miR-582-5P induces colorectal cancer cell proliferation by targeting adenomatous polyposis coli
© The Author(s). 2016
Received: 1 April 2016
Accepted: 17 August 2016
Published: 6 September 2016
microRNA (miRNAs) dysregulation is widely involved in cancer progression and contributed to sustained cell proliferation by directly targeting multiple targets. Therefore, better understand the underlying mechanism of miRNA in carcinogenesis may improve diagnostic and therapeutic strategies for malignancy.
We assessed microRNA-582 (miR-582-5P) expression in colorectal cancer (CRC) specimens and cell lines by real-time PCR. Luciferase reporter assay was used to confirm the target associations. Colony formation assay and anchorage-independent growth assay were used to analyze the effect of miR-582-5P on cell proliferation. Adenomatous polyposis coli (APC) gene and protein expression were examined using real-time PCR and western blotting, respectively.
miR-582-5P was upregulated in the CRC specimens and cell lines and targeted the 3′ untranslated region of APC directly. miR-582-5P overexpression increased cyclin D1 and c-MYC expression, which subsequently induced CRC cell proliferation in an APC-dependent manner.
Our findings suggest that miR-582-5P plays an important role in the progression of CRC by inducing proliferation and may identify new targets for anti-cancer treatment.
KeywordsmiR-582-5P APC Proliferation Colorectal cancer
Colorectal cancer (CRC) is one of the most prevalent malignant cancers and affects men and women almost equally. Currently, approximately 1.25 million people in China are diagnosed with CRC, and the incidence of CRC increases annually and it will continue to rise in the next few years . Furthermore, CRC is a major cause of cancer-associated mortality, and more than 600,000 patients will die from it every year worldwide . In the USA and Europe, CRC is the second most frequent cancer that leads to death . In recent years, significant advances have been made in targeted therapies of CRC. However, better targeted drugs are required because the effects of existing drugs are not satisfactory.
The adenomatous polyposis coli (APC) gene located at 5q21–q22 encodes a tumor suppressor protein that acts as an antagonist of the Wnt/β-catenin pathway, which controls the CRC cell fate during the maintenance phase of tumors in patients [4, 5]. It is also involved in other processes, including cell cycle control and cell migration, adhesion, differentiation, apoptosis, and transcriptional activation . Defects in this gene may cause familial adenomatous polyposis, an autosomal dominant pre-malignant disease that usually progresses to malignancy. APC mutation has been found in over 80 % of CRC cases and significantly less frequently in sporadic high microsatellite instability cancers than in low microsatellite instability or microsatellite instability cancers . Furthermore, APC mutation-induced upregulation of the survivin/ABK cascade is associated with crypt cell maturation, expansion of proliferative cell populations, and promotion of tumorigenesis .
microRNAs (miRNAs) are a class of endogenous, small, non-coding RNAs involved in multiple biological processes. They negatively regulate post-transcriptional gene expression to act as tumor suppressors or oncogenes by binding to the 3′ untranslated region (UTR) of a target gene [8–11]. miRNAs have been widely proposed as potential targets for anti-cancer therapies because a number of findings have indicated that some miRNAs, such as miR-150 [12, 13], miR-153 , miR-561 , and miR-622 , are involved in the development of human CRC. Publicly available algorithms have indicated that miR-582-5P may directly target the 3′ UTR of APC. miR-582-5P reduces the proliferation and invasion of human bladder cancer by suppressing the expression of target genes such as protein geranylgeranyltransferase type I beta subunit (PGGT1B), leucine-rich repeat kinase 2 (LRRK2), and DIX domain containing 1 (DIXDC1) . However, the role of miR-582-5P in CRC progression has not been determined. In this study, we searched for the possible relationship between miR-582-5P and APC and the role of miR-582-5P in the development of CRC.
Patients and tissues
The eight malignant CRC tissues and matched adjacent noncancerous tissues used in this study were obtained from patients who had undergone surgery at the China-Japan Union Hospital of Jilin University of the People’s Republic of China. The CRC tissues and matched adjacent noncancerous tissues were frozen and stored in liquid nitrogen until used.
A normal colonic mucosal epithelial cell line (normal control) was isolated and purified from the adjacent noncancerous tissues obtained from the patients. The human CRC cell lines HT29, SW403, SW480, COLO205, SW620, COLO320DM, and KM202L were purchased from American Type Culture Collection (Manassas, VA, USA) and cultured in Dulbecco’s modified Eagle’s medium (Invitrogen, Carlsbad, CA, USA) supplemented with 10 % fetal bovine serum (Invitrogen) at 37 °C in a 5 % CO2 atmosphere in a humidified incubator.
