Abstract
Variants in microRNA genes may affect their expression by interfering with the microRNA maturation process and may substantially contribute to the risk of breast cancer. Recent studies have identified miR-10b as an interesting candidate because of its close association with the metastatic behavior of breast cancer. However, the roles of miR-10b-related single nucleotide polymorphisms in breast cancer susceptibility remain unclear. This case-control study evaluated the associations between variants in the upstream transcription regulation region of miR-10b and the risk of breast cancer among Chinese women. Seven potentially functional SNPs were investigated using genotyping assays. The potential biological functions of the identified positive SNPs were further evaluated using in silico databases. We found that rs4078756, which was located at the promoter region of miR-10b, was significantly associated with breast cancer risk (rs4078756 AG/GG versus AA, adjusted odds ratio: 1.17, 95% confidence interval: 1.02–1.35). The other six single nucleotide polymorphisms exhibited negative associations. Based on the in silico prediction, rs4078756 potentially regulated miR-10b expression through promoter activation or repression. These findings indicate that a potentially functional SNP (rs4078756) in the promoter region of miR-10b may contribute to breast cancer susceptibility among Chinese women.
1. Introduction
Breast cancer is the most common malignancy among women, with an estimated 1.7 million cases diagnosed worldwide in 2012 [1]. In China, breast cancer is the most common cancer among women and is the sixth most common cause of death among Chinese women [2]. The precise mechanisms underlying breast cancer have not been fully explored, although several strong genetic and environmental risk factors for breast cancer have been identified and have been addressed in public awareness campaigns and clinical monitoring strategies [3, 4].
Recent research has revealed that microRNAs (miRNAs) participate in human carcinogenesis as either tumor suppressors or oncogenes, and the disruption of specific miRNA expression levels and functions might play a key role in the genesis of diverse cancer types [5–7]. Abnormal expressions of many miRNAs, including miR-34a, miR-210, miR-567, and miR-10b, were also associated with breast cancer tumorigenesis or progression [8–11]. As a key molecule in the development of breast cancer, miR-10b was first identified as being downregulated in primary breast tumors, compared to normal breast samples [11]. However, Ma et al. reported conflicting findings in 2007, as they observed that miR-10b was upregulated in metastatic breast cancer [12]. Subsequent studies have revealed that overexpression of miR-10b triggered migration and invasion processes in various cancer cell lines, as well as distant metastasis in xenotransplantation models [12–18]. Furthermore, miR-10b exerted its oncogenic effects by directly targeting various tumor-associated genes, such as HOXD10, TBX5, KLF4, and PTEN, in breast cancer, pancreatic cancer, glioblastoma, and bladder cancer [12–19]. These findings indicate that miR-10b plays a central role in cancer metastasis and may be used as a biomarker for breast cancer carcinogenesis.
A growing number of studies have revealed that single nucleotide polymorphisms (SNPs) in miRNA genes may interfere with the miRNA transcription or maturation processes and are associated with susceptibility to cancer development [20–26]. For example, rs116159732 in the miR-6826 primary sequence was associated with breast cancer among women of African ancestry [22]. In addition, rs11614913 in the miR-196a2 precursor sequence may affect the miRNA-196a2 maturation process and is associated with the risk of breast cancer among Chinese and American women [23–25]. Furthermore, rs2682818 in the stem-loop sequence of the miR-618 precursor may alter the secondary stem-loop structure and is associated with an increased breast cancer risk in a South American population [26]. However, we are not aware of any studies regarding the role of miR-10b SNPs in breast cancer risk. Nevertheless, given the important biological functions of miR-10b in breast cancer, polymorphisms in the miR-10b gene could potentially confer a risk of disease. Therefore, the present study used a case-control design to evaluate 7 potentially functional SNPs in the upstream transcription regulation region of the miR-10b gene. All candidate SNPs had a minor allele frequency (MAF) of ≥0.05 among Han Chinese women. We hope that the results can provide useful insights for breast cancer prevention and personalized treatment.
