J Cancer 2014; 5(9):804-812. doi:10.7150/jca.10456 This issue Cite

Research Paper

MicroRNA-21 Down-regulates Rb1 Expression by Targeting PDCD4 in Retinoblastoma

Fengmei Shen1*, Meng-Hsuan Mo2*, Liang Chen2, Shejuan An2, Xiaohui Tan2, Yebo Fu2, Katayoon Rezaei3, Zuoren Wang4, Lin Zhang1 Corresponding address, Sidney W. Fu2 Corresponding address

1. Department of Ophthalmology, Xi'an Jiaotong University First Affiliated Hospital, Xi'an, China
2. Department of Medicine, Division of Genomic Medicine, and Department of Microbiology, Immunology and Tropical Medicine, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA
3. Department of Pathology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA
4. Department of Surgery, Xi'an Jiaotong University First Affiliated Hospital, Xi'an, China
* These authors contributed equally to this work.

Shen F, Mo MH, Chen L, An S, Tan X, Fu Y, Rezaei K, Wang Z, Zhang L, Fu SW. MicroRNA-21 Down-regulates Rb1 Expression by Targeting PDCD4 in Retinoblastoma. J Cancer 2014; 5(9):804-812. doi:10.7150/jca.10456. https://www.jcancer.org/v05p0804.htm
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Retinoblastoma (RB) is a children's ocular cancer caused by mutated retinoblastoma 1 (Rb1) gene on both alleles. Rb1 and other related genes could be regulated by microRNAs (miRNA) via complementarily pairing with their target sites. MicroRNA-21 (miR-21) possesses the oncogenic potential to target several tumor suppressor genes, including PDCD4, and regulates tumor progression and metastasis. However, the mechanism of how miR-21 regulates PDCD4 is poorly understood in RB. We investigated the expression of miRNAs in RB cell lines and identified that miR-21 is one of the most deregulated miRNAs in RB. Using qRT-PCR, we verified the expression level of several miRNAs identified by independent microarray assays, and analyzed miRNA expression patterns in three RB cell lines, including Weri-Rb1, Y79 and RB355. We found that miR-19b, -21, -26a, -195 and -222 were highly expressed in all three cell lines, suggesting their potential role in RB tumorigenesis. Using the TargetScan program, we identified a list of potential target genes of these miRNAs, of which PDCD4 is one the targets of miR-21. In this study, we focused on the regulatory mechanism of miR-21 on PDCD4 in RB. We demonstrated an inverse correlation between miR-21 and PDCD4 expression in Weri-Rb1 and Y79 cells. These data suggest that miR-21 down-regulates Rb1 by targeting PDCD4 tumor suppressor. Therefore, miR-21 could serve as a therapeutic target for retinoblastoma.

Keywords: Retinoblastoma, miRNA, miR-21, PDCD4.


Retinoblastoma (RB) is a common pediatric intraocular tumor represented by a mutation of the retinoblastoma gene (Rb1) on both alleles. There are about 250-350 newly diagnosed RB cases every year in the United States [1, 2]. Retinal tumors develop rapidly in early childhood, usually before the age of five. Common treatments now include chemotherapy, focal therapy such as laser or cryotherapy, and enucleation [3]. Metastasis of RB is often fatal, despite the high cure rate in children [4]. Later in life, survivors with bilateral RB, an inheritable form, will face increased risk of developing other RB-related nonocular cancers [5, 6], and a trilateral RB, known as pineoblastoma, a tumor in pineal gland [7]. Previous report indicates that 30-40% of all RBs were found to be bilateral [8, 9]. The metastasis could be seen in both heritable and inheritable cases, as tumor cells frequently invade the optic nerve, orbit and choroid [10, 11]. Thus, methods to minimize the requirement of enucleation, decrease the risk of tumor metastasis and the development of secondary cancers, preserve vision and prevent systemic toxicity are crucially needed [1].

