Abstract
The insulin-like growth factor (IGF) pathway has been implicated as risk modifier in premenopausal breast cancer. In this study, associations between single nucleotide polymorphisms (SNPs) and diplotypes in the IGFBP1 and IGFBP3 genes and circulating IGFBP-3 levels, BRCA family status and breast cancer among women from high-risk breast cancer families were investigated. Nine IGFBP1 and IGFBP3 SNPs were genotyped with PCR-based methods in 323 women. Nine IGFBP1 and ten IGFBP3 diplotypes were identified. Plasma IGFBP-3 levels obtained during cycle day 18–23 were available for 231 women, 87 current users of combined oral contraceptives and 144 non-users. IGFBP1 (rs1995051 and rs4988515) and IGFBP3 (rs2471551 and rs2854744) SNPs were associated with circulating IGFBP-3 levels (P < 0.05). IGFBP1 low diplotypes were associated with lower IGFBP-3 levels and were more common in BRCA2 families OR 2.05 (95%CI 0.97–4.30). IGFBP3 high diplotypes were associated with higher IGFBP-3 levels and were more common in BRCAX families OR 1.68 (95%CI 1.04–2.74). After adjusting the models for BRCA family status, both the BRCA1 and BRCA2 family status (P ≤ 0.006) and the IGFBP1 diplotype GTAC/ACAT (P = 0.004) were associated with lower IGFBP-3 levels. Similarly, both the BRCA1 and BRCA2 family status (P ≤ 0.03) and the IGFBP-3 diplotypes GCA/GCG (P = 0.007) and GCG/CCG (P = 0.002) were significantly associated with lower IGFBP-3 levels, adjusted for age, weight, OC use, and other IGFBP diplotypes. No individual SNP was associated with breast cancer. There were 23 cases of breast cancer and one IGFBP1 diplotype was associated with a decreased risk of breast cancer after age 18 (log rank P=0.05). In conclusion, independent effects from IGFBP1, IGFBP3 diplotypes, and BRCA family status on IGFBP-3 levels were observed. These factors may influence the risk of breast cancer among women from high-risk breast cancer families.
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Introduction
Breast cancer is the most commonly diagnosed cancer among women in the Western world and the lifetime risk is approximately 12%. Women with one first-degree relative with breast cancer have an approximately twofold greater risk compared to women in the general population. Mutations in the high-penetrance BRCA1 or BRCA2 genes confer 60–80% lifetime risk of breast cancer [1]. Still, >50% of the genetic predisposition to hereditary breast cancer remains unexplained and the influence of other low-penetrance genetic or non-genetic factors is under intense investigation [2].
Insulin-like growth factor I (IGF-I) is a polypeptide growth hormone that promotes cell proliferation and inhibits apoptosis of both normal and malignant breast epithelial cells [3]. Given the high circulating IGF-I concentration and wide tissue distribution, tight regulation and control of its actions is required to maintain homeostasis. The vast majority of circulating IGF-I is bound to IGF-binding proteins, predominantly IGFBP-3 in complex with an acid-labile subunit, which restrict the bioactive IGFs and limit their interaction with receptors. Dysregulation of this control resulting in increased IGF-I levels or altered IGF-I/IGFBP-3 ratios may contribute to an increased risk of breast cancer. IGFBP-3 has a well-defined role in sequestering IGF-I and thereby, attenuating its mitogenic actions. However, in addition to this regulatory role on IGF-I actions, IGFBP-3 may exert IGF-I independent effects promoting cellular growth [4, 5]. High circulating IGFBP-3 levels have been associated with proliferative benign breast disease and increased breast cancer risk [6, 7].
Non-genetic factors such as oral contraceptives (OC) have been shown to increase IGFBP-3 levels in most women [8, 9]. In addition to lifestyle and environmental factors, IGFBP-3 plasma levels are likely to be influenced by genetic variation in the IGFBP1 and IGFBP3 genes [10]. The gene for IGFBP3 is located at chromosome 7p14-p12, in a tail-to-tail configuration with IGFBP1 at 7p13-p12 [11]. Twin studies indicate that genetic variants may account for up to 60% of the inter-individual variation in circulating IGFBP-3 levels [12–14]. Our group has previously reported significant associations between the AA genotype of the IGFBP3 SNP rs2854744 (A-202C) in the promoter region of IGFBP3 and higher circulating IGFBP-3 levels, especially in women from BRCAX families, in the present study population [8]. This polymorphism may directly influence IGFBP3 gene promoter activity [15, 16]. To our knowledge, associations between multiple genetic polymorphisms and diplotypes in IGFBP1 and IGFBP3, and circulating IGFBP-3 levels among women from BRCA1, BRCA2, or BRCAX families have not been previously investigated. The aims of this study were to examine the associations between genetic variation in the IGFBP1 and IGFBP3 genes and IGFBP-3 plasma levels, BRCA status, and breast cancer risk among women from high-risk breast cancer families.