2. Materials and Methods
2.1. Study Population
This case-control study's protocol was approved by the Institutional Review Board of Nanjing Medical University. A total of 1,064 breast cancer cases and 1,073 cancer-free controls were included in this study, which has been described previously [27]. Briefly, the patients were recruited between January 2004 and April 2010 at the First Affiliated Hospital of Nanjing Medical University, Gulou Hospital, and Cancer Hospital of Jiangsu Province (Nanjing, China). The diagnosis of breast cancer was confirmed using pathological examination. Patients with a history of cancer, radiotherapy, or chemotherapy were excluded. Cancer-free controls were randomly selected from a pool of individuals who voluntarily participated in a community-based screening program that was performed in Jiangsu Province during the same time period. The controls had no self-reported history of cancer and were frequency-matched with the cases according to age and residential area. All subjects were genetically unrelated Han Chinese women. Approximately 95% of the eligible population provided written informed consent for participation. Each participant completed an interview using a structured questionnaire to collect information regarding the demographic characteristics, menstrual history, reproductive history, and environmental exposure history. Information regarding the estrogen receptor (ER) and progesterone receptor (PR) statuses of breast cancer cases was extracted from their medical records. After each interview, a 5 mL venous blood sample was collected from each participant.
2.2. SNP Selection and Genotyping Assays
The miR-10b gene is located at 2q31.1, which is in an intergenic region between HOXD4 and HOXD8 genes. Its promoter has recently been identified in human mammary cells and is located approximately 12 kb upstream of precursor miR-10b (pre-miR-10b) [28]. We searched the International HapMap Project (http://www.hapmap.org), dbSNP (http://www.ncbi.nlm.nih.gov/projects/SNP/), SNAP (http://archive.broadinstitute.org/mpg/snap/), and UCSC (http://genome.ucsc.edu/) databases for SNPs that were located between the promoter and pre-miR-10b. The linkage disequilibrium (LD) value (r2 < 0.8) and MAF value (≥0.05) in the Chinese Han population were also applied to select candidate SNPs. We ultimately identified nine SNPs (rs3731795, rs79025511, rs4078756, rs1348807, rs1018827, rs6736786, rs10196832, rs4972806, and rs1867863) in the upstream region of pre-miR-10b, although we omitted rs3731795 and rs79025511 because of their high LD with rs4078756 (r2 > 0.8) to optimize the assay. Thus, seven SNPs in the miR-10b transcript were genotyped for the present case-control study (Table 1).
Table 1.
SNP | Chr | Position | Location | Allelesa | Casesb N = 1,064 |
Controlsb N = 1,073 |
Call rate (%) | MAFc (case/control) |
HWEd | OR (95% CI)e | P valuee |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4078756 | 2q31.1 | 177,004,115 | 11 kb upstream of pre-mir-10b | A/G | 540/436/84 | 582/425/66 | 97.80 | 0.285/0.260 | 0.341 | 1.17 (1.02–1.35) | 0.027 |
rs1348807 | 2q31.1 | 177,005,757 | 9.3 kb upstream of pre-mir-10b | A/G | 403/499/156 | 391/507/171 | 97.52 | 0.383/0.398 | 0.750 | 0.91 (0.80–1.03) | 0.148 |
rs10188827 | 2q31.1 | 177,007,664 | 7.5 kb upstream of pre-mir-10b | A/G | 514/448/99 | 502/471/99 | 97.85 | 0.304/0.312 | 0.477 | 0.92 (0.80–1.05) | 0.210 |
rs6736786 | 2q31.1 | 177,008,914 | 6 kb upstream of pre-mir-10b | A/G | 419/495/148 | 446/495/132 | 97.89 | 0.372/0.354 | 0.79 | 1.13 (0.99–1.29) | 0.066 |
rs10196832 | 2q31.1 | 177,011,655 | 3.5 kb upstream of pre-mir-10b | A/G | 936/127/1 | 920/143/7 | 97.89 | 0.061/0.073 | 0.502 | 0.87 (0.68–1.12) | 0.281 |
rs4972806 | 2q31.1 | 177,012,578 | 2.5 kb upstream of pre-mir-10b | A/G | 352/512/197 | 361/529/183 | 97.85 | 0.427/0.417 | 0.706 | 1.03 (0.91–1.17) | 0.643 |
rs1867863 | 2q31.1 | 177,014,970 | 161 bp upstream of pre-mir-10b | A/C | 434/488/140 | 403/519/151 | 97.89 | 0.362/0.383 | 0.477 | 0.90 (0.79–1.02) | 0.105 |
aMajor/minor allele; bmajor homozygote/heterozygote/rare homozygote between cases and controls; cminor allele frequency (MAF); dPvalues for the Hardy-Weinberger equilibrium (HWE) test; elogistic regression analysis with adjustment for age, age at menarche, and menopausal status in the additive model; Chr: chromosome, OR: odds ratio, CI: confidence interval.
