ARNTL hypermethylation promotes tumorigenesis and inhibits cisplatin sensitivity by activating CDK5 transcription in nasopharyngeal carcinoma
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Increasing evidence support an important role for DNA methylation in nasopharyngeal carcinoma (NPC). Here, we explored the role of circadian clock gene Aryl Hydrocarbon Receptor Nuclear Translocator-Like (ARNTL) methylation in NPC.
We employed bisulfite pyrosequencing to determine the epigenetic change of ARNTL in NPC cell lines and tissues. ARNTL mRNA and protein expression in cell lines and tissues were detected by real-time PCR and western blotting. Then, we constructed cell lines overexpressing ARNTL and knocked down ARNTL to explore its function and effect on chemotherapy sensitivity of NPC cell lines to cisplatin in vitro and vivo. Finally, we investigated the potential molecular mechanism of ARNTL by gene set enrichment analysis (GSEA), dual Luciferase reporter assay and chromatin immunoprecipitation assay.
ARNTL was hypermethylated, and its mRNA and protein were significantly down-regulated in NPC cell lines and tissues. When treated by 5-aza-2′-deoxycytidine, mRNA expression was up-regulated. Overexpression of ARNTL could suppress NPC cells proliferation in vitro and vivo while silencing of ARNTL using shRNA achieved opposite results. GSEA assay found that ARNTL was associated with cell cycle and ectopic ARNTL overexpression could induce G2-M phase arrest. Then, we identified and validated cyclin-dependent kinase 5 (CDK5) as the targeting gene of ARNTL by dual Luciferase reporter assay and chromatin immunoprecipitation assay. When transiently infected ARNTL-overexpression cells with PENTER-vector or PENTER-CDK5 plasmids, the later could reverse the suppressive effects of ARNTL on NPC cell proliferation. Moreover, ARNTL significantly enhanced sensitivity to cisplatin in NPC cells.
ARNTL suppresses NPC cell proliferation and enhances sensitivity to cisplatin by targeting CDK5. ARNTL may represent a novel therapeutic target for NPC.
KeywordsNasopharyngeal carcinoma ARNTL Methylation Proliferation CDK5 Chemotherapy sensitivity
Aryl Hydrocarbon Receptor Nuclear Translocator-Like
Cyclin-dependent kinase 5
Fetal bovine serum
Gene set enrichment analysis
SDS-polyacrylamide gel electrophoresis
Short hairpin RNA
Nasopharyngeal carcinoma (NPC) is a malignancy arising from the nasopharynx epithelium, and it is mainly endemic in Southeast Asia but relatively rare in white population . Radiotherapy with or without chemotherapy has emerged as the standard care for non-disseminated disease. Although the advance in radiotherapy technique and chemotherapy strategies have improved prognosis of NPC to some extent, there are still approximately 30% of cases suffering treatment failure [2, 3, 4]. Identifying novel and effective treatments is essential for further improvement of survival outcomes. Given this, we should have a better understanding of the molecular mechanism underlying the pathogenesis and progression of NPC first.
There is a mass of evidence showing that DNA methylation, one kind of epigenetic alterations, plays an important role in cancer initiation and progression [5, 6, 7]. In NPC, dysregulated methylation of specific genes could facilitate tumor cell proliferation and metastasis [8, 9]. Since DNA methylation is a dynamic modification which could be formed or reversed by plenty of enzymes, it represents a promising biomarker for future diagnosis, prognosis prediction and therapeutic target in cancer [10, 11]. In our previous study, we identified that Aryl Hydrocarbon Receptor Nuclear Translocator-Like (ARNTL) is one of the top-ranked hypermethylated genes between 24 normal nasopharynx epithelium and 24 NPC tissues by Illumina Human Methylation 450 K Beadchips (GSE52068) . ARNTL, also called Bmal1, is an indispensable core component of clock system , which forms a heterodimer with circadian genes and activates transcription of upstream genes [14, 15].
Circadian system consists of a series of genes including Clock, Bmal1, Per1, Per2, Cry1, Cry2, Cry3 and CK1e . In mammals, many physiological and behavioral processes display circadian rhythm which was controlled by endogenous clock system . Disruption of circadian rhythm has been found to be associated with various human disease including cancer [18, 19, 20]. Among these genes, Previous studies found that abnormal expression of ARNTL was associated with tumor proliferation, cell cycle, survival outcomes as well as chemotherapy sensitivity in various cancers [16, 21, 22, 23, 24], suggesting that ARNTL could act as a potential therapeutic target. However, the role of ARNTL in NPC remains unclear.
