MicroRNA-623 inhibits tumor progression and is a predictor of poor prognosis of breast cancer.

Dysregulated microRNAs (miRNAs) serve vital roles in the progression and prognosis of breast cancer. miR-623 has been reported to influence the progression of numerous other cancers, such as lung adenocarcinoma and hepatocellular carcinoma, however, its role in breast cancer remains unclear. In the present study, the mRNA expression of miR-623 was studied in 121 pairs of breast cancer and adjacent normal tissues and cultured cell lines by reverse-transcription quantitative PCR. The association between miR-623 expression and clinical characteristics or the overall survival rate of patients was investigated by the χ2 test or Cox regression analysis, respectively. The role of miR-623 in cell proliferation, migration and invasion of breast cancer cells was evaluated by cell transfection to regulate miR-623 expression and the CCK8 and Transwell assays, respectively. miR-623 was downregulated in breast cancer tissues and cell lines compared with normal tissues and breast epithelial cell lines. The χ2 test demonstrated that the downregulation of miR-623 was associated with the tumor node metastasis (TNM) stage of patients with breast cancer. miR-623 and TNM stage were considered as two independent prognostic factors for breast cancer. Additionally, cell proliferation, migration, and invasion of breast cancer cells were promoted by the downregulation of miR-623, while upregulation of miR-623 led to inhibition of the aforementioned processes. Downregulation of miR-623 in breast cancer is associated with the development of breast cancer and indicates a poor prognosis of patients. The downregulation of miR-623 promotes cell proliferation, migration and invasion of breast cancer. The findings of the present study indicate that miR-623 functions as a prognosis biomarker and a tumor suppressor in breast cancer, which provides a potential therapeutic target for patients with breast cancer. Copyright: © Wang et al.

Introduction

Although the management and therapy of cancers has improved in the past decades, cancer remains one of the leading causes of death worldwide, especially breast cancer among women (1,2). Globally, over 1,000,000 people are diagnosed with breast cancer annually and 400,000 females died from breast cancer every year (3). In China, the incidence of breast cancer among women was ~20-30% in 2016 and annually grows by 3–5% according to Chinese urban cancer registries (4). The number of patients newly diagnosed with breast cancer is still increasing annually, while the therapeutic effect of breast cancer is unsatisfactory (5,6). Distant metastasis and recurrence are the main factors that result in death and poor prognosis of patients with breast cancer (7). Therefore, an improved understanding of tumor progression in breast cancer and the identification of novel biomarkers, which are associated with the development of breast cancer are essential for improved disease stratification and clinical management choices.

Studies have demonstrated that microRNA (miRNA) expression profiling studies have provided a lot of evidence for the regulatory role of miRNAs in tumor progression (8–10). miRNAs are a group of small non-coding RNAs, which are involved in tumorgenesis and regulate a variety of cellular pathways including proliferation, differentiation, migration, and invasion (11,12). miRNA expression profiling can screen dysregulated miRNAs in various cancers, such as prostate cancer, hepatocellular carcinoma, and gastric cancer, which provides potential functional miRNAs for the diagnosis and prognosis of cancers (13). Differentially expressed miRNAs being expressed in distinguishable patterns allows them to be used as potentially novel clinical and prognostic biomarkers (14). Downregulation of miR-143 can promote cell apoptosis and regulate the progression of pancreatic cancer (15). miR-558 serves as a biomarker for gastric cancer as its upregulation promotes tumorigenesis and aggressiveness of gastric cancer by targeting heparinase (16). miR-425, miR-132, miR-145 have been reported to serve roles in the progression of breast cancer with different degrees of dysregulation reported (17–19).

miR-623 is a demonstrated downregulated miRNA in breast cancer and has also been reported to serve roles in a number of other cancers, such as gastric cancer, pancreatic cancer, and lung adenocarcinoma (20–22). Reduced or increased expression of miR-623 regulates the progression of various cancers; hence, it was hypothesized that the dysregulation of miR-623 may act as a regulator during the development of breast cancer. The present study aimed to estimate the clinical significance and functional role of miR-623 in breast cancer.