Materials and methods
Study Population
The study population included 323 women from 192 families from two inclusion arms, all belonging to high-risk breast cancer families in the South Swedish Health Care Region with DNA available for genotyping. The first inclusion arm has been described in detail elsewhere [17]. In brief, 267 young healthy women with no previous cancer history or prophylactic mastectomy or bilateral oophorectomy were enrolled in the study between 1996 and 2006. Eligible participants had to belong to high-risk breast cancer families and be either (1) known BRCA1 or BRCA2 mutation carriers or (2) first or second-degree relatives of a breast cancer case or (3) first- or second-degree relatives of a known male or female BRCA1 or BRCA2 mutation carrier. In the second inclusion arm, an additional 40 BRCA1 and 16 BRCA2 mutation carriers born between 1950 and 1988 were included irrespective of cancer status, in order to include all BRCA1/2 mutation carriers in the South Swedish Health Care Region with DNA available for SNP testing. Information on BRCA mutation status was obtained through medical records from the Oncogenetic Clinic at the Department of Oncology, Lund. Written informed consent was obtained from all participating women and the study was approved by the local ethics committee at Lund University. Extensive questionnaire data with information on reproductive factors, the use of combined OCs, and other medications, etc., were obtained from the majority of cohort members. Characteristics of the women are presented in Table 1.
IGFBP-3 plasma levels
IGFBP-3 levels were measured in plasma samples obtained between 07:15 am and 12:15 pm 5–10 days before the predicted onset of the next menstrual period, i.e., during cycle day 18–23 in most women, using the IMMULITE 2000 IGFBP-3 enzyme-labeled chemiluminescent immunometric assay (Siemens) in Uppsala University Hospital (Uppsala, Sweden) as previously described [8]. The assay sensitivity was 0.02 μg/ml. The intra-assay and inter-assay variations were 4.1 and 7.3%, respectively.
SNP selection and genotyping
Four IGFBP1 (rs1995051, rs3763497, rs1065780, and rs4988515) in one haplotype block and three IGFBP3 haplotype-tagging (ht)SNPs (rs2471551, rs2854744, and rs2132572) in another haplotype block were selected to capture 95% of the genetic diversity of the IGFBP1 and IGFBP3 genes in a Swedish population, based on personal communication with Dr Mattias Johansson (International Agency for Research against Cancer, IARC, Lyon, France) and data from a Swedish cancer cohort [18]. Two additional IGFBP3 SNPs (rs6670 and rs2453839) between the blocks were also included.
Genomic DNA was extracted from peripheral blood using Wizard Genomic DNA Purification Kit (Promega, Madison, WI, USA). Genotyping was performed in the Department of Genotyping and Sequencing at Region Skåne’s Competence Center of Clinical Research (RSKC, Malmö, Sweden).
The SNP (rs3763497, rs1065780, rs4988515, rs6670, rs2471551, rs2854744, and rs2132572) analyses were performed on a matrix-assisted laser desorption/ionization time-of-flight mass spectrometry on a Sequenom MassARRAY® platform (Sequenom, San Diego, CA, USA), using iPLEX reagents according to the manufacturers’ protocol. The Sequenom MassARRAY® designer software was used for multiplex SNP analysis design. The SNPs (rs1995051 and rs2854744) were genotyped using a Taqman SNP allelic discrimination assay in 384-well format on ABI PRISM 7900 Sequence Detection System (Applied Biosystems, Foster City, CA, USA). Six out of 323 women were not successfully genotyped for IGFBP3 rs2854744 SNP using TaqMan. For those six women, rs2854744 genotypes were available from iPLEX and DNA sequencing from the previous study [8] (100% concordance) and used in the study models. For quality control of genotype data, more than 10% of the samples were run in duplicates, with 100% concordance. The genotyping success rate was ≥95% for all SNPs.