Plasmids and transfection
The human APC 3′ UTR was PCR-amplified from genomic DNA from SW480 cells and cloned into pGL3 vectors (Promega, Madison, WI, USA). Transfection of miR-582-5P mimic, miR-582-5P inhibitor (miR-582-5P-in), negative control (NC), NC inhibitor (NC-in) (RiboBio, Guangzhou, China), and plasmids was performed using Lipofectamine 2000 (Invitrogen) according to the manufacturer’s instructions.
RNA extraction and real-time quantitative PCR
Total miRNA from cultured cells and cancer tissue samples was extracted using the mirVana miRNA Isolation Kit (Ambion, Austin, TX, USA) according to the manufacturer’s manual. The expression level of miR-582-5P was performed using miR-582-5P-specific primer and probe (TaqMan MicroRNA Assay Kit; Applied Biosystems, Foster City, CA, USA) on an ABI 7900 system (Applied Biosystems). The expression of miR-582-5P was defined based on Ct, and relative expression levels were calculated as 2−[(Ct of miR-582-5p) − (Ct of U6)] after normalization with reference to the quantification of U6 small nuclear RNA expression. The following primers (RiboBio, Guangzhou, China) were synthesized and used in this study: GAPDH forward: 5′-AATCTCCACTTTGCCACTG-3′, GAPDH reverse: 5′-CCTCGTCCCGTAGACAAAA-3′; cyclin D1 forward: 5′-AGGAGAACAAACAGATCA-3′, cyclin D1 reverse: 5′-TAGGACAGGAAGTTGTTG-3′; and c-MYC forward: 5′-TCAAGAGGTGCCACGTCTCC-3′, c-MYC reverse: 5′-TCTTGGCAGCAGGATAGTCCTT-3′.
Western blotting was performed according to a previously reported method . The membranes were probed with polyclonal mouse antibodies: anti-APC (ab15270; 1:1000; Abcam, Cambridge, UK), anti-cyclin D1 (1:1000; Cell Signaling Technology, Danvers, MA, USA), and anti-c-MYC (1:1000; Cell Signaling Technology). The membranes were stripped and re-probed with anti-α-tubulin mouse monoclonal antibody (1:1000; Cell Signaling Technology) as the loading control.
Cells were seeded in 24-well plates and allowed to settle for 24 h. PGL3-APC-luciferase plasmid or pGL3-Mut-luciferase plasmid (100 ng) was transfected into CRC cells using Lipofectamine 2000 according to the manufacturer’s instructions. Luciferase and control signals were measured 48 h after transfection using a Dual Luciferase Reporter Assay Kit (Promega) according to a protocol provided by the manufacturer. Three independent experiments were performed, and the data are presented as the mean ± SD.
3-(4,5-Dimethyl-2-thiazolyl)-2, 5-diphenyl-2H-tetrazolium bromide assay
Cells were seeded on 96-well plates and stained at the indicated time points with 100 μl sterile 3-(4,5-dimethyl-2-thiazolyl)-2, 5-diphenyl-2H-tetrazolium bromide (MTT) dye (0.5 mg/ml, Invitrogen) for 4 h at 37 °C, followed by the removal of the culture medium and the addition of dimethyl sulfoxide (Sigma-Aldrich, St. Louis, MO, USA). The absorbance at 450 nm was measured using a microplate reader (Bio-Rad, La Jolla, CA, USA). Three independent repeat experiments were performed, and the data are presented as the mean ± SD.
Colony formation assay
Cells were seeded on a 6-well plate (1 × 103 cells per well) and cultured for 10 days. The colonies were stained with 1.0 % crystal violet for 5 min after a 15-min fixation with 10 % formaldehyde. All experiments were performed in triplicates.
Anchorage-independent growth assay
Five hundred cells were trypsinized and suspended in 2 ml complete medium plus 0.3 % agar (Sigma-Aldrich). The agar-cell mixture was plated on top of a bottom layer containing 1 % complete medium agar mixture. After 10 days, viable colonies that were larger than 0.1 mm (diameter) were counted with an ocular micrometer (Xintu Photonics Co., Ltd, Fuzhou, China). The experiment was performed three times independently for each cell line.