The seven SNPs were genotyped using the Illumina Infinium® HumanExome BeadChip platform (Illumina, USA) and 2,137 DNA samples, which have been reported in the previous study [27]. Genotype calling was performed using Illumina's GenTrain clustering algorithm (version 1.0) in GenomeStudio (V2011.1). The genotyping call rates for all SNPs were >97% among the 1,064 breast cancer cases and the 1,073 controls. Genotyping was performed without knowledge of the individual's case or control status, and approximately equal numbers of case and control samples were tested during each assay, with two blank controls.
2.3. Statistical Analyses
Differences in demographic characteristics, selected variables, and genotype frequencies were compared between the cases and controls. These differences were evaluated using Student's t-test (equal variance assumed) for continuous variables and the χ2 test for categorical variables. The Hardy-Weinberg equilibrium was tested using the goodness-of-fit χ2 test to compare the observed and expected genotype frequencies among the control subjects.
Associations between the genotypes and breast cancer risk were estimated using logistic regression analyses adjusted for age, age at menarche, and menopausal status. The effects were reported as odds ratios (ORs) and 95% confidence intervals (CIs). All statistical analyses were performed using SAS software (version 9.1.3; SAS Institute, Cary, NC, USA). P values of ≤0.05 were considered statistically significant.
3. Results
3.1. Associations between the Selected SNPs and Breast Cancer Risk
The included individuals' basic characteristics are presented in Supplementary Table 1 in Supplementary Material available online at https://doi.org/10.1155/2017/2352874. After frequency matching, the cases and controls had comparable ages (P > 0.05). Compared to the controls, patients with breast cancer had significantly earlier menarche and later first live births (P < 0.0001). Among the 1,064 breast cancer cases, 490 cases (46.05%) were ER-positive and 506 cases (47.56%) were PR-positive.
The loci information and association results for the seven SNPs are described in Table 1. The multivariate logistic regression models revealed that rs4078756 was significantly associated with breast cancer risk (rs4078756 AG/GG versus AA, adjusted OR: 1.17, 95% CI: 1.02–1.35). The remaining six SNPs were not significantly associated with breast cancer risk (Table 1).
We also performed stratification analysis of the associations between rs4078756 and breast cancer risk according to age, age at menarche, age at first live birth, and menopausal status. As shown in Table 2, the breast cancer risk associated with variant AG/GG genotypes (versus the AA genotype) was significantly higher among older women (adjusted OR: 1.32; 95% CI: 1.08–1.61), postmenopausal women (adjusted OR: 1.26; 95% CI: 1.03–1.54), women with later menarche (adjusted OR: 1.29; 95% CI: 1.06–1.56), ER-positive women (adjusted OR: 1.27; 95% CI: 1.07–1.52), and PR-positive women (adjusted OR: 1.34; 95% CI: 1.12–1.60). No heterogeneity was detected for each paired comparison (P > 0.05).
Table 2.