Diplotype assignment
The htSNPs were used to predict the most likely haplotypes and their corresponding diplotypes, i.e., paired haplotypes. Each of the htSNPs within IGFBP1 or IGFBP3 was cross-tabulated against the remaining htSNPs within their respective genes to generate possible linkage combinations and to identify non-existing or unlikely combinations. The most likely haplotypes were created and compared with previously published data [18]. The women were subsequently assigned to their most likely diplotypes. Diplotypes with an assignment of five women or fewer were combined together into a composite “rare diplotypes” category.
Follow-up
Women were considered at risk for breast cancer from age 18 and were followed until the development of a first breast cancer according to the Regional Cancer Registry, until the date of a self-reported prophylactic mastectomy or oophorectomy, or until May 31, 2009, whichever came first. The women in the study who were considered to have a high-risk of developing breast cancer were offered clinical follow-up including annual mammograms, ultrasounds or magnetic resonance imaging, and physical examination of the breasts. The report rate of the Swedish cancer registries is close to 100%.
Statistical analysis
The statistical software SPSS 17.0 was used for most analyses and the multivariate linear regression models were also adjusted for family clustering by using the cluster option of the regress command in STATA. For analyses of IGFBP-3 levels, the authors excluded women who were breast-feeding at blood draw (n = 4), women using hormonal contraceptives other than combined OCs (n = 19), or both (n = 1), as well as one woman who had not answered the question on hormonal contraceptive use, leaving 87 current OC users and 144 non-users. For SNP and diplotype analyses, frequencies and associations with circulating levels were calculated for all women as well as stratified according to OC status. Multivariate linear regression models were used to estimate the standardized [age (29 years), weight (ln 67 kg), and no current OC use] mean IGFBP-3 levels for each SNP. Non-linear additive effects for the minor allele were accounted for in the analyses through the use of dummy variables for each copy of the minor allele and the wild type allele as reference. An interaction term between OC status and cumulative number of SNP alleles was created.
Non-standardized means for circulating IGFBP-3 levels for each diplotype were obtained using one-sample t-tests. Kaplan–Meier survival analyses were used to investigate incident breast cancers after 18 years of age in relation to htSNPs or diplotypes. For healthy women, the authors censored at the woman’s age on May 31, 2009, or at the age of a prophylactic mastectomy. Nominal P values are presented. All P values were two-tailed.
Results
Frequencies of htSNPs in IGFBP1 and IGFBP3 and associations with IGFBP-3 levels
Several SNPs in IGFBP1 and IGFBP3 were associated with circulating IGFBP-3 levels (Table 2). The strongest associations with IGFBP-3 levels were observed with IGFBP1 (rs1995051 and rs4988515) and IGFBP3 (rs2471551 and rs2854744) (P < 0.05 for all). The minor alleles of IGFBP1 SNPs rs1995051 and rs4988515 were associated with lower IGFBP-3 levels. These minor alleles segregated at a higher frequency among women from BRCA2 families (35.5 and 20.6%, respectively) than among women from BRCA1 (25.4 and 7.5%, respectively) or BRCAX families (27.3 and 10.9%, respectively) (additional data given in Online Resource 1). Similarly, the heterozygous variant of the IGFBP3 rs2471551 was associated with lower IGFBP-3 levels. In contrast, the minor allele of the IGFBP3 rs2854744 was associated with higher IGFBP-3 levels. Women from BRCA2 families were less frequently homozygous for this variant allele (5.9%) than women from BRCA1 or BRCAX families (12.9 or 18.2%, respectively) (additional data given in Online Resource 1). These four SNPs were associated with changes in mean circulating IGFBP-3 levels ranging from 4% (rs2471551) to 12% (rs2854744). However, only rs2854744 remained significantly associated with circulating IGFBP-3 levels (nominal P = 0.0002) after adjustment for multiple testing. The differences in standardized mean IGFBP-3 levels according to rs2854744 genotype were 271 ng/ml (6%, P = 0.009) for heterozygotes (CA) and 547 ng/ml (12%, P = 0.0002) for homozygotes (AA) compared with the wild type (CC).
OC use influences IGFBP-3 levels and was considered as effect modifier of the SNP and IGFBP-3 level relationship. Hence, analyses were also stratified for OC use (Table 2). The mean IGFBP-3 levels were lower in the 144 non-users 4,768 ng/ml (95%CI: 4,636–4,899) than in the 87 current OC users 5,190 ng/ml (95%CI: 5,039–5,341). An interaction was observed between cumulative number of IGFBP1 SNP (rs3763497) and OC use (P interaction = 0.034).