Materials and methods

Patients and samples

A total of 121 paired samples were used the present study, which included breast cancer tissues and adjacent normal tissues (>5 cm from tumor tissues) with histopathological diagnosis. The inclusion criteria for the patients were: i) Female confirmed diagnosed of breast cancer; ii) underwent mastectomy or breast-conserving surgery; and iii) complete clinical data and follow-up status. The exclusion criteria were as follows: i) Patients underwent chemotherapy, radiotherapy or other types of anticancer therapy; ii) diagnosis with other malignant tumor; and iii) family history of breast cancer. Patients had an average age range of 34–66 years with an average age of 50.18±6.82 years. All samples were obtained from patients with breast cancer who underwent surgery at The Second Hospital of Liaocheng affiliated to Shandong First Medical University (Linqing, China) from January 2011 to December 2013. The characteristics of patients are summarized in Table I. The TNM stage was recorded according to the 2010 tumor-node metastasis classification recommended by the American Joint Committee on Cancer (AJCC 7th edition) (23). Samples were immediately frozen in liquid nitrogen and stored at −80°C for subsequent experimentation and analysis. Written informed consent was obtained from every patient, and the present study was approved by the Ethics Committee of The Second Hospital of Liaocheng affiliated to Shandong First Medical University (approval no. 201033). In addition, all patients participated in a 5-year follow-up survey for the collection of the survival information. Patients were followed-up at 6, 9, 12, 15, 18, 21, 24, 30, 36, 42, 48, and 60 months after surgery over the telephone.

Table I.

Association between miR-623 expression and the characteristics of patients with breast cancer.

		miR-623 expression
Characteristics	Patients (n=121)	Low (n=68)	High (n=53)	P-value
Age, years				0.162
≤50	54	30	24
>50	67	38	29
Tumor size, cm				0.247
≤5	62	32	30
>5	59	36	23
Lymph node metastasis				0.162
Negative	69	40	29
Positive	52	28	24
TNM stage				0.028
I–II	71	36	35
III–IV	50	32	18
HER 2 status				0.255
Negative	55	29	26
Positive	66	39	27
ER status				0.341
Negative	58	35	23
Positive	63	33	30
PR status				0.276
Negative	57	37	23
Positive	64	31	33

HER 2, human epidermal growth factor receptor 2; ER, estrogen receptor; PR, progesterone receptor; TNM, tumor node metastases.

Cell culture and transfection

Four human breast cancer cell lines, MCF-7, MDA-MB-231, HCC1954, and HCC1937, and the normal human breast epithelial cell line MCF-10A were used in the present study. All cell lines were purchased from Shanghai Cell Bank of the Chinese Academy of Medical Sciences and cultured in Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% fetal bovine serum (FBS) (both Gibco; Thermo Fisher Scientific Inc.). All cell cultures were maintained at 37°C in a humidified incubator with 5% CO2 for 24 h.

To regulate the expression of miR-623 and explore its effects on the cellular processes of breast cancer, breast cancer cells were transfected with 20 nM miR-623 mimic, miR-623 inhibitor, mimic negative control (mimic NC), or inhibitor negative control (inhibitor NC) purchased from Guangzhou RiboBio Co., Ltd. Lipofectamine 2000® reagent (Invitrogen; Thermo Fisher Scientific Inc.) was used for transfection at 37°C for 24 h. Untransfected cells were defined as control group. The sequences of transfections are as follows: miR-623 mimic, 5′-AUCCCUUGCAGGGGCUGUUGGGU-3′; miR-623 inhibitor, 5′-ACCCAACAGCCCCUGCAAGGGAU-3′; mimic NC, 5′-UUCUCCGAACGUGUCACGUTTACGUGACACGUUCGGAGAATT-3′ and inhibitor NC, 5′-CAGUACUUUUGUGUAGUACAA-3′. After 48 h of transfection, subsequent experimentation was performed.