Characteristics | Cases | Controls | OR (95% CI)a | P | P b | ||||
---|---|---|---|---|---|---|---|---|---|
AA (%) | AG (%) | GG (%) | AA (%) | AG (%) | GG (%) | ||||
Age | |||||||||
<51 years | 312 (53.0) | 242 (41.1) | 35 (5.9) | 289 (53.3) | 226 (41.7) | 27 (5.0) | 1.05 (0.86–1.28) | 0.648 | 0.111 |
≥51 years | 228 (48.4) | 194 (41.2) | 49 (10.4) | 293 (55.2) | 199 (37.5) | 39 (7.3) | 1.32 (1.08–1.61) | 0.007 | |
Menopausal status | |||||||||
Premenopausal | 266 (51.9) | 211 (41.1) | 36 (7.0) | 267 (53.0) | 212 (42.1) | 25 (5.0) | 1.15 (0.93–1.42) | 0.197 | 0.540 |
Postmenopausal | 217 (48.2) | 194 (43.1) | 39 (8.7) | 286 (54.5) | 201 (38.3) | 38 (7.2) | 1.26 (1.03–1.54) | 0.028 | |
Age at menarche | |||||||||
<16 years | 320 (53.5) | 236 (39.5) | 42 (7.0) | 217 (52.8) | 172 (41.9) | 22 (5.4) | 1.03 (0.84–1.26) | 0.799 | 0.115 |
≥16 years | 211 (47.5) | 192 (43.2) | 41 (9.2) | 363 (55.0) | 253 (38.3) | 44 (6.7) | 1.29 (1.06–1.56) | 0.010 | |
Age at first live birth | |||||||||
<24 years | 119 (49.6) | 104 (43.3) | 17 (7.1) | 204 (55.0) | 140 (37.7) | 27 (7.3) | 1.18 (0.90–1.53) | 0.229 | 0.831 |
≥24 years | 392 (52.0) | 301 (39.9) | 61 (8.1) | 358 (53.4) | 276 (41.1) | 37 (5.5) | 1.14 (0.96–1.36) | 0.141 | |
ER status | |||||||||
Positive | 237 (48.6) | 211 (43.2) | 40 (8.2) | 1.27 (1.07–1.52) | 0.008 | 0.713 | |||
Negative | 194 (51.5) | 146 (38.7) | 37 (9.8) | 1.21 (1.0–1.46) | 0.055 | ||||
PR status | |||||||||
Positive | 237 (46.9) | 223 (44.2) | 45 (8.9) | 1.34 (1.12–1.60) | 0.001 | 0.204 | |||
Negative | 192 (53.3) | 136 (37.8) | 32 (8.9) | 1.13 (0.93–1.37) | 0.235 |
aPer-allele odds ratio (OR) and 95% confidence interval (CI) adjusted for age, age at menarche, and menopausal status where appropriate; bP value for the heterogeneity test; ER: estrogen receptor; PR: progesterone receptor.
3.2. Bioinformatics Analysis of the Potentially Biological Functions of rs4078756
The potential biological functions of rs4078756 were evaluated using bioinformatics analysis with HaploRegV4.1 and the UCSC database. As shown in Table 3, rs3731795 and rs79025511 exhibited strong linkage with rs4078756 (r2 > 0.8) in Chinese and Japanese population and were strongly modified by histone H3K27Ac, which might lead to aberrant transcription of miR-10b (Figure 1). Based on the JASPAR database for predicting transcription factor binding, we found that the G allele of rs3731795 might increase the binding of transcription factors, such as TCF3, TFAP2A, and TCF4, to the promoter of miR-10b, compared to the C allele (Table 4).
Table 3.
Chr | Pos (hg19) |
LD (r2) |
Variant | Ref | Alt | ASN freq | Promoter histone marks | DNAse | Proteins bound | Motifs changed |
---|---|---|---|---|---|---|---|---|---|---|
2 | 177000616 | 1.00 | rs1348808 | T | C | 0.23 | 15 tissues | 12 tissues | CTBP2 | Ets, LF-A1, NF-E2 |
2 | 177001145 | 1.00 | rs76652183 | G | T | 0.23 | 19 tissues | 18 tissues | 5 bound proteins | EBF |
2 | 177001378 | 1.00 | rs3731795 | A | G | 0.27 | 19 tissues | 7 tissues | CTCF, p300 | |
2 | 177001962 | 0.96 | rs79025511 | C | T | 0.23 | 19 tissues | MUS, MUS | Gcm1 | |
2 | 177004689 | 0.92 | rs72927149 | G | C | 0.23 | 12 tissues | 6 tissues | Pax-5 | |
2 | 177005519 | 1.00 | rs79120932 | G | T | 0.23 | 19 tissues | 32 tissues | 5 bound proteins | 4 altered motifs |
2 | 177007102 | 1.00 | rs67435554 | G | T | 0.23 | ||||
2 | 177007527 | 1.00 | rs76363873 | A | G | 0.23 | IPSC | GATA, MZF1::1–4 | ||
2 | 177008484 | 1.00 | rs79440139 | T | A | 0.23 | 6 altered motifs |
Chr: chromosome, Pos: position, LD: linkage disequilibrium in CHB + JPT population, Ref: reference, Alt: alternative, freq: frequency, MUS: musculus, and IPSC: induced pluripotent stem cell.
