Research Article | Open Access
Jing Ke, Chunming Gu, Heyan Zhang, Yang Liu, Wenhao Zhang, Huiling Rao, Shan Li, Fuyun Wu, "Nucleolin Promotes Cisplatin Resistance in Cervical Cancer by the YB1-MDR1 Pathway", Journal of Oncology, vol. 2021, Article ID 9992218, 11 pages, 2021. https://doi.org/10.1155/2021/9992218
Nucleolin Promotes Cisplatin Resistance in Cervical Cancer by the YB1-MDR1 Pathway
Purpose. Cervical cancer is the fourth most common cancer in women worldwide and is the main cause of cancer-related deaths in women. Cisplatin (DDP) is one of the major chemotherapeutic drugs for cervical cancer patients. But, drug resistance limits the effectiveness of cancer therapy. Nucleolin (NCL) is a nucleocytoplasmic multifunctional protein involved in the development of cancer. It has been reported that NCL may be a potential target for modulation of drug resistance. However, the precise molecular mechanisms are poorly understood. Materials and Methods. Human cervical cancer Hela cells and their cisplatin-resistant cell line Hela/DDP were used in this study. The protein level of NCL in cervical cancer cells was measured by western blot analysis. Hela cells and Hela/DDP cells were transfected with NCL overexpression plasmid or NCL siRNA separately. MTT and EdU assay were performed to evaluate the cell viability and sensitivity to cisplatin. The drug efflux function of MDR1 protein was assessed by intracellular rhodamine-123 accumulation assay.The promoter activity of MDR1 was assessed by using a dual-luciferase reporter assay. Results. We found that the protein level of NCL was elevated in Hela/DDP cells. Overexpression of NCL increased cervical cancer cell proliferation and attenuated the sensitivity to cisplatin. Overexpression of NCL increased Multidrug resistance (MDR1) gene expression and drug efflux. Our results demonstrated that NCL was highly related with cisplatin resistance in cervical cancer. NCL played an important role in MDR1 gene transcription through regulation of the transcription factor YB1. Conclusion. Our findings revealed the novel role of NCL in cisplatin-resistant cervical cancer and NCL may be a potential therapeutic target for chemoresistance.
Cervical cancer is the fourth most common cancer in women worldwide and the second most common cancer in women living in less-developed regions . Cisplatin-based chemotherapy is an important treatment option for cervical cancer, but resistance to cisplatin often results in chemotherapy failure [2, 3]. As so far, the mechanism of cisplatin resistance in cervical cancer is not clear. NCL is a multifunctional phosphoprotein involved in ribosome assembly, rRNA maturation, mRNA stability, and so on [4, 5]. It is mainly located in the nucleolus, but also found in the nucleoplasm, cytoplasm, and cell membrane . Many studies have shown that NCL plays an important role in tumor development [7, 8]. NCL is upregulated in a variety of tumor cells and promotes the proliferation, invasion, and migration of tumor cells through its action on different cellular pathways [9, 10]. In recent years, it was found that the expression of NCL was significantly increased in etoposide- and mitoxantrone-resistant breast cancer cells . Recent reports have demonstrated that high NCL expression promotes drug resistance in acute lymphoblastic leukemia .These results indicate that NCL may be involved in drug resistance of tumor cells, but whether NCL is involved in cisplatin resistance in cervical cancer has not been reported. Here, we explored the relationship between NCL and cisplatin resistance in cervical cancer. We found a new mechanism of cisplatin resistance mediated by NCL via stimulating YB1-induced MDR1 transcription. Our results indicated that NCL may be a potential drug-resistant target.
2. Materials and Methods
The human NCL gene was amplified by PCR from the cDNA of Hela cells and cloned into the pcDNA4/TO vector. To construct MDR1-luciferase reporter plasmid, the nt −201 to nt +43 fragment of the MDR1 promoter was inserted into the pGL3-basic vector at the KpnI and HindIII sites. Y-Box mutated MDR1-luciferase reporter plasmid was generated by overlap extension PCR using the primer. Forward: 5′-GGTGAGGCTGATCAACTGGGCAGGAAC-3′ Reverse: 5′-GTTCCTGCCC AGTTGATCAG CCTCACC-3′
2.2. Cell Culture and Transfection
The Hela cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM, Invitrogen) supplemented with 10% fetal bovine serum (Hyclone), 50 U/mL penicillin, and 50 μg/mL streptomycin (Invitrogen) at 37°C with 5% CO2, and cisplatin-resistant cervical cancer cells Hela/DDP were treated with DDP at 0.5 µg/ml in the complete medium to maintain their resistant phenotypes. Hela cells were transfected with pcDNA4/TO-NCL plasmid using lipofectamine 3000 (Invitrogen) based on the manufacturer’s instructions. After 48 h, cells were selected with zeocin (200 μg/ml) for one week, and then, the cells were used to assay proliferation.