Diplotype associations with circulating IGFBP-3 levels
Eight IGFBP1 and nine IGFBP3 diplotypes were created from four IGFBP1 and three IGFBP3 htSNPs, respectively, based on assignment to >5 women (Fig. 1). One additional composite group of each rare IGFBP1 and rare IGFBP3 diplotypes (≤5 women) were included in the analyses. Two IGFBP3 SNPs outside of the haplotype blocks (rs6670 and rs2453839) were excluded from the diplotype analyses.
Four IGFBP1 diplotypes and four IGFBP3 diplotypes were associated with changes in mean IGFBP-3 levels of >200 ng/ml relative to the mean level of 4,927 ng/ml for all women (Fig. 1). Among the four IGFBP1 diplotypes, GTAC/ACAT and the composite rare IGFBP1 diplotypes group were associated with decreased mean IGFBP-3 levels (−654 and −427 ng/ml, respectively), while two IGFBP1 diplotypes (GCGC/GCGC and GTAC/GTAC) were associated with increased mean IGFBP-3 levels (201 and 227 ng/ml, respectively). Among the IGFBP3 diplotypes, GCG/CCG and GCA/GCG were associated with decreased IGFBP-3 levels (−488 and −301 ng/ml, respectively), while GAG/GAG and the composite rare IGFBP3 diplotypes group were associated with increased IGFBP-3 levels (314 and 673 ng/ml, respectively). Using linear regression models, the adjusted mean IGFBP-3 level associated with the IGFBP1 diplotype GTAC/ACAT was significantly lower compared with the reference diplotype GCGC/GTAC (P = 0.004), adjusted for age, weight, OC use, and other IGFBP1 diplotypes. Similarly, the adjusted mean IGFBP-3 levels associated with the IGFBP3 diplotypes GCA/GCG and GCG/CCG were significantly lower compared with the reference diplotype GAG/GCA (P = 0.004 and P = 0.002, respectively). The associations between diplotypes and IGFBP-3 levels differed between OC users and non-users (Fig. 1). The IGFBP1 diplotype GCGC/ACGC had opposing associations on IGFBP-3 levels dependent on OC use, while the IGFBP-3 levels in GTAC/ACGC carriers was similar irrespective of OC status.
After adjusting the models for BRCA family status, both the BRCA1 and BRCA2 family status (P ≤ 0.006) and the IGFBP1 diplotype GTAC/ACAT (P = 0.004) were associated with lower IGFBP-3 levels, adjusted for age, weight, OC use, and other IGFBP diplotypes. Similarly, both the BRCA1 and BRCA2 family status (P ≤ 0.03) and the IGFBP3 diplotypes GCA/GCG (P = 0.007) and GCG/CCG (P = 0.002) were significantly associated with lower IGFBP-3 levels, adjusted for age, weight, OC use, and other IGFBP diplotypes. This suggests independent effects from IGFBP1, IGFBP3 diplotypes, and BRCA family status on IGFBP-3 levels. After adjustment for family clustering, all statistical associations between IGFBP1 and IGFBP3 diplotype data and IGFBP-3 levels remained.
Diplotype co-segregation with BRCA1/2 mutation status
Possible co-segregation of diplotype frequencies and BRCA family status were examined in all women (Figs. 2a, 3a) and in the first included woman from each family (Figs. 2b, 3b). GCGC/GTAC was the most common IGFBP1 diplotype across the BRCA1, BRCA2 and BRCAX families (Fig. 2a, b). As previously reported, IGFBP-3 levels were higher in BRCAX than in BRCA1/2 families [8]. Based on the corresponding IGFBP-3 levels, the diplotypes were sub-grouped into IGFBP1 low, IGFBP1 high, IGFBP3 low, and IGFBP3 high compared with the overall mean IGFBP-3 level. No evident co-segregation of IGFBP1 or IGFBP3 diplotypes was observed among the BRCA1 families. Women from BRCA2 families more frequently carried IGFBP1 diplotypes associated with lower IGFBP-3 levels (60.6%) OR 2.05 (95%CI 0.97–4.30) than women from BRCA1 or BRCAX families (40.8 or 45.5%, respectively) (Fig. 2a). In contrast, IGFBP3 diplotypes associated with higher IGFBP-3 levels (IGFBP3 high) co-segregated among BRCAX families (57.3%) OR 1.68 (95%CI 1.04–2.74) compared with women from BRCA1 or BRCA2 families (45.1 or 41.2%, respectively) (Fig. 3a).