The critical role of Rb1 in cell proliferation attracted much attention after it was first discovered in RB. The Rb1 gene is located at chromosome 13q14 and functions as a tumor suppressor, which regulates the cell cycle, specifically cell proliferation and apoptosis. The retinoblastoma protein (pRb) binds to the transcription factor of the E2F family to mediate the succession of the G1/S phase [12]. As described in Knudson's “two-hit theory” model of tumorigenesis [13], the heritable form of RB is derived from one germ line mutation and one somatic mutation. On the other hand, the non-heritable or sporadic form is due to two somatic mutations. Loss of the Rb1 gene in RB is necessary for tumorigenic initiation as well as subsequent genetic and epigenetic alterations causing tumor metastasis [1, 12, 14, 15].

miRNA is a small non-coding single-stranded RNA (18-24nt), widespread throughout the human genome. It is well documented for their post-transcriptional modifications on gene expression [16-18]. According to miRBase Release 21 (June 2014), 2,588 mature human miRNAs have been identified [19, 20]. Primary miRNA (pri-miRNA) is transcribed by RNA polymerase II and then cleaved by endonuclease RNase III Drosha in the nucleus to release stem-loop shaped pre-miRNA, which are approximately 70 nucleotides in length [14, 21]. After being exported into the cytoplasm and processed by another endonuclease, Dicer, pre-miRNA becomes mature double-strand miRNA. One strand of mature miRNA is integrated into the RNA-induced silencing complex (RISC) to regulate target genes [16, 22]. Imperfectly or perfectly base pairing the 3' UTR of a target mRNA with the conserved seed region (~5 nucleotides) in the 5' end of a miRNA caused genomic instability and transcriptional degradation, as well as translational repression [18, 21, 23, 24]. Furthermore, due to important features of miRNAs, a single miRNA can target more than one mRNA molecule and single target mRNA can be recognized by multiple miRNAs. The interaction between miRNAs and its targets creates a complex regulatory network [18, 22, 25].

miRNA transcripts are often located at fragile genomic sites related to cancer and are expressed abnormally because of alterations in cancer genome [26, 27]. Several cancer-related miRNAs and their target genes in tumor cells have been identified [14, 25] and their disposition clarified as either towards tumor suppression or oncogenesis [16, 18]. For instance, loss of miRNA-15/-16 in chronic lymphocytic leukemia [16, 18, 27, 28], miRNA let-7 in lung cancer [16, 18, 27, 29], and miRNA-143/ miRNA-145 in colon cancer [30], miR-638 in breast cancer [31] provided some evidences towards the tumor suppressing capabilities of miRNA. Similarly, over-expressed miRNA-21/ miRNA-155 in human breast cancer [16, 18, 32] showed the oncogenic potential of miRNAs. Recently, we found that a number of miRNAs, including miR-21, are involved in early breast cancer progression using microarray assay on microdissected formalin-fixed paraffin-embedded (FFPE) samples [33].

Targeting miRNAs could be a novel therapeutic option due to its regulatory role during cancer development and progression. miRNA-34a was reported as a tumor suppressor in RB cell lines [14]. The inverse correlation between down-regulated hsa-let-7b and overexpressed HMGA-1 and HMGA-2 was found in FFPE RB tumor samples [15]. By profiling miRNA expression in RB cell line HXO-RB44 under normal and hypoxic conditions, researchers identified miR-181 as a hypoxia-related miRNA and that the inhibition of miR-181b impeded cell growth in RB cells under hypoxia conditions [34].

In this study, we first tried to determine the expression of a set of miRNAs related to RB in three RB cell lines, Weri-Rb1, Y79 and RB 355. We found a list of five miRNAs: miR-19b, miR-21, miR-26a, miR-195 and miR-222, which might be involved in the proliferation and metastasis in RB. Then we analyzed the predicted target genes of these miRNA in RB pathologies by miRNA and mRNA interactions. Among them, miR-21 is well studied and is a known onco-miR that is highly expressed in cancers, such as breast cancer [35-37], glioblastoma [38, 39], glioma [40], colorectal cancer [41], prostate cancer [42, 43], hepatocellular cancer [44], non-small cell lung cancer [45], papillary thyroid carcinoma [46], gastric cancer [47], osteosarcoma [48], diffuse large B-cell lymphoma [49] and laryngeal carcinoma [50]. However, to the best of our knowledge, there is no report on the role of miR-21 in RB initiation and development. In this study, we focused on elucidating the role of miR-21 in regulating one of its target genes, the programmed cell death 4 (PDCD4), a tumor suppressor involving cell cycle regulation.