In this study, we provide our findings that ARNTL was downregulated in NPC cell lines and tumor tissues due to its promoter hypermethylation. Overexpression of ARNTL inhibited NPC cell proliferation by inducing G2/M phase arrest in vitro, and vice versa. Mechanism study revealed that ARNTL could suppress tumorigenicity through inhibiting cyclin-dependent kinase 5 (CDK5) transcription. Furthermore, ARNTL enhanced the sensitivity of NPC cells to cisplatin, suggesting that ARNTL may guiding the therapeutic timing of cisplatin in NPC.
Cell culture and clinical specimens
Human immortalized nasopharyngeal epithelial cell line NP69 was cultured in keratinocyte serum-free medium (Invitrogen, Life technologies, Grand Island, NY) supplemented with bovine pituitary extract (BD influx, Bioscience, USA). Human NPC cell lines (CNE1, CNE2, SUNE1, HONE1, HNE1, 5-8F, 6-10B) were maintained in RPMI-1640 (Invitrogen) supplemented with 5% fetal bovine serum (FBS, Gibco-BRL, Carlsbad, CA, USA). 293 T cells were grown in DMEM supplemented with 10% FBS. Additionally, 12 pairs of normal nasopharyngeal epithelial and freshly frozen NPC samples were obtained from our center. This study was authorized by the Institutional Ethical Review Boards of Sun Yat-sen University Cancer Center (YB2017–70), and written informed consents were provided by all patients for using their biopsy tissue samples.
RNA extraction and reverse transcription quantitative PCR (RT-qPCR)
Total RNA was extracted from cultured cell lines using TRIzol Reagent (Invitrogen) according to the manufacturer’s instructions and reverse-transcribed to cDNA with M-MLV reverse transcriptase (Promega, Madison, WI, USA). Quantitative PCR reactions were performed using the Platinum SYBR Green qPCR SuperMix-UDG reagents (Invitrogen) and the CFX96 sequence detection system (Bio-Rad, Hercules, CA, USA) with the following primers: ARNTL forward, 5’-GATGGTTCAGTTTCATGAACC-3′ and reverse, 5’-CCTCTTATCCTGTGGATTTCC-3′; CDK5 forward, 5’-CATCGTCAGGCTTCATGACG-3′ and reverse, 5’-CACCTCAGCTGAGTAACAGC-3′. GAPDH was applied as the endogenous control for normalization, and the 2-△△CT was used to calculate the relative mRNA expression.
Western blotting assay
Proteins were extracted from cells by using RIPA lysis buffer (Beyotime, Shanghai, China) and Bradford method was applied to test the concentration. A total of 20 μg proteins were separated by SDS-polyacrylamide gel electrophoresis (SDS-PAGE, Beyotime) and then transferred onto PVDF membranes (Millipore, Billerica, MA, USA). After transfer, the membrane was blocked in 5% defatted milk for 1 h and then incubated with primary anti-ARNTL (1,5000; Proteintech, Chicago, IL, USA) or anti-CDK5 (1,1000; Abcam, Cambridge, UK) antibody overnight at 4 °C, followed by species-matched secondary antibodies for 1 h at room temperature. Finally, protein bands were visualized using enhanced chemiluminescence (Thermo, USA).
DNA isolation and bisulfite pyrosequencing analysis
NPC cell lines (6 × 105cells) were seeded on 100 mm culture dishes. After culturing for 24 h, the cells were treated with or without 10 μmol/L 5-aza-2′-deoxycytidine (DAC, Sigma Aldrich, Munich, Germany) for 72 h with replacing the drug and medium every 24 h. Subsequently, DNA was extracted using the EZ1 DNA Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturer’s instructions. For bisulfite pyrosequencing analysis, 1–2 μg DNA was treated by sodium bisulfite using the EpiTect Bisulfite Kit (Qiagen). The PyroMark Assay Design Software 2.0 (Qiagen) was employed to design bisulfite pyrosequencing primers for ARNTL as follow: PCR forward: 5′-GGAAGGGGAGTGTTGGATAT-3′; PCR reverse: 5’-CCAAAACAACCCTAAATAACC-3′; sequencing primer: 5′- GGATATAGGAGTTTGTTGTTAA-3’.The PyroMark Q96 System (Qiagen) was adopted to conduct sequencing reaction and quantify methylation level.