2.3. Western Blotting
The whole cell lysates were extracted using RIPA buffer supplemented with protease inhibitors, and the concentration of isolated protein was determined using the BCA protein assay. Samples were resolved by SDS-PAGE and transferred to PVDF membranes. Membranes were blocked in 5% nonfat dry milk in TBST for 1 h at room temperature and then incubated with the primary antibodies overnight at 4°C, followed by Horseradish-Peroxidase-linked secondary antibodies for 1 h at room temperature. Protein signals were detected by using the ECL western blotting substrate. The following antibodies were used in immunoblotting: rabbit monoclonal antibodies against NCL, YB1, MDR1, and GAPDH purchased from Proteintech Group.
2.4. siRNA Transfection
To knockdown NCL expression, the double-stranded small interfering RNA against human NCL (target sequence: 5′-UUUCUCAAACGAAGUAAGCUUdTdT-3′) and nonspecific siRNA (target sequence: 5′-UUCUCCGAACGUGUCACGU-3′) (purchased from GenePharma Company Ltd.) were used for transient transfection. Hela/DDP cells were plated into a 6-well plate. After 24 h, cells were transfected with 5 μg NCL siRNA or control siRNA with Lipofectamine 3000 reagent according to the manufacturer’s instructions. Gene silencing was assessed after 36 h by western blotting.
2.5. Cell Proliferation Assay
Cell proliferation was assessed by both MTT and EdU assays. For MTT assay, 3000 Hela cells transfected with NCL vector or Hela/DDP cells transfected with siNCL were seeded into a 96-well plate for overnight. After 36 h, cells were treated with different concentrations of cisplatin for 24 h. MTT was added to each well and incubated for 4 h at 37°C, and then, 100 μl dimethyl sulfoxide (DMSO) was added to each well with plate shaking for 30 minutes. Absorbance was read at 540 nm using a 96-well plate reader. For EdU assay, Hela cells transfected with NCL vector or Hela/DDP cells transfected with siRNA were seeded in 24-well plates. After treated with DDP for 24 h, cell proliferation was detected using the EdU Cell Proliferation Assay Kit (KeyGEN, China). The EdU positive cells were determined by fluorescence microscopy and calculated from five different fields. Each experiment was repeated at least three times.
2.6. Quantitative Real-Time PCR Analysis
Total cellular RNA was extracted using Trizol (Invitrogen) according to the manufacturer’s instructions. First-strand cDNA was generated with the HiScript 1 Strand cDNA Synthesis Kit (vazyme, China).Quantitative real-time PCR was conducted using a HiScript one-step qRT-PCR SYBR Green Kit (vazyme, China) and performed on the Bio-Rad CFX96 TM Real-time system. Gene expression in each sample was normalized to GAPDH expression. Primer sequences were as follows: NCL, 5′-GATCACCTAATGCCAGAAGCCAGC-3′; 5′-CAAAGCCGCCTCTGCCTCCACCAC-3′; MDR1, 5′-TGACTACCAGGCTCGCCAATGAT-3′; 5′-TGTGCCACCAAGTAGGCTCAAA-3′; GAPDH, 5′-GGAGTCAACGGATTTGGT-3′; 5′-GTGATGGGATTTCCATTGAT-3′.
2.7. Intracellular Rhodamine-123 Accumulation Assay
Hela cells transfected with NCL overexpression or empty vector were plated at 1 × 105/well in 12-well plates and incubated for 24 h, cells were treated with or without DDP (2.5 μg/mL) for 12 h, and then, Rh123 was added at a final concentration of 10 μg/ml and incubated with cells at 37°C for 30 min. Cells were harvested and resuspended with cold PBS. The fluorescence intensity of the cells was measured at 488/575 nm using the FACS Calibur flow cytometer (Becton Dickinson, USA).
