1. Department of Clinical Laboratory, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & the Affiliated Cancer Hospital of Nanjing Medical University, Nanjing 210009, P. R. China.
2. Department of Clinical Laboratory, Nanjing Qixia District Hospital, Nanjing 210000, P. R. China.
3. Department of Surgery, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & the Affiliated Cancer Hospital of Nanjing Medical University, Nanjing 210009, P. R. China.
4. Department of Pathology, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & the Affiliated Cancer Hospital of Nanjing Medical University, Nanjing 210009, P. R. China.
Background: DC-STAMP domain containing 1-antisense 1 (DCST1-AS1) is a long noncoding RNA (lncRNA) that is up-regulated in triple-negative breast cancer (TNBC) tissues. Here, we attempt to investigate the oncogenic property of DCST1-AS1.
Methods: LncRNA microarrays were used to detect differentially expressed lncRNA in cancerous tissues. Fluorescence in situ hybridization assay was used to detect the distribution of DCST1-AS1 in BT-549 and MDA-MB-231 cells. Lentiviral systems, inhibitors, siRNA and overexpression plasmids were used for gain- and loss-of-function experiments. Colony formation assay, wound healing assay, CCK8 assay, transwell assay, and flow cytometry assay were used to study the function of DCST1-AS1. Luciferase assay was used to verify the binding of MYC to the promoter region and the binding of miR-873-5p to DCST1-AS1. RNA immunoprecipitation assay was used to verify that argonaute 2 binds to both miR-873-5p and DCST1-AS1. Western blotting was used to measure changes in protein expression.
Results: Consistent with the microarray results, we found that DCST1-AS1 was up-regulated in both TNBC tissue samples and cell lines. DCST1-AS1 was positively correlated with distant metastasis and histopathological grades. DCST1-AS1 is distributed in both nucleus and cytoplasm. Knockdown of DCST1-AS1 inhibits TNBC cell proliferation and metastasis, while overexpression of DCST1-AS1 promotes TNBC cell proliferation and metastasis. We confirmed that DCST1-AS1 expression in TNBC cells is regulated by MYC. Furthermore, we found that DCST1-AS1 is negatively correlated with miR-873-5p in TNBC tissues and is a direct target gene of miR-873-5p. Argonaute 2 is involved in the binding of DCST1-AS1 and miR-873-5p and promotes the degradation of DCST1-AS1. The interaction of DCST1-AS1 with miR-873-5p ultimately up-regulated the expression of insulin-like growth factor 2 mRNA binding protein 1 (IGF2BP1), MYC, CD44 and lymphoid enhancer binding factor 1 (LEF1).
Conclusions: DCST1-AS1 is activated by MYC and is degraded by binding to miR-873-5p, thereby upregulating the expression of miR-873-5p downstream proteins IGF2BP1, MYC, LEF1 and CD44. MYC, DCST1-AS1 and miR-873-5p form a positive regulatory loop to promote TNBC cell proliferation and metastasis.
Keywords: long noncoding RNA, MYC, miR-873-5p, IGF2BP1, metastasis.
Triple-negative breast cancer (TNBC) is a heterogeneous disease in which the estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2) are absent. TNBC has the characteristics of early onset and high rates of invasion and distant metastasis, making it a more aggressive subtype of breast cancer [1, 2]. Due to the lack of expression of hormone receptors and HER2, endocrine therapy and trastuzumab treatment are ineffective in TNBC. Therefore, it is urgent to elucidate the molecular mechanisms underlying TNBC metastasis and identify available therapeutic targets .
Recent studies have shown that long noncoding RNA (lncRNA), with a length of more than 200 nt, has a wide range of regulatory functions and can regulate gene expression at the level of modification, transcription, and post-transcriptional regulation [4-6]. LncRNAs can interact with DNA, RNA, or proteins and are widely involved in the regulation of tumor signaling pathways [7, 8]. For example, the lncRNA MAYA promotes breast cancer cell bone metastasis through the ROR1/HER3-LLGL2-MAYA-NSUN6 signaling axis . The LncRNA LINP1 can be used as a scaffold for Ku80 and DNA-PKcs to promote double-strand DNA breakage repair . Although emerging evidence has shown the paramount role of lncRNAs in tumor development, only a small portion of them have been well characterized in various carcinomas [11-13]. The number of lncRNAs expressed in TNBC, and whether they have important biological functions, remains largely unknown.