RNA isolation and reverse-transcription quantitative (RT-q)PCR assay

Total RNA from collected tissues and cultured cells was extracted by using TRIzol reagent (Invitrogen; Thermo Fisher Scientific Inc.) and reverse transcribed into cDNA by using miRNA First-Strand cDNA Synthesis kit (Invitrogen; Thermo Fisher Scientific Inc.). The reverse transcription protocol was: 37°C for 1 h and 85°C for 5 min. SYBR Green I Master Mix kit (Invitrogen; Thermo Fisher Scientific Inc.) was used to perform RT-qPCR on the 7300 Real-Time PCR System (Applied Biosystems; Thermo Fisher Scientific Inc.). The thermocycling conditions were as follows: 95°C for 10 min followed by 40 cycles of 95°C for 15 sec and 60°C for 15 sec. The expression of miR-623 was normalized to that of U6 with relative quantification by the 2−ΔΔCq calculation method (24). The primer sequences of miR-623 were: Forward. 5′-ATCCCTTGCAGGGGCTGTTGGGT-3′ and reverse, 5′-GCCAGCACAGAATTAATACGAC-3′. The primer sequences of U6 were: Forward 5′-CTCGCTTCGGCAGCACA-3′; reverse 5′-AACGCTTCACGAATTTGCGT-3′.

CCK8 assay

To measure the proliferation ability of breast cancer cells, a CCK8 assay was performed according to the manufacturer's instructions. Cells were plated in 96-well plates at a density of 5×103 cells/well and cultured at 37°C with 5% CO2 for 0, 24, 48 and 72 h. Cells were then incubated with 10 µl cell counting kit-8 (CCK-8) reagent (Dojindo Molecular Technologies Inc.) per well for 4 h at 37°C with 5% CO2. Absorbance at 450 nm was measured with a microplate reader (Thermo Fisher Scientific Inc.).

Transwell assay

Matrigel-uncoated and coated transwell (for invasion) inserts (8-mm pore size; Thermo Fisher Scientific Inc.) were used for the detection of cell migration and invasion. Matrigel precoating was performed at 37°C for 1 h for the invasion assay. A total of 2×105 transfected cells were seeded into the upper chamber with serum-free medium and culture medium with 10% FBS was placed in the lower chamber as a chemoattractant. The Transwell was incubated at 37°C for 24 h, after that, transwells were removed and stained with 0.1% crystal violet (Sigma; Merck KGaA) at 37°C for 5 min. The number of migrated and invaded cells in the lower chamber was detected by a fluorescence microscope (magnification, ×100).

Statistical analysis

All data were represented as the mean value ± SD obtained from 3 repeats and were analyzed by SPSS 20.0 software (IBM Corp.) and GraphPad Prism 5.0 software (GraphPad Software, Inc.) The differences in the expression of miR-623 in breast cancer tissues and adjacent normal tissues were analyzed using a paired Student's t-test. The differences between multiple groups was assessed by one-way ANOVA followed by the post hoc Tukey's test. The association between miR-623 expression and clinical characteristics of patients was evaluated by the χ2 test. The survival curves of patients were generated using the Kaplan-Meier method and were compared using the log-rank test. Additionally, the prognostic value of miR-623 was further assessed by the Cox regression analyses. P<0.05 was considered to indicate a statistically significant difference.

Results

Expression level of miR-623 in breast cancer tissue and cells

In the collected breast cancer and adjacent normal tissues, the expression of miR-623 was detected by RT-qPCR. miR-623 demonstrated significantly decreased expression in breast cancer tissues compared with adjacent normal tissues (P<0.001; Fig. 1A). Similarly, miR-623 was significantly downregulated in breast cancer cell lines (HCC1954, HCC1937, MCF-7 and MDA-MB-231) compared with MCF-10A cells (P<0.001; Fig. 1B). The relatively lower expression of miR-623 in HCC1937 and MCF-7 cells compared to the other cancer cell lines indicated that they are more sensitive to the dysregulation of miR-623, hence they were chosen for subsequent cell experiments.

Figure 1.

miR-623 is downregulated in breast cancer tissues and cell lines. (A) Relative expression of miR-623 in 121 paired breast cancer and adjacent normal tissues detected by reverse-transcription quantitative PCR. ***P<0.001 compared with normal tissues. (B) Relative expression of miR-623 in breast cancer cell lines (HCC1954, HCC1937 MCF-7, MDA-MB-231) and a normal human breast epithelial cell line MCF-10A. ***P<0.001 compared with MCF-10A. miR, microRNA.