Table 4.
Motif | Relative score | Start | End | Strand | Predicted | |
---|---|---|---|---|---|---|
A allele | G allele | site sequence | ||||
TCF3 | 0.610 | 0.804 | 11 | 20 | −1 | GTGACTG |
TFAP2A | 0.685 | 0.873 | 11 | 19 | 1 | CGGTGA |
TCF4 | 0.649 | 0.807 | 11 | 20 | −1 | TCCAGTCACC |
NRF1 | 0.648 | 0.805 | 8 | 18 | −1 | AGCCGGTGA |
TFAP2A | 0.767 | 0.875 | 8 | 16 | −1 | AGCCGGTGACT |
TFAP2A | 0.757 | 0.801 | 10 | 20 | −1 | TGACTGG |
4. Discussion
The present study investigated the associations between breast cancer and seven potentially functional SNPs that were located in the upstream transcription regulation region of the miR-10b gene. The results indicate that an A-to-G base change at rs4078756 increased the risk of breast cancer among a group of Han Chinese women. To the best of our knowledge, this is the first study to evaluate the associations between breast cancer susceptibility and genetic variations in the potential regulatory region of miR-10b.
Previous research has indicated that miR-10b appears to play a key role in breast cancer invasion and metastasis. Ma et al. reported that miR-10b was highly expressed in clinical samples of metastatic breast cancer, and the ectopic upregulation of miR-10b in nonmetastatic breast cancer cells initiated invasion and metastasis [12]. Moreover, miR-10b silencing inhibits breast cancer metastasis in a mouse mammary tumor model [12, 13]. Additional studies have suggested that miR-10b regulates invasion and metastasis in breast cancer by suppressing the translation of a targeting gene (HOXD10) [12]. In this context, HOXD10 is an mRNA encoding a transcriptional repressor that inhibits the expression of several genes that are involved in cell migration and extracellular matrix remodeling, such as RhoC, uPAR, α3 integrin, and MT1-MMP [12]. Furthermore, miR-10b could target the syndecan-1 gene and promoted breast cancer cell motility and invasiveness through a Rho-GTPase-dependent and E-cadherin-dependent mechanism [29]. Another study revealed that miR-10b promotes cell proliferation, migration, and invasion by inhibiting the expression of the TBX5 transcription factor, which led to repression of the DYRK1A and PTEN tumor suppressor genes [19]. In addition, miR-10b could respond to vascular endothelial growth factor stimulation and was expressed at high levels in the human high-grade breast tumor vasculature, which suggested that vascular expression of miR-10b might reflect the metastatic progression of breast cancer [30].