DC-STAMP domain containing 1-antisense 1 (DCST1-AS1) is an up-regulated lncRNA identified by microarray analysis. The function of DCST1-AS1 has not been previously reported. In this study, we verified the results of lncRNA microarrays, elucidated the subcellular localization of DCST1-AS1, and explored its diagnostic efficiency and clinical significance. We demonstrated that DCST1-AS1 is activated by MYC and binds directly to miR-873-5p, ultimately upregulating the expression of insulin-like growth factor 2 mRNA binding protein 1 (IGF2BP1) and its downstream protein MYC, CD44, lymphoid enhancer binding factor 1 (LEF1). DCST1-AS1 forms a positive feedback loop with miR-873-5p and MYC to promote TNBC cell proliferation and metastasis. This study sheds light on the potential utilization of DCST1-AS1 as a novel therapeutic target for TNBC.
Six pairs of matched primary tumor and adjacent normal tissues were selected from the tissue sample bank. The cancer tissues were confirmed by immunohistochemical staining to be negative for ER, PR, and HER2. The Arraystar Human LncRNA Microarray v4.0 was used to detect lncRNA and mRNA in TNBC tissues. The original signal file of the probe was imported into the GeneSpring GX v12.1 software and standardized to obtain lncRNA expression information. Data is available through the Gene Expression Omnibus GSE115275.
Thirty pairs of primary TNBC and adjacent normal tissues were obtained from the tissue bank of Jiangsu Cancer Hospital. All tissues were from female patients and were diagnosed between 2017 and 2018. Two experts from the Department of Pathology of Jiangsu Cancer Hospital confirmed by immunohistochemistry that all cancer tissue samples included in the study were ER negative, PR negative, and HER negative. The study was approved by the Ethics Committee of Nanjing Medical University. Informed consent was obtained from all patients. Tissues were frozen in liquid nitrogen until RNA extraction. The TNBC cell lines (MDA-MB-453, BT-549, MDA-MB-231, and HCC1937) and mammary epithelial cell line HBL-100 were obtained from the Chinese Academy of Sciences Cell Bank (Shanghai, China) and cultured according to the ATCC protocols. These cell lines were tested before the study by methods of morphology check, growth curve assay, and mycoplasma detection.
Total RNA was extracted from the cells using Trizol reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's protocol and assessed for quality by One-Drop (Eppendorf, Hamburg, Germany). Mature miRNAs were quantified using the Bulge-Loop miRNA RT-qPCR starter kit and the Bulge-Loop miRNA RT-qPCR primer set (RIBOBIO, Guangzhou, China). The 2-fold Ct method was used to calculate the fold change in gene expression. Primer sequences were shown in Table 1.
DCST1-AS1 RNA probes were labeled with Cy3; BT-549 and MDA-MB-231 cells were fixed and incubated with RNA probes. All manipulations were performed according to the instructions of the FISH kit (Gene Pharma, Shanghai, China). After hybridization, nuclear staining was performed using DAPI staining and the intracellular distribution of DCST1-AS1 was observed with a fluorescence microscope.
The primer sequences used for RT-qPCR.
|Gene name||Forward primer sequences (5'-3')||Reverse primer sequences (5'-3')|
The lentiviral interference vector of DCST1-AS1 and the negative control were synthesized and packaged by Genechem (Shanghai, China). The lentiviral overexpression vector of DCST1-AS1 and the negative control were synthesized and packaged by GenePharma. The original titers of all infectious viruses were > 108 TU/ml. Gradient dilution was used to determine the multiplicity of infection, puromycin (10μg/ml) was used to screen stably transfected cell lines, and RT-qPCR was used to detect the knockdown or overexpression efficiency. MYC overexpression vector and interference fragment were purchased from GenePharma.
The cells were plated in 96-well culture plates (3 × 103 cells per well). At intervals of 24 hours, 10 μl of CCK8 (Dojindo, Kyushu, Japan) was added to each well and incubated for 2 hours, and the absorbance was read at 450 nm. Five replicate wells were set at each time point and the experiment was repeated at least 3 times.
The cells were seeded into a 6-well plate at a gradient density of 800 cells per dish and gently rotated to uniformly disperse the cells. When macroscopic colonies appeared, the supernatant was discarded and the cells were washed twice with PBS. Cells were then fixed with 2 ml of 4% paraformaldehyde for 15 minutes, stained with 1% crystal violet for 20 minutes, then washed with running water.
A sterile 200 μl pipette tip was used to create a wound on a monolayer of cells and the floating cells were washed away with PBS. Microscopic examination of cell migration near the wound was performed regularly. Each experiment was repeated at least 3 times.
