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Department of Experimental Pathology and Oncology, University of Florence, Florence, Italy (L.P., E.W., M.D., M.L., E.B., A.T., A.L., N.S., S.C.); Program in Biomolecular Research, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia (K.A.K.); and Department of Pharmacology, University of Milan, Italy (A.M.B, A.N.)
Received May 21, 2007; accepted November 6, 2007
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Abstract |
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). To undergo apoptosis, cells need to switch-off the bcl-2 gene expression (Haldar et al., 1994). Therefore, preventing bcl-2 down-regulation could be, at least in principle, a very suitable strategy to treat diseases characterized by excessive apoptosis and, particularly in the neurodegenerative pathologies, to promote conditions that could slow down neuron loss (Belcredito et al., 2001; Yi et al., 2006). Furthermore, stabilizing bcl-2 expression could rescue cells committed to apoptosis by hypoxia/ischemia-related stress (Cao et al., 2002). Recently, simvastatin has been found to protect neurons from excitotoxicity by up-regulating bcl-2 mRNA and protein by a still-to-be-clarified mechanism (Johnson-Anuna et al., 2007).
Differentiation and cell cycle are other cellular programs in which bcl-2 plays a role. Evidence indicates that bcl-2 expression is involved in promoting and accelerating neuronal differentiation (Abe-Dohmae et al., 1993; Suzuki and Tsutomi, 1998; Eom et al., 2004). On the other hand, bcl-2 up-regulation is also known to have an inhibitory effect on cell cycle entry independently from its antiapoptotic activity (Mazel et al., 1996; Vairo et al., 1996; Huang et al., 1997).
Increased knowledge of molecular determinants of apoptosis regulation and execution is now offering new molecular targets suitable to repair apoptosis dysfunctions (Nicholson, 2000; Hersey et al., 2006). Several antiapoptotic molecules have been proposed as therapeutics for neurodegenerative diseases (Garber, 2005). Post-transcriptional control of gene expression based on mRNA half-life or translation regulation has been known for many years for a variety of genes. A number of cis-acting elements are known to stabilize or destabilize the relevant mRNA, among which adenine and uracil-rich elements (AU-rich elements, AREs) located in the 3'-UTR of many mRNAs modulate mRNA stability via interaction with stabilizing or destabilizing ARE-binding proteins (AUBPs) (Bevilacqua et al., 2003; Barreau et al., 2005). The ability of AREs to interact with endogenous AUBPs has suggested that these sequences could be also accessible to exogenously vehiculated molecules (Bevilacqua et al., 2003; Luzi et al., 2003). An ARE-based mechanism of post-transcriptional control of bcl-2 expression accounting for mRNA half-life regulation and its reduction during apoptosis has been described previously by us (Schiavone et al., 2000; Lapucci et al., 2002; Donnini et al., 2004).
In a previous work, in an attempt to stabilize the bcl-2 mRNA by hampering its degradation machinery, we have targeted the ARE of bcl-2 mRNA with peculiar 2'-O-methyl oligoribonucleotides (ORNs) in antisense orientation (Ghisolfi et al., 2005). Unlike standard DNA oligonucleotides, which form DNA/RNA heteroduplexes that can be cleaved by the RNase H (Schiavone et al., 2004), RNA oligonucleotides form stable RNA/RNA homoduplexes that are not cleaved by the RNase H (Schiavone et al., 2004). These bcl-2 ARE-targeting antisense ORNs (bcl-2 ARE asORNs), transported by cationic lipids into neuroblastoma and hematopoietic cell lines (i.e., SHSY-5Y and HL60, respectively), stabilized bcl-2 mRNA and increased the level of Bcl-2 protein in a dose-dependent manner. The effect was confirmed in cell-free experiments evaluating mRNA decay. In a second work, the same effects were obtained with oligoribonucleotides homologous to the bcl-2 ARE and therefore were acting as decoy-aptamers (Bevilacqua et al., 2007).
