Introduction
MicroRNAs (miRNAs) are a class of multifunctional, small (18 to 25 nucleotides) non-coding RNA molecules [
1,
2]. To date, approximately 940 miRNAs have been described [
3]. Their functions include epigenetic control of gene expression, mRNA degradation, and suppression of mRNA translation [
4]. These diverse functions of miRNAs are necessary for normal development, metabolism, cellular differentiation, proliferation, cell cycle control, and cell death. Aberrant miRNA expression or activity or both have been implicated in a variety of human diseases, including cancer [
5].
Several studies have analyzed miRNA expression patterns in primary tumors of various types, and specific subtypes of cancers could be easily differentiated on the basis of the expression pattern of these miRNAs [
6]. Recent studies have identified miRNAs in extracellular space, mainly through ceramide-dependent secretory exosomes or microvesicles [
7‐
9]. Additionally, secreted miRNAs have been shown to be in the Argonaute2 protein complex, which confers stability [
10]. These secreted miRNAs are transported through high-density lipoprotein (HDL) and enter heterotypic cells to alter migration/invasive properties [
7,
8,
11‐
13]. However, secretion or packaging of miRNAs into the exosomes is a selective process as the level of miRNA in exosomes secreted by a cell type does not always correlate with the intracellular levels of the corresponding miRNA [
14]. Specific cellular proteins, most of which are RNA-binding proteins, are suggested to be involved in exosomal secretion of miRNAs and their stability in circulation [
15].
Several reports describe differential blood/plasma/serum miRNA levels between healthy people and those with various diseases, including cancer [
7‐
9,
14,
16‐
25]. Serum miRNA was first reported in diffuse large B-cell lymphoma; sera of patients contained higher levels of miR-155, miR-210, and miR-21 [
25]. Elevated serum miR-21 levels correlated with good prognosis. Similar studies in prostate cancer revealed elevated levels of miR-141 in the plasma of patients with cancer compared with healthy subjects [
24], although the same result was not obtained in another study [
23]. A four-miRNA predictive profile from serum was described recently for non-small-cell lung cancer [
22]. There are limited studies on breast cancer. One study reported higher serum levels of miR-155 in patients with progesterone receptor-positive (PR
+) breast cancer compared with patients with PR
- breast cancer [
26]. Two recent studies reported elevated levels of miR-195 and let-7a in the whole blood of patients with breast cancer; levels of these miRNAs declined after surgical removal of tumors, suggesting that they were tumor-derived [
20,
21]. Elevated levels of miR-195 in the whole blood appear to be unique to breast cancer [
21]. Elevated levels of plasma miR-122 and miR-192 were reported after acetaminophen-induced liver injury, suggesting that tissues that are enriched for specific miRNAs may release them upon injury [
27]. Patients with atherosclerosis display an HDL-associated miRNA profile that is distinct from that of healthy subjects [
11].
It is postulated that the miRNAs are released into circulation either actively by the tumor cells or passively as a result of tumor cell death and lysis [
28]. However, this does not explain low serum levels of some miRNAs in patients with cancer compared with healthy controls. For example, plasma of patients with acute myeloid leukemia shows low levels of miR-92a compared with healthy subjects despite high levels of this miRNA in leukemic cells [
19]. In the sera of patients with lung cancer, 28 miRNAs are missing and 63 new miRNA species are detectable compared with healthy subjects [
18]. Similarly, sera of patients with ovarian cancer show elevated levels of five miRNAs and decreased levels of three miRNAs compared with healthy subjects [
17]. These observations raise questions of whether serum miRNAs in patients with cancer are directly derived from tumor cells or an indirect consequence of effects of cancer on other tissues, which then release miRNA into circulation. Given that the tumor often represents a very tiny portion of the body mass, microvesicles/exosomes secreted from the tumor cells are less likely to be sufficient enough to change the miRNA profile in a large volume of blood (5 L in a 72-kg person). Systemic effects of cancer on distant organs could easily result in a differential serum miRNA profile in patients with cancer. More importantly, these changes in serum profile could persist even after the patient is 'disease-free' if an epigenetic mechanism is involved in the systemic effects. In the latter situation, miRNAs would be poor markers of active disease.
