Osteosarcoma (OS) is the most common type of primary malignant neoplasm of the skeleton in children and young adolescents 1. Despite significant advances have been achieved in chemotherapeutics and surgical management, the long-term survival for OS patients remains dismally poor. Now near 30-40 percent of patients after the successful resection of primary tumors may develop metastases, moreover approximately 80 percent of the OS patients with metastatic disease at diagnosis 2. Generally, the standard multimodal therapy failure for OS is associated with a very poor prognosis. Thus, it is imperative to reveal novel molecular markers in the diagnosis, treatment and prognosis of osteosarcoma 3.Ubiquitination is involved in post-translational modification and plays vital roles in different biological and pathological processes in eukaryotes 4. E3 ubiquitin ligases (E3s) are critical importance due to not only transfer ubiquitin to specific substrates 5. Ring finger protein 187 (RNF187), a RING domain-containing ubiquitin E3 ligase, was lately verified to overexpressed in hepatocellular carcinoma and non-small cell lung carcinoma and advanced tumor development by inducing tumor cell epithelial-mesenchymal transition (EMT) 6, 7. Furthermore, RNF187 knockout was revealed to suppress the cellular proliferation via inhibiting the transcription of AP-1-related genes, and RNF187 overexpression activated Wnt and Ras pathways to accelerate the tumor formation in colon epithelial tumor 8. Moreover, RNF187 was originally demonstrated to be a co-activator of JunD by a yeast two-hybrid screen 9. Together, the aforementioned data indicate that the abnormal RNF187 may be an important booster in tumor development 10. However, the expression and roles of RNF187 in OS are largely uncharacterized.Here, we tried to determine the RNF187 expression in OS tissues and cells, and assess the role of RNF187 in biological behaviors of OS cells via RNF187 knockdown and cDNA transfection. Finally, the clinical implications of RNF187 in OS patients were studied in TMAs including 51 OS cases.
Materials and Methods
Cell lines, plasmids and chemotherapeutic agents
OS cells lines , U-2OS, MG-63, Saos and HOS, and a human osteoblastic cell line, hFOB1.19 (from the Cell bank of Chinese Academy, Shanghai, China), were conventionally cultured in DMEM and RPMI 1640 (Gibco; Waltham, MA, USA) supplied with 10 percent heat-inactivated fetal calf serum (FCS) (Gibco; Waltham, MA, USA), 1% L-glutamine, and penicillin/streptomycin (10,000 U/mL and 10,000 µg/mL) (Yesen, Shanghai, China), and kept at 37°C in a humidified incubator under 5% CO2.The pGPU6-GFP-vshRNA-RNF187s and pGMLV-RFP-cDNA-RNF187 was constructed by genomeditech biological company (Genomeditech, Shanghai, China). Paclitaxel (Yesen, Shanghai, China) and Docetaxel (Yesen, Shanghai, China) were kept in our laboratory.
Patients and follow-up
The data of OS patients who underwent surgical therapy at the Second Affiliated Hospital of Nanchang University between January 2006 and December 2012 were summarized and re-examined according to our previous study 11. The pathological diagnosis was affirmed by two pathologists. The frozen specimens were storage at -80°C. Paraffin-embedded OS samples were conventionally prepared by the pathologist and kept in the department of pathology of our hospital. Written agreement from patients or their guardians was obtained and approved by the Nanchang University Ethics Committee. Clinicopathologic features of the present series of OS patients are shown in Table .
RNA Extraction and qRT-PCR
Fifteen OS and their matched nontumorous specimens were used to determine the RNF187 expression, and the RNAs were extracted routinely according to the description elsewhere 12. The DNA amplification and revelation were accomplished by applying the ABI PRISM 7900 Sequence Detection System (Applied Biosystems, Foster City, CA). β-action was availed as an internal reference. Primers for RNF187 were: 5'-TGGAAATCATGAGAACTTG-3' and: 5'-ACGGTCCATCACGTGTCC-3′; and β-action: 5'-AGAGCTACGAGCTGCCTGAC-3' and 5'-AGCACTGTGTTGGCGTACAG-3'. The PCR amplification were in accordance with our previous study 11. This test was repeated three times.
Western blot
Thirty mg protein extracted from the OS cell lines were used for western blot as described elsewhere 13, 14. All antibodies used in this study were listed in . β-action (1:2000, Abcam, Cambridge, UK) was used as an internal reference. This test was repeated in triplicate. All the antibodies employed in our experiment were displayed in.
Cell proliferation, cell migration, and invasion assays
Cell proliferation was determined by the Cell Counting Kit-8 (CCK8) (Yesen, Shanghai, China) according to the manufacturer's protocol.The scratch and cell invasion assays were carried out in accordance with our previous reports 11. This experiment was performed in triplicate.