Similar to other protein-coding genes, the miR-10b gene has its own promoter. The putative promoter of human miR-10b was initially characterized by Zhou et al., who found that it spanned between –111 bp and –460 bp upstream of pre-miR-10b [31]. Ma et al. also found that the Twist transcription factor could activate transcription of the miR-10b gene by binding to an E-box sequence that is proximal to its putative promoter [12]. Vrba et al. subsequently performed H3K4me3 chromatin immunoprecipitation assays using human mammary cells and redefined the promoter region of miR-10b as being located approximately 12 kb upstream of pre-miR-10b [28]. Several researchers have also suggested that SNPs in the promoter region of important miRNA genes may be ideal disease biomarkers. For example, our group reported that two SNPs (rs4938723 and rs999885) in the promoter region of the miR-34b/c and miR-106b-25 cluster were significantly associated with the risk of hepatocellular carcinoma [32, 33]. Luo et al. also identified and confirmed an association between the rs57095329 promoter variant of miR-146a and systemic lupus erythematosus. Combined functional assays revealed that the risk-associated G allele of the rs57095329 had decreased binding to the Ets-1 transcription factor, which contributed to the reduced levels of miR-146a in patients with systemic lupus erythematosus [34]. Furthermore, the results of the present study revealed a significant association between rs4078756 in the miR-10b promoter region and an increased risk of breast cancer. Moreover, we found that the risk effects of the rs4078756 variant genotypes were statistically significant in some subgroups, such as women who were older, postmenopausal, ER-positive, and PR-positive and had later menarche. However, the heterogeneity tests revealed no significant heterogeneity for each paired comparison (P > 0.05), which suggests that these variables did not modify the risk effect.
The present study also revealed that rs4078756 is located approximately 11 kb upstream of pre-miR-10b, and is a SNP that has strong linkage with rs3731795 in the defined promoter region of miR-10b (r2 = 1). Based on the UCSC and ENCODE databases, rs3731795 lies in the maximum peak of the H3k27me3 histone mark in seven cell lines, and this mark is often found near active regulatory elements. In addition, according to JASPAR database, we observed that the G allele of rs3731795 might increase the binding of transcription factors, such as TCF3, TFAP2A, and TCF4, to the promoter of miR-10b. These transcription factors are involved in gene regulation through promoter activation or repression, depending on the specific interacting protein. However, these speculations are based on computer simulations and require confirmation using biological assays in future studies.
In conclusion, the present results suggest that rs4078756 in the promoter region of the miR-10b gene is associated with a significantly increased risk of breast cancer among Han Chinese women. Larger well-designed epidemiological studies with ethnically diverse populations and functional evaluations are warranted to confirm these findings.
Supplementary Material
Acknowledgments
The authors thank the study participants and research staff for their contributions. Funding was provided by the Natural Science Foundation of Jiangsu Province (BK20151553), the Natural Science Foundation for Outstanding Youth of Jiangsu Province (BK20160095), the National Natural Science Foundation of China (81521004, 81230067), the Priority Academic Program for the Development of Jiangsu Higher Education Institutions (Public Health and Preventive Medicine), and the Top-notch Academic Programs Project of Jiangsu Higher Education Institutions (PPZY2015A067).
Conflicts of Interest
The authors declare that there are no conflicts of interest.
References
- 1.Torre L. A., Bray F., Siegel R. L., Ferlay J., Lortet-Tieulent J., Jemal A. Global cancer statistics, 2012. CA:A Cancer Journal for Clinicians. 2015;65(2):87–108. doi: 10.3322/caac.21262. [DOI] [PubMed] [Google Scholar]
- 2.Chen W., Zheng R., Baade P. D., et al. Cancer statistics in China, 2015. CA:A Cancer Journal for Clinicians. 2016;66(2):115–132. doi: 10.3322/caac.21338. [DOI] [PubMed] [Google Scholar]