Association between miR-623 expression and clinical characteristics of patients with breast cancer

A total of121 breast cancer patients were divided into miR-623 high or low expression groups based on the mean value of the miR-623 level (0.375) in breast cancer tissues. Results of the χ2 test demonstrated a significant association between miR-623 expression and the TNM stage of patients (P=0.028), while age, tumor size, lymph node metastasis, and the status of human epidermal growth factor receptor 2, estrogen receptor (ER) and progesterone receptor of patients demonstrated no significant association with the expression of miR-623 (P>0.05, Table I).

Prognostic value of miR-623 in breast cancer

Fig. 2 demonstrates the survival rate of patients with breast cancer with low or high miR-623 expression levels 5 years after surgery. Patients with low miR-623 expression demonstrated a shorter overall survival time compared with patients with high miR-623 expression (Log-rank P=0.020; Fig. 2). Additionally, the results of Cox regression analysis indicated that miR-623 expression [hazard ratio (HR) factor=2.743; 95% confidence interval (CI)=1.260–5.971; P=0.011] and TNM stage (HR factor=2.191; 95% CI=1.082–4.434; P=0.029) are two independent prognostic factors for breast cancer due to their close association with the survival rate of patients (Table II).

Figure 2.

Kaplan-Meier curve of patients with breast cancer with different miR-623 expression levels. Low miR-623 expression predicts a poor prognosis of patients with breast cancer (Log-rank P=0.020 relative to patients with high miR-623 expression). miR, microRNA.

Table II.

Cox regression analysis of the association between characteristics of patients with breast cancer and survival rate.

Characteristics	HR factor	95% CI	P-value
miR-623 expression	2.743	1.260–5.971	0.011
Age	1.250	0.602–2.598	0.549
Tumor size	1.633	0.789–3.377	0.186
Lymph node metastasis	1.694	0.831–3.453	0.147
TNM stage	2.191	1.082–4.434	0.029
HER2 status	1.594	0.765–3.320	0.213
ER status	1.447	0.698–3.003	0.321
PR status	1.504	0.741–3.049	0.258

HER 2, human epidermal growth factor receptor 2; ER, estrogen receptor; PR, progesterone receptor; HR, hazard ratio; CI, confidence interval.

Effect of miR-623 expression on cell proliferation of breast cancer cells

miR-623 mimic, miR-623 inhibitor and corresponding negative controls were transfected into HCC1937 and MCF-7 cells for the overexpression or knockdown of miR-623. In addition, the proliferation ability of transfected cells was analyzed by the CCK8 assay to investigate the effect of miR-623 expression on cell proliferation of breast cancer cells. Following the transfection of miR-623 mimic, miR-623 was significantly upregulated, while the transfection of miR-623 inhibitor significantly downregulated miR-623 in HCC1937 and MCF-7 cells compared with cells in control group (P<0.001; Fig. 3A).

Figure 3.

Downregulation of miR-623 promotes cell proliferation of HCC1937 and MCF-7. (A) Relative expression of miR-623 in HCC1937 and MCF-7 cells transfected with miR-623 mimic, miR-623 inhibitor and corresponding NC. ***P<0.001 compared with Control. (B) Proliferation of HCC11937 and MCF-7 cells after transfection. *P<0.05 compared with Control. miR, microRNA; control, untransfected cells; NC, negative control; OD, optical density; ns, not significant.

The results of CCK8 assay revealed that the proliferation of HCC1937 and MCF-7 cells was significantly inhibited by the miR-623 mimic and promoted by the miR-623 inhibitor (P<0.05 relative to control group; Fig. 3B). This suggests that miR-623 may be involved in the proliferation of breast cancer cells.

Role of miR-623 in cell migration and invasion of breast cancer cells

Transwell assays were performed to evaluate the migration and invasion of HCC1937 and MCF-7 cells with different expression levels of miR-623. The results demonstrated that the migration and invasion of cells transfected with the miR-623 mimic was significantly lower compared with cells transfected with miR-623 inhibitor, which revealed the inhibitory role of miR-623 in the migration and invasion of breast cancer cells (P<0.001; Fig. 4A and B).

Figure 4.

Downregulation of miR-623 promotes cell migration and invasion of HCC1937 and MCF-7. (A) Migration of HCC1937 and MCF-7 after the transfection of miR-623 mimic, miR-623 inhibitor and corresponding NC. ***P<0.001 compared with control. (B) Invasion of HCC1937 and MCF-7 after the transfection of miR-623 mimic, miR-623 inhibitor and corresponding NC. ***P<0.001 compared control. miR, microRNA; control, untransfected cells; NC, negative control.