Construction of stable cell line and ARTNL short hairpin RNA (shRNA)
The pSin-EF2-puro-ARNTL, pSin-EF2-puro-vector and psin-EF2-puro-CDK5 plasmids were obtained from Land. Hua Gene Biosciences (Guangzhou, China), and the psin-EF2-puro-vector plasmid served as a control. To generate stable cell lines, lentivirus packing expression plasmids were co-transfected into 293 T cells for 48 h. Then, SUNE1 and HONE1 cell lines were infected with the supernatants containing virus for 48 h. After infection, stably infected cells were selected by puromycin (1 μg/ml) and further confirmed by RT-qPCR assay. Two shRNAs targeting ARNTL were purchased from Invitrogen and connected to pLKO.1 plasmid. The nucleotide sequences of shRNA#1 and shRNA#2 were shown in Additional file 1: Table S1.
Cell proliferation and colony-formation assay
Cell proliferation assay was performed using CCK-8. Briefly, cells (1 × 103) in 100 μl medium were seeded into 96-well plates and incubated for 0–4 days. Ten microliters CCK-8 (Dojindo, Tokyo, Japan) were added into each well, and the absorbance values were measured using a spectrophotometer at 450 nm. With regard to DDP treatment in vitro, 1 × 103cells in 100 μl medium were incubated for 24 h first. Subsequently, the cells were treated with DDP at different concentrations (0, 0.625, 1.25, 2.5, 5 and 10 μg/ml) for 72 h according to our previous study , and the cell viability was determined. For the colony formation assay, 300 cells (600 cells for NP69) were seeded into 6-well plates with HONE1 cell line cultured for 1 week and SUNE1 cell line for 2 weeks. Then, the colonies were fixed in methanol and stained by crystal violet.
Wound healing assay
SUNE-1 or HONE-1 cells were seeded into six-well plates for culture. When growing to almost confluent, the cells were subjected to serum-free medium starvation for 24 h. A sterile 200 μl tip was used to create artificial wounds by scraping the monolayers, and the cells were washed with PBS and then subjected to serum-free medium for another 24 h starvation. Images of cells migrating into wounds were captured at 0 h and 24 h by microscope (Olympus IX73, Japan).
Transwell migration and invasion assays
Transwell chambers (8 μm pores, Corning, USA) coated with (invasion assay) or without (migration assay) Matrigel (BD Bioscience) were used to perform cell invasion and migration assays. SUNE-1 or HONE-1 cells (5 × 104) in 200 μl serum-free medium were added into upper chambers, and the lower chambers were filled with 500 μl medium supplemented with 10% FBS. After incubating, the cells on upper membrane filter were fixed with methanol, stained with haematoxylin and counted.
Cell cycle assay
For cell cycle analysis, 6 × 105 cells were cultured onto 100 mm dishes for 24 h and then starved for 24 h by serum-free medium to synchronize cell cycle (G1/S). Thereafter, the cells were cultured using RPMI-1640 supplemented with 5% FBS for 9 h. Finally, cells were trypsinized, washed by cold PBS, fixed in 70% ethanol and stored at 4 °C for further analysis. A Cell Cycle Detection Kit (KeyGene BioTech, Nanjing, China) was used to conduct cell cycle analysis according to manufacturer’s instruction. Before staining, cells were washed twice by PBS, and thereafter RNase A and Propidium lodide (PI) mixture (1:9) was used to resuspend and incubate cells for 30–60 min at room temperature. The fluorescence intensity of the cells was determined using flow cytometry (Gallios; Beckman-Coulter, Germany).
Gene set enrichment analysis (GSEA)
The GSEA (version 2.0.13, www.broadinstitute.org/gsea/) was applied to identity ARNTL expression related pathways in GSEA12452, and an enrichment score was calculated for each gene set (i.e., cell cycle pathway) by ranking each gene by their expression difference using computing a cumulative sum of each ranked in each gene set and recording the maximum deviation from zero as the enrichment score. We found that an overrepresentation of up- or downregulated genes between high and low ARNTL expression groups was associated with G2/M arrest pathway.
Luciferase reporter assay
PGL3-based luciferase reporter plasmids (Promega) which contained wild type and mutant type of CDK5 promoter were constructed. Thereafter, 2 × 105 cells were seeded in 6-well plate for 24 h, and then each well were co-transfected with pGL3-basic (2 μg) and Renilla luciferase (20 ng) for 24 h using Lipofectamine 3000 (Invitrogen). The cells were harvested using Passive lysis buffer (Promega), and Dual Luciferase Reporter Assay System (Promega) was used to measure luciferase activity.