Student’s t test was used to evaluate the significant difference between the two groups of data in all pertinent experiments. P < 0.05 (Student’s t test) was considered statistically significant.
miR-582-5P is upregulated in CRC cells and tumor tissues
miR-582-5P overexpression induces cell proliferation
Downregulation of miR-582-5P inhibits cell proliferation
miR-582-5P targets APC in CRC cells directly
Subsequently, real-time PCR demonstrated that miR-582-5P overexpression significantly increased the expression of cyclin D1 and c-MYC mRNA in SW480 cells (Fig. 4d). Additionally, the western blotting results were consistent with the real-time PCR data (Fig. 4e). These findings indicate that miR-582-5P may play an important role in regulating the proliferation of CRC cells.
miR-582-5P induces SW480 cell proliferation in an APC-dependent manner
microRNAs, a class of small regulatory RNA molecules that negatively regulate their mRNA targets in a sequence-specific manner, play important roles in multiple biological processes such as cell differentiation, proliferation, oncogenesis, angiogenesis, invasion, and metastasis and may function as either tumor suppressors or oncogenes [18–20]. Uchino et al. found that miR-582-5P reduced human bladder cancer proliferation and invasion by suppressing the expression of target genes such as PGGT1B, LRRK2, and DIXDC1 . Furthermore, Floyd et al. found that miR-582-5P directly targeted caspase 3 (CASP3), caspase 9 (CASP9), and BIM, consequently influencing glioblastoma cell survival . Liu et al. suggested that miR-582-5P can inhibit monocyte apoptosis by downregulating forkhead box O1 (FOXO1) expression and that it plays an important role in regulating anti-Mycobacterium tuberculosis-directed immune responses . However, there has been no research on the role of miR-582-5P in CRC progression. In our study, we found that miR-582-5P was significantly overexpressed in CRC cells as compared to normal colonic mucosa epithelial cells. Additionally, miR-582-5P was upregulated in CRC tissues when compared with the matched adjacent noncancerous tissues. Furthermore, ectopic expression of miR-582-5P significantly increased cell growth, while inhibiting miR-582-5P had the opposite effect. These results indicate that upregulation of miR-582-5P may correlate with the progression of CRC and that miR-582-5P may function as an onco-miRNA in CRC.
Mutations in APC are believed to be one of the earliest events that contribute to CRC initiation. APC I1307K germline mutation is the most common and important mutation. Firstly, the APC I1307K germline mutation is associated with increased risk for CRC development, tumor location, and tumor stage . Secondly, compared with non-carriers, APC I1307K carriers had increased numbers of adenomas and tumors per patient, as well as younger age at diagnosis. The APC I1307K allele is associated with an estimated relative risk of 1.5–1.7 for colorectal neoplasia . However, Figer et al. suggested that these mutations contribute little to disease pathogenesis [25, 26]. In addition, methylation of the APC gene promoter region in cancerous tissue in combination with the predominance of methylation in normal tissue may serve as a prognostic factor in patients with CRC [27, 28]. In this study, we used three methods to confirm that APC is a predicted target gene of miR-582-5P. Western blotting showed that overexpression of miR-582-5P downregulated APC protein expression but upregulated cyclin D1 and c-MYC expression. The luciferase activity assay and point mutation analysis demonstrated that APC downregulation was mediated by miR-582-5P specifically targeting the APC 3′ UTR. The mechanism of miR-582-5P induction of cell proliferation is currently under investigation in our laboratory.
Our results show that miR-582-5P is markedly upregulated in the CRC cells and clinical tissues as compared with matched adjacent noncancerous tissues from the same patient. Furthermore, APC is a direct target gene of miR-582-5P, and overexpression of miR-582-5P reduced the expression of APC and inhibited CRC cell proliferation, whereas downregulation had the opposite effect. Further investigation is required to fully characterize the biological function of miR-582-5P and its clinical relevance in the development of CRC. Collectively, although the precise mechanisms are not yet fully understood, this finding suggests that miR-582-5P may play an important role in regulating the proliferation of CRC cells and represent a therapeutic target for colorectal cancer.
We thank the staff of the Department of Gastrointestinal Colorectal and Anal Surgery at the China-Japan Union Hospital of Jilin University for their great support.
This manuscript received no funding.
Availability of data and materials
The datasets during and analyzed during the current study are available from the corresponding author on reasonable request.
ZS and DD conceived the study and design. ZS and LC undertook the experiment. LC performed the analysis and interpretation of data. ZS drafted the manuscript. DD critically reviewed the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
The Institutional Ethical Board of Jilin University and the China-Japan Union Hospital approved the use of clinical materials for research purposes in this study, and written informed consent was obtained from all patients. This research does not involve the use of any animal data or tissue.
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