Discussion

Due to the increasing number of new cases and the death rate resulting from recurrence and metastasis, breast cancer is still considered as the most malignant tumor in women (25). The exploration of novel biomarkers in breast cancer has received increasing attention in recent decades (26). miRNAs have been identified as biomarkers for the diagnosis or prognosis of various cancers, such as gastric cancer, lung cancer, colorectal cancer, and numerous other cancers and diseases, such as acute myeloid leukemia and Alzheimer's disease (16,27–29). For example, overexpressed miR-675 in non-small cell lung cancer promotes the progression of the disease by activating the NF-κB signaling pathway (30). A number of miRNAs, such as miR-145-5p, miR-940, and miR-205-3p (19,31,32), which serve roles in the progression of breast cancer have been considered as potential biomarkers for breast cancer.

Previously, miR-623 was reported to be dysregulated in breast cancer (33) and to serve roles in various cancers (20–22). For example, miR-623 was demonstrated to inhibit cell migration, invasion, and metastasis of pancreatic cancer in vitro and in vivo by directly targeting MMP1 (22). In gastric cancer, miR-623 can function as a tumor suppressor and enhance chemosensitivity (20). miR-623 has also been demonstrated to suppress the progression of lung adenocarcinoma by targeting MMP-2 and MMP-9 (21). The present study was performed to identify the role of miR-623 in the progression and prognosis of breast cancer. miR-623 was found to be downregulated in breast cancer tissues and cell lines compared with normal breast tissues and cell lines. In the present study, overexpression of miR-623 by miR-623 mimic transfection was demonstrated to exert inhibitory effects on cell proliferation, migration and invasion of breast cancer, indicating the tumor suppressor role of miR-623 in the progression of breast cancer.

Recently, the biological function of miR-623 has been revealed by Li et al (34) in MCF-7 and MDA-MB-453 cells. The exogenous overexpression of miR-623 inhibited cell proliferation and promoted cell apoptosis of breast cancer by targeting X-ray repair cross-complementing protein 5 (34), which is consistent with the biological function of miR-623 in MCF-7 and HCC1937 cells in the present study. In the present study, in addition, to miR-623 function in cell progression of breast cancer, the clinical significance of miR-623 was also assessed. miR-623 expression had a close relationship with the TNM stage of patients. Additionally, in the present study patients who had low miR-623 mRNA expression demonstrated poorer prognosis compared with patients with high miR-623 expression, indicating that the downregulation of miR-623 was associated with poor prognosis of breast cancer. Based on the findings of the present study, miR-623 expression and TNM stage were considered as two independent prognostic factors for breast cancer. miRNAs have been reported to predict the prognosis of a variety of cancers and serve as independent prognostic factors for cancers. For instance, overexpression of miR-153 in prostate cancer can predicate the poor prognosis of patients (35). Downregulation of miR-1247-5p in breast cancer is associated with poor prognosis of patients (36). All the aforementioned findings of the present study, indicate that miR-623 participated in and suppressed the progression of breast cancer.

However, in addition to the investigation of the function of miR-623 in the progression of breast cancer, it is also necessary to determine the mechanism underlying the functional role of miR-623. Previously, MMP1 and Cyclin D1 were demonstrated to be direct targets of miR-623, regulating how miR-623 participates in the progression of pancreatic cancer and gastric cancer (20,22). Hence, it was speculated that miR-623 may regulate the progression of breast cancer by targeting these genes or other potential targets, which is a limitation of this study and needs further experiments to validate this hypothesis.

In conclusion, the results of the present study demonstrated that miR-623 was downregulated in breast cancer tissues and cells, which was associated with the TNM stage of patients and predicted poor prognosis of patients with breast cancer. miR-623 participated in the progression of breast cancer and was an independent prognostic factor together with TNM stage. In addition, knocking down of miR-623 significantly promoted cell proliferation, migration and invasion of breast cancer, while its overexpression significantly suppressed these cellular processes, which indicated the tumor inhibitor role of miR-623 in breast cancer. Malignant tumor is a multifaceted disease with important differences among diverse types of cancers (37). This research is an expanding study that applied regular methods to investigate the role of miR-623 in breast cancer.