Materials and Methods

Cell culture

The human RB cell lines Y79, Weri-RB1 and RB355 were provided by Dr. Hakim Djaballah at the Memorial Sloan-Kettering Cancer Center. They were cultured in RPMI-1640 (Lonza) with 1% penicillin-streptomycin, 2 mM glutamine and 20% fetal bovine serum (HyClone, Thermo Scientific) [51]. All cell lines were grown in suspension at a concentration of 105 - 106 cells/ml and incubated at 37 ˚C with 5% CO2.

Isolation of total RNAs and miRNAs

Total RNAs and miRNAs from the cell lines were isolated using TRIzol® Reagent (Invitrogen) and the mirVana miRNA Isolation Kit (Ambion) respectively. Concentration and purity of the RNA samples were assayed using the NanoDrop ND-1000 Spectrophotometer (NanoDrop, Wilmington, DE).

qRT-PCR for miRNAs and mRNAs

The Taqman MiRNA Reverse Transcript Kit (Applied Biosystems), wherein a stem-loop RT primer specifically hybridizes with a miRNA molecule and a MultiScribe™ Reverse Transcriptase, was used for reverse transcription (RT). The RT reaction mixture was incubated at 16˚C for 30 minutes, 42˚C for 30 minutes, 85˚C for 5 minutes, and then stored at 4˚C. The RT products were subsequently amplified with the mature miRNA-specific Taqman® MiRNA Assay Kit (Applied Biosystems) using the ABI 7300 Real-Time PCR system. The PCR was performed at 95 ˚C for 10 minutes, followed by 40 cycles of 95 ˚C for 15 seconds and 60 ˚C for 60 seconds. U6 small nuclear RNA was used as an internal control for normalization. PDCD4 primers were synthesized by the Integrated DNA Technologies (IDT) and the sequences were as follows: Forward, 5'-GGC CTC CAA GGA GTA AGA CC-3'; Reverse, 5'-AGG GGT CTA CAT GGC AAC TG-3'. The cDNAs were synthesized via iScript cDNA Synthesis Kit (Bio-Rad Laboratories) and amplified with SYBR® GreenER™ qPCR Supermix Universal (Invitrogen) using the ABI 7300 Real-Time PCR system. The RT reactions were carried out at 25˚C for 5 minutes, 42˚C for 30 minutes, 85˚C for 5 minutes and then held on 4˚C. The PCR reactions were performed under the following conditions, 50˚C for 2 minutes, 95˚C for 10 minutes and then 40 cycles of 95˚C for 15 seconds and 60˚C for 60 seconds. 18S rRNA gene was used for normalization. The qRT-PCR analyses for each miRNA and mRNA in three cell lines were performed in quadruplicates and triplicates respectively. Relative quantitation was calculated using the 2-Δ(ΔCt) method where fold change is equal to 2-[(Mean ΔCt Target Gene) - (Mean ΔCt Internal Control)].

Transfection of miR-21 mimic and inhibitor in RB cell lines

The miR-21 mimic is a small double-strand RNA that mimics endogenous precursor miRNA, and the miR-21 inhibitor is a single-strand RNA that is designed to bind to and inhibit endogenous miRNA. Transfection of Weri-Rb1, Y79 and RB355 cell lines was executed with Lipofectamine™ 2000 (Invirtrogen) according to the manufacturer's protocol. Briefly, cells were plated in 6-well plates at 30-50% confluence in antibiotics-free growth medium one day before transfection. To make the transfection complex, we diluted 70pmole of Pre-miR™ miRNA precursor, Anti- miR™ miRNA inhibitors (hsa-miR-21) or miRNA negative control (Ambion) with 5µl Lipofectamine™ 2000 (Invirtrogen) in 2ml of Opti-MEM® I Reduced Medium (Invitrogen). Medium were changed to complete growth medium (20%FBS) after 4-6 hours. After 48 h transfection, total RNA and protein were isolated.