The cell cycle was analyzed using PI Staining Kit (KeyGEN, Nanjing, China). Apoptosis was analyzed using Annexin-V APC/7-AAD Double Staining Kit (KeyGEN). The stained cells were then analyzed using a BD LSRFortessaTM flow cytometer (BD Biosciences, Franklin Lake, NJ, USA). Each experiment was repeated at least 3 times.
Transwell chambers (MilliporeSigma, Burlington, MA, USA) and BD BioCoat Matrigel Invasion Chambers (Franklin Lake, NJ, USA) were used for cell migration and invasion assays. After incubation, the upper chamber residual cells were removed with cotton-tipped swabs, and the cells that passed through the membrane were fixed with 4% paraformaldehyde and stained with 0.5% crystal violet. For each experiment, the number of migrating tumor cells was counted from 5 randomly selected fields. Each experiment was repeated at least 3 times.
The reporter vectors containing wild type and mutant MYC binding sites were constructed separately. The interaction between MYC and the promoter binding site was confirmed by the increase in relative fluorescence of the reporter gene. The wild type and mutant type of DCST1-AS1 were cloned into the reporter vector, and the miR-873-5p mimics were co-transfected with the constructed reporter gene vector into 293T cells. The interaction of miR-873-5p with DCST1-AS1 was confirmed by the decrease in relative fluorescence of the reporter gene. Luciferase activity was measured by Dual-Luciferase Reporter Assay System (Promega, Mannheim, Germany) according to the manufacturer's instructions.
The cells were lysed in RIPA Lysis Buffer (Beyotime, Shanghai, China) containing 1 mM PMSF (Beyotime), and total protein from the cell lysate was extracted. The primary antibodies for MYC (1:1000 dilution; Abcam, ab32072), CD44 (1:1000 dilution; Abcam, ab51037), LEF1 (1:1000 dilution; Abcam, ab53293), IGF2BP1 (1:1000 dilution, Abcam, ab184305), AGO2 (1:1000 dilution, Abcam, ab186733), and GAPDH (1:1000 dilution, Abcam, ab181602), were incubated with the transfer membrane for 2 hours at room temperature. The bands were detected using a SuperSignal West Femto Maximum Sensitivity Substrate Kit (Thermo Scientific, Rockford, USA), the images were acquired using a SYNGENE G: BOX chemiXR5 system (Cambridge, UK), and the results were analyzed using Gel-Pro32 software. GAPDH was used as an internal reference to standardize the relative expression of the proteins.
Sufficient cells were harvested and lysed. RNA immunoprecipitation was performed using the Magna RIP RNA-Binding Protein Immunoprecipitation Kit (Millipore, Billerica, MA, USA) according to the manufacturer's instructions. Immunoprecipitation was performed using an AGO2 antibody (Abcam, ab186733) [or immunoglobulin G (IgG) control]. After washing, the AGO2-bound RNAs were eluted and quantified. RT-qPCR was performed to examine whether miR-873-5p and DCST1-AS1 were co-immunoprecipitated.
All data presented are representative of at least 3 independent experiments. Wilcoxon signed rank test was used to compare the matched TNBC and adjacent normal samples. The Mann-Whitney U test was used to analyze the correlation between DCST1-AS1 expression levels and clinicopathological features. Student's t test and one-way analysis of variance (ANOVA) were used to finish the comparisons. P values less than 0.05 were considered statistically significant ( #, P < 0.05; *, P < 0.01, **; P < 0.001). All statistical analyses were performed using SPSS version 22.0 (SPSS, Chicago, IL, USA).
Hierarchical cluster analysis revealed systematic changes in transcriptional expression levels between cancer tissues and adjacent normal tissues (Figure 1A, B). DCST1-AS1 is an antisense lncRNA that we screened via microarray detection and bioinformatics analysis. We used RT-qPCR to detect DCST1-AS1 in 30 pairs of TNBC tissues and adjacent normal tissues, and found that DCST1-AS1 in cancer tissues was significantly higher than adjacent normal tissues, which was consistent with microarray results (Figure 1C). In addition, receiver operating characteristic (ROC) curve showed that the area under the curve (AUC) was 0.952, [95% confidence interval (CI), 0.906 - 0.998, P = 0.023], suggesting that DCST1-AS1 detection has high sensitivity and specificity (Figure 1D).
