 3214-3225. 10.1091/mbc.12.10.3214.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Protopopov A, Kashuba V, Zabarovska VI, Muravenko OV, Lerman MI, Klein G, Zabarovsky ER: An integrated physical and gene map of the 3.5-Mb chromosome 3p21.3 (AP20) region implicated in major human epithelial malignancies. Cancer Res. 2003, 63 (2): 404-412.

    CAS  PubMed  Google Scholar 

  16. Carey LA, Perou CM, Livasy CA, Dressler LG, Cowan D, Conway K, Karaca G, Troester MA, Tse CK, Edmiston S, Deming SL, Geradts J, Cheang MC, Nielsen TO, Moorman PG, Earp HS, Millikan RC: Race, breast cancer subtypes, and survival in the Carolina Breast Cancer Study. JAMA. 2006, 295 (21): 2492-2502. 10.1001/jama.295.21.2492.

    Article  CAS  PubMed  Google Scholar 

  17. Schneider BP, Winer EP, Foulkes WD, Garber J, Perou CM, Richardson A, Sledge GW, Carey LA: Triple-negative breast cancer: risk factors to potential targets. Clin Cancer Res. 2008, 14 (24): 8010-8018. 10.1158/1078-0432.CCR-08-1208.

    Article  CAS  PubMed  Google Scholar 

  18. Wedlund PJ: The CYP2C19 enzyme polymorphism. Pharmacology. 2000, 61 (3): 174-183. 10.1159/000028398.

    Article  CAS  PubMed  Google Scholar 

  19. De Morais SM, Wilkinson GR, Blaisdell J, Meyer UA, Nakamura K, Goldstein JA: Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese. Mol Pharmacol. 1994, 46 (4): 594-598.

    CAS  PubMed  Google Scholar 

  20. Roddam PL, Rollinson S, Kane E, Roman E, Moorman A, Cartwright R, Morgan GJ: Poor metabolizers at the cytochrome P450 2D6 and 2C19 loci are at increased risk of developing adult acute leukaemia. Pharmacogenetics. 2000, 10 (7): 605-615. 10.1097/00008571-200010000-00004.

    Article  CAS  PubMed  Google Scholar 

  21. Sim SC, Risinger C, Dahl ML, Aklillu E, Christensen M, Bertilsson L, Ingelman-Sundberg M: A common novel CYP2C19 gene variant causes ultrarapid drug metabolism relevant for the drug response to proton pump inhibitors and antidepressants. Clin Pharmacol Ther. 2006, 79 (1): 103-113. 10.1016/j.clpt.2005.10.002.

    Article  CAS  PubMed  Google Scholar 

  22. Baldwin RM, Ohlsson S, Pedersen RS, Mwinyi J, Ingelman-Sundberg M, Eliasson E, Bertilsson L: Increased omeprazole metabolism in carriers of the CYP2C19*17 allele; a pharmacokinetic study in healthy volunteers. Br J Clin Pharmacol. 2008, 65 (5): 767-774. 10.1111/j.1365-2125.2008.03104.x.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Goldstein JA, Blaisdell J: Genetic tests which identify the principal defects in CYP2C19 responsible for the polymorphism in mephenytoin metabolism. Methods Enzymol. 1996, 272: 210-218.

    Article  CAS  PubMed  Google Scholar 

  24. Hsu HL, Woad KJ, Woodfield DG, Helsby NA: A high incidence of polymorphic CYP2C19 variants in archival blood samples from Papua New Guinea. Hum Genomics. 2008, 3 (1): 17-23. 10.1186/1479-7364-3-1-17.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Kaaks R, Berrino F, Key T, Rinaldi S, Dossus L, Biessy C, Secreto G, Amiano P, Bingham S, Boeing H, de Mesquita HB B, Chang-Claude J, Clavel-Chapelon F, Fournier A, van Gils CH, Gonzalez CA, Gurrea AB, Critselis E, Khaw KT, Krogh V, Lahmann PH, Nagel G, Olsen A, Onland-Moret NC, Overvad K, Palli D, Panico S, Peeters P, Quiros JR, Roddam A, et al: Serum sex steroids in premenopausal women and breast cancer risk within the European Prospective Investigation into Cancer and Nutrition (EPIC). J Natl Cancer Inst. 2005, 97 (10): 755-765. 10.1093/jnci/dji132.

    Article  CAS  PubMed  Google Scholar 

  26. Lupski JR, Stankiewicz P: Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes. PLoS Genet. 2005, 1 (6): e49-10.1371/journal.pgen.0010049.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Justenhoven C, Hamann U, Pierl CB, Baisch C, Harth V, Rabstein S, Spickenheuer A, Pesch B, Bruning T, Winter S, Ko YD, Brauch H: CYP2C19*17 is associated with decreased breast cancer risk. Breast Cancer Res Treat. 2009, 115 (2): 391-396. 10.1007/s10549-008-0076-4.

    Article  CAS  PubMed  Google Scholar 

  28. Pierobon M, Frankenfeld CL: Obesity as a risk factor for triple-negative breast cancers: a systematic review and meta-analysis. Breast Cancer Res Treat. 2013, 137 (1): 307-314. 10.1007/s10549-012-2339-3.

    Article  PubMed  Google Scholar 

  29. Bulun SE, Chen D, Moy I, Brooks DC, Zhao H: Aromatase, breast cancer and obesity: a complex interaction. Trends Endocrinol Metab. 2012, 23 (2): 83-89. 10.1016/j.tem.2011.10.003.

    Article  CAS  PubMed  Google Scholar 

  30. Federico A, Morgillo F, Tuccillo C, Ciardiello F, Loguercio C: Chronic inflammation and oxidative stress in human carcinogenesis. Int J Cancer. 2007, 121 (11): 2381-2386. 10.1002/ijc.23192.

    Article  CAS  PubMed  Google Scholar 

Pre-publication history

Download references


We thank all patients for volunteering to participate in this study, and Kari Mononen for his help in collecting clinical data. This study was supported by the Academy of Finland (grant number 250083, 122715 and the Center of Excellence grant number 251314), the Finnish Cancer Foundation, the Sigrid Juselius Foundation, the University of Oulu, the University of Oulu Support Foundation and the special Governmental EVO funds for Oulu University Hospital -based research activities.

Author information

Authors and Affiliations


Corresponding authors

Correspondence to Robert Winqvist or Katri Pylkäs.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

KP and RW conceived the study. KP and AT performed the breakpoint mapping, AT multiplex analysis and CYP2C19 genotyping. AJV provided the clinical information for the patients. KP and AT analyzed the statistics and drafted the manuscript. All authors read and approved the final manuscript.

Electronic supplementary material


Additional file 1: Table S1: Primers used in multiplex PCR. Table S2. Primers used for the detection of other metabolizer phenotypes described in CYP2C19. Table S3. Correspondence of microarray based and sequencing confirmed genomic coordinates for the breakpoints. Table S4. Tumor characteristics of CDH19 deletion allele carriers compared with the tumors of non-carrier unselected breast cancer cases. (DOCX 28 KB)

Additional file 2: Figure S1: Sequence of the CYP2C19 deletion breakpoint. (PPTX 321 KB)

Rights and permissions

Open Access  This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made.

The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.

To view a copy of this licence, visit

The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Tervasmäki, A., Winqvist, R., Jukkola-Vuorinen, A. et al. Recurrent CYP2C19 deletion allele is associated with triple-negative breast cancer. BMC Cancer 14, 902 (2014).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: