Down-regulation of miR-210-3p encourages chemotherapy resistance of renal cell carcinoma via modulating ABCC1

Background ATP-binding cassette transporter super-family including ABCC1 and MDR-1 were involved in multi-drug resistance (MDR) of renal cell carcinoma (RCC) patients. Several miRNAs were confirmed to promote the MDR and the survival of tumor cells. Methods The RCC cell lines Caki-2 with vinblastine-resistant (Caki-2/VBL) or doxorubicin-resistant (Caki-2/DOX) were constructed, respectively. The expressions of miR-210-3p, ABCC1 and MDR-1 protein were determined by qRT-PCR and Western blot assays. The viability of RCC cells was assessed by MTT assay. The regulatory relationship between miR-210-3p and ABCC1 was analyzed by Dual Luciferase assay. The effect of miR-210-3p in vivo was investigated with a tumor xenograft model in mice. Results MiR-210-3p expression was observed to significantly decrease in Caki-2/VBL and Caki-2/DOX cells. Meanwhile, ABCC1 and MDR-1 were significantly increased in Caki-2/VBL and Caki-2/DOX cells. ABCC1 was a novel target of miR-210-3p and negatively regulated by miR-210-3p. And miR-210-3p improved drug-sensitivity of RCC cells. Down-regulation of ABCC1 could reverse the effect of miR-210-3p knockdown on the drug-resistance and the level of MDR-1 in drug-sensitive RCC cells. Conclusion We confirmed that down-regulation of miR-210-3p increased ABCC1 expression, thereby enhancing the MRP-1-mediated multidrug resistance of RCC cells.


Background
Renal cell carcinoma (RCC) is one of the most lethal urologic malignancies worldwide with significant morbidity, mortality and poor prognosis [1]. The surgical therapy, including radical resection or nephron-sparing surgery, was commonly used as the preferred method for RCC. For those with advanced or recurring RCC patients, chemotherapy is the mainstream method for RCC in clinic, but it has unsatisfactory results in RCC patients [2]. The main reason for chemotherapy failure is that RCC cells develop multidrug resistance (MDR) to chemotherapy agents, such as vinblastine and doxorubicin [3]. MDR expanded the ability of RCC cells to resist the cytotoxicity induced by chemotherapy agents, which was also accurately regulated by non-coding RNAs, proteins and signaling pathways [4]. The exploration of MDR mechanisms in RCC has become a new research direction in this field.
RCC patient with insensitivity to conventional chemotherapy agents may attribute to the intrinsic or acquired multi-drug resistance. ABCC1 and MDR-1, two numbers of ATP-binding cassette transporter super-family related to multi-drug resistance, were documented to increase in RCC patients and served as the efflux pumps to promote chemotherapeutic drugs out of cancer cells via the assistance of ATPase activity [5,6]. The expression of ABCC1 and MDR-1 could act as the MDR markers in RCC [6].
However, the relative contributions and causative roles of ABCC1 and MDR-1 in MDR of RCC cells have not been completely clarified.
MicroRNAs (miRNAs), a class of non-coding RNAs with the length of 18-25nt, are implicated in various fundamental biological processes and cancer pathological processes [7] through binding with 3′UTR of target mRNAs, thereby causing the inhibition of translation and the degradation of mRNA, eventually to modulate gene expression at the post-transcriptional level [8]. More and more evidences have indicated that the aberrant miRNA expression is related to drug resistance/sensitivity and pathology of RCC [9,10]. MiR-210-3p was reported to be depleted by CRISPR/Cas9 to promote tumorigenesis through TWIST1 revival in RCC [11]. Moreover, miR-210-3p was predicted to have the binding site on the 3′UTR of ABCC1. Hence, we hypothesized that miR-210-3p was involved in the underlying mechanism of MDR in RCC.

Cell culture and induction of drug-resistant cell lines
Caki-2 cells, a human RCC cell line, were purchased from American Type Culture Collection (ATCC; Manassas, VA, USA) and were cultured in the McCoy's 5A medium (Thermo Fisher scientific, Massachusetts, USA) supplied with 10% FBS and 100 µg/ml double-antibody at 37 °C with the humidified 5% CO 2 . Caki-2/DOX (doxorubicinresistant) and Caki-2/VBL (vinblastine-resistant) cells, the drug-resistant RCC cell lines, were constructed via Caki-2 cell lines (their independent parental cell lines) being exposed to the IC 50 concentration of DOX and VBL for 3 months, and then exposed to tenfold higher dose of IC 50 for 6 months with the same cultural conditions as Caki-2 cell lines [12].