DCST1-AS1 is up-regulated in TNBC tissues. (A) Hierarchical cluster analysis of lncRNAs in 6 pairs of tumor samples and adjacent normal tissue samples. (B) Analysis of 6484 lncRNAs that were differentially expressed (≥ 2-fold; P < 0.05) using volcano plots. Of these, 2,464 were up-regulated and 4,020 were down-regulated. (C) DCST1-AS1 expression was analyzed by RT-qPCR in tumor samples and adjacent normal tissues (n = 30). DCST1-AS1 expression level was normalized to GAPDH. Horizontal lines in the box plots represent the medians; the boxes represent the interquartile range. The significant differences between samples were analyzed using the Wilcoxon signed rank test. **, P < 0.0001. (D) ROC curve for prediction of TNBC using RT-qPCR based DCST1-AS1 expression level. The AUC was 0.952, with 95% CI and P value indicated, P = 0.023.
DCST1-AS1 is a bona fide lncRNA and is distributed both in the nucleus and cytoplasm. (A) Analysis of coding capacity of DCST1-AS1, MYC as a coding gene control and HOTAIR as a noncoding gene control. (B) RT-qPCR was used to detect the expression of DCST1-AS1 in BT-549, MDA-MB-231, HCC1937, MDA-MB-453, and HBL-100 cells. The mammary epithelial cell line HBL-100 was used as a reference. Values represent averages and bars represent S.D. of three independent experiments. (C) RT-qPCR was used to determine the nuclear/cytoplasmic expression ratio of DCST1-AS1 in BT-549 and MDA-MB-231 cells. U6 was used as an internal reference for the quality of nuclear RNA extracted, and GAPDH was used as an internal reference for the quality of cytoplasmic RNA extraction. Values represent averages and bars represent S.D. of three independent experiments. (D) FISH was used to detect the subcellular localization of DCST1-AS1. Nuclei were detected with DAPI staining and DCST1-AS1 was detected with a Cy3 labeled probe.
Patients with pathologically confirmed TNBC were included in this study according to the selection criteria. We grouped these 30 pairs of tissue specimens according to age, menopause, tumor size, histopathological grade, lymph node metastasis, distant metastasis, and histopathological grade. According to the median DCST1-AS1 detection, the RT-qPCR results of DCST1-AS1 in TNBC tissues and adjacent normal tissues were divided into a high expression group and a low expression group. The results showed that DCST1-AS1 was positively correlated with distant metastasis (P = 0.024) and histopathological grade (P = 0.026) (Table 2).
The analysis of the Coding Potential Calculator  shows that DCST1-AS1 is a typical noncoding RNA lacking protein coding ability and a complete open reading frame (ORF) (Figure 2A). DCST1-AS1 was significantly increased in TNBC cell lines (BT-549, HCC1937, MDA-MB-231, and MDA-MB-453) compared to the mammary epithelial cell line HBL-100 (Figure 2B). HBL-100 cells originally derived from a normal source of breast tissue, established by primary cultures of healthy female milk epithelial cells, and whose transformed phenotype is attributed to integrated simian virus 40 (SV40) genetic information. HBL-100 is an immortalized non-tumorigenic mammary epithelial cell line that is negative for estrogen and progesterone receptors and is used as a source of normal human mammary epithelial cells in many studies [15-17]. The RT-qPCR showed that DCST1-AS1 was expressed both in the nucleus and in the cytoplasm, with a slightly higher expression in the nucleus at a distribution ratio of approximately 6:4 (Figure 2C). The subcellular localization of DCST1-AS1 was detected by fluorescence in situ hybridization assay, and results showed that the fluorescence intensity in the nucleus was higher than in the cytoplasm, which was consistent with the nuclear/cytoplasmic RT-qPCR assay (Figure 2D).
Relationship between DCST1-AS1 expression and pathological features in TNBC patients.
|Parameter||Number||Relative expression of DCST1-AS1|
#P < 0.05. LN, lymph node.