2.8. Luciferase Reporter Assay
The pGL3-MDR1-promoter-luc plasmid or Y-Box mutated MDR1-luc plasmid and NCL overexpression plasmid or empty vector were cotransfected into Hela cells. After 24 h, cells were treated with cisplatin for 24 h. Luciferase activity was measured using the Dual-Luciferase Reporter Assay System (Promega).
2.9. Statistical Analysis
Data analysis was performed using GraphPad Prism 5. All results are expressed as means ± S. E. M. Differences between the two groups were determined using Student’s t-test. was considered statistically significant.
3.1. NCL Is Involved in Cisplatin-Resistant Cervical Cancer Cells
To determine whether NCL was associated with cisplatin resistance in cervical cancer, the expression of NCL was detected by western blotting in Hela cells and cisplatin-resistant cervical cancer cells Hela/DDP. As shown in Figures 1(a) and 1(b), NCL was expressed more abundant in Hela/DDP cells than in Hela cells. We then test the effect of overexpression and knockdown of NCL on the sensitivity to cisplatin of cervical cancer cells. NCL overexpression vector (NCL) or empty vector (NC) were transfected into Hela cells. Western blot results showed that the expression level of NCL was remarkably elevated in cells transfected with NCL overexpressing vector compared with the control (Figure 1(c)), and MTT assay result indicated that overexpression of NCL increased cervical cancer cell proliferation and attenuated the sensitivity to cisplatin (Figure 1(d)). Consistently, siRNA knockdown of NCL inhibited cell proliferation and enhanced the sensitivity of Hela/DDP cells to cisplatin (Figures 1(e) and 1(f)). We then performed the EdU assay, in which Hela/DDP cells transfected with siRNA were treated with or without DDP, then exposed to EdU (10 μM) for 12 h, and visualized under a fluorescent microscope. As expected, knockdown of NCL attenuated the cell proliferation and enhanced the sensitivity of cisplatin (Figures 1(g) and 1(h)).These results suggested that NCL was involved in the cisplatin resistance to cervical cancer.
3.2. NCL Regulates MDR1 Expression
Mechanisms of multidrug resistance in cancer are very complicated. One of the most important mechanisms responsible for multidrug resistance is the overexpression of multidrug resistance protein 1 (MDR1), also known as P-glycoprotein 1 (P-gp) or ATP-binding cassette subfamily B member 1 (ABCB1), which acts as an efflux pump for a wide spectrum of anticancer drugs. So, MDR1 proteins may be involved in the mechanism of cisplatin resistance mediated by NCL. To test this possibility, we detected the effect of overexpression and knockdown of NCL on MDR1 protein expression level. NCL overexpression plasmid or vector control was transfected in the Hela cells, and MDR1 and NCL were detected by western blotting. As shown in Figures 2(a) and 2(b), the MDR1 protein level was increased in NCL expressing cells, compared with that of cells expressing empty vector control. Conversely, a significantly decreased MDR1 level was observed after NCL knockdown cells when compared with the control (Figures 2(c) and 2(d)). Furthermore, we measured the mRNA level of MDR1 in the Hela cells transfected with NCL siRNA by qRT-PCR. Compared with the siNC group, the mRNA level of MDR1 was markedly decreased (Figure 2(e)).
3.3. NCL Overexpression Increases Drug Efflux
It has been reported that MDR1 functions as a drug efflux pump and extrudes multiple anticancer drugs contributing to multidrug resistance in many human cancers. So, we investigated whether overexpression of NCL affected the function of drug efflux. Rhodamine-123 accumulation assay was carried out by flow cytometry. As shown in Figure 3, the fluorescence intensity of rhodamine-123 was lower in NCL overexpression cells than control cells.
3.4. NCL Regulates Transcription Factor YB1 Expression
Transcriptional activation is generally accepted to be the principle mechanism for upregulating MDR1 gene expression. Many transcription factors play a role in the regulation of MDR1 gene expression. YB1 (Y-Box binding protein 1) has been demonstrated to be involved in multidrug resistance and regulation of downstream gene MDR1 (Figure 4(a)).So, we tested whether NCL may affect the expression of YB1. Results showed a significant increase of YB1 after NCL overexpression (Figures 4(b) and 4(c)).Similarly, NCL knockdown dramatically attenuated the expression of YB1 (Figures 4(d) and 4(e)).