Chromatin immunoprecipitation assay
Chromatin immunoprecipitation (ChIP) assay was performed in the SUNE1-ARNTL and HONE1 ARNTL cells using an EZ-Magna ChIP kit (Millipore) according to manufacturer’s protocol. Briefly, cells were induced crosslinking by 1% formaldehyde solution and then quenching crosslinking with 140 mM glycine. The nucleoprotein complexes were sheared to about 200–500 bp to yield DNA fragments and then immunoprecipitated with anti-ARNTL, IgG (negative control) or anti-RNA Pol II (positive control) antibodies overnight at 4 °C. PCR and real-time PCR assays were applied to detect the enrichment of DNA fragments in the binging sites of CDK5 promoter. The primers used in PCR assay for detecting CDK5 promoter sequence were as follow: forward: 5’-TGCCCAACGAAATCACAAAGTCT-3′; reverse: 5’-CTTGAGGGCTATGGACCGAGGGA-3′. The percentage of binding DNA fragments was quantified related to input.
Xenograft tumor models
Female BALB/c nude mice (4–5 weeks old) were purchased from Charles River Laboratories (Beijing, China) and bred at the Animal Experiment Center of Sun Yat-sen University. For tumor growth model, 1 × 106 SUNE1-ARNTL or SUNE1-Vector cells were injected into the dorsal flank of mice (n = 7 in each group). Tumor size was measured every 3 days. Four weeks later, mice were sacrificed and tumors were weighted. For chemosensitivity assay in vivo, 1 × 106 HONE1-ARNTL or HONE1-Vector cells were injected. After tumor formed in palpable mass 6 days after transplantation, the mice were randomly assigned to four groups (n = 5 in each group) which received intraperitoneal DDP (4 mg/kg) or normal saline injection every 3 days: ARNTL + DDP; ARNTL + saline; Vector + DDP; Vector + saline. Tumor size was also measured every 3 days. Two weeks later, mice were sacrificed and tumors were weighted. All tumor volumes were calculated as follow: volume = D × d2 × π/6, where D represents the longest diameter and d represents the shortest diameter. All animal assays were carried out in accordance with the detailed rules of the Animal Care and Use Ethics Committee of Sun Yat-sen University and we tried our best to minimize animal suffering.
Formalin-fixed paraffin-embedded (FFPE) slices of xenograft mice tissues were used to perform Immunohistochemistry (IHC). Briefly, the tissues were deparaffinized at 60 °C for 30 min and then rehydrated. The endogenous peroxidase was blocked by 3% H2O2, and the tissues were treated by high-temperature citrate for antigen retrieval. Subsequently, non-specific binding was blocked and tissues were incubated with primary antibodies at 4 °C overnight. All slices were reviewed and scored by two experienced pathologists employed at our hospital.
All data in our study were obtained from at least three independent experiments for each assay. Continuous variables were expressed as mean ± SD, and the difference was compared by non-parametric test. Spearman correlation analysis was used to analyze the relationship between ARNTL and CDK5 mRNA expression in the GEO GSE12452 dataset and the TCGA dataset. The study data underlying current findings were deposited at the Research Data Deposit (RDDB2018000394, available at http://www.researchdata.org.cn). All tests were two-sided, and P < 0.05 was considered significant. Statistical analysis was conducted via SPSS 18.0 version (SPSS Inc., Chicago, IL, USA) software.
ARNTL promoter is hypermethylated in NPC
ARNTL promoter hypermethylation results in its downregulation in NPC
ARNTL suppresses NPC cell viability and colony formation in vitro
ARNTL suppresses xenograft tumor growth in vivo
ARNTL suppresses NPC cell proliferation by inducing G2-M phase arrest
Flow cytometry assay showed that overexpression of ARNTL significantly increased the proportion of cells in G2/M phase (31.03% ± 0.91% vs. 19.12% ± 0.30% in HONE1 cells; 45.36% ± 0.55% vs. 30.09% ± 1.06% in SUNE1 cells; P < 0.05) and reduced the percentage of cells in S phase (27.15% ± 0.87% vs. 36.13% ± 0.27% in HONE1 cells; 17.04 ± 0.33% vs. 25.11% ± 0.53% in SUNE1 cells; P < 0.05) (Fig. 5b, c). However, knocking down ARNTL could decrease the proportion of cells in G2/M phase (31.63% ± 0.33% vs. 21.24% ± 1.09% vs. 21.93% ± 0.48% in HONE1 cells; 33.06% ± 0.45% vs. 23.14% ± 0.58% vs. 22.20% ± 0.90% in SUNE1 cells; P < 0.05) and increase the percentage in S phase (33.99% ± 0.14% vs. 46.0% ± 0.94% vs. 46.66% ± 0.67% in HONE1 cells; 21.12% ± 1.18% vs. 35.73% ± 0.37% vs. 36.99% ± 0.26% in SUNE1 cells; P < 0.05; Fig. 5d-e). Collectively, these results suggested ARNTL suppress cell proliferation by inducing G2/M phase arrest.
