μ-Opioid receptor gene (OPRM1) polymorphism in patients with breast cancer

The GLOBOCAN 2012 International Agency for Research on Cancer database shows breast cancer (BC) is the most common cancer in females worldwide, at approximately 25 % of all female cancers, and the second most commonly occurring malignancy. It ranks as the fifth major global cause of cancer death and the second in developed countries [1]. It is currently believed that tumor development in the majority of cases is associated with a genetic background, and this includes sporadic tumors [2]. This resulted from increased focus on natural gene population variability as a determinant of cancer susceptibility. At least 80 different genes with 145 variants were investigated to determine the relationship between single nucleotide polymorphisms (SNPs) and breast cancer risk, with polymorphism considered significant in approximately 35 genes with 46 variants [3]. Herein, the previously untested μ-opioid receptor gene (OPRM1) is examined as the newest candidate in this regard.

Opioids form part of the extensive physiological system of neuronal, hormonal, and immune regulation essential for bodily homeostasis maintenance. Their pain perception control and analgesia is moderated by endogenous and exogenous opioid peptide interaction with receptors situated in the central and peripheral nervous systems, in the immunologic system, and on the endothelial cell surface [4‐7].

While opioid influence on tumor growth and cancer progression is less established, there is increasing evidence for its support [8‐13]. μ-Opioid receptor (MOR) expression in breast cancer cells has been demonstrated in both the MCF-7 and T47D ER-positive BC cell lines and in patient biopsy specimens [14‐17]. Chatikhine and coworker’s immunohistochemical studies [18] showed that the most common type of BC invasive ductal carcinomas can prove positive for β-endorphin and Met-enkephalin opioid peptides [18]. Further research has revealed that clinically relevant doses of analgesic opioids, such as morphine, promote basal cell proliferation and migration, and accompanying angiogenesis results in direct tumor growth and metastasis [9, 19, 20] or in indirect morphine-induced immunosuppression [13]. In contradistinction, however, morphine and other opioids also promote tumor cell death [15, 16, 21]. While these facts suggest that the endogenous opioid system can participate in breast cancer development and progression, many results on opioid and BC interrelationships are contradictory. One reason for this discord may be genetic variation in the OPRM1 gene.

The human OPRM1 gene is located on chromosome 6q24–q25. It spans 236 kb with at least 11 exons and 17 different splice variants under the control of multiple promoters [22]. The most commonly occurring MOR polymorphism is A118G variant (rs1799971). This is located in the first exon of gene and consists of non-synonymous substitution of guanine (G) for adenine (A), resulting in the exchange of aspartic acid for asparagine at MOR protein position 40 (N40D). This leads to loss of the N-glycosylation site in the G protein-coupled receptor’s extracellular region and associated change in its molecular level function [23]. Clinical observations have demonstrated a relationship between A118G polymorphism frequency and response to exogenous opioids, with resultant pain threshold variation [24‐28]. Further studies suggest that G allele carriers exhibit decreased breast cancer-specific mortality [29] and significantly lowered risk of esophageal carcinoma development [30].

Our previous research identified opioid peptides in lactating women’s milk, where concentrations of cryptopeptides derived from human β-casein β-casomorphin-5 and β-casomorphin-7 were dependent on lactation phase [31]. This result combined with lactation as a protective factor in breast cancer risk and the abovementioned opioid participation in tumor biology prompted our examination of the relationship between the A118G polymorphism in the OPRM1 μ-opioid receptor gene and breast cancer occurrence.

The study population consisted of 151 histopathologically confirmed breast cancer patients and 590 healthy controls (287 female and 303 male). The distribution of selected characteristics in breast cancer females and healthy volunteers is listed in Table 1, with no statistically significant differences in the majority of compared features. All subjects were Caucasians, of approximately the same age. Both healthy and breast cancer female groups (HF and BCF, respectively) had similar fertility rates, and they reached sexual maturity, menopausal status, and gave birth at equivalent ages. Most HF and BCF were breast-fed, with a slightly less percent in the BCF group. While 10 % of both groups were nulliparous, more BC females were postmenopausal (p = 0.03) and more were smokers (p = 0.03). In addition, while both female groups, and only a few more BC than HF, reported a positive breast cancer family history, healthy males recorded BC occurrence in their female relatives twice less frequently (p = 0.02). Clinical evidence and histopathology classified all BCs herein invasive, with 58 % in stage I and 42 % in stage II (data not shown).