To assess the possible role of DCST1-AS1 in TNBC cells, we obtained two sets of TNBC cell lines stably expressing DCST1-AS1 siRNA or negative control using lentivirus, labeled BT-549-si, BT-549-NC and MDA-231-si, MDA-231-NC, respectively. Our data indicate that lentiviral interference vectors can effectively knock down endogenous DCST1-AS1 levels in these cells (Figure 3A). The growth curve detected by CCK8 showed that DCST1-AS1 knockdown significantly reduced TNBC cell growth (Figure 3B). Cell colony formation assay showed that down-regulation of DCST1-AS1 significantly inhibited anchor-independent growth of BT-549 and MDA-MB-231 cells, resulting in fewer and smaller colonies (Figure 3C). To explore the underlying mechanism of growth inhibition after DCST1-AS1 knockdown, we evaluated its effect on cell cycle and apoptosis in BT-549 and MDA-MB-231 cells. Analysis of the cell cycle distribution showed that DCST1-AS1 down-regulation resulted in a decrease in the G0/G1 phase ratio and an increase in the G2/M ratio in BT-549-si and MDA-231-si, whereas G2/M arrest may contribute to DCST1-AS1 silence-induced growth inhibition (Figure 3D). Annexin V staining showed that the percentage of early apoptotic cells after DCST1-AS1 knockdown was not significantly changed relative to the control group (Figure 3E). Wound healing assay showed a reduced migration capacity of the DCST1-AS1 knockdown cell line (Fig. 3F). Using the transwell system, we found that the invasive ability of TNBC cells was significantly reduced after down-regulation of DCST1-AS1 (Fig. 3G).
We still used the lentiviral overexpression system to assess the effect of DCST1-AS1 overexpression in these hormone receptor negative cells. We selected cell lines with moderate (MDA-MB-231) or very low (HBL-100) endogenous DCST1-AS1 levels and labeled DCST1-AS1 overexpressing cell lines as MDA-231-exp and HBL-100-exp, respectively. The expression of DCST1-AS1 in MDA-MB-231 and HBL-100 cells was significantly increased 96 hours after infection with lentivirus compared to the negative control. The DCST1-AS1 is up-regulated by 105 times in the MDA-MB-231 cells and up by 266 times in the HBL-100 cells (Figure 4A). The CCK8 assay showed that upregulation of DCST1-AS1 promoted cell proliferation of MDA-231-exp, but there was no significant change in HBL-100-exp (Figure 4B). Cell cycle analysis indicated that overexpression of DCST1-AS1 did not alter the distribution of MDA-MB-231 cell cycle (Figure 4C). In the colony formation assay, the number of colonies formed by MDA-231-exp in the overexpressed group was significantly increased after 1 week of culture (Figure 4D). Furthermore, transwell experiments indicated that enhanced expression of DCST1-AS1 promoted cell invasion of MDA-MB-231 cells (Figure 4E). Although HBL-100 cells overexpressed DCST1-AS1, there was no significant change in cell proliferation and invasion ability.
By analyzing the Cancer Genome Atlas (TCGA) data, we found high expression of MYC in TNBC (Figure 5A). Recent studies have confirmed that MYC can regulate lncRNAs . To confirm whether MYC can regulate DCST1-AS1 transcription, the MYC-MAX-specific inhibitor 10058-F4 and MYC siRNA were used to interfere with MYC expression. RT-qPCR showed inhibition or interference with MYC in BT-549 and MDA-MB-231 cells, also accompanied by a significant decrease in DCST1-AS1 (Figure 5B, C). In contrast, DCST1-AS1 in these cells was significantly up-regulated when the MYC overexpression plasmid was transfected (Figure 5D). We predicted the MYC binding site in the 2,000 bp promoter region upstream of the DCST1-AS1 gene using the JASPAR. The mutated sequence was designed, and the dual luciferase assay was used to detect the binding specificity of the transcription factor and the promoter site. We found that the binding of MYC to the wild type site increased the fluorescence intensity by 3.15-fold, confirming that MYC regulates DCST1-AS1 transcription (Figure 5E).
Knockdown of DCST1-AS1 inhibits proliferation and migration. (A) RT-qPCR was used to detect the expression level of DCST1-AS1 in TNBC cells after lentivirus transfection. *, P < 0.01, compared with the NC group. (B, C) CCK8 assay and colony formation assay were used to examine cell proliferation in DCST1-AS1 knockdown TNBC cells. *, P < 0.01, compared with the NC group. (D, E) Flow cytometry was used to detect cell cycle and apoptosis rates of BT-549-si, MDA-231-si cells after lentiviral transfection. *, P < 0.01, compared with the NC group. (F, G) Wound-healing assay and transwell assay were used to determine the migration ability of DCST1-AS1 knockdown TNBC cells. In the migration assay, BT-549 and MDA-MB-231 cells were incubated for 18 hours, whereas in the invasion assay, cells were incubated for 24 hours. *, P < 0.01, compared with the NC group.