Western blot assays

Proteins were extracted from transfected cells using 10X RIPA lysis buffer (Millipore). Protein concentration was measured using the Pierce® BCA protein assay kit (Thermo). The primary anti-PDCD4 (rabbit) antibody was purchased from Rockland (Gilbertsville, PA) and anti-β-actin (mouse) antibody was obtained from Sigma-Aldrich. Protein with 1X Laemmli buffer was denatured at 95˚C for 5 minutes before electrophoresis using the 10% Mini-PROTEAN® TGX Precast Gels (BIO-RAD), under the condition of 120V, for 1 - 1.5 hours. Protein was transferred onto the nitrocellulose membrane. The membrane was blocked with 5% non-fat milk/ PBST for one hour at RT and incubated with the primary antibody (1:5,000 dilution) at 4 ˚C overnight. The secondary antibody (1:100,000 dilution) was applied for 1-1.5h at RT. The blot signals were detected using the SuperSignal West Dura Chemiluminescent Substrate (Thermo) and visualized via Image Lab™ system software (BIO-RAD). β-actin was used as an internal control. The band intensity was quantified using the Image J software.

Statistical analysis

Data were presented as the mean ± standard deviation (S.D.). The one-way analysis of variance (ANOVA) was performed for the miRNA differential expression in cell lines. The Student's t-test was applied to compare two transfected groups. P-value ≤ .05 or .01 was considered statistically significant and presented with one and two asterisks respectively.

Results and Discussion

Differentially expressed miRNAs in three RB cell lines

miRNAs, such as miR-19b, 93, -141 and 181c, miR-181a, -183, -222 and let-7a were identified earlier as RB-related miRNAs using a Human miRNA 2k custom array (Agilent) [24]. A separate study identified 11 over-expressed miRNAs in RB compared to normal retina, most notably a fourfold increase in miR-320, miR-373 and miR-503 using the miRCURYTM array microarray (Exiqon) [27]. To explore the relative expression of miRNAs in three RB cell lines, Weri-Rb1, Y79 and RB355, we selected a list of 23 candidate miRNAs (miR-19b, -21, -26a, -29b, -93, -96, -141, -181a, -181c, -183, -187,-195, -200b, -200c, -205, -214, -222, -381,-556-3p, -557, -644, -1287 and let-7a) from aforementioned studies for qRT-PCR analysis.

Interestingly, those miRNAs, such as miR-19, -21, -26, -29, -93, -96, -141, -181, -183, -195, -200b, -205 and -222, were predicted to target one or more of the 320 retinal genes, which are known to be involved in visual functions or related to inherited retinal diseases [52]. These target genes were identified by a combination of the RetinaCentral, the Retinal Information Network databases, and the comparison of retinal/ RPE dbEST libraries between five tissue-specific libraries [52].

In addition, we found that the expression of some miRNAs, such as miR-141, -187, -200b, 200c, -214 and -381, was very low in all three RB cell lines (data not shown). Others, such as miR-195, miR-19b, miR-26a, miR-21 and miR-222 were extensively over-expressed in one cell line as compared to the other two (Figure 1). miR-19b was deregulated as previously reported [24] in RB cell lines, with greater expression in Weri-Rb1 than in Y79 cells and low levels in RB355 cells. miR-26a, which is expressed in normal retina [52], appeared with significantly different expression levels among the three cell lines, with the highest expression being found in Y79 cells and a comparable expression level in both Wer-Rb1 and RB355 cells. Others, such as miR-21 and miR-222, were well documented by independent studies in regards to their regulatory activity within a number of cancers and also showed differential expression in RB cells. It should be noted that four of the five miRNAs were commonly overexpressed in Y-79 cells as compared to Rb-1 and Rb-355 cells. Alongside our previous observation of Y-79 cells as having increased potency in metastasis and proliferation, we suggest those four miRNAs might have the ability to predict metastasis and proliferation of the RB. However, miR-19b was expressed higher exclusively in Rb-1 cells and required further investigation.

 Figure 1 

The differential expression patterns of miRNAs in three RB cells. Five miRNAs were identified by ANOVA tests to be overexpressed in one cell line compared to the other two. Four of the five miRNAs had a common increase in expression level in Y-79 cells, whereas miR-19b had a higher expression level in Weri-Rb1 cells (Rb1). All data were measured in triplicate and presented as the mean ± standard deviation (S.D.).