Here we demonstrate that bcl-2 ARE asORNs were able to inhibit apoptosis by partially preventing the degradation of bcl-2 mRNA and consequently the reduction of Bcl-2 protein levels in response to apoptotic stimuli. Apoptosis inhibition was accompanied by neuronal differentiation, as evaluated by counts of neurites and cell morphology, and inhibition of cell proliferation. These effects render bcl-2 ARE asORNs as potential candidates for pharmacological interventions, particularly in the field of ischemic stress and neurodegenerative diseases.
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Materials and Methods |
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J-bcl-2 or pCJ-SV2 empty vector (Tsujimoto, 1989) were carried out with Lipofectamine reagent (Invitrogen, Carlsbad, CA) according to the manufacturer's instructions 48 h before treatment with the oligonucleotides described below.
2'-O-Methyl Antisense Oligonucleotides. Three synthetic 26- to 27mer chemically modified asORNs sequentially overlapping the bcl-2 ARE asORN1 from 1020 to 994 nt, asORN2 from 993 to 967 nt, and asORN3 from 966 to 943 nt of b-RNA (GenBank number M14745
[GenBank]
) were synthesized and polyacrylamide gel electrophoresispurified by Dharmacon (Chicago, IL) as described previously (Ghisolfi et al., 2005). A degenerated 25-mer oligoribonucleotide (degORN) was used as control (Ghisolfi et al., 2005). The sequences of the asORNs are the following: asORN1 (27-mer), 5'-UGUCUUAAAUAAAUAAAUCUUUUUUUC-3'; asORN2 (26-mer), 5'-UUAAUAAUGUAAAAAAUAAAUGAUAU-3'; asORN3 (26-mer), 5'-UUCCCUUUGGCAGUAAAUAGCUGAUU-3'; and degORN (26-mer), 5'-NNNNNNNNNNNNNNNNNNNNNNNNNN-3', where N is any nucleotide. ORNs were 2'-O-methyl-modified, which increased their stability with respect to the natural RNA derivatives (Yoo et al., 2004). ORN cellular uptake and stability were increased by their vehiculation with the cationic lipid DOTAP (Roche, Mannheim, Germany), used as lipofection reagent, as reported previously (Luzi et al., 2003; Ghisolfi et al., 2005).
Treatments. SHSY-5Y cells were seeded at a density of 5 x 105 cells/60-mm dish 1 day before lipofection with ORNs. The lipofection mixtures were prepared by mixing 1 mM DOTAP (Roche Diagnostics) with 1 mM concentration of either the three bcl-2 ARE asORNs or the degORN and incubated at room temperature for 20 min before adding to cells as described previously (Capaccioli et al., 1993). The final concentration of each ORN was 0.5 µM. Apoptosis was induced 3 days after ORN lipofection either by replacing the culture medium without serum and glucose, namely Locke medium (Martínez de la Escalera et al., 1992), or by culturing cells in a hypoxic atmosphere (i.e., containing 1% oxygen). The transcriptional block was obtained by treating cells with the transcription blocker 5,5-dichloro-1-β-D-ribofuranosylbenzimidazole (DRB; Sigma-Aldrich, St. Louis, MO) at 20 µg/ml added at hour 3 after application of apoptotic stimuli.