ARNTL suppresses NPC cell proliferation by inhibiting CDK5 transcription
Then, we performed dual luciferase reporter gene assay to further validate our findings. The wild-type or mutant sequences of the CDK5 promoter were cloned into luciferase reporter vectors. When transfected into ARNTL- or Vector-overexpression cells, the luciferase activity of wild-type reporter gene in ARNTL-overexpression cells was significantly lower than that in Vector-overexpression cells, while the luciferase activity of mutant reporter gene did not significantly differ between the two groups (Fig. 6g). Moreover, the ChIP assay also showed that ARNTL could bind to the promoter region of CDK5 (Fig. 6h). Given these findings, CDK5 was a potential target gene of ARNTL.
CDK5 reverses ARNTL-mediated proliferation suppression
To explore whether CDK5 was a functional target in ARNTL-mediated tumor cell proliferation suppression, we transiently infected the SUNE1 or HONE1 ARNTL-overexpression cells with PENTER-vector or PENTER-CDK5 plasmids (Fig. 6i, j). The CCK-8 (Fig. 6k, l) and colony formation (Fig. 6m, n) assays demonstrated that the cells infected with CDK5 achieved significantly stronger viability and colony formation ability compared with the cells transfected with Vector. Furthermore, we evaluated whether ARNTL could affect cell proliferation ability in CDK5 downregulated cells. Western blot assay confirmed that CDK5 was downregulated in NP69 cells compared with SUNE1 and HONE1 cell lines (Additional file 7: Figure S6A). Therefore, we knocked down ARNTL expression in NP69 cell (Additional file 7: Figure S6B). The CCK-8 (Additional file 7: Figure S6C) and colony formation (Additional file 7: Figures. S6D-E) assays showed that NP69 cells transfected with ARNTL ShRNAs achieved significantly stronger viability and colony formation ability compared with the cells transfected with control ShRNA. These results revealed that CDK5 serves as a functional target of ARNTL and ectopic expression of CDK5 could partially reverse the suppressive effect of ARNTL.
ARNTL enhances sensitivity of NPC cells to cisplatin
In our current study, we validate that ARNTL is downregulated in both NPC cell lines and freshly frozen tissues as a result of its promoter hypermethylation. Overexpression of ARNTL could reduce NPC cell viability and colony formation while silencing of ARNTL produces inverse effect in vitro. Xenograft tumor model also shows that ARNTL suppress NPC cell proliferation in vivo. Then, we identify that ARNTL induces G2/M phase arrest by targeting CDK5. Moreover, ARNTL could enhance the sensitivity of NPC cells to cisplatin in both vitro and vivo. Our findings provide new insights into potential mechanism of ARNTL regulating cell proliferation and clinical treatment for NPC.
Distant metastasis are the main failure patterns in NPC. Although the application of intensity-modulated radiotherapy has improved the management of NPC, there are still almost 30% of patients experiencing treatment failure [3, 4, 29, 30]. Therefore, better understanding of the molecular mechanisms underlying distant metastasis could facilitate future treatments for NPC. There is increasing evidence supporting that epigenetic processes play a vital role in cell biology and tissue physiology. With regard to cancer in human, these epigenetic processes are mainly exemplified by aberrant DNA methylation [11, 31]. Also, aberrant epigenetic changes play an important role in NPC . Recently, numerous studies have uncovered the diagnostic and prognostic value of hypermethylation of some genes in NPC [8, 9, 12, 33]. Given these knowledge, it’s worth exploring the mechanism of specific gene methylation which contributes to disease progression or recurrence in NPC.