3.5. NCL Regulates the Promoter Activity of MDR1 in an YB1‐Dependent Manner
To further address the mechanisms that control MDR1 gene expression by NCL, firstly, we determined whether NCL modulated the activity of the MDR1 promoter. We constructed the MDR1 promoter/luciferase reporter plasmid and Y-Box mutated MDR1-luc plasmid (Figure 5(a)), then they were cotransfected with NCL overexpression vector or empty vector into Hela cells as described in Section 2. After treatment with or without DDP, luciferase activities were measured. As shown in Figure 5(b), MDR1 promoter activity was increased by about 2-fold after NCL overexpression compared with the control, and luciferase activity was markedly increased by about 4-fold following DDP treatment, while no change was observed in the NC group. As expected, NCL failed to activate luciferase activity in transfectants containing Y-Box mutated MDR1-luciferase vector. In contrast, MDR1 promoter activity was dramatically rEduced in NCL-silenced cells. Moreover luciferase activity was at a much lower level when cotransfected with Y-Box mutated MDR1-luciferase vector (Figure 5(c)). These results suggest that NCL regulates the expression of MDR1 by controlling its promoter activity in a YB1-dependent manner.
3.6. NCL Induces Cisplatin Resistance in Cervical Cancer Cells by the YB1-MDR1 Pathway
To further test whether NCL induces cisplatin resistance in cervical cancer cells by the YB1-MDR1 pathway, we also performed the EdU assay. As shown in Figure 6(a), NCL overexpression promoted cell proliferation and attenuated the sensitivity of cells to DDP compared with the NC control. However, a significant decrease in cell proliferation and increase in the sensitivity to DDP was observed after YB1 knockdown in NCL overexpression cells.
Chemotherapy resistance is one of the main obstacles to successful clinical cancer therapy, and drug resistance can be obtained by different mechanisms, including drug efflux, apoptosis suppression, enhancing DNA repair, altering drug metabolism and persistence of cancer stem cells (CSCs), and epithelial-mesenchymal transition (EMT) [13–15]. Cisplatin is the major chemotherapeutic drug for cervical cancer, but cisplatin resistance has been a common and serious problem in the treatment of cervical cancer. Several reports have been published showing that overexpression of MDR1 gene enhancing drug efflux is associated with multidrug resistance in cervical cancer [16–18]. NCL, as a multifunctional protein with oncogenic properties involved in many key cellular processes, has attracted attention as a potential therapeutic target [19, 20]. NCL was able to traffic from the nucleus to the cytoplasm and cell surface, acting as a surface receptor for a variety of ligands implicated in tumorigenesis and angiogenesis. AS1411, an NCL-targeted DNA aptamer, has antiproliferative activity against a wide range of cancer cells [21–23]. It was reported that the NCL gene was upregulated in etoposide- and mitoxantrone-resistant breast cancer cells and associated with the drug resistance in acute lymphoblastic leukemia. However, the role of NCL in cisplatin resistance in cervical cancer is not clearly understood. In this study, we found that NCL was overexpressed in cisplatin-resistant cervical cancer cells and NCL expression was closely related to cisplatin sensitivity in cervical cancer cells. Overexpression of NCL significantly attenuated the sensitivity of cisplatin resistance in Hela cells, while NCL knockdown inhibited cell proliferation and reversed the cisplatin-resistant in Hela/DDP cell lines (Figure 1).Furthermore, we investigated the relationship between NCL and the expression level of MDR1 protein because one of the best characterized drug resistance mechanisms is overexpression of MDR1 which acts as a drug efflux and reduces the drug accumulation. We observed that knockdown of NCL expression with siRNA dramatically decreased MDR1 expression levels in protein and mRNA levels. Conversely, a significantly increased MDR1 level and intracellular accumulation of Rhodamine-123 were observed in NCL overexpression cells (Figures 2 and 3).It suggested that NCL contributed to the drug resistance by regulation the expression and function of MDR1. Transcriptional activation is the principle mechanism for upregulating MDR1 gene expression . YB1, as a major transcription factor for the MDR1 gene, has been reported to regulate the expression of MDR1 and mediated multidrug resistance in a variety of tumors [25–27]. Here, we provided evidence that overexpression of NCL led to a markedly increased level of YB1 expression. Moreover, the results of luciferase reporter assay showed that NCL could modulate MDR1 promoter activity in a YB1-dependent manner (Figures 4 and 5). Furthermore, we demonstrated that NCL overexpression in cervical cancer cells led to cisplatin resistance depending on YB1 (Figure 6). Taken together, NCL is closely associated with drug resistance, so NCL inhibitor or the combination of NCL and MDR1 inhibitors may provide a potential therapeutic option for the treatment of multipdrug resistance in cervical cancer.
