miR-639 promotes the proliferation and invasion of breast cancer cell in vitro
© Li et al.; licensee BioMed Central Ltd. 2014
Received: 22 February 2014
Accepted: 1 May 2014
Published: 10 May 2014
Breast cancer is characterised by an elevated capacity for tumour invasion and lymph node metastasis, but the cause remains to be determined. Recent studies suggest that microRNAs can regulate the evolution of malignant behaviours by regulating multiple target genes. In this study, we have first confirmed that miR-639 is up-regulated in metastatic breast cancer tissues and cell line with highly invasive capacity. Furthermore, we provided evidence to demonstrate that up-regulation of miR-639 contributes breast cancer invasion and metastasis. These data reveal a key role of miR-639 in breast cancer metastasis and support biological and clinical links between miR-639 and breast cancer.
KeywordsmiR-639 Breast cancer Invasion Metastases
Breast cancer-related deaths are caused by cancer metastases rather than the primary tumor. Different subtypes of breast cancer exhibit distinct metastases behaviors in terms of the temporal kinetics and anatomic sites. Estrogen receptor–positive (ER+) breast cancer, predominantly recurs in bone after the diagnosis of the primary tumor . The main mechanisms underlying these observations, however, remain to be elucidated.
MicroRNAs (miRNAs) are small, endogenous, non-coding RNAs which play important gene-regulatory roles in animals via sequence-specific interactions with the 3′UTR of cognate mRNA targets, causing suppression of translation and mRNA decay . It has been firmly established that miRNAs regulate many key cellular processes such as cell growth, differentiation and apoptosis [3, 4]. About 50% of annotated human miRNAs are detected in regions of fragile sites, which are associated with cancer. Experiments have confirmed that miRNAs participate in the tumorigenesis progression of many types of cancers, including the breast cancer . Although the number of verified human miRNAs is still expanding, the functions of only a few have been described. Subsets of miRNAs have been identified as potential diagnostic and prognostic markers in malignant tumors [6–8]. MiR-639 has been reported to have disrupted expression in pathological states [9, 10]. Similarly, miR-639 has been proven to be dysregulated in in serum of patients with bladder cancer. Therefore, the role of miR-639 in breast cancer caused us a great interest.
In this study, we examined the expression of miR-639 in breast cancer tissue samples and breast cancer cell lines. We found that miR-639 levels were up-regulated in metastatic breast cancer tissues and highly invasive cell lines. Furthermore, we have investigated the mechanism of miR-639 in breast cancer cell lines. These results show that exogenous overexpression of miR-639 promotes the invasion and migration of breast cancer cells in vitro.
Materials and methods
MCF-7 cancer cells are breast cancer derived and display an epithelial phenotype and low invasive capacity. MDA-MB-231 (MD231) cancer cells are also breast cancer derived but these cells have a mesenchymal phenotype and high invasive capacity. Both these breast cancer cell lines were obtained from the American Type Culture Collection (ATCC). These cell lines were cultured in DMEM supplemented with 10% heat-inactivated FBS (GIBCO BRL, NY, USA), penicillin (100 units/ml) and streptomycin (100 μg/ml) at 37°C in a humidified 5% CO2 atmosphere.
Tissue samples and reagents
All samples were obtained by surgery and quickly frozen in liquid nitrogen and stored at -80°C. Informed consent was obtained in advance for all patients selected in this study. In parallel, a separate cohort of 84 patients was assembled from a large pool of patients in the database based on histological diagnosis of breast cancer between 2001 and 2005. We retrospectively reviewed the medical records of patients. Total RNAs were extracted from paraffin blocks using the high pure miRNA isolation kit according to the manufacturer’s protocol (Roche, Switzerland) before further analysis.
Both the miR-639 inhibitor and its mimics were purchased from GenePharma (Shanghai, China). The high pure miRNA isolation kit was purchased from Roche (Basel, Switzerland). The miRcute miRNA qPCR detection kit and miRcute miRNA qPCR detection kit were purchased from TIANGEN BIOTECH (Beijing, China).
Real-time PCR analysis
Real-time PCR reactions were performed using an ABI 7500 real-time PCR system (Applied Biosystems, CA). Reverse transcription of the extracted miRNA was performed with miRNA-specific primers using the miRcute miRNA first-strand cDNA synthesis kit, and real-time PCR of miRNAs was performed using the miRcute miRNA qPCR detection kit according to the manufacturer’s protocol (TIANGEN BIOTECH, China), the primer is provided by the miRcute miRNA qPCR detection kit.