Total RNA Extraction and Real-Time Reverse-Transcriptase Polymerase Chain Reaction. After treatments, total cellular RNA was extracted from approximately 106 cells collected at 0, 30, 60, 120, 180, 240, and 360 min after induction of apoptosis. The RNeasy Mini Kit (Qiagen, Valencia, CA) was used according to the manufacturer's instructions. In brief, total RNA isolated from SHSY-5Y cells lipofected with asORNs or degORN was treated with RNase-free DNase (Invitrogen) and analyzed spectroscopically and by gel electrophoresis for purity and integrity, respectively. Total RNA (0.1 µg/µl) was reverse-transcribed with high-capacity cDNA Archive Kit (Applied Biosystems, Foster City, CA) using standard manufacturer's conditions in a total volume of 50 µl. Levels of bcl-2 and GAPDH cDNAs of each sample were determined by quantitative real-time PCR applying TaqMan Universal MasterMix (Applied Biosystems) standard manufacturer's conditions: 5 µl of total cDNA was amplified with 2x TaqMan Universal Master Mix buffer, 20x PDAR System target bcl-2, 20x PDAR System control GAPDH, and Nuclease-Free Water (Promega, Madison, WI) to a total volume of 25 µl. Each reaction was triplicated for a better statistical reliability of results. The PCR reactions were carried out in an ABI PRISM 7000 Sequence Detection System under the following conditions: 50°C for 2 min, 95°C for 10 min, 95°C for 15 s, and 1 min at 60°C (40 cycles). Amplification plot and CT data were elaborated with ABI PRISM 7000 SDS Software 1.1 updated version. GAPDH data were used to normalize bcl-2 cDNA values.
Western Blotting. The assays were performed according to standard conditions. In brief, after treatments, cells were washed twice in ice-cold phosphate-buffered saline and resuspended in 100 µl of ice-cold RIPA lysis buffer, vortexed for 3 s, and incubated on ice for 30 min. The protein lysates were obtained by centrifugation at a high speed for 20 min at 4°C to separate nonsoluble cell debris. Proteins (20 µg/lane) were analyzed by 12% SDS-polyacrylamide gel electrophoresis, blotted onto nitrocellulose membrane (Hybond-ECL; GE Healthcare, Chalfont St. Giles, Buckinghamshire, UK) in a Transblot apparatus (Bio-Rad Laboratories, Hercules, CA) at 100 V for 90 min. Blots were processed by an enhanced chemoluminescence (ECL Plus) detection kit according to the supplier's instructions (GE Healthcare). The blots were probed with a mouse monoclonal anti-Bcl-2 antibody (Upstate Biotechnology, Charlottesville, VA), rabbit polyclonal anti-Bax antibody (Santa Cruz Biotechnology, Santa Cruz, CA), and mouse monoclonal anti-caspase-3 antibody (Santa Cruz). A mouse monoclonal anti-
-tubulin antibody (Sigma-Aldrich) was used as a protein loading control.
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).
Evaluation of Cell Growth. SHSY-5Y cells were lipofected with bcl-2 ARE asORNs or degORN control as described above and cultured in 100-mm Petri dishes in growth medium. Each day during a 5-day period, cells were detached and evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyltetrazolium bromide (MTT) colorimetric assay (van de Loosdrecht et al., 1994).
Evaluation of Cell Proliferation by Fluorescence-Activated Cell Sorting Analysis. The number of cell divisions was assessed with the carboxyfluorescein diacetate succinimidyl ester (CFSE; Invitrogen) assay and evaluated by fluorescence-activated cell sorting analysis (BD Biosciences, San Jose, CA). CFSE covalently binds cellular components, yielding a fluorescence (measured by flow cytometry) that is divided equally between daughter cells at each division (Lyons et al., 2001) and allows for calculating successive rounds of replication. Confluent cultures of SHSY-5Y cells were starved for 14 h in the growth medium described above but containing only 0.5% fetal bovine serum. Cells were then harvested and labeled for 10 min with 10 µM CFSE at 37°C and washed twice with culture medium. Labeled cells were plated (6 x 104/60-mm dish) and lipofected with asORNs or degORN the following day as described above. An aliquot of freshly labeled cells was used to measure the starting fluorescence level (day 0). Cells were harvested on day 5 to determine a decrease in fluorescence. These values were used to calculate the number of replicative rounds elapsed from day 0 in response to treatments (ModFit LT for Macintosh, Proliferation Protocol; Verity Software House Inc., Topsham, ME).