Overexpression of DCST1-AS1 promotes TNBC cell proliferation and invasion. (A) RT-qPCR was used to detect changes in the expression of DCST1-AS1 in MDA-MB-231 and HBL-100 cells after lentiviral transfection. Transcript levels were normalized to GAPDH. *, P < 0.01, compared with the NC group. (B) CCK8 assay was performed to determine the effect of ectopic expression of DCST1-AS1 on TNBC cell proliferation. #, P < 0.05, compared with the NC group. (C) Flow cytometry was used to detect changes in the cell cycle of MDA-MB-231 cells overexpressing DCST1-AS1. (D) Colony formation assays were used to determine the effect of DCST1-AS1 overexpression on TNBC cells anchorage-dependent growth. *, P < 0.01, compared with the NC group. (E) Transwell assays were used to determine the effect of up-regulation of DCST1-AS1 on cells invasion. In the migration assay, MDA-MB-231 cells were incubated for 12 hours and HBL-100 cells were incubated for 24 hours. In the invasion assay, MDA-MB-231 cells were incubated for 24 hours and HBL-100 cells were incubated for 48 hours. *, P < 0.01, compared with the NC group.
We predicted that miR-873-5p could bind to DCST1-AS1 using miRBase (Figure 6A). RT-qPCR assay confirmed that miR-873-5p was down-regulated in TNBC and negatively correlated with DCST1-AS1 (Figure 6B, C). Overexpression of miR-873-5p in BT-549 and MD-MB-231 cells significantly down-regulated DCST1-AS1, whereas knockdown of DCST1-AS1 in these cells up-regulated miR-873-5p (Figure 6D, E). We designed the mutant sequence based on the "seed region" of miR-873-5p and confirmed that miR-873-5p binds to DCST1-AS1 through the predicted site by dual luciferase assay (Figure 6F).
MicroRNAs are known to bind in an argonaute 2(AGO2)-dependent manner and cause RNA translational inhibition and/or degradation . To understand how miR-873-5p acts on DCST1-AS1, we performed mRNA stability experiments. We treated the TNBC cells transfected with miR-873-5p using the RNase inhibitor actinomycin D, and then detected the remaining DCST1-AS1 in the cells using RT-qPCR. Our results showed that the half-life of DCST1-AS1 was significantly shortened (Figure 6G), indicating that miR-873-5p affects the stability of DCST1-AS1 at the post-transcriptional level. Subsequently, we designed the siRNA fragment to knock down AGO2 and found that DCST1-AS1 was up-regulated by about 19-fold, indicating that AGO2 is involved in the degradation of DCST1-AS1 (Figure 6H, I). To confirm this inference, we treated BT-549 cells with a miR-873-5p inhibitor or a negative control for RNA immunoprecipitation. We detected DCST1-AS1 and miR-873-5p in both AGO2 antibody immunoprecipitates, and DCST1-AS1 was significantly reduced in the miR-873-5p inhibitor group (Figure 6J).
DCST1-AS1 is activated by MYC. (A) Analysis of MYC expression levels in breast cancer subtypes using TCGA data. **, P < 0.0001. (B, C) DCST1-AS1 expression was decreased when MYC siRNA or the MYC-MAX inhibitor 10058-F4 (50 μg/ml) were added to BT-549 and MDA-MB-231 cells. *, P < 0.01, compared with the NC group. (D) DCST1-AS1 expression was up-regulated when MYC-overexpression plasmids were transferred into BT-549 and MDA-MB-231 cells. *, P < 0.01, compared with the NC group. (E) Dual luciferase assay confirmed that MYC binds to the DCST1-AS1 promoter locus. Pro, promoter. *, P < 0.01, compared with the NC group.
Since DCST1-AS1 can affect the expression of miR-873-5p in TNBC cells, can it affect the downstream target genes of miR-873-5p? We searched the literature to find that IGF2BP1 is a direct target gene of miR-873-5p . Further analysis of TCGA data, we found that IGF2BP1 is highly expressed in breast cancer (Figure 7A, B). Patients with high IGF2BP1 expression in breast cancer have a worse prognosis (Figure 7C). In the above studies we have confirmed that DCST1-AS1 is a direct target of miR-873-5p. MYC, CD44 and LEF1 are known downstream proteins of IGF2BP1 and are involved in the regulation of cell proliferation and metastasis. Using Western blotting experiments, we found that knockdown of DCST1-AS1 effectively down-regulated IGF2BP1, MYC, CD44 and LEF1 protein levels in TNBC cells (Figure 7D). Our study found that DCST1-AS1 can adsorb miR-873-5p, knockdown of DCST1-AS1 can increase miR-873-5p in BT-549 cells, thereby reducing the expression of the pro-cancerous factor IGF2BP1. To validate our findings, we designed a series of rescue experiments in which miR-873-5p inhibitors were transfected into BT-549-si cells, and we found that IGF2BP1 expression was up-regulated (Figure 7E). CCK8 detection and wound healing experiments confirmed partial recovery of cell proliferation and migration (Figure 7F, G).