Xenograft model
In order to analyze the effects of miR-210-3p on drugresistant renal tumor growth in vivo, a nude mouse tumor xenograft model was established. The present study was approved by Animal Care and Experimentation Committee of The First Affiliated Hospital of Zhengzhou University. Nude mice were transplanted subcutaneously with 2.5 × 10 6 Caki-2/DOX cells with/without miR-210-3p over-expression into the right flank [pre-NC group (n = 8) and miR-210-3p mimic group (n = 8)]. After 10 days, the mice of two groups were treated with DOX (2 mg/kg/day) via intraperitoneal injections. Every 3 days, the length (L) and width (W) of tumor in mice were measured, and the tumor volume was calculated using the following equation: (L × W 2 )/2. After 30 days, the mice were killed and tumor tissues were removed for the following study.
In the following experiment, Mice were transplanted subcutaneously with 2.5 × 10 6 Caki-2 cells with/without miR-210-3p knockdown into the right flank [NC group (n = 8) and miR-210-3p inhibitor group (n = 8)]. After 10 days, the mice of two groups were treated with DOX (2 mg/kg/day) via intraperitoneal injections. Every 3 days, the length (L) and width (W) of tumor in mice were measured, and the tumor volume was calculated using the following equation: (L × W 2 )/2. After 30 days, the mice were killed and tumor tissues were removed for the following study.

Statistical analysis
All data from three independent repeated experiments were exhibited as the mean ± SD and statistically analyzed with Student's t test for single comparison between two groups and one-way ANOVA for comparison of multiple groups on SPSS 17.0 (SPSS Inc., Chicago, IL, USA). A value of P less than 0.05 was considered statistically significant.

The expression of miR-210-3p could decline the drug resistance of RCC cells
MiR-210-3p levels were up-regulated in Caki-2/DOX and Caki-2/VBL cells via transfection with miR-210-3p mimic, followed by treated with different concentration of DOX and VBL, respectively. The viabilities of Caki-2/ DOX and Caki-2/VBL cells with miR-210-3p overexpression were declined, which suggested that up-regulation of miR-210-3p could elevate the drug-sensitivity of RCC cells (Fig. 2a). In addition, Caki-2 cells with miR-210-3p knockdown were treated with different concentrations of DOX or VBL. The increased viability of Caki-2 cells indicated that the drug-resistance of RCC cells was enhanced by miR-210-3p down-regulation (Fig. 2b).

MiR-210-3p promoted the drug-sensitivity of RCC in mice
DOX was used to inject into the mice injected by Caki-2/DOX cells with/without miR-210-3p overexpression. The tumor volume was markly reduced in the mice of miR-210-3p mimic group, which exhibited that the miR-210-3p effectively enhanced the DOX-sensitivity of RCC to inhibit the growth of tumor (Fig. 6a). The levels of ABCC1 and MDR-1 were also declined in the mice of miR-210-3p mimic group (Fig. 6b). On the other hand, DOX was used to inject into the mice injected by Caki-2 cells with/without miR-210-3p inhibition. The DOX-resistance of RCC enhanced the speed of tumor growth in the mice of miR-210-3p inhibitor group (Fig. 7a). The levels of ABCC1 and MDR-1 were also remarkably elevated in the mice of miR-210-3p inhibitor group (Fig. 7b).