Evaluation of Apoptotic Events. After cell transfer to Locke medium, apoptotic events were counted by the time-lapse videomicroscopy using a Zeiss inverted phase-contrast microscope (Carl Zeiss Inc., Thornwood, NY) equipped with a 10x objective, Panasonic charge-coupled device cameras, and JVC BR9030 time-lapse video recorders as reported previously (Luzi et al., 2003). An apoptotic event was scored at the moment the cell became fully contracted and fragmented in apoptotic bodies. Apoptotic cells were also evaluated by flow cytometry with GUAVA Personal Cell Analysis System with Guava Nexin Assay (GUAVA Technologies, Hayward, CA) that uses Annexin V-PE to detect phosphatidyl serine on the external membrane of apoptotic cells. The cell-impermeant dye 7-aminoactinomycin D is included in the kit as an indicator of membrane structural integrity and for the differential assessment of the Annexin V-reactive cells into the early and late stages of apoptosis. 7-aminoactinomycin D is excluded from live, healthy cells and early apoptotic cells but permeates late-stage apoptotic and dead cells. The assay was performed according to the manufacturer's instructions.
Statistical Analysis. The statistical evaluation of the data was performed with the two-tailed Student's t test for unpaired values. Differences were considered statistically significant when p 
0.05. The data are reported as a percentage of the maximal value.
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Results |
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) 3 days before the application of apoptotic stimuli. Apoptosis was induced by culturing cells either in Locke minimal medium, mimicking condition of glucose/growth factor deprivation, or in condition of hypoxia. Bcl-2 ARE asORNs Markedly Attenuated the Decrease of bcl-2 mRNA Half-Life and Bcl-2 Protein Level in Response to Growth Factor Deprivation. Transfection of the SHSY-5Y cell line with bcl-2-specific asORNs resulted in Bcl-2 protein increase as shown in Fig. 1, whereas no effect was observed on expression of Bax, a proapoptotic member of the bcl-2 family.
The effect of bcl-2 ARE asORNs on bcl-2 mRNA stability after glucose/growth factor deprivation as an apoptotic stimulus (Locke medium) in SHSY-5Y is shown in Fig. 2. Bcl-2 mRNA stability was evaluated by quantification of bcl-2 mRNA levels at various times after application of a transcriptional block (20 µM DRB added 3 h after transfer to Locke medium). The bcl-2 mRNA half-life decreased from 3 h in conventional medium to 30 min in the Locke medium. The addition of asORNs to the Locke medium counteracted the decrease, increasing the bcl-2 mRNA half-life from 30 min to 2 h. The degORN used as control did not elicit any effect on the mRNA levels. This indicates that asORNs are endowed with strong stabilizing activity toward bcl-2 mRNA also in condition of apoptotic stress.
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We then evaluated the effect of asORNs on Bcl-2 protein levels by Western blot analysis in response to Locke medium (Fig. 3). On the third day of culturing in the Locke medium, the Bcl-2 protein levels underwent a marked decrease in SHSY-5Y cells with respect to controls cultured in normal medium (Fig. 3A). The addition of asORNs to the Locke medium markedly attenuated this decrease, whereas the addition of degORN did not have significant effects. Histograms in Fig. 3B were obtained by the densitometric analysis of bands in Fig. 3A and are means of three independent experiments.