We found a new mechanism of cisplatin resistance mediated by NCL in cervical cancer. NCL contributed to the drug resistance by regulation the expression and function of MDR1 in a YB1-dependent manner. Our results indicated that NCL may be a potential drug-resistant target, and blocking its function may be a potential strategy to enhance the treatment efficacy in cisplatin-resistant cervical cancer.
The data that support the findings of this study are available from the corresponding author upon reasonable request.
Conflicts of Interest
The authors report no conflicts of interest in this work.
Jing Ke and Chunming Gu contributed equally to this work.
This work was supported by the National Natural Science Foundation of China (Grant nos. 81702639 and 81502637), Health Commission of Hubei Province Scientific Research Project (Grant no. WJ2019M052), Free Exploration Project of Hubei University of Medicine (Grant no. FDFR201901), and Innovative Research Program for Graduates of Hubei University of Medicine (Grant no. YC2020007).
- M. Arbyn, E. Weiderpass, L. Bruni et al., “Estimates of incidence and mortality of cervical cancer in 2018: a worldwide analysis,” The Lancet Global Health, vol. 8, no. 2, pp. e191–e203, 2020.
- S.-H. Chen and J.-Y. Chang, “New insights into mechanisms of cisplatin resistance: from tumor cell to microenvironment,” International Journal of Molecular Sciences, vol. 20, no. 17, p. 4136, 2019.
- X. Zhu, H. Zhu, H. Luo, W. Zhang, Z. Shen, and X. Hu, “Molecular mechanisms of cisplatin resistance in cervical cancer,” Drug Design, Development and Therapy, vol. 10, pp. 1885–1895, 2016.
- W. Jia, Z. Yao, J. Zhao, Q. Guan, and L. Gao, “New perspectives of physiological and pathological functions of nucleolin (NCL),” Life Sciences, vol. 186, pp. 1–10, 2017.
- D. Ishimaru, L. Zuraw, S. Ramalingam et al., “Mechanism of regulation of bcl-2 mRNA by nucleolin and A + U-rich element-binding factor 1 (AUF1),” Journal of Biological Chemistry, vol. 285, no. 35, pp. 27182–27191, 2010.
- C. M. Berger, X. Gaume, and P. Bouvet, “The roles of nucleolin subcellular localization in cancer,” Biochimie, vol. 113, pp. 78–85, 2015.
- Z. Chen and X. Xu, “Roles of nucleolin. focus on cancer and anti-cancer therapy,” Saudi Medical Journal, vol. 37, no. 12, pp. 1312–1318, 2016.
- M. Koutsioumpa and E. Papadimitriou, “Cell surface nucleolin as a target for anti-cancer therapies,” Recent Patents on Anti-cancer Drug Discovery, vol. 9, no. 2, pp. 137–152, 2014.
- C. Xu, Y. Wang, Q. Tu et al., “Targeting surface nucleolin induces autophagy-dependent cell death in pancreatic cancer via AMPK activation,” Oncogene, vol. 38, no. 11, pp. 1832–1844, 2019.
- S.-H. Shin, G. Y. Lee, M. Lee et al., “Aberrant expression of CITED2 promotes prostate cancer metastasis by activating the nucleolin-AKT pathway,” Nature Communications, vol. 9, no. 1, p. 4113, 2018.
- Z. Fu and C. Fenselau, “Proteomic evidence for roles for nucleolin and poly[ADP-ribosyl] transferase in drug resistance,” Journal of Proteome Research, vol. 4, no. 5, pp. 1583–1591, 2005.
- J. Hu, Y. Chen, Z. Wu et al., “Targeting nucleolin for reversal of chemotherapy resistance in acute lymphoblastic leukemia,” Blood, vol. 134, no. S1, p. 5058, 2019.