DCST1-AS1 is direct target of miR-873-5p. (A) Prediction of binding sites for miR-873-5p and DCST1-AS1. (B) Expression of miR-873 in 30 pairs of TNBC tissues and adjacent normal tissues. miR-873-5p expression levels were normalized to U6. The significant differences between samples were analyzed using the Wilcoxon signed rank test. *, P < 0.01. (C) The inverse relationship between the expression of DCST1-AS1 and miR-873-5p. Expression was normalized and correlation was analyzed by Pearson correlation coefficient, R2 = 0.6249, P < 0.0001 (D) RT-qPCR analysis showed that DCST1-AS1 expression was decreased in BT-549 and MDA-MB-231cells transfected with miR-873-5p mimics. *, P < 0.01. (E) qPCR analysis showed that miR-873-5p expression was up-regulated by interference with DCST1-AS1 in BT-549 and MDA-MB-231 cells. *, P < 0.01. (F) Dual luciferase assay confirmed that miR-873-5p binds to the predicted binding site of DCST1-AS1. WT, wild type. Mut, mutant. *, P < 0.01. (G) mRNA stability analysis: The half-life of DCST1-AS1 in BT-549 cells was shortened by 6.22 hours and the half-life of DCST1-AS1 in MDA-MB-231 cells was shortened by 3.46 hours; 18S rRNA was used as an internal reference. *, P < 0.01. (H) The relative expression levels of miR-873-5p and DCST1-AS1 in BT-549 cells after interference with AGO2 were detected by RT-qPCR. GAPDH was used as an internal reference for DCST1-AS1, and U6 was used as an internal reference of miR-873-5p. *, P < 0.01. (I) Western blotting was used to detect IGF2BP1 protein levels in BT-549 cells after AGO2 interference. (J) The amount of DCST1-AS1 and miR-873-5p bound to anti-AGO2 or IgG was measured by RT-qPCR in the presence of a miR-873-5p inhibitor or a negative control. *, P < 0.01.
Metastasis is the leading cause of death in solid tumor patients and is considered to be the last step in progressive breast cancer . Patients with TNBC have a lower survival rate due to the high invasiveness, metastasis, and rapid recurrence of the tumor . The lack of a new treatment for TNBC reflects, in part, a lack of full understanding of its development and progress.
The identification and characterization of cancer-associated lncRNAs is a critical step toward a thorough understanding of cancer biology and subsequent diagnosis and treatment [22, 23]. Studies have shown that lncRNAs can regulate many important cancer phenotypes and can also be used as diagnostic or prognostic markers [24-26]. We found that DCST1-AS1 is an oncogenic lncRNA and its expression level is associated with disease progression. Gain- and loss-of-function approaches confirmed that DCST1-AS1 is involved in regulating cell proliferation and metastasis. To date, there have been no reports on the biological function of DCST1-AS1; therefore, this research is innovative.
DCST1-AS1 regulates the downstream proteins of miR-873-5p. (A) The expression level of IGF2BP1 in BRCA was analyzed by TCGA data. **, P < 0.0001. (B) TCGA data analysis showed that IGF2BP1 expressed higher levels in TNBC and luminal subtypes than normal controls, with significant differences. #, P < 0.05, *, P < 0.01. (C) The relationship between the expression of IGF2BP1 and the prognosis of BRCA patients was analyzed by TCGA data. P = 0.0054. (D) Western blotting showed a decrease in the expression of IGF2BP1, MYC, LEF1 and CD44 in DCST1-AS1 interfering cells. (E) The miR-873-5p inhibitor was transfected into BT-549-si cells, and the expression of IGF2BP1 protein was measured by Western blotting. (F) The miR-873-5p inhibitor was transfected into BT-549-si cells and cell proliferation was measured by CCK8 assay. *, P < 0.01. (G) The miR-873-5p inhibitor was transfected into BT-549-si cells and cell migration was measured by wound healing assay. *, P < 0.01.
MYC is a central regulator of tumorigenesis and affects a variety of cellular biological processes [27, 28]. It is worth noting that MYC is disproportionately up-regulated in TNBC, and its specific functions are not fully understood. Our results indicate that DCST1-AS1 is consistent with MYC expression and that MYC can promote DCST1-AS1 transcription.