To address these issues, we determined the levels of breast cancer-associated miRNAs in the sera of healthy subjects and breast cancer patients who were considered clinically cancer-free at the time of serum collection. Further validation of significant initial results was performed (a) with an independent sample set comprising serum from healthy subjects, clinically disease-free patients with breast cancer, and patients with overt metastasis and (b) with a set with serum from healthy subjects and patients with active metastasis. We report that SNORD44, a small nucleolar RNA (also called RNU44), is similar in the sera of healthy subjects and clinically cancer-free patients with breast cancer. However, levels of U6 (also called RNU6-1), which is commonly used for the purpose of normalization between samples, and U6/SNORD44 ratio were elevated in the sera of breast cancer patients who did not have active disease. Elevated U6 was detected in the sera of patients with estrogen receptor alpha-positive (ERα+) and of those with ER- breast cancer. Sera of patients with overt metastasis also showed elevated U6 or U6/SNORD44 ratio when compared with healthy women. Taken together, these results suggest that elevated U6 serum levels represent persistent systemic effects of breast cancer attained during cancer progression.
Materials and methods
Sample processing and RNA extraction
All sera were obtained from Indiana University Simon Cancer Center's Komen Tissue Bank. Patients gave informed consent to participate in the study, and the Indiana University institutional review board that evaluates studies involving human subjects approved the study. All samples were collected in accordance with standard operating procedure, which is detailed in the tissue bank website [
29]. More information on serum collection is provided as Additional file
1. RNA was isolated from 250 μL of serum by using the mirVana kit (Ambion, part of Applied Biosystems, Foster City, CA, USA) in accordance with the protocol of the manufacturer. RNA was eluted with 70 μL of RNase-free water, and a NanoDrop ND-1000 (NanoDrop, Wilmington, DE, USA) was used to measure the concentration of RNA. Although it was reported previously that serum miRNAs are stable and can withstand repeated freeze-thawing [
24], consistent results were obtained only when samples from healthy subjects and patients with cancer were handled similarly.
Quantitative reverse transcription-polymerase chain reaction
In the first series of experiments, 5 μL of RNA was reverse-transcribed to cDNA in a final volume of 15 μL by using a Taqman miRNA reverse transcription kit (Applied Biosystems). In the additional cohorts, 25 ng of RNA was used for reverse transcription. Quantitative polymerase chain reaction (qPCR) was performed by using Taqman universal PCR mix (Applied Biosystems) and specific primers on the qPCR instrument (Applied Biosystems). Primers for U6 (catalog number 001973), miR-16 (#000391), miR-21 (#000397), miR-155 (#000479), and miR-195 (#000494) were purchased from Applied Biosystems, whereas 5S primer (#201509) was purchased from Exiqon (Vedbaek, Denmark). SNORD44 primers (MPH01658A-200) were purchased from SABiosciences (Frederick, MD, USA). In some experiments, SNORD44 primers from Applied Biosystems (also called RNU44, #001094) were used. Each amplification reaction was performed in duplicate in a final volume of 20 μL containing 2 μL of the cDNA. qPCR of sera from healthy subjects and patients with cancer for a particular probe was in the same plate in all but extended cohort 2 to limit mechanical errors. The expression levels of miRNAs, U6, and 5S were normalized to SNORD44 or miR-16 and were calculated using the 2-ΔΔCt method.
Statistical analysis
Expression levels of serum miRNAs were compared by using the Mann-Whitney U test. A P value of less than 0.05 was considered statistically significant.
Discussion
This study was designed to address two critical issues related to circulating miRNAs as a biomarker in breast cancer: the first concerned normalization control and the second was related to persistence of miRNA changes in patients who are clinically cancer-free. Although analysis of candidate miRNAs did not reveal major cancer-specific changes in serum profile, our results clearly showed elevated levels of U6 RNA, which is often used for normalization, in the sera of patients with breast cancer. With SNORD44 as a normalization control, we could demonstrate upregulation of U6 in the sera of both ER/PR+ and ER/PR- breast cancer patients who were in remission. This also indicates that the type of treatment has no effect on serum U6 levels as ER/PR+ and ER/PR- patients receive different therapies. Disease activity did not appear to influence the levels of serum U6 as sera from ER/PR+ versus ER/PR- or node-positive versus node-negative patients did not show a statistically significant difference in U6 levels. Sera of patients with active disease also showed elevated levels of U6. Further studies assessing U6 levels before and after treatment are required to test the temporal effects of treatment on serum U6 levels.