Diplotypes associated with breast cancer
Against a background of a limited number of breast cancer cases (n=23), there was a non-significant tendency toward increased breast cancer incidence among women carrying a combination of IGFBP1 high and IGFBP3 high diplotypes (9/88, 10.2%) compared with IGFBP1 low and IGFBP3 low diplotypes (4/68, 5.9%). The incidences of breast cancer found among women carrying IGFBP1 low/IGFBP3 low diplotypes (4/69, 5.8%) and IGFBP1 high/IGFBP3 low diplotypes (6/91, 6.6%) were similar to the incidence of breast cancer among women with the IGFBP1 low/IGFBP3 low diplotypes. Among the 23 breast cancer cases, nine (39.1%) carried a IGFBP1 high/IGFBP3 high diplotype and only four (17.1%) carried a IGFBP1 low/IGFBP3 low diplotype (Fig. 4a). One IGFBP1 diplotype (GTAC/ACGC) showed a tendency toward being associated with decreased risk of breast cancer (log rank P = 0.050) (Fig. 4b).
Discussion
To our knowledge, this is the first study to examine genetic variants (SNPs) and diplotypes in the IGFBP1 and IGFBP3 genes in relation to both circulating IGFBP-3 levels and risk of breast cancer among women from BRCA1, BRCA2, or BRCAX families. Two SNPs in IGFBP1 and two SNPs in IGFBP-3 were associated with circulating IGFBP-3 levels, but no associations between individual SNPs and breast cancer incidence were found. Several diplotypes in IGFBP1 and IGFBP3 were associated with circulating IGFBP-3 levels. Breast cancer incidence was non-significantly higher among women carrying a combination of IGFBP1 high/IGFBP3 high diplotypes associated with higher circulating IGFBP-3 levels. The frequency of IGFBP1 high and IGFBP3 high diplotypes differed between women from BRCA1, BRCA2, or BRCAX families, which further reflected in significant differences in mean circulating IGFBP-3 levels.
The IGF axis plays important roles in normal physiology by regulating cell proliferation, differentiation, and apoptosis [3]. In addition, considerable evidence from laboratory, clinical, and epidemiological research demonstrates important roles of the IGF-I and its major binding protein IGFBP-3 in the development and progression of several tumor types, including breast cancer [3]. Large inter-individual variations in circulating levels of IGF-I and IGFBP-3 exist, which in part may be related to different genotypes. Previous studies have evaluated associations between circulating IGFBP-3 levels and risk of sporadic breast cancer in relation to individual IGFBP1 and IGFBP3 SNPs or haplotypes and reported conflicting results. Although many SNPs have been associated with the corresponding IGFBP-3 plasma levels, their respective associations with breast cancer risk have been inconsistent across studies. Reports from the Nurses Health Study II and from the NCI Breast and Prostate Cancer Cohort Consortium found associations between IGFBP3 polymorphisms and circulating IGFBP-3 levels, but no substantial influence on breast cancer risk [19, 20]. In some studies, genetic variants and IGFBP-3 levels were inversely associated with breast cancer risk [21, 22], while in other studies, IGFBP-3 levels were positively associated with breast cancer risk [7, 23]. In addition, meta-analyses report that high circulating IGFBP-3 levels were associated with increased risk of premenopausal breast cancer [24, 25].
The results presented herein suggest that women carrying the heterozygous variant of IGFBP1 SNPs rs1995051, rs4988515 or IGFBP3 SNP rs2471551 have lower IGFBP-3 levels, consistent with results observed by others [26]. Notably, these all heterozygous variants co-segregated among women from BRCA2 families. A recent study reported positive associations for the rare allele of the extensively studied IGFBP3 rs2854744 (A-202C) with both IGFBP-3 levels and proliferative benign breast disease, a marker of increased breast cancer risk [6]. The higher circulating IGFBP-3 levels observed with the AA genotype are consistent with the functional differences between the A and C alleles indicated in vitro, describing significantly higher promoter activity of the A allele compared to the C allele [15, 16]. Consistent with these findings, our group has previously reported that women carrying the AA genotype have higher IGFBP-3 levels and that this genetic variant segregated at a higher frequency among women from BRCAX families in the present study population [8], while the CC genotype segregated among women from BRCA1 families [8]. However, there were residual effects of BRCA family status on IGFBP-3 levels beyond the effect of the rs2854744 genotype and beyond the effects of diplotypes.