Invasion assays and wound-healing experiment
In vitro invasion assays, a total of 4 × 104 cells in 200 μl serum-free DMEM medium were plated onto BD BioCoat™ Matrigel™ Invasion Chambers (8 μm pore size; BD Biosciences), and the lower chamber was immediately filled with 500 μl of DMEM medium with 10% FBS as a chemoattractant. After 24 hrs of incubation in a humidified atmosphere containing 5% CO2 at 37°C, the membranes were then fixed with methanol and stained by 0.2% crystal violet. For wound-healing experiments, cells were plated in 6-well plates, transfected as indicated, and cultured to confluency. Cells were serum-starved and scraped with a P200 tip (time 0), and pictures (5 fields) were taken at the 24 h time points.
Informed consent and ethical approval
This study was approved by Institutional Ethic Committee Office of the First Affiliated Hospital of Zhengzhou University. Written informed consent was obtained from the patient for the publication of this article and accompanying images.
The categorical variables were compared among the groups using the X-squared test. The continuous variables were analyzed using the two-tailed Student’s t-test. A P value of <0.05 was considered statistically significant.
The association of miR-639 expression with metastatic rates in patients with breast cancer
Associtions between miR-639 and clinical parameters (n = 158)
No. of patients
miR-639 ΔCt a
Mean ± SD
1.71 ± 0.17
1.64 ± 0.21
1.69 ± 0.21
1.86 ± 0.14
1.98 ± 0.15
1.54 ± 0.27
1.65 ± 0.24
1.33 ± 0.17
1.19 ± 0.14
2.11 ± 0.31
Histologic signs of severity (vascular emboli, perineural invasion, diffuse infiltration)
1.57 ± 0.23
1.73 ± 0.17
1.37 ± 0.23
1.47 ± 0.21
1.35 ± 0.29
1.27 ± 0.36
We next analyzed mature miR-639 levels in the collection of breast cancer patients with clinical characteristics. Patients were divided into two groups with high or low levels of miR-639. Remarkably, when tested using the Kaplan-Meier survival analysis, the miR-639 “low expression” group displayed a significantly longer disease-free survival rates when compared to the “high expression” group (Figure 1B). These data suggest a possible link between miR-639 expression and breast cancer progression.
miR-639 promotes cell proliferation
Ectopic expression of miR-639 promotes cancer metastasis
Although a global reduction of miRNA abundance appears to be a general trait of human cancers, playing a causal role in the metastatic phenotype [11–13], several miRNAs are up-regulated in tumors , Recently, miRNAs have been shown to be related to tumor metastasis , providing a new perspective on the metastatic process. Nonetheless, The role of miRNAs in breast cancer has been widely investigated. Here, we will focus on miRNA-639 promotes breast cancer metastasis.
In this study, we described for the first time the miR-639 is markly upregulated in metastatic breast cancer in large samples. We also found that miR-639 is closely related to the cancer metastasis and miR-639 “high expression” group displayed a significantly poorer disease-free survival rates. We have proven that the down-regulation of miR-639 is crucial in breast cancer metastasis and demonstrated that miR-639 acts as a putative oncogene. MD231 cells, which stably express miR-639 ectopically, were transiently transfected with the miR-639 inhibitor, and MCF-7 cells were transfected with miR-639 mimics. This could be in line with the internal environment of the cells.
The genetic and epigenetic silencing of tumor suppressor genes is considered a vital molecular event in the development and progression of breast cancer . This study first proves that miR-639 is up-regulated in metastatic breast cancer. Aberrant patterns of miRNA expression are implicated in human diseases including breast cancer. Recent studies have identified miRNAs regulated by estrogens in human breast cancer cells, human endometrial stromal and myometrial smooth muscle cells, rat mammary gland, and mouse uterus. The decline of estradiol levels in postmenopausal women has been implicated in various age-associated disorders . The role of estrogen- regulated miR-639 expression has yet to be explored. As miRNAs function mainly through the inhibition of target genes and Wu et al.  showed p21Cip1/Waf1 expression was reduced by miR-639. This result may preliminary explain the mechanism of miR-639.
In conclusion, our results have proven that miR-639 plays a causal role in the metastases of breast cancer. These findings have implications for understanding the mechanism of breast cancer metastasis, and miR-639 may be a valuable maker and target for prevention or adjuvant therapy in breast cancer patients.
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