Background
Retinoblastoma (RB) is the most frequent pediatric retinal tumor and is initiated by biallelic inactivation of
RB1, the first discovered tumor suppressor gene [
1]. This primary intraocular pediatric cancer is gaining increasing attention from researchers with approximately 8000 new cases diagnosed every year, particularly in Asia and Africa [
2,
3]. Children diagnosed early with RB are commonly treated with photocoagulation, cryotherapy, or irradiation and tumor enucleation [
4,
5]. Survival of children with RB is markedly dependent on an early diagnosis shortly after the detection of symptom [
5,
6].
However, in contrast to the excellent survival rates of malignant childhood RB in Europe and the United states, that in China is very low; children diagnosed with RB in China are always in the advanced D or E stage, and the survival rate is only 26% [
5]. Additional chemotherapy before or after enucleation is necessary to prevent cases of hematogenous spreading or involvement of the central nervous system [
5,
7]. Recurrence and metastasis of high-risk advanced RB is still a major obstacle for successful therapy in China [
5,
8].
Chemotherapy resistance to antineoplastic agents, including carboplatin, etoposide and vincristine, is a major problem in the treatment of high-risk advanced RB [
5,
8,
9]. Etoposide is well known for its use in the treatment of many malignancies, such as Hodgkin’s disease, lung cancer, ovarian cancer, myeloma, gastric cancer and breast cancer [
10‐
13]; the drug is a DNA topoisomerase-II inhibitor that can directly bind to DNA and cause DNA damage [
14]. Previously, we successfully generated an etoposide drug-resistant subline (Y79/EDR) from the parental human retinoblastoma cell line Y79 and explored potential mechanisms related to etoposide resistance. Preliminary results indicated that Y79/EDR cells showed significant resistance to etoposide mediated by the PI3K/AKT and p53 signaling pathways, which promoted cell proliferation and apoptosis inhibition [
15].
In the present study, to elucidate the chemoresistance mechanism and identify potential biomarkers in RB, we generated transcriptome profiles of Y79/EDR and parental Y79 cells and distinguished any candidate differentially expressed genes (DEGs) between the two lines before performing functional and technical validation studies.
Methods
Cell cultures and treatments
The human retinoblastoma cell line Y79 was obtained from the Cancer Hospital of the Chinese Academy of Medical Sciences and was cultured in RPMI-1640 medium (Thermo Fisher Scientific, Waltham, MA, USA) with 20% (v/v) fetal bovine serum (Thermo Fisher Scientific, Waltham, MA, USA), penicillin G (100 U/mL) and streptomycin (100 μg/mL) under a humidified atmosphere of 5% CO
2 at 37 °C. Y79/EDR cells were maintained by treating parental Y79 human retinoblastoma cells with a tolerance concentration of etoposide (Sigma-Aldrich, MO, USA) as previously described [
15].
Detection of drug resistance
Cell Counting Kit-8 (CCK-8) (Dojindo, Kumamoto, Japan) was used to detect drug resistance. Y79/EDR and parental Y79 cells were seeded at a density of 2.0 × 10
4 cells per well with 200 μL of medium in 96-well plates and treated with different concentrations of etoposide (Sigma-Aldrich, MO, USA), carboplatin (Sigma-Aldrich, MO, USA) and vincristine (Sigma-Aldrich, MO, USA) for 48 h, respectively. Cells treated with phosphate-buffered saline (PBS) served as the controls. Then, 20 μL of CCK-8 solution was added to each well and incubated for 4 h at 37 °C. The absorbance was measured at 450 nm using a microplate reader (BioTek, Vermont, USA). GraphPad Prism 5 was used to plot the drug concentration-cell survival curves. SigmaPlot 10.0 was used to calculate IC
50, and resistance index (RI) was calculated according to IC
50 as the following formula:
$$ \mathrm{RI}={\mathrm{IC}}_{50}\ \left(\mathrm{Y}79/\mathrm{EDR}\right)/{\mathrm{IC}}_{50}\ \left(\mathrm{Y}79\right) $$
Total RNA was extracted from Y79/EDR and parental cells with TRIzol (Thermo Fisher Scientific, Waltham, MA, USA) according to the manufacturer’s protocol and purified with a NucleoSpin RNA Clean-up kit (Macherey-Nagel, NucleoSpin®, Germany). RNA degradation and contamination were assessed on 1% agarose gels. RNA purity and concentrations were detected using a NanoPhotometer spectrophotometer (Implen, CA, USA) and a Qubit RNA Assay Kit in a Qubit 2.0 Fluorometer (Thermo Fisher Scientific, Waltham, MA, USA), respectively. RNA integrity was assessed using the RNA 6000 Nano Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, Santa Clara, CA, USA).