Metastasis assays in vivo
The OS cells (Including 2.0 × 106 shRNA-RNF187-MG-63 and HOS-RNF187 cDNA cells and their control cells were suspended in 100 μL serum-free RPMI 1640 medium with Matrigel™ (1:1) (BD Biosciences, San Jose, CA, USA), and then injected into the flank of nude mice (s.c.). The implanted tumor volume and total number of lung metastases were evaluated according to our and other previous reports 11, 15.
Tissue microarrays and immunohistochemistry
Tissue microarrays (TMA) and immunohistochemistry (IHC) and were constructed and performed as our pervious report 11. Polyclonal rabbit anti-humanRNF187 (1:200; Novus Biologicals, Cambridge, UK) was used to detect the RNF187 protein. RNF187 expression was evaluated according to the intensity and ratio of positive tumor cells as the previously described 6, 13, 16. The two levels of RNF187 intensity of were classified according to the mean area of positive staining, and the cutoff value was 50% of tumor section, the ≥50 percent was positive, and negative was < 50 percent.
Statistical analysis
The SPSS 21.0 software (SPSS) was employed to analyze the data. Values were showed as the mean ± standard deviation. The Fisher's exact probability, χ2 test, and Student's t test were used for comparison between groups. Overall survival and recurrence free survival (RFS) were defined as described previously 20. Prognostic significance was analysed by Kaplan-Meier survival analysis and log-rank tests. The P <0.05 was considered statistically significant.
Results
RNF187 expression is elevated in OS tissues
Expression of RNF187 was examined by qRT-PCR in OS and matched nontumorous tissues. Low expression of RNF187 was detected in matched nontumorous compared with OS tissues. As shown in Fig. and 1B, the relative RNF187 expression was 3.83 ± 0.79 and exhibited considerable variation in OS samples (range 1.28 - 6.27), while mean expression level was only 1.70 ± 0.63 in matched nontumorous tissues (range 0.59 - 2.64). The difference in RNF187 expression between OS and matched nontumorous tissues was statistically significant (p < 0.01). IHC also showed a high level of RNF187 in OS samples compared with matched nontumorous tissues (Fig. ).
RNF187 promotes metastasis and invasion of OS in vitro
To explore the biological role of RNF187 in OS, we firstly evaluated the RNF187 expression in hFOB1.19, Saos, HOS, U-2OS and MG-63 cell lines, and found that RNF187 expression in OS cells was higher than that in hFOB1.19 cells at the level of mRNA and protein (p < 0.05). Then MG-63 cells were transfected with pGPU6-GFP-vshRNA-RNF187s. Of three vshRNA-RNF187s tested, #2 was found to be the most efficient downregulation of RNF187 by qRT-PCR and western blot assays. The pGMLV-RFP-cDNA-RNF187 vectors were transfected to HOS cells, and the RNF187 was obviously up-regulated in HOS cells (Figs. ) and selected for following experiments. The OS cells proliferation were inhibited by the interference of RNF187, while increased by RNF187 cDNA transfection (p > 0.05, Fig. ). The scratch assay showed that an distinctly postponement in the wound closure rate of MG-63-shRNA-RNF187 and HOS-RNF187 cells was found at 48 h, compared with their control cells (Fig. ). The transwells assay showed that down-regulated RNF187 expression was associated by weaken invasiveness of MG-63 a cells, while was enhanced by RNF187-cDNA transfection (Fig. ). Moreover, the cells with high level of RNF187 showed enhanced ability of clone formation (Fig. ). These results indicated that overexpression of RNF187 was along with increased metastatic and proliferative potential of OS cells.
Elevated RNF187 induces the drugs resistance of OS cells, increased the activation of ERK1/2 and BCL-2 expression
The chemoresistance to anti-OS therapy is one of the major obstacles in the treatment of OS, including paclitaxel and docetaxel which were routinely used in the therapy of OS 3, 17, 18. Here, we further explored the roles of RNF187 on the effect of paclitaxel and docetaxel in OS cells. We found that proliferation decreased significantly upon treatment with paclitaxel and docetaxel in OS cells with low level of RNF187 compared with the OS cells with high level of RNF187(Figure ). Additionally, we revealed that high level of RNF187 was associated with the activation of ERK1/2 signaling, and elevated expression of BCL-2(Figure ). In vivo analysis showed that the tumor volumes of in the MG-63-shRNA-RNF187 or HOS group were smaller compared to their controls (p<0.05, Figure ), and the incidences of lung metastasis were 40% and 20% in the MG-63-shRNA-RNF187 and HOS groups compared to 100% in the control groups, respectively (Figure
Expression of RNF187 was positively associated with malignant phenotypes of OS
Positive RNF187 staining was located in the cytoplasm of tumor cells and showed substantial heterogeneity in the different tumor specimens (Figure . A proportion of 47.05% (24/51) was RNF187high in the total number of patients. Patients with high RNF187 expression exhibit aggressive phenotype. As shown in Table , RNF187high was significantly correlated with high Enneking stage (p = 0.001), a poor response to chemotherapy (p = 0.004) and metastasis (p = 0.001) compared to the patients with low expression of RNF187. However, additional clinical features, containing age, sex, and site of primary tumor, were not significantly relevant to the RNF187 expression.