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5% of viable cells) compared with controls cultured in standard atmosphere. Treatment with bcl-2 ARE asORNs markedly counteracted this effect, protecting cells from apoptosis: the percentage of viable cells in hypoxic conditions was substantially at the level of untreated controls at hour 12 and decreased to 80 and 50% of viable cells at the hours 24 and 48, respectively. Treatment with the degORN did not have any significant effect on the viability compared with the untreated control. Bcl-2 ARE asORNs Inhibited Caspase-3 Activation in Response to Locke Medium. Caspase-3 has been reported to activate death effector molecules resulting in the fragmentation of genomic DNA in association with structural and morphological changes characteristic of apoptosis. Caspase-3 is initially present as a proenzyme of 32 kDa that is cleaved in the cell undergoing apoptosis into its enzymatically active form composed of two subunits of 17 (p17) and 11 kDa (p11). Activity of the caspase-3 in SHSY-5Y cells lipofected with bcl-2 ARE asORNs or with degORN was evaluated by Western blot analysis after 0, 24, 48, and 72 h in Locke medium (Fig. 5). The activity of caspase-3 in SHSY-5Y cells maintained in normal growth medium provided untreated control. As expected, the cleaved 17-kDa active caspase-3 subunit, undetectable in untreated controls, was evident in SHSY-5Y cells cultured in Locke medium but was markedly lowered when bcl-2 ARE asORNs were added. The degORN did not elicit any effect. The SHSY-5Y cells transiently transfected with a bcl-2-harboring plasmid did not show significant caspase activation in response to Locke medium with respect to mock transfected cells, untransfected cells, and degORN-transfected cells.
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; Vairo et al., 1996; Huang et al., 1997). We have evaluated the possibility that bcl-2 ARE asORNs affect cell proliferation by MTT assay and by flow cytometry (Fig. 6). The cell proliferation was evaluated by analysis of cell viability every day for 5 days with the MTT assay. The bcl-2 ARE asORNs markedly reduced the rate of SHSY-5Y cell proliferation compared with untreated or degORN-treated controls (Fig. 6A). The distribution of cell divisions in bcl-2 ARE asORN-treated SHSY-5Y cells compared with untreated or degORN-treated controls was determined by flow cytometry on the basis of the CFSE dye dilution (Fig. 6B). This assay allows counting the subsequent rounds of cell divisions (generations) that start from fully labeled SHSY-5Y cells on day 0. On the 5th day, approximately 70% of untreated cells approached the ninth generation, 20% of these reached the 10th generation, and only 17% were still at the eighth generation. Similar results were obtained in cells lipofected with the degORN. Instead, only 8% of bcl-2 ARE asORN-treated cells reached the 10th generation, 50% were at the ninth generation, and 30% of cells were at the eighth generation. Furthermore, 10% of cells treated with bcl-2 ARE asORNs were arrested at the seventh generation, demonstrating significant inhibition of SHSY-5Y proliferation rate.
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Bcl-2 ARE asORNs Induced Neuronal Differentiation. In addition to its antiapoptotic function, bcl-2 has been reported to have differentiating and neuroprotective properties, promoting dendrite branching and regeneration of damaged neurons. We have evaluated the ability of bcl-2 ARE asORNs to induce neuronal differentiation in SHSY-5Y cells, assuming neuron length and number as differentiation index. The morphology of SHSY-5Y cells treated for 5 days with asORNs or the degORN or untreated controls is shown in the Fig. 7. Most asORN-treated cells assumed the differentiated phenotype, characterized by the presence of numerous relatively long and interconnected neurites (Fig. 7A). Instead, untreated cells and degORN-treated cells maintained the undifferentiated phenotype, characterized by very small number or even total absence of neurites (Fig. 7A). As expected, the transient transfection of a bcl-2-harboring plasmid but not of an empty vector was able to promote neurite formation in SHSY-5Y cells (Fig. 7A). The median length of neurites and the median number of neurites per cell are reported in Fig. 7B, top, and in Fig. 7B, bottom, respectively.
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Discussion |
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In a previous work, we have shown that three contiguous synthetic asORNs targeting the bcl-2 mRNA regulative ARE stabilize bcl-2 mRNA and enhance Bcl-2 protein levels in a dose-dependent fashion (Ghisolfi et al., 2005). The effectiveness of this strategy relies on the accessibility of any mRNA cis-acting element by the relevant transacting factors modulating the RNA decay machinery that assembles on it (Bevilacqua et al., 2003). Therefore, up-regulation of bcl-2 gene expression by targeting its destabilizing bcl-2 ARE with synthetic modified single-strand RNAs could be a paradigm for any gene regulated by AREs or to any other gene carrying cis-acting elements in their RNA.