The observed genotype distribution of OPRM1 A118G polymorphism in both control subgroups and cancer patients conformed to the Hardy–Weinberg equilibrium (p > 0.05). This suggests no population stratification and no sampling bias. The AA, AG, and GG genotypes were identified, with 0.1 G allele frequency in the entire research population. Of the total 741 participants, 609 had genotype AA, 119 had AG, and 13 had GG. These latter 13 GG genotypes were in 5 healthy individuals and 8 cancer-diagnosed patients. All healthy GG homozygous carriers were females under 50 years of age, and 3 of these were premenopausal. The AG genotype was present in 75 healthy control individuals and 44 BC patients. The respective genotype distribution and A/G allele frequencies are listed in Table 2.

Our results suggest a strong association between the presence of the G allele at position 118 of the μ-opioid receptor gene and increased breast cancer incidence (OR = 3.3, 95 % CI 2.2–5.0, p < 0.0001). Significant difference was also identified in G allele occurrence in the female gender (OR = 2.0, 95 % CI 1.4–2.9, p = 0.0004).

Although the endogenous opioid system’s precise role in tumor initiation and development remains undetermined, a relationship with cancer is anticipated because it plays a regulatory function in organism homeostasis, and opioid peptides and receptors are present in cancer cells [14, 17, 18]. The identification of functionally significant genetic variation in the opioid system compounds this issue. Global reports indicate that OPRM1 A118G allele frequencies are highly dependent on ethnicity, where the overall G allelic frequency varies between 0.8 and 48 % in different ethnic groups [23]. Genotypic distribution analysis of our entire population identified 10 % G allele frequency, thus approximating the established global Caucasian frequency of 11–17 % [23].

Herein, we investigated the association between A118G OPRM1 gene polymorphism and breast cancer risk. We found that female G allele carriers had more than three times increased breast cancer risk than both healthy female and the entire control group. The one previous study on the relationship between A118G OPRM1 gene and breast cancer by Bortsov et al. recorded that breast cancer-specific mortality was significantly reduced in patients possessing the OPRM1 118G variant allele [29]. Additionally, while the protective effect of this SNP was limited only to invasive cases, it increased with increasing cancer diagnosis stage. These authors concluded this was due to reduced opioid response in patients who possessed one or both G alleles. In contrast, we examined only primary invasive breast cancer patients with no history of opioid use. The μ-opioid G variant receptor may therefore play a protective role by decreasing opioid drug action in cancer progression and metastasis, and simultaneously increase the risk of endogenous opioid peptide action in the carcinogenic process. Mura et al.’s [23] summary of research into the molecular consequences of A118G OPRM1 polymorphism indicates that this phenomenon is possible because, in contrast to the wild-type A variant N40 receptor effect, the G variant receptor can be associated with both decreased and increased signal transduction. It is important to note here that females can also be influenced by β-casomorphin-5 and β-casomorphin-7 opioid peptides in lactation milk. While both β-casomorphin peptide concentrations changed with lactation phase in healthy breast-feeding females [31], concentrations remained the same throughout lactation in the breast milk of females with food allergies [33]. While this expected time-dependent β-casomorphin gradient in healthy lactating females inspires a comparative study of the interrelationships between breast-feeding period, respective genotypes, and breast cancer diagnosis, our current study group has inappropriate stratification to pursue this herein. Future research will establish study population stratification which identifies interrelationships between the number of live births, maternal lactation duration, feeding periods, and food allergy status.

Mainstream clinical A118G OPRM1 polymorphism analysis focuses on opioid-induced analgesia and opioids, vulnerability to alcohol and nicotine addiction, and therapy response. It is interesting here that our female OPRM1 G allele frequency is approximately twice that of males. No males were GG homozygous and only 40 carried one G allele. Some studies indicate gender-specific associations [34‐36], and Fillingim et al.’s allelic distribution of tested SNP in healthy people specifies only females [28]. Although these authors’ population was more ethnically diverse than ours, their G allele overrepresentation in females is consistent with our results. This may constitute one explanation why breast cancer is so rare in males; accounting for only 0.6 % of all breast cancer patients worldwide [37]. It is acknowledged that male BC does not significantly differ from female BC, except in obvious gender-specific differences, and also that breast cancer is more likely to be estrogen receptor (ER)-positive in males than in females [38]. It should be noted that functional relationship between ERα and MOR has been reported recently. It was shown that MOR activation leads to ERα activation and mediates its translocation to the plasma membranes. The synergistic induction of breast cancer cell proliferation has been observed as the final effect [39]. Moreover, it has also been shown that expression of ERβ can be regulated by opioids [40]. In conclusion, since the MOR G allele (40D variant) proves more sensitive to endogenous opioid peptides and promotes the recently reported estrogen receptor interaction, our results highlight the significance of the OPRM1 G allele as a serious risk factor in breast cancer development.