Overexpression of RNF187 was associated with poor prognosis of OS patients
Up to the final follow-up, the 5-year overall survival and relapse-free survival (RFS) in the whole population were 69.44%, and 62.35%, respectively. The 2- and 5-year overall survival in the RNF187low group was apparently higher than that in the RNF187high group (Fig. ). The 2- and 5-year RFS in the RNF187low group were apparently higher than those in the RNF187high group (Fig. ), indicating that RNF187 expression predicts an unfavorable prognosis for patients with osteosarcoma. Univariate analysis showed that overexpression of RNF187, high Enneking stage, poor response to chemotherapy, and lymphatic metastasis were predictors of overall survival and RFS. Additional features containing age and sex had no prognostic significance for overall survival or RFS (Table ).
Discussion
OS has a strong tendency to metastasize, and metastasis is the key cause of therapy disappointment and death for OS patients 19. In this study, we showed that RNF187 overexpressed in OS compared to matched nontumorous tissues. By RNA interference and cDNA transfection, we presented that OS cells with high levels of RNF187 appeared the high invasive and metastatic potential both in vitro and in vivo. Furthermore, we also confirm that OS cells expressing high levels of RNF187 showed drugs resistance to chemotherapeutic agents. Clinically, we found that the elevated expression of RNF187 correlates with poor survival and with disease recurrence in TMA including 51 OS cases. The above results indicated RNF187 functioned as a promoter for the proliferation and invasion of RNF187-overexpressing OS cells.Now, it is acknowledged that ubiquitination plays an important role in posttranslational protein modification, regulating a host of crucial cellular processes, such as cell cycle, apoptosis, and DNA repair 20, 21. Thus, it is easy to understand that dysfunction of ubiquitin has been identified to be related to the tumorigenesis and progression of various tumors 20, including lung cancer 22-24, colorectal cancer 25, hepatocellular carcinoma 26, 27 and OS. Our results indicated that high level of RNF187 promote OS progression, which was concluded the following facts. Firstly, the expression of RNF187 is higher in OS tissues and cells than that in matched nontumorous tissues and the fetal osteoblastic cell, and low level of RNF187 decreased accordingly the capacity for tumor metastasis and invasion both in vitro and in vivo. Secondly, we show that high expression of RNF187 is associated with drugs resistance in OS cells. Lastly, we demonstrate that RNF187 overexpression occurs more frequently in various OS with poor prognosis-associated clinical variables. Importantly, we also show that elevated expression of RNF187 is correlated with poor survival and early disease recurrence in a cohort of OS patients. Thus, we consider that RNF187 overexpression promotes OS progression.In summary, our findings identify RNF187 as a predictor of overall survival and recurrence in patients with OS, and RNF RNF187 may be a potential therapeutic target for OS patients.Supplementary table S1.Click here for additional data file.
Table 1
Correlation between RNF187 expression and OS clinicopthological parameters
Result of immunostaining (No. of patients)
Parameter
RNF187-negative (n =27/51)
RNF187-positive (n=24/51)
p
Age (yrs)
<19
17
14
≥19
10
10
0.937
Gender
Male
18
16
Female
9
8
0.052
Site of primary tumor †
Femur
19
15
Tibia
4
4
Humerus
3
3
Pelvis
0
1
Other
1
1
0.103
Histologic differentiation ††
Osteoblastic
14
22
Chondroblastic
2
2
Fibroblastic
7
0
Telangiectatic
3
0
Other
1
0
0.001
Enneking stage ‡
I
3
0
IIA
8
2
IIB
15
17
III
1
5
0.001ª
Response to chemotherapy*
Good
20
8
Poor
5
16
NA
2
0
0.004
Metastasis
Negative
18
6
Positive
9
18
0.001
Note:
† Femur vs. Tibia/ Humerus/Pelvis/Other; †† Osteoblastic vs. Chondroblastic/ Fibroblastic/ Telangiectatic/Other; ‡ I/IIA vs. IIB/III; * good vs. poor/NA; ª Fisher's exact probability.
Table 2
Univariate analysis of factors associated with OS survival and recurrence