Library construction for RNA sequencing
A total of 1 μg of RNA per sample was used as input material for RNA sample preparation. All procedures for cDNA library construction were performed using an NEBNext UltraTM RNA Library Prep Kit for Illumina (NEB, Ipswich, MA, USA) following the manufacturer’s recommendations. Sequencing of the libraries was carried out on an Illumina HiSeq 2500 platform, and paired-end reads were generated (raw data).
Sequencing data analysis
Quality control of the raw data was performed, including removal of reads containing adapter and poly-N sequences and removal of low-quality reads, to obtain clean data. In addition, the quality score and GC content of the clean reads were calculated. Clean reads with a perfect match or only one mismatch were mapped to the Genome Reference Consortium assembly GRCh37 using TopHat2 [
16] for further analysis and annotation. Quantification of gene expression levels was estimated based on fragments per kilobase of transcript per million fragments mapped (FPKM) with the following formula: FPKM = cDNA fragments/mapped fragments (millions) × transcript length (kb). We performed RNAseq analysis on the platform BMKCloud (
www.biocloud.net).
Determination and clustering analysis of DEGs
Prior to differential gene expression analysis, for each sequenced library, the read counts were adjusted with the edgeR program package through one scaling normalized factor. Differential expression analysis of two samples was performed using the DESeq (2010) R package.
P values were adjusted using q values [
17]. Fold change (FC) ≥ 2 and q value < 0.005 were set as the threshold for significant DEGs.
Pathway enrichment analysis
Gene Ontology (GO) enrichment analysis of DEGs was executed with the R package GOseq based on Wallenius’ noncentral hypergeometric distribution [
18], which can adjust for gene length bias in DEGs. Terms with KS value < 0.05 (Kolmogorov–Smirnov) were considered significantly enriched. The Kyoto Encyclopedia of Genes and Genomes [
19] (KEGG,
http://www.genome.jp/kegg/) was used to predict the enriched pathways of the DEGs. KOBAS software was used to test the statistical enrichment of DEGs in KEGG pathways [
20].
Real-time quantitative reverse transcription polymerase chain reaction (real time QRT-PCR) validation
To validate the expression levels of the DEGs obtained from RNAseq, we selected 7 genes for real time QRT-PCR analysis. Total RNA from parental Y79 and Y79/EDR cells was isolated with TRIzol reagent (Thermo Fisher Scientific, Waltham, MA, USA), and then cDNA was synthesized with a Transcriptor First Strand cDNA Synthesis Kit (Roche, Mannheim, Germany). Real time QRT-PCR was conducted with a SYBR® Premix Ex Taq™ II kit (TaKaRa, Kusatsu, Japan). All procedures were performed according to the manufacturer’s instructions. The 2
-ΔΔCt method was used to determine relative expression levels with the GAPDH gene as an internal control [
21]. To further calculate log
2 FC (fold change) between Y79/EDR and Y79 cell lines from real time QRT-PCR, an equation of log
2 [2
-ΔΔCt (Y79/EDR)/ 2
-ΔΔCt (Y79)] was used to compare with that from RNAseq. The primers used are listed in Additional file
1: Table S1.