ARNTL, a member of the bHLH-PAS structural domain transcription factor family, mainly regulates cell circadian rhythm. Promoter hypermethylation of ARNTL was observed in breast cancer and hematologic malignancies [16, 34]. Consistent with these findings, our study also validated that ARNTL was hypermethylated in NPC. We found that ARNTL mRNA and protein expression were significantly downregulated in NPC cell lines and tissues. Overexpression of ARNTL could suppress NPC cells proliferation both in vitro and vivo while silencing of ARNTL substantially promoted NPC cells viability and colony formation. These findings suggest that ARNTL serve as a tumor suppressor in NPC, which is consistent with its role in other malignancies [21, 22, 24, 35].
Normal physiological cell cycle is mainly controlled by the protein kinase complexes consisting of cyclins and cyclin-dependent kinases (CDKs). Cyclins act as the regulatory subunit and CDKs serve as the catalytic subunit to activate the heterodimer complexes, which regulate entry into the S phase of cell cycle . Aberrant expression of cell cycle components could lead to uncontrolled cell cycle, therefore resulting in uncontrolled cell proliferation and cancer . Recent studies demonstrate that ARNTL is correlated with cell cycle [16, 22, 24, 38, 39]. Mullenders et al. and Grechez-Cassiau et al. revealed ARNTL affect the cell cycle and proliferation through p53/p21 signaling pathway [22, 39]. Zeng et al. found that ARNTL could regulate G2-M phase arrest by activating the ATM signaling pathway . Our study also validated that ARNTL could induce G2-M phase arrest, further validating its role in cell cycle.
CDK5, a member of CDK family which binds to ATP sandwiched between N- and C-terminal lobes  and is activated by binding to non-cyclin CDK5 activators CDK5R1 (p35) and CDK5R2 (p39) . Recent evidence found that CDK5-induced G2/M arrest played an important role in cancer progression [42, 43, 44, 45]. In our study, GSEA and flow cytometer found overexpression of ARNTL could induce G2-M phase arrest. To further clarify the underlying downstream ARNTL, luciferase reporter system and function rescue experiments validated ARNTL could inhibit NPC cell proliferation by directly regulating CDK5 transcription. Combining these studies with our findings, it’s reasonable to infer that ARNTL induces G2-M phase arrest by binding to CDK5 to inhibit NPC cell proliferation.
Chemotherapy is one of the most important treatments for malignancies, and resistance to chemotherapy could result in tumor recurrence or distant metastasis. Therefore, identifying potential target genes which correlate with chemotherapy sensitivity is of great importance to cancer care. Cisplatin has been the most widely and effective chemotherapy reagent for NPC for the past decades. Therefore, we explored whether ARNTL affected chemotherapy sensitivity of NPC cell to cisplatin. The results suggested that ARNTL could increase sensitivity to cisplatin both in vitro and vivo, consistent with previous findings that ARNTL-overexpression tumors showed improved sensitivity to anticancer drugs [24, 28, 46]. Our findings suggested that ARNTL could serve as a molecular target to increase cisplatin sensitivity in NPC.
In summary, our study demonstrates that ARNTL could suppress NPC cell proliferation by targeting CDK5 and inducing G2-M phase arrest. Moreover, ARNTL could enhance chemotherapy sensitivity of NPC cell to cisplatin. Our findings provide new insights into molecular mechanism of NPC progression and identify ARNTL/CDK5 pathway as a novel target for treatment.
This work was funded by Natural Science Foundation of Guangdong Province (No. 2017A030310227 and 2017A030312003), Health & Medical Collaborative Innovation Project of Guangzhou City, China (201803040003), Innovation Team Development Plan of the Ministry of Education (No. IRT_17R110) and Overseas Expertise Introduction Project for Discipline Innovation (111 Project, B14035).
Availability of data and materials
All the original data underlying our findings of this study was deposited at the Research Data Deposit public platform (RDDB2018000394, available at www.researchdata.org.cn). The study data was available from the corresponding author for scientific research purpose.
HP, JZ, Y-QL and JM designed the study. HP, JZ, P-PZ, XW, X-JY, Q-MH and NL carried out all experiments. HP, JZ, LC and L-LT participated in data analysis and interpretation of results. HP and JZ wrote the manuscript. NL and YS contributed to quality control and review of the manuscript. All authors read and approved the final version of manuscript.
Ethics approval and consent to participate
This study was performed in accordance with the ethical standards and the Declaration of Helsinki and according to national and international guidelines. Our study has been approved by the ethics committee of Sun Yat-sen University Cancer Center.
Consent for publication
The authors declared that they have no competing interest.
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