Discussion
Chemotherapeutic unresponsiveness, metastatic spread and recurrence of RCC are mainly resulted from MDR. MiR-210-3p has been detected to be differently expressed between the drug-resistant and drug-sensitive RCC cells and involved in the drug-sensitivity of RCC cells. In our study, we focused on the role of miR-210-3p in the occurrence of RCC drug-resistance and further explored its underlying mechanism.
Emerging researches have indicated that several miR-NAs were significantly associated to the recurrence and survival of patients with RCC and might act as biomarkers for the diagnosis of RCC patients with high risk in early recurrence phase after surgical resection in kidney [25]. In like manner, miRNAs promoted the phenotype of drug-resistant and the survival of tumor cell via directly targeting MDR family members to regulate the multi-drug resistance. MiR-210-3p was reported to highly express in clinical ccRCC specimens (compared to adjacent non-cancerous tissues) and RCC cell lines 786-o, A498 and Caki-2 (compared to normal kidney cells). However, Yoshino et al. reported that the higher expression of miR210-3p found in the ccRCC clinical samples and the cell lines was probably inhibitory to tumor progression, as shown by an accelerated cell invasiveness and an increased number of colonies in the miR-210-3p-depleted cells in comparison to the controls [11]. In the present study, the expression of miR-210-3p was decreased in Caki-2/DOX and Caki-2/VBL cells, compared to the RCC cell line Caki-2, suggesting the correlativity between miR-210-3p and drug-resistance of RCC cells. We further confirmed that miR-210-3p improved drug-sensitivity of RCC cells through inhibiting ABCC1. And up-regulation of miR-210-3p could decrease the drug-resistance and the levels of ABCC1 and MDR-1 in (See Figure on previous page.) Fig. 3 The mechanism of miR-210-3p regulating ABCC1. a The binding site of miR-210-3p on ABCC1 3′UTR was predicted by bioinformatics software. b In the Caki-2 cells, knockdown of miR-210-3p up-regulated the 3′UTR activity of wild type ABCC1 and the expression of ABCC1. c Overexpression of miR-210-3p inhibited the 3′UTR activity of wild type ABCC1 and the expression of ABCC1 in drug-resistant RCC cells. *P < 0.05 vs. NC, #P < 0.05 vs. pre-NC Fig. 4 MiR-210-3p modulated MDR-1 expressions of RCC cells via ABCC1. a Caki-2 cells were transfected with si-ABCC1 or si-control, the knockdown efficiency of ABCC1 was detected using qRT-PCR and Western blot assays. Caki-2 cells were transfected with miR-210-3p inhibitor or miR-210-3p inhibitor + si-ABCC1, and then the levels of MDR-1 were assessed by Western blot assays. b Caki-2/DOX and Caki-2/VBL cells were transfected with pcDNA-ABCC1 or pcDNA, the overexpression efficiency of ABCC1 was detected using qRT-PCR and Western blot assays. Caki-2/DOX and Caki-2/VBL cells were transfected with miR-210-3p mimic or miR-210-3p mimic + pcDNA-ABCC1, and then the levels of MDR-1 were assessed by Western blot assays. *P < 0.05 vs. si-control or pcDNA inhibitor + si-control, and then cell viabilities were assessed by MTT assays. b Caki-2/DOX and Caki-2/VBL cells were transfected with miR-210-3p mimic or miR-210-3p mimic + pcDNA-ABCC1, then cell viabilities were assessed by MTT assays. *P < 0.05 vs. NC or pre-NC, # P < 0.05 vs. miR-210-3p inhibitor + si-control or miR-210-3p mimic + pcDNA Fig. 6 MiR-210-3p increased the drug-sensitivity of RCC. DOX was used to inject into the mice injected by Caki-2/DOX cells with/without miR-210-3p over-expression. a The tumor volume was markly reduced in the mice of miR-210-3p mimic group. b The levels of ABCC1 and MDR-1 were also declined in the mice of miR-210-3p mimic group. *P < 0.05 vs. pre-NC drug-resistant RCC cells. Hence, we confirmed that miR-210-3p mediated multi-drug resistance of RCC cells via binding with ABCC1. Moreover, miR-210-3p improved drug-sensitivity of RCC cells through inhibiting ABCC1. We identified the existence of miR-210-3p/ABCC1 axis in multidrug resistance of RCC cells, which also were proved in vivo.
In conclusion, we confirmed that down-regulation of miR-210-3p increased ABCC1 expression, thereby enhancing the MRP-1-mediated multidrug resistance of RCC cells, as shown by an increase in MDR1 expression and in cell viability with DOX or VBL treatment. Fig. 7 MiR-210-3p decreased the drug resistance of RCC. DOX was used to inject into the mice injected by Caki-2 cells with miR-210-3p inhibition. a The tumor volume was markly enhanced in the mice of miR-210-3p inhibitor group. b The levels of ABCC1 and MDR-1 were also enhanced in the mice of miR-210-3p inhibitor group. *P < 0.05 vs. NC