Transfection and RNA interference of selected genes
To explore the relationship between the 7 identified genes and etoposide resistance, we knocked down these genes in parental Y79 cells to determine their effects on drug sensitivity. Three short interfering RNA (siRNA) sequences targeting different regions of each gene were transiently transfected at a concentration of 100 nM into parental Y79 cells with Lipofectamine RNAiMAX (Thermo Fisher Scientific, Waltham, MA, USA). The siRNA sequences are listed in Additional file
2: Table S2. Scrambled siRNA was used as a negative control (RiboBio, Guangzhou China). Then, some of the cells were collected 6–8 h after transfection and seeded into 96-well plates for drug sensitivity analysis, while others were harvested for real time QRT-PCR after 48 h.
Cytotoxicity assay
Parental Y79 cells transfected with siRNA of 7 candidate genes were seeded in 96-well plates, respectively, and treated with different concentrations of etoposide, carboplatin and vincristine for 48 h. Then, CCK-8 was used to analyse changes of drug sensitivity after knockdown of candidate genes.
To observe drug-induced changes in ARHGAP9 mRNA expression, parental Y79 cells were seeded at a density of 5.0 × 105cells per well with 2 mL of medium into 6-well plates and treated with IC50 of carboplatin and etoposide for 24 h, following with detection of ARHGAP9 mRNA expression by real time QRT-PCR.
Statistical analysis
Statistical analyses of the transcriptome profiles were described in above subsections, respectively. The rest analyses were conducted using Student’s t-test for functional validation studies. The quantitative data were presented as mean ± SEM.
Discussion
In the present study, RNAseq technology and gene expression profile analysis revealed that etoposide significantly altered the transcriptomic profile of Y79/EDR cells. GO and KEGG pathway enrichment analyses identified several key pathways involved in etoposide-induced acquired resistance. These pathways were linked to cellular processes and environmental information processing involving regulation of the actin cytoskeleton, focal adhesion and tight junctions, AMPK signaling, calcium signaling, ARVC, FoxO signaling, PI3K-AKT signaling and cancer pathways, providing us with insights into potential new molecular therapeutic targets in RB treatment. The results were also demonstrated in our previous report, which indicated that Y79/EDR cells showed significant resistance to etoposide that was mediated via the PI3K/AKT and p53 signaling pathways [
15]. Thus, we have successfully experimentally confirmed our study design and hypothesis.
As well known, acquired drug resistance appears to be a relatively common issue throughout the administration of treatment, leading to cancer treatment failure and a patient relapse. As evolving of cancer cells during drug treatment, it is possible that a variety of related molecules in cancer cells can be altered by aberrant microenvironment due to genomic instability or intratumor heterogeneity, leading to MDR to cancer therapy [
23]. For instance, levels of reactive oxidative species (ROS) in cancer cells were modulated during chemotherapy, further resulting in MDR regulated by various associated molecules including NADPH oxidases (NOXs), thioredoxin reductases (TrxRs) and nuclear factor erythroid 2-related factor 2 (Nrf2), and so on [
24,
25]. Other molecules such as P-gp, multidrug resistance protein 1 (MRP1) and BCRP have also been demonstrated to be involved [
26]. Moreover, it suggests that resistance to therapy may occur through multiple somatic events simultaneously within the same tumor [
27]. For example [
28], following BRAF inhibitor therapy in BRAF V600 mutant melanoma, individual tumors were found to develop multiple resistance events, including NRAS and MEK1 mutations in one patient and two distinct NRAS mutations in another. It was not surprising that Y79/EDR cells showed significant resistance not only to etoposide, but also to carboplatin and vincristine, suggesting some molecules altered in genetic status or expression. Accumulating evidence shows that the expression of markers related to stemness is crucial for tumor maintenance and the mediators of resistance. Polygenic resistance mechanisms might contribute to multiple chemoresistance [
27]. Our finding with regarding to MDR in Y79/EDR cells encouraged us to elucidate intrinsic mechanism of MDR in Y79/EDR cell line. Therefore, we performed RNA sequencing to discover any MDR-associated genes and identify potential prognostic markers or therapeutic targets for RB treatment. That would be important for clinical significance and targeted drug development to overcome acquired chemoresistance.