- 3.Lichtenstein P., Holm N. V., Verkasalo P. K., et al. Environmental and heritable factors in the causation of cancer: analyses of cohorts of twins from Sweden, Denmark, and Finland. The New England Journal of Medicine. 2000;343(2):78–85. doi: 10.1056/NEJM200007133430201. [DOI] [PubMed] [Google Scholar]
- 4.Shields P. G., Harris C. C. Cancer risk and low-penetrance susceptibility genes in gene-environment interactions. Journal of Clinical Oncology. 2000;18(11):2309–2315. doi: 10.1200/JCO.2000.18.11.2309. [DOI] [PubMed] [Google Scholar]
- 5.Lu J., Getz G., Miska E. A., et al. MicroRNA expression profiles classify human cancers. Nature. 2005;435(7043):834–838. doi: 10.1038/nature03702. [DOI] [PubMed] [Google Scholar]
- 6.Calin G. A., Croce C. M. MicroRNA signatures in human cancers. Nature Reviews Cancer. 2006;6(11):857–866. doi: 10.1038/nrc1997. [DOI] [PubMed] [Google Scholar]
- 7.Adams B. D., Kasinski A. L., Slack F. J. Aberrant regulation and function of microRNAs in cancer. Current Biology. 2014;24(16):R762–R776. doi: 10.1016/j.cub.2014.06.043. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Bertoli G., Cava C., Diceglie C., et al. MicroRNA-567 dysregulation contributes to carcinogenesis of breast cancer, targeting tumor cell proliferation, and migration. Breast Cancer Research and Treatment. 2016;161(3):605–616. doi: 10.1007/s10549-016-4079-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Peurala H., Greco D., Heikkinen T., et al. MiR-34a expression has an effect for lower risk of metastasis and associates with expression patterns predicting clinical outcome in breast cancer. PLoS ONE. 2011;6(11) doi: 10.1371/journal.pone.0026122.e26122 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Rothé F., Ignatiadis M., Chaboteaux C., et al. Global microRNA expression profiling identifies MiR-210 associated with tumor proliferation, invasion and poor clinical outcome in breast cancer. PLoS ONE. 2011;6(6) doi: 10.1371/journal.pone.0020980.e20980 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Iorio M. V., Ferracin M., Liu C.-G., et al. MicroRNA gene expression deregulation in human breast cancer. Cancer Research. 2005;65(16):7065–7070. doi: 10.1158/0008-5472.CAN-05-1783. [DOI] [PubMed] [Google Scholar]
- 12.Ma L., Teruya-Feldstein J., Weinberg R. A. Tumour invasion and metastasis initiated by microRNA-10b in breast cancer. Nature. 2007;449(7163):682–688. doi: 10.1038/nature06174. [DOI] [PubMed] [Google Scholar]
- 13.Ma L., Reinhardt F., Pan E., et al. Therapeutic silencing of miR-10b inhibits metastasis in a mouse mammary tumor model. Nature Biotechnology. 2010;28(4):341–347. doi: 10.1038/nbt.1618. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Xiao H., Li H., Yu G., et al. MicroRNA-10b promotes migration and invasion through KLF4 and HOXD10 in human bladder cancer. Oncology Reports. 2014;31(4):1832–1838. doi: 10.3892/or.2014.3048. [DOI] [PubMed] [Google Scholar]
- 15.Liao C.-G., Kong L.-M., Zhou P., et al. MiR-10b is overexpressed in hepatocellular carcinoma and promotes cell proliferation, migration and invasion through RhoC, uPAR and MMPs. Journal of Translational Medicine. 2014;12(1, article 234) doi: 10.1186/s12967-014-0234-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Tian Y., Luo A., Cai Y., et al. MicroRNA-10b promotes migration and invasion through KLF4 in human esophageal cancer cell lines. Journal of Biological Chemistry. 2010;285(11):7986–7994. doi: 10.1074/jbc.M109.062877. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Li G., Wu Z., Peng Y., et al. MicroRNA-10b induced by Epstein-Barr virus-encoded latent membrane protein-1 promotes the metastasis of human nasopharyngeal carcinoma cells. Cancer Letters. 2010;299(1):29–36. doi: 10.1016/j.canlet.2010.07.021. [DOI] [PubMed] [Google Scholar]
- 18.Liu S., Sun J., Lan Q. TGF-β-induced miR10a/b expression promotes human glioma cell migration by targeting PTEN. Molecular Medicine Reports. 2013;8(6):1741–1746. doi: 10.3892/mmr.2013.1709. [DOI] [PubMed] [Google Scholar]