The above observations raise two important questions: one is related to the source of serum U6 RNA and the other is related to the mechanism(s) leading to altered U6 levels in serum. It is generally believed that tumor cells are the primary source of serum miRNAs [
28]. Reduction of miR-92 in sera of patients with acute myeloid leukemia [
19], reduction of 28 miRNAs in sera of patients with lung cancer [
18], and our observation of elevated U6 RNA in sera of patients with metastasis-free breast cancer favor the possibility that cancer alters the release of miRNAs from distant organs or the immune system. The majority of plasma microvesicles are derived from leukocytes; therefore, cancer-induced alteration in leukocyte functions may potentially contribute to miRNA profile changes in the serum of patients with cancer [
14].
Our observation of persistent change in U6 levels even after a patient is cancer-free is slightly surprising. It is possible that cancer-derived growth factors/cytokines, stress, host response to cancer, or carcinogens result in stable epigenetic changes in distant organs. In this context, it was recently reported that chronic stress induces epigenetic changes, which impact DNA methylation patterns and consequent effects on gene expression in both germline and somatic tissues [
30]. Furthermore, neonatal experiences altering ERα levels in the adult mammary gland and consequent effects on mammary tumor incidence have been reported using animal models [
31]. In addition, a recent study showed that individuals with a persistent asymptomatic hepatitis B virus (HBV) infection and patients with active HBV infection share a serum miRNA profile, which is distinct from a healthy individual [
32]. Thus, a chronic infection/inflammatory condition may prompt certain organs to undergo permanent change in gene expression pattern. An alternative possibility, which may be provocative, is that upregulation of serum U6 levels is a preamble to cancer initiation or suggestive of a pre-cancerous state, similar to the creation of a niche for metastasis by the vascular endothelial growth factor receptor-1-positive (VEGFR-1
+) hematopoietic bone marrow progenitor cells before the arrival of cancer cells [
33].
RNAP-III transcribes both U6 and 5S RNA [
34,
35]. Aberrant RNAP-III-mediated transcription during cancer progression is just beginning to be recognized. RNAP-III upregulation is essential for cMyc-induced transformation [
36]. The major signaling pathways activated in cancer, including Ras, Raf, PI3K, and AKT, enhance RNAP-III activity, whereas several tumor suppressors, including retinoblastoma, PTEN, p53, and BRCA1, decrease RNAP-III activity [
35]. Inactivation of BRCA1 alone is sufficient to increase U6 levels in cancer cells [
37]. Since we observed elevated U6 levels in the sera of patients who are cancer-free at the time of sample collection as well as in the sera of patients with metastasis, alteration in the RNAP-III transcription machinery may be one of the systemic changes that occur during cancer progression prior to diagnosis and treatment. Recent serum protein biomarker profiling studies have shown a 'chronic inflammatory state' in patients with breast cancer [
38]. Whether such an inflammatory state alters serum U6 levels by modulating RNAP-III activity is not known. Unlike RNA polymerase II, RNAP-III has not been targeted for cancer therapy. It is not known whether serum U6 influences the course of the disease or whether blocking it will impact progression of the disease. It is also not known whether serum U6 is complexed with Argonaute2 or HDL and is delivered to heterotypic cells to modulate gene expression through alternative splicing [
10,
11]. We hope that our observations will prompt additional studies using inhibitors that can modulate (but not eliminate) the activity of RNAP-III to control cancer cell growth or the secondary effects of cancer or both.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
HNA carried out sample preparation and qPCR. CPG and YL performed the statistical analysis. LAM, SB, and GWS participated in patient recruitment, data interpretation, and editing of the manuscript. HN designed the experiments, interpreted results, and wrote the manuscript. All authors read and approved the final manuscript.