Although mutations in the high-penetrance BRCA1 and BRCA2 genes predispose to early-onset breast cancer, considerable individual variation in tumor incidence and onset exist. In addition, only one-third of women from Swedish high-risk breast cancer families carry disease-causing mutations in BRCA1 and BRCA2. Considering that differences in individual breast cancer susceptibility probably result from the additive effect of multiple genetic variants, where each variant contribute but a modest risk increase [2], associations between in vivo IGFBP-3 levels and IGFBP1 and IGFBP3 diplotypes were investigated. The diplotype analyses revealed significant variation in circulating IGFBP-3 levels between the highest and lowest IGFBP1 diplotypes (range ~900 ng/ml). Interestingly, the homozygous IGFBP1 diplotypes were all associated with the highest IGFBP-3 levels. Similar variation was observed for the IGFBP3 diplotype associations with circulating IGFBP-3 levels (range ~1,100 ng/ml). Two out of three homozygous IGFBP3 diplotypes, of which one contained the AA genotype of IGFBP3 SNP rs2854744, were associated with the highest IGFBP-3 levels.
By applying diplotype analyses in preference to individual SNP analyses, a tendency toward increased breast cancer incidence among women carrying a combination of IGFBP1 high /IGFBP3 high diplotypes was found. The higher frequency of IGFBP3 high diplotypes among BRCAX families implies that the subgroup of these women who carry a combination of IGFBP1 high/IGFBP3 high diplotypes may have an increased breast cancer risk related to high IGFBP-3 levels. This is the first study where IGFBP1 and IGFBP3 diplotype analyses have been applied to examine influence on breast cancer risk; previous studies have only examined haplotype data [19–21]. One IGFBP1 diplotype (GTAC/ACGC) was borderline associated with decreased breast cancer incidence after age 18. However, these observations warrant replication in larger study populations.
Current OC use increases the overall mean circulating IGFBP-3 levels [8, 9]. However, the associations between diplotypes and IGFBP-3 levels differed between OC users and non-users. The variations present at position 2 and 3 in the IGFBP1 GCGC/ACGC and GTAC/ACGC diplotypes suggest that the CC and GG genotypes of these polymorphisms may causally influence IGFBP-3 levels during OC use, or tag for other unknown functional SNPs. These data suggest that women from high-risk families carrying specific combinations of IGFBP1 and IGFBP3 diplotypes may be more susceptible to IGFBP-3 level modulation by OC use, which could further modify their risk of breast cancer. Further studies and the identification of causal mechanisms are needed to better understand how these genotypes and diplotypes may modify non-genetic factors related to IGFBP-3.
In conclusion, this is the first study to investigate associations between multiple genetic polymorphisms and diplotypes in IGFBP1 and IGFBP3, and circulating IGFBP-3 levels among women from BRCA1, BRCA2, or BRCAX families. The present findings suggest that individual SNPs and diplotypes are associated with circulating IGFBP-3 levels. These associations vary according to OC status and may influence the risk of breast cancer among women from high-risk breast cancer families. A co-segregation of IGFBP1 low diplotypes among BRCA2 families and of IGFBP3 high diplotypes among BRCAX families was observed. This study highlights the informative advantage of applying diplotype analyses over individual SNPs or haplotypes. The findings warrant confirmation in independent study populations.
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Acknowledgments
We thank our research nurses Kerstin Nilsson, Monica Pehrsson, and Anita Schmidt-Casslén for their assistance with body measurements and blood drawing and Johanna Wagenius, Johanna Frenander, Helen Sundberg, Malin Sternby, and Susanna Holmquist for their assistance with recruitment. We also thank Dr Pär-Ola Bendahl for assistance with the family clustering analyses and Dr. Eric T. Dryver for proofreading the manuscript. This study was supported by grants from Vetenskapsrådet (the Swedish Research Council, K2001-27GX-14120-01A and K2008-68X20802-01-3), the Medical Faculty, Lund University, the Mrs. Berta Kamprad’s Foundation, the Gunnar Nilsson Foundation, the Crafoord Foundation, the South Swedish Health Care Region (Region Skåne), Lund Hospital Fund and the Swedish Cancer Society.
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Rosendahl, A.H., Hietala, M., Henningson, M. et al. IGFBP1 and IGFBP3 polymorphisms predict circulating IGFBP-3 levels among women from high-risk breast cancer families. Breast Cancer Res Treat 127, 785–794 (2011). https://doi.org/10.1007/s10549-010-1277-1
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DOI: https://doi.org/10.1007/s10549-010-1277-1