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Target gene prediction of the candidate miRNAs

In order to understand how these five miRNAs function in RB tumor development and progression, predicted target genes of those five miRNAs were obtained via three computational algorithms, miRanda (http://www.microrna.org/), TargetScan (http://www.targetscan.org/), and DianaMicroT (http://diana.cslab.ece.ntua.gr/microT/). For each miRNA, predicted target genes were displayed if at least predicted by two algorithms. The predicted miR-21 target genes are presented in Figure 2.

 Figure 2 

Program prediction of target genes of miR-21. The Venn-diagram displays the putative targets genes of miR-21 as predicted by Diana MicroT, TargetScan, and Miranda. There were 202 candidates predicted by at least two programs and 46 candidates by all three algorithms.

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miR-21 and one of its target genes, PDCD4 in RB

To study the biological significance of the differentially expressed miRNAs, we predicted putative target genes, which were documented in previous studies. PDCD4 is one of the well reported targets of miR-21. Reduction or loss of PDCD4 expression was often seen in various cancers, including lung cancer [53], heptocellular carcinoma [54], ductal breast cancer [55], oral squamous cell carcinoma [56], and colorectal cancer [57]. PDCD4 protein levels were found to be inversely correlated with miR-21 levels in human glioblastoma cell lines [58], colorectal samples [41] and cell lines [59], and breast tumor specimens [35].

Furthermore, the conserved target site for miR-21 in the 3'-UTR of PDCD4 was perfectly matched through bioinformatics predictions. The suppression of reporter gene activity with the 3'-UTR of PDCD4 verified the down-regulatory effect of miR-21 in colorectal cells [59], cervical carcinoma cells [60], glioblastoma cells [58], breast cancer cells [61], and myelogenous leukemia cells [62-64]. The TargetScan program was applied to confirm the miR-21 binding site in the 3'-UTR of PDCD4 and the sequence for the binding site was well conserved among species as shown in Figure 3.

In glioblastoma T98G cells, high levels of miR-21 repressed PDCD4 [58]. We reasoned that similar interactions might also exist in RB. Thus, we assessed both PDCD4 mRNA and protein levels in RB cell lines, Rb1, Y79 and Rb355. We expected that PDCD4 expression might be inversely correlated with miR-21 expression. The implication being, cell lines with high endogenous miR-21 might contain a low level of PDCD4 protein, and vice versa. When compared between Rb1 and Y79 cells, miR-21 was barely detectable and the most abundant amount of PDCD4 protein was found in Rb1, whereas Y79 cells displayed a higher miR-21 level and low PDCD4 mRNA and protein (Figure 4.). Rb-355 cells have similarly low expression levels of miR-21 and high levels of PDCD4 mRNA. However, Rb-355 rarely expressed the PDCD4 protein, indicating PDCD4 might be subject to more complex post-transcriptional regulation.

Overexpression of PDCD4 could inhibit cell invasion in MDA-MB-231 breast cancer cells [35] as well as OSCC cells [56]. We hypothesize that higher miR-21 levels accompanied by attenuated PDCD4 protein levels in Y79 cell lines might be closely related to its more aggressive nature in tumor growth and metastasis. Meanwhile, lower miR-21 and up-regulated expression of PDCD4 protein in Rb1 cells denotes its non-metastasis feature. As for RB355 cells, knowledge is limited on the invasive ability and metastatic propensity.

 Figure 3 

miR-21 seed sequence matches the target site in the 3' UTR of PDCD4. The seed sequence of miR-21 was identified by TargetScan and accurately matched to the 3' UTR of PDCD4 in six different species.

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 Figure 4 

Expression of miR-21 and PDCD in RB cells. Total RNA and total protein were isolated from three RB cell lines by mirVana and RIPA respectively. qRT-PCR was performed to measure the expression level of miR-21 and PDCD4 mRNA. Western blot analysis was performed to measure the protein level of PDCD4. Y79 cells had the highest miR-21 level along with a low PDCD4 mRNA and protein level. Rb1 had a lower miR-21 expression level, but the highest PDCD4 protein level. RB355 cells had a low miR-21 expression level along with the highest PDCD4 mRNA level, but barely expressed any PDCD4 protein.