It is well known that microRNAs can interact with mRNA by sequence complementarity to induce inhibition of protein translation levels. Recent studies have shown that microRNAs can also bind to noncoding RNAs and play regulatory roles [29, 30]. miR-873-5p is a microRNA that is down-regulated in colorectal cancer, gastric cancer, ovarian cancer and breast cancer, and acts as a negative regulator of tumor proliferation and metastasis [31, 32]. We found that miR-873-5p is negatively correlated with DCST1-AS1 in TNBC tissues, and that miR-873-5p binds directly to DCST1-AS1. microRNA mainly forms RNA-induced silencing complex (RISC) to negatively regulate target genes, and AGO2 is the core protein that exhibits enzyme cleavage activity . We found that DCST1-AS1 and miR-873-5p bind to the same RISC, and miR-873-5p exerted an mRNA cleavage function at the post-transcriptional level.
IGF2BP1 plays an important role in embryogenesis and carcinogenesis. As a post-transcriptional regulator, IGF2BP1 regulates the expression of some mRNAs required to control tumor cell proliferation and invasion, and is associated with poor overall survival and metastasis in cancer . Therefore, IGF2BP1 is considered to be a potential therapeutic target for oncogenes and cancer [35, 36]. IGF2BP1 can bind to the unstable determinant in the ORF coding region and prevents the cleavage of MYC mRNA by endonucleases and microRNAs . IGF2BP1 can increase the stability of CD44 mRNA and promotes cell adhesion and invadopodia formation in cancer cells . IGF2BP1 can prevent LEF1 mRNA degradation, leading to the up-regulation of LEF1 expression . LEF1 is an important transcription factor involved in the activation of the Wnt signaling pathway, and facilitates the synthesis of mesenchymal fibronectin and promotes epithelial-mesenchymal transition in breast cancer . We found that the interaction between DCST1-AS1 and miR-873-5p dilutes the regulation of IGF2BP1 expression by miR-873-5p, upregulating the expression of MYC, CD44 and LEF1, which play important roles in cell proliferation and metastasis. Here, we were pleasantly surprised to find a positive feedback regulation: MYC promotes DCST1-AS1 transcription, and DCST1-AS1 increases MYC translation.
We believe that the conclusions of this study are not all the functions and mechanisms of DCST1-AS1. In future studies, we will validate the function of DCST1-AS1 using in vivo experiments and screen for potential cellular signaling cascades regulated by DCST1-AS1 using high-throughput sequencing.
In summary, we confirmed that DCST1-AS1 is an oncogenic lncRNA and its expression level is positively correlated with TNBC progression. DCST1-AS1 is activated by MYC and is degraded by binding to miR-873-5p. DCST1-AS1 forms a positive regulatory loop with miR-873-5p and MYC to promote TNBC cell proliferation and metastasis. Our research on DCST1-AS1 will help broaden the understanding of the complex regulatory mechanisms among key molecules in cancer cells and provides a new perspective on the molecular mechanisms of TNBC cell proliferation and metastasis.
TNBC: triple-negative breast cancer; ER: estrogen receptor; PR: progesterone receptor; HER2: human epidermal growth factor receptor 2; lncRNA: long noncoding RNA; DCST1-AS1: DC-STAMP domain containing 1-antisense 1; IGF2BP1: insulin-like growth factor 2 mRNA-binding protein 1; AGO2: argonaute 2; LEF1: lymphoid enhancer-binding factor 1; RISC: RNA-induced silencing complex; EMT: epithelial-mesenchymal transition.
This work was founded by National Natural Science Foundation of China (21475063, 81802898), Natural Science Foundation of Jiangsu Province (BK20181090), Innovative Team of Jiangsu Province (CXTDA2017017).
LT: design experiments, analyze data, and draft the manuscript. YC and XT: conduct experiments. DW and XX: collect breast cancer tissue specimens and perform pathological identification. FY revised the manuscript. All authors read and approved the final manuscript.
This study involved patient tissue specimens. This study was approved by the Ethics Committee of Nanjing Medical University. All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent was obtained from all individual participants included in the study.
The authors have declared that no competing interest exists.
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Corresponding author: Feng Yan, Department of Clinical Laboratory, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & the Affiliated Cancer Hospital of Nanjing Medical University; No. 42 Baiziting Road, Nanjing 210009, P.R. China. Tel: +86 25 83283397; E-mail: yanfeng1895com