The
ARHGAP9 gene encodes a member of the Rho-GAP family of GTPase-activating proteins that has substantial GAP activity towards several Rho-family GTPases in vitro, converting them to an inactive GDP-bound state. ARHGAP9 has been implicated in regulating adhesion of hematopoietic cells to the extracellular matrix, which is correlated with cell proliferation, migration and invasion in several cancers [
29‐
35]. A previous report indicated that ARHGAP9 expression in breast cancer was correlated with poor patient survival, implying that
ARHGAP9 could act as an oncogene. Their findings revealed that silencing
ARHGAP9 inhibited proliferation, migration, invasion and induced cell cycle G0/G1 arrest and apoptosis in breast cancer cells, effects that might be mediated by significant inhibition of ERK and p38 activity [
34,
35]. Sun et al. also demonstrated that
ARHGAP9 knockdown suppressed gastric cancer cell proliferation, migration and invasion [
36].
Different from the above findings, another study indicated that
ARHGAP9 expression was significantly lower in hepatocellular carcinoma (HCC) tissues than that in normal liver tissues, and the overall survival time of patients with lower
ARHGAP9 expression was significantly shorter than those with its higher expression. Further experimental overexpression of
ARHGAP9 significantly inhibited cell proliferation, migration and invasion in HCC, as well as lung metastases in vivo [
33]. Furthermore, Takefuji et al. found that the mRNA level of
ARHGAP9 was strongly detected in hematopoietic cells, which inhibited cell migration, spreading and adhesion [
32]. Recent results from a bioinformatics analysis of patients with breast cancer and healthy individuals revealed that high levels of
ARHGAP9 expression were associated with better prognosis, including preferable relapse-free survival and overall survival. They concluded that
ARHGAP9 might be a promising target for precision treatment of breast cancer [
37]. In another report, weighted gene co-expression network analysis (WGCNA) was used to predict the intrinsic relationship or correlation between gene expression in head and neck squamous cell carcinoma (HNSCC).
ARHGAP9 were identified to be used as a biomarker and therapeutic target of HNSCC [
38]. These above findings suggested that ARHGAP9 had controversial effects on cell proliferation, migration and invasion among those different cancer types. This inconsistence might be attributed to difference in action mechanisms of ARHGAP9 in various cancers where genetic instability, cellular response and formation of the tumor microenvironment might also differ owing to tissue-derived specificities and heterogeneity. Certainly, more research and clinical studies are required to explore ARHGAP9 functions in different tumors. In addition, we had also noticed that the levels of
ARHGAP9 mRNA expression in Y79/EDR cells were significantly lower than that in the parental Y79 cells. Therefore, to determine if ARHGAP9 may play an important role in RB progression and chemoresistance, we next selected
ARHGAP9 as the candidate gene and validated its effect on drug resistance experimentally.
In our study, we first observed that
ARHGAP9 downregulation significantly altered cellular susceptibility to antineoplastic agents (Fig.
6a, b) and that etoposide and carboplatin decreased the mRNA levels of
ARHGAP9 (Fig.
6c). These results imply that
ARHGAP9 may be a diagnostic and prognostic marker or a potential new molecular therapeutic target. We speculate that its functions differ mainly due to cell type specificity and different development stages of tumor progression, although more clinical data are needed to draw definitive conclusions. Furthermore, our transcriptome profiling and enrichment analysis results for Y79/EDR cells showed that the top ranked DEGs were involved in regulation of the actin cytoskeleton, focal adhesion and tight junctions. Such findings imply that the
ARHGAP9 gene might also play a very important role in those functions in cell proliferation, migration and invasion of RB tumors and in chemoresistance, similar to the suggestions of previous reports [
36].