- 19.Kim J., Siverly A. N., Chen D., et al. Ablation of miR-10b suppresses oncogene-induced mammary tumorigenesis and metastasis and reactivates tumor-suppressive pathways. Cancer Research. 2016;76(21):6424–6435. doi: 10.1158/0008-5472.CAN-16-1571. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Ryan B. M., Robles A. I., Harris C. C. Genetic variation in microRNA networks: the implications for cancer research. Nature Reviews Cancer. 2010;10(6):389–402. doi: 10.1038/nrc2867. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Cammaerts S., Strazisar M., De Rijk P., Del Favero J. Genetic variants in microRNA genes: impact on microRNA expression, function, and disease. Frontiers in Genetics. 2015;6, article 186 doi: 10.3389/fgene.2015.00186. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Qian F., Feng Y., Zheng Y., et al. Genetic variants in microRNA and microRNA biogenesis pathway genes and breast cancer risk among women of African ancestry. Human Genetics. 2016;135(10):1145–1159. doi: 10.1007/s00439-016-1707-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Hu Z., Liang J., Wang Z., et al. Common genetic variants in pre-microRNAs were associated with increased risk of breast cancer in Chinese women. Human Mutation. 2009;30(1):79–84. doi: 10.1002/humu.20837. [DOI] [PubMed] [Google Scholar]
- 24.Hu Z., Chen J., Tian T., et al. Genetic variants of miRNA sequences and non small cell lung cancer survival. Journal of Clinical Investigation. 2008;118(7):2600–2608. doi: 10.1172/JCI34934. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Hoffman A. E., Zheng T., Yi C., et al. microRNA miR-196a-2 and breast cancer: A genetic and epigenetic association study and functional analysis. Cancer Research. 2009;69(14):5970–5977. doi: 10.1158/0008-5472.CAN-09-0236. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Upadhyaya A., Smith R. A., Chacon-Cortes D., et al. Association of the microRNA-single nucleotide polymorphism rs2910164 in miR146a with sporadic breast cancer susceptibility: a case control study. Gene. 2016;576(1, part 1):256–260. doi: 10.1016/j.gene.2015.10.019. [DOI] [PubMed] [Google Scholar]
- 27.Qin Z., Xue J., He Y., et al. Potentially functional polymorphisms in ATG10 are associated with risk of breast cancer in a Chinese population. Gene. 2013;527(2):491–495. doi: 10.1016/j.gene.2013.06.067. [DOI] [PubMed] [Google Scholar]
- 28.Vrba L., Garbe J. C., Stampfer M. R., Futscher B. W. Epigenetic regulation of normal human mammary cell type-specific miRNAs. Genome Research. 2011;21(12):2026–2037. doi: 10.1101/gr.123935.111. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Ibrahim S. A., Yip G. W., Stock C., et al. Targeting of syndecan-1 by microRNA miR-10b promotes breast cancer cell motility and invasiveness via a Rho-GTPase- and E-cadherin-dependent mechanism. International Journal of Cancer. 2012;131(6):E884–E896. doi: 10.1002/ijc.27629. [DOI] [PubMed] [Google Scholar]
- 30.Plummer P. N., Freeman R., Taft R. J., et al. MicroRNAs regulate tumor angiogenesis modulated by endothelial progenitor cells. Cancer Research. 2013;73(1):341–352. doi: 10.1158/0008-5472.CAN-12-0271. [DOI] [PubMed] [Google Scholar]
- 31.Zhou X., Ruan J., Wang G., Zhang W. Characterization and identification of microRNA core promoters in four model species. PLoS Computational Biology. 2007;3(3):0412–0423. doi: 10.1371/journal.pcbi.0030037. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Xu Y., Liu L., Liu J., et al. A potentially functional polymorphism in the promoter region of miR-34b/c is associated with an increased risk for primary hepatocellular carcinoma. International Journal of Cancer. 2011;128(2):412–417. doi: 10.1002/ijc.25342. [DOI] [PubMed] [Google Scholar]
- 33.Liu Y., Zhang Y., Wen J., et al. A genetic variant in the promoter region of mir-106b-25 cluster and risk of hbv infection and hepatocellular carcinoma. PLoS ONE. 2012;7(2) doi: 10.1371/journal.pone.0032230.e32230 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Luo X., Yang W., Ye D.-Q., et al. A functional variant in microRNA-146a promoter modulates its expression and confers disease risk for systemic lupus erythematosus. PLoS Genetics. 2011;7(6) doi: 10.1371/journal.pgen.1002128.e1002128 [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.