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Previous studies also implied that the Y79 cell line represents more metastatic potential as compared to the Rb1 cell line. The metastatic characteristics of Y79 cells were observed after intravitreous cavity injections in immune-deficient mice, while Rb1 cells represented a less-metastatic model [65]. Tumors formed in Y79-injected mice aggressively invaded subretinal and choroidal space, and then migrated to the optic nerve as well as the brain and contralateral optic nerve. On the other hand, the mice injected with Rb1 cells developed localized tumors located in the anterior uveal tissue. In vitro, suspended Y79 cells adhered to monkey choroid and rat C6 glioma cells, but not to human embryonic kidney cells. The binding of Y79 RB cells to the choroid and glioma cells, which were derived from target sites of invasion, were confirmed as true cell-cell interactions since trypsin treatment interrupted the binding of Y79 cells, but neuraminidase did not. Few Rb1 cells interacted with choroidal and glioma cells. It was believed that the distinct ability and inclination to metastasize in Rb1 and Y79 RB cells might result from differences in membrane protein structure. Moreover, the invasive Y79 cells lost expression of N-cadherin and cadherin-11 proteins, contributing to RB tumor progression [66, 67]. Rb1 cells relied on cadherin-mediated cell-cell interaction [66], which is calcium-dependent [67]. Ectopic expression of N-cadherin and cadherin-11 in Y79 cells transplanted into the vitreous of mice showed a less extensive optic nerve invasion, which was similar to Rb1 cell xenografts as compared to Y79 cell controls.

In a previous study, Dalgard et al. discovered that precursor and mature miR-34a in RB cell lines were expressed in different levels: they were higher in Rb1 cells and lower in Y79 cells [14]. In Y79 cells, the level of miR-34a rose after adding p53-activating agents. Overexpression of miR-34a diminished cell growth and increased caspase-3/7 activity in both RB cells, particularly in Y79 cells. It is likely that miR-34a expression levels represent the aggressiveness of both cells, due to the miRNAs' epigenetic manipulation on RB cell lines contributing to invasion variability. Thus, Y79 seems to be more aggressive when compared to Weri-Rb1 cells, and higher expression level of miR-21 along with diminished PDCD4 level might serve as an indicator of its aggressive nature.

Inhibition or overexpression of miR-21 in RB cell lines

We sought to explore whether or not miR-21 regulates endogenous PDCD4 in RB cell lines Rb1 and Y79, as well as to observe the miR-21 and PDCD4 expression levels after transient transfections. The negative regulation of miR-21 on its target gene, PDCD4, has been established in other cancers. The protein expression level of PDCD4 could be down- and up-regulated by a miR-21 inhibitor and precursor respectively in OSCC cells [56] and cervical carcinoma Hela cells [60]. A similar study showed that anti-miR-21 transfected in leukemia HL60 and K562 cells increased the mRNA and protein expression of PDCD4 [62-64].

To validate the similar alterations of miR-21 and PDCD4, we performed qRT-PCR and Western blotting to compare RB cells with miR-21 inhabitation and overexpression to negative controls. The transfection with the miR-21 inhibitor and mimic were efficient and could elevate miR-21 to more than 100-fold levels in cell lines when compared to negative controls in both Rb1 and Y79 cells (Figure 5).

The PDCD4 protein level significantly decreased in Rb-1 and Y-79 cells when miR-21 is overexpressed. Meanwhile, inhibition of miR-21 successfully restored PDCD4 protein levels; eliminating the possibility that miR-21 overexpression silences PDCD4 due to the non-specific off-target binding effect.