According to recent reports in China, the failure of adjuvant therapy in most patients post enucleation is mainly due to chemoresistance, leading to bottle-necks in treatment for high-risk advanced RB. In a retrospective study to observe the treatment and prognosis for different degrees of invasion of eye tissue in RB and identify the indications for post-enucleation adjuvant therapy, 537 children were recruited who had been diagnosed with unilateral RB and had received enucleation from January 2006 to December 2012 in Beijing Tongren Hospital which is the Top one rank of Ophthalmic hospitals in China, and were divided them into three groups according to their number of histopathologic high-risk factors including invasion of the optic nerve posterior to the ethmoid plate and extensive invasions of the choroid, sclera, anterior chamber, iris, and ciliary body. Chemotherapy was not recommended for patients with no risk factors following enucleation, while patients with at least one risk factor received corresponding treatment. As a result, of the 537 RB patients who received enucleation, 28 had recurrences (5.2%), and 25 died (4.7%), resulting in an overall survival rate of 95.3%. On the contrary, of the 168 with histopathologic risk factors, 26 had recurrences, and 24 died, suggesting much higher irresponsive frequency of chemotherapy at 29.8% (50 patients) [
39]. A total of 202 unilateral RB patients post enucleation without prior treatment were enrolled in a retrospective study from Zhongshan Ophthalmic Center as one of the best famous Ophthalmic hospitals in China between January 2003 and February 2011, followed with or without adjuvant therapy. The locations of tumor invasion, treatment and survival condition of patients were recorded. In the end of study, the 5-PEFS (5 year probability event-free survival) in total was 88.6% (179 cases) with 23 patients died of relapse or invasion and metastasis, whereas the 5-PEFS of the patients with transection line of optic nerve involvement were only 40.0%.Among those, the 5-PEFS of patients accepted treatment was significantly higher than that of untreated ones (54.5% versus 0%), however, the irresponsive frequency of chemotherapy (45.5%) was still high for high-risk advanced RB even with treatment mainly due to drug resistance [
40]. Another similar retrospective study in the same hospital between January 1997 and December 2001 showed that the 5-PEFS of a total of 102 RB patients recruited post enucleation was 79.41% (81 cases) and 20.59% (21 cases). However, the 5-PEFS of the patients with transection line of optic nerve involvement was only 14.29% in Log-rank analysis including 7 cases, among which 6 having adjuvant chemotherapy died mostly because of chemoresistance with 85.7% of the frequency of drug resistance [
41].
Our confirmatory experiments validated our RNAseq results (Fig.
5). Further experimental studies are warranted to verify the results of the present study. We realize that the limitation of this study is that the transcriptomic data were obtained from only one resistant subline of Y79 cells. It is more convincible to create etoposide-resistant cell models and interpret drug resistance for RB therapy by using more than one cell line. In fact, we initially selected two common human RB cell lines (Y79 and WERI-Rb1) to prepare for etoposide-resistant cell lines, however, we found that WERI-Rb1 cell susceptibility to etoposide is much lower than that of Y79. Few WERI-Rb1 cells remained alive after treated even with 1 nM of etoposide, which didn’t allow us to create its resistant cell model. Therefore, we only used Y79 cells and successfully constructed an Y79/EDR cell line previously for the follow-up studies. More biologically representative RB cell lines, as well as a large cohort of patient samples, would be needed to generate genomic, transcriptomic, epigenomic and proteomic profiles for the complex molecular signatures of RB. Interestingly, in another ongoing study, we have recruited advanced high-risk RB patients post enucleation and chemotherapy to collect peripheral blood samples from both cured and relapse/or metastasis patients. After determined patient prognosis, we compared whole exome sequencing (WES) data between those two groups of patients followed with validation by using more clinical samples. The result from the association analysis indicated that one SNP in
ARHGAP9 was significantly associated with good prognosis (
P < 0.01), consistent with the observation from WES data. The above results from clinical validation further convinced us to conduct research on
ARHGAP9 identified from the transcriptomic data using the in vitro resistant cell line model in the present study, confirming that
ARHGAP9 may indeed play an important role in RB chemoresistance [
42]. Clearly, more in vitro and in vivo functional studies should be performed to elucidate the etoposide-induced chemoresistance mechanism in advanced RB. The use of multiple drug-resistant sublines or models will be necessary to deepen understanding of the mechanisms of drug-induced cytotoxicity and acquired resistance. Finally, deep sequencing of genetic loci involved in
ARHGAP9 mutations and amplifications will be needed to identify more predictive biomarkers for diagnosis and treatment in the future. Further mechanistic studies will be helpful in determining the functions of
ARHGAP9 in RB cell proliferation, migration, invasion and metastasis, as well as chemoresistance.
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