Here we show that this innovative approach, stabilizing bcl-2 mRNA and leading to increased Bcl-2 protein level without affecting the bcl-2 family member Bax, in SHSY-5Y cells, inhibits bcl-2 gene down-regulation in response to apoptotic stimuli. As a consequence, this approach prevents apoptosis and modifies fundamental cellular programs. Indeed, the three synthetic bcl-2 ARE asORNs protected bcl-2 mRNA from the fast degradation triggered by the deprivation of growth factors and glucose or by hypoxic stress and maintained the Bcl-2 protein at relatively high levels in SHSY-5Y cells compared with degORN-treated or untreated controls. The relatively high steady-state level of Bcl-2 protein in asORN-treated cells, in line with the relatively high bcl-2 mRNA level (Ghisolfi et al., 2005), counteracted activation of apoptotic program. Counteraction of apoptosis was maximal in the initial phases of the apoptotic program but was still apparent at 48 h.
Although the main function of Bcl-2 protein is to increase the apoptotic threshold of the cells, Bcl-2 has also another fundamental activity that is the inhibition of cell proliferation. Moreover, in proper settings, the above biological property of Bcl-2 can be associated with the activation of the differentiation program (Grossmann et al., 2000). Both effects have been obtained in the SHSY-5Y neuronal cell line as a result of Bcl-2 overproduction induced by treatment with bcl-2 ARE asORNs or by transient transfection of a bcl-2 harboring plasmid. Clearly, bcl-2 ARE asORNs reduced cell number without affecting cell viability and lowered proliferative kinetics compared with untreated controls. It is most relevant that bcl-2 ARE asORNs induced neuronal cell differentiation evaluated on the basis of the length of neurites and their number per cell, albeit at a lower degree than exogenously expressed bcl-2. The impact of synthetic singlestrand RNAs complementing the cis-acting AU-rich element of bcl-2 mRNA on proliferation and differentiation of human cells suggests the high pharmacological potential of an innovative strategy able to modify cellular programs by acting at the post-transcriptional level of the gene expression.
The hypothesis that short bcl-2 ARE-targeting single-strand RNAs could modulate bcl-2 expression was in part inspired by our discovery in t(14;18) lymphoma cells that a hybrid bcl-2/IgH antisense transcript caused bcl-2 overexpression by overlapping the bcl-2 ARE of the bcl-2/IgH mRNA (Capaccioli et al., 1996). This hypothesis is strongly supported by evidences obtained by Meisner et al. (2004), analyzing the effects of synthetic ORNs on the secondary structure and stability of ARE-controlled transcripts. They demonstrated in peripheral blood mononuclear cells that ARE accessibility of synthetic ARE-controlled transcripts (tumor necrosis factor- and interleukin-2) by the stabilizing AUBP HuR can be either opened or closed by computationally designed ORNs. This property decides the fate (stabilization or decay) of the transcripts, indicating the possibility to manipulate ARE-controlled gene expression by exogenous ARE openers or closers. It is conceivable that pairing of the bcl-2 ARE with asORNs in our cellular model could have opened the bcl-2 ARE accessibility to stabilizing AUBPs or closed the bcl-2 ARE accessibility to destabilizing AUBPs, or could have done both.
Short 2'-O-methyl-oligonucleotides designed to target a complementary region within an endogenous messenger RNA are not supposed to activate ribonuclease activities, and they are not known to induce RNA degradation by heteroduplex ribonucleases (Schmitz et al., 2001). Actually, 2'-O-methyl ORNs have been used to temporarily interfere with translation or other mRNA-involving processes, such as enforced exon skipping (Schmitz et al., 2001). In addition, 2'-O-methyl modified small interfering RNA duplexes show reduced efficacy in down-regulating gene expression, even when the modification is restricted to as few as 3 of 20 positions on the antisense strand (Prakash et al., 2005). We have shown previously that our bcl-2 ARE asORNs mask the bcl-2 mRNA ARE with respect to the relevant transacting AUBPs and inhibit their functions in a reversible fashion (Ghisolfi et al., 2005). Furthermore, their application to SHSY-5Y cells did not induce obvious toxic effects other than the specific action at the level of the target gene.