By targeting PDCD4, miR-21 could manage tumor growth and invasion. In colorectal RKO cells that endogenously expressed high levels of miR-21, anti-miR-21 transfection caused PDCD4 protein levels to increase and also blocked cell invasion and distal metastasis [59]. In a similar vein, pre-miR-21-transfected Colo206f cells that were naturally low in miR-21 displayed decreased PDCD4 protein levels and increased cell invasion. In cervical carcinoma Hela cells, the knockdown of miR-21 restrained cell proliferation and colony formation [60]. In parallel, elevated expression of miR-21 in RB via a precursor might consistently lessen PDCD4 expression, a responder to apoptosis in cancer, thus stimulating cell proliferation. In contrast, miR-21 inhibition might contribute to restoring PDCD4 expression in RB cells, resulting in suppression of tumor cell growth and invasion. These imply that miR-21 may serve as a therapeutic target by suppressing tumor growth and triggering apoptosis pathways by regulating PDCD4 gene expression in RB.


Our data suggests that miR-21 may play a significant regulatory role in RB tumor cell migration and invasion. Therefore, it may serve as a therapeutic target in RB as it regulates Rb1 gene expression by directly targeting PDCD4.

 Figure 5 

Expression of PDCD4 mRNA and protein in Rb1 and Y79 cells when transfected by miR-21 mimic or inhibiotor. Rb1 and Y79 cells were transfected with miR-21 mimic and inhibitor respectively. Two days after transfection, total RNA and protein were isolated. qRT-PCR showed the inhibition and overexpression were successful in comparison with the wild type control. PDCD4 mRNA levels in Rb1 cells did not show a significant change, but a sigifnicant fold change was present in Y79 cell data. Western blotting revealed PDCD4 proteins in both cells as having an inverse correlation with the miR-21 level, in which miR-21 overexpression reduced the PDCD4 protein while miR-21 inhibition restored the PDCD4 protein level.

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We are grateful to Dr. Hakim Djaballah (Memorial Sloan-Kettering Cancer Center, US) for providing the Weri-RB1, Y-79 and RB355 cell lines and Dr. Gail M. Seigel (State University of New York at Buffalo, US) for the gift of RB143, Y79 and WERI-RB27 cell lines. This research was supported in part by the Wendy Will Case award (to SWF), the Hao Foundation Award (to SWF) and the Elaine H. Snyder Cancer Research Award (to SWF).

Competing Interests

The authors have declared that no competing interest exists.


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Author contact

Corresponding address Corresponding authors: Sidney W. Fu, MD. PhD. Department of Medicine, Division of Genomic Medicine, The George Washington University School of Medicine and Health Sciences, 2300 Eye Street, N.W. Ross Hall 402C, Washington, DC 20037 Email: sfuedu Tel: 202-994-4767 Fax: 202-994-8924 or Lin Zhang, MD. Department of Ophthalmology, Xi'an Jiaotong University First Affiliated Hospital, Xi'an, China. Email: zhanglinxjtucom Tel: +86-189-9123-2235.

Received 2014-9-1
Accepted 2014-9-28
Published 2014-11-21

Citation styles

Shen, F., Mo, M.H., Chen, L., An, S., Tan, X., Fu, Y., Rezaei, K., Wang, Z., Zhang, L., Fu, S.W. (2014). MicroRNA-21 Down-regulates Rb1 Expression by Targeting PDCD4 in Retinoblastoma. Journal of Cancer, 5(9), 804-812. https://doi.org/10.7150/jca.10456.

Shen, F.; Mo, M.H.; Chen, L.; An, S.; Tan, X.; Fu, Y.; Rezaei, K.; Wang, Z.; Zhang, L.; Fu, S.W. MicroRNA-21 Down-regulates Rb1 Expression by Targeting PDCD4 in Retinoblastoma. J. Cancer 2014, 5 (9), 804-812. DOI: 10.7150/jca.10456.

Shen F, Mo MH, Chen L, An S, Tan X, Fu Y, Rezaei K, Wang Z, Zhang L, Fu SW. MicroRNA-21 Down-regulates Rb1 Expression by Targeting PDCD4 in Retinoblastoma. J Cancer 2014; 5(9):804-812. doi:10.7150/jca.10456. https://www.jcancer.org/v05p0804.htm

Shen F, Mo MH, Chen L, An S, Tan X, Fu Y, Rezaei K, Wang Z, Zhang L, Fu SW. 2014. MicroRNA-21 Down-regulates Rb1 Expression by Targeting PDCD4 in Retinoblastoma. J Cancer. 5(9):804-812.

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