- B. Mansoori, A. Mohammadi, S. Davudian, S. Shirjang, and B. Baradaran, “The different mechanisms of cancer drug resistance: a brief review,” Advanced Pharmaceutical Bulletin, vol. 7, no. 3, pp. 339–348, 2017.
- L. Galluzzi, L. Senovilla, I. Vitale et al., “Molecular mechanisms of cisplatin resistance,” Oncogene, vol. 31, no. 15, pp. 1869–1883, 2012.
- S. N. Aleksakhina, A. Kashyap, and E. N. Imyanitov, “Mechanisms of acquired tumor drug resistance,” Biochimica et Biophysica Acta (BBA)—Reviews on Cancer, vol. 1872, no. 2, Article ID 188310, 2019.
- Z. Chen, K. Ling, Y. Zhu, L. Deng, Y. Li, and Z. Liang, “Rucaparib antagonize multidrug resistance in cervical cancer cells through blocking the function of ABC transporters,” Gene, vol. 759, Article ID 145000, 2020.
- K. Zhu, L. Chen, X. Han, J. Wang, and J. Wang, “Short hairpin RNA targeting twist1 suppresses cell proliferation and improves chemosensitivity to cisplatin in HeLa human cervical cancer cells,” Oncology Reports, vol. 27, no. 4, pp. 1027–1034, 2012.
- F. Yang, B. Gao, R. Li et al., “Expression levels of resistant genes affect cervical cancer prognosis,” Molecular Medicine Reports, vol. 15, no. 5, pp. 2802–2806, 2017.
- S. Romano, N. Fonseca, S. Simões, J. Gonçalves, and J. N. Moreira, “Nucleolin-based targeting strategies for cancer therapy: from targeted drug delivery to cytotoxic ligands,” Drug Discovery Today, vol. 24, no. 10, pp. 1985–2001, 2019.
- T. Watanabe, K. Hirano, A. Takahashi et al., “Nucleolin on the cell surface as a new molecular target for gastric cancer treatment,” Biological and Pharmaceutical Bulletin, vol. 33, no. 5, pp. 796–803, 2010.
- S. Soundararajan, L. Wang, V. Sridharan et al., “Plasma membrane nucleolin is a receptor for the anticancer aptamer AS1411 in MV4-11 leukemia cells,” Molecular pharmacology, vol. 76, no. 5, pp. 984–991, 2009.
- J. E. Rosenberg, R. M. Bambury, E. M. Van Allen et al., “A phase II trial of AS1411 (a novel nucleolin-targeted DNA aptamer) in metastatic renal cell carcinoma,” Investigational New Drugs, vol. 32, no. 1, pp. 178–187, 2014.
- E. Wolfson, S. Solomon, E. Schmukler, Y. Goldshmit, and R. Pinkas-Kramarski, “Nucleolin and ErbB2 inhibition reduces tumorigenicity of ErbB2-positive breast cancer,” Cell Death & Disease, vol. 9, no. 2, p. 47, 2018.
- S. Labialle, L. Gayet, E. Marthinet, D. Rigal, and L. G. Baggetto, “Transcriptional regulators of the human multidrug resistance 1 gene: recent views,” Biochemical Pharmacology, vol. 64, no. 5-6, pp. 943–948, 2002.
- R. Chattopadhyay, S. Das, A. K. Maiti et al., “Regulatory role of human AP-endonuclease (APE1/Ref-1) in YB-1-mediated activation of the multidrug resistance gene MDR1,” Molecular and Cellular Biology, vol. 28, no. 23, pp. 7066–7080, 2008.
- T. Shibata, K. Watari, A. Kawahara et al., “Targeting phosphorylation of Y-box-binding protein YBX1 by TAS0612 and everolimus in overcoming antiestrogen resistance,” Molecular Cancer Therapeutics, vol. 19, no. 3, pp. 882–894, 2020.
- M. Kuwano, T. Shibata, K. Watari, and M. Ono, “Oncogenic Y‐box binding protein‐1 as an effective therapeutic target in drug‐resistant cancer,” Cancer Science, vol. 110, no. 5, pp. 1536–1543, 2019.
Copyright © 2021 Jing Ke et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.