Despite the success of the bcl-2 ARE asORNs in up-regulating bcl-2 expression in a neuronal cell line, the pharmacological potential of these tools requires some general considerations. Indeed, the molecular and phenotypic effects of modified bcl-2 expression are far from being obvious. Despite that bcl-2 overexpression is commonly associated with tumor onset and progression, the role of Bcl-2 protein in tumors needs to be further clarified. Indeed, rapid tumor progression and bad prognosis are often paradoxically associated with loss of Bcl-2 function, an effect that could be in part explained by the ability of Bcl-2 to inhibit the cell cycle. Likewise, bcl-2 overexpression is usually associated with unspecific drug resistance in most tumors (Kiechle and Zhang, 2002).
Furthermore, studies and even clinical trials conducted to evaluate the anticancer effectiveness of combined application of bcl-2 down-regulating antisense molecules with conventional chemotherapeutics gave controversial results. Numerous evidences indicated a synergism between antisense oligodeoxyribonucleotide-mediated bcl-2 down-regulation and classic anticancer compounds (Milella et al., 2004). Whatever is the role of Bcl-2 in tumors, maintaining the basal level of Bcl-2 above the threshold that triggers apoptosis execution might represent a new therapeutic strategy to treat those humans diseases in which deficient bcl-2 expression plays a key role and to prevent tissue damages in the case of ischemic and stress conditions.
Particularly attractive is the potential application of bcl-2 ARE asORNs to neurodegenerative conditions, in which induction of high level of Bcl-2 protein has already shown therapeutic values (Lawrence et al., 1996). The recent finding that statins are implied in neuroprotection by a bcl-2-dependent mechanism (Johnson-Anuna et al., 2007) further supports our approach. Authors suggest that transcriptional and post-transcriptional mechanisms can be involved in simvastatin-induced up-regulation of bcl-2. In particular, statins have already been demonstrated to positively modulate mRNA stability (Bonetti et al., 2003) and can be thus considered for synergic therapeutic effects.
Besides asORN-mediated up-regulation of bcl-2 expression by the specific targeting of its ARE, this work might open a new avenue for the pharmacological enhancement of any gene expression, provided a destabilizing element is harbored on its mRNA. Besides enhancement of oncosuppressor functions in cancer gene therapy, the restoration of depressed activity of specific genes is a common requirement for the treatment of human diseases. Although oligonucleotides are still facing substantial difficulties entering into cells and explicating activity in experimental animals, the reversibility of their action and their apparent low toxicity could encourage developing a general modality to apply these molecules to positively regulate gene expression in a very specific fashion.
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Footnotes |
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ABBREVIATIONS: AU, adenine and uracil; ARE, adenine and uracil-rich element; AUBP, adenine and uracil-rich element binding proteins; ORN, 2'-O-methyl oligoribonucleotide; asORN, antisense 2'-O-methyl oligoribonucleotide; nt, nucleotide; degORN, degenerated 2'-O-methyl oligoribonucleotide; DOTAP, N-[1-(2,3-dioleoyloxy)propyl]-N,N,N-trimethylammonium methylsulfate; DRB, 5,5-dichloro-1-β-D-ribofuranosylbenzimidazole; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyltetrazolium bromide; CFSE, carboxyfluorescein diacetate succinimidyl ester.
Address correspondence to: Dr. Nicola Schiavone, Department of Experimental Pathology and Oncology, University of Florence, Viale G.B. Morgagni 50, 50134 Florence, Italy. E-mail: nicola{at}unifi.it
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