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Introduction

Activating transcription factor (ATF) 2 is a member of the ATF/cyclic AMP-responsive element binding protein family of transcription factors, which harbors leucine zipper and DNA binding domains (1), and exhibits both oncogenic and tumor-suppressor functions (2–4). ATF2 is important for normal cellular development and survival, and is also involved in the response to stress and DNA damage in the context of normal and tumorigenesis processes (5). The transactivating potential of ATF2 is stimulated to a higher level by a broad group of agents causing DNA damage and other types of cellular stress, including short-wavelength ultraviolet (UV) light, osmotic stress and inflammatory cytokines (6,7). ATF2 is expressed ubiquitously, and elevated expression of ATF2 was detected in skin carcinomas (8) and melanoma (9). It was reported that the ATF2 expression levels were significantly induced under oxidative stress in immortalized human urothelial cells treated with arsenic (10).

Translational control is important in the control of gene expression, by which, cells can respond to rapid changes in physiological conditions, including DNA damage and cellular stress (11,12). One of the common mechanisms of translational control is the induction of changes in the translation initiation site on the messenger RNA (mRNA) molecule, which may occur via two distinct mechanisms, cap-dependent scanning and internal ribosome entry (IRE) (13). The latter mechanism requires the formation of a complex RNA structural element termed IRE segment (IRES), which is located in the 5′-untranslated region (UTR) of the mRNA molecule (14). To date, IRES elements have been mainly identified in mRNAs involved in regulating gene expression during development, differentiation, cell cycle progression, cell growth, apoptosis and stress, including nuclear factor-κB repressing factor, X-chromosome linked inhibitor of apoptosis protein (XIAP), vascular endothelial growth factor, c-Myc, fibroblast growth factor-2 and Smad mRNAs (15–19). The most notable difference in cellular IRES sequence from the UTR data sets is that IRES-containing UTRs are generally long (>150 bases) and GC rich (20).

Multiple cellular stresses lead to the inhibition of translation; however, there are certain cellular mRNAs that are selectively translated under these conditions to protect cells from stress, the majority of which contain an IRES element (21). Yang et al noticed that tumor necrosis factor receptor-associated factor 1 protein expression can be stimulated under cellular stress conditions, and its translation is regulated by IRES (22). In addition, it was reported that ATF4 splice variant, whose protein expression was induced by thapsigargin and tunicamycin in THP-1 cells, contains an IRES structure (23).

Adriamycin (ADM) and paclitaxel (PTX) are two effective antitumor agents that are widely used in hepatocellular carcinoma therapy (24,25). Both can induce cell apoptosis and cause cellular stress (26). In the present study, ATF2 protein expression in the human hepatoma cell line Bel7402 was observed to be induced following treatment with ADM or PTX, and it was demonstrated that the 5′-UTR of ATF harbors a bona fide IRES structure localized between nt −299 to nt −269 upstream of the start codon. The IRES activity of ATF2 was low in the mouse embryo fibroblast cell line National Institutes of Health (NIH)-3T3 and in the human colon carcinoma cell line HCT-8, while it was high in the human embryonic kidney (HEK) 293 cell line and in the human hepatoma cell line Bel7402. Furthermore, the present study was demonstrated that ATF2 IRES activity was also elevated following treatment with cellular stress-inducing chemotherapeutic drugs such as PTX and ADM.

Materials and methods

Plasmid construction

The bicistronic vector pRF was constructed by inserting the firefly luciferase (FL or FLUC) gene from the plasmid pGL-6 (Beyotime Institute of Biotechnology, Haimen, China) into the linker region of the plasmid pRL-SV4 (Promega Corporation, Madison, WI, USA) downstream of the Renilla luciferase (RL or RLUC) gene. To insert the FLUC fragment, a polymerase chain reaction (PCR) was performed on the pGL-6 plasmid with primers FLUCF 5′-GCTCTAGACTCGAGCATATGGAATTCGGCGCGCCCATGGAAGATGCCAAAAACATTAAGAAGGGCCC-3′ (forward) and FLUCR 5′-AAATATGCGGCCGCTTACACGGCGATCTTGCCGCCCTT-3′ (reverse). The PCR was conducted in a 50-µl reaction mixture containing 2X PrimeSTAR Max Premix (Takara Biotechnology Co., Ltd., Dalian, China), 0.2 µM forward and reverse primers, and 200 ng genomic DNA, which was purchased from the Beyotime Institute of Biotechnology. The PCR was conducted at 98°C for 3 min, followed by 32 cycles of 98°C for 1 min, 55°C for 10 sec and 72°C for 1 min, and 72°C for 5 min. The amplified product was digested with Bsp119 and XbaI, and subsequently cloned into pRL-SV40, thus generating pRF. In this vector, the two cistrons were separated by ~20 base pairs (bp) of the intercistronic linker region containing several unique endonuclease restriction sites. The expression of bicistronic mRNA is driven by a simian virus (SV) 40 promoter. The full length 5′-UTR complementary DNA (cDNA) of ATF2, nuclear respiratory factor (NRF) and XIAP were obtained by gene synthesis (Sangon Biotech Co., Ltd., Shanghai, China), while serial truncations of ATF2 were produced by PCR amplification with forward and reverse primers (Table I) containing EcoRI and NdeI endonuclease restriction sites, respectively. The PCR was conducted in a 50-µl reaction mixture containing 2X PrimeSTAR Max Premix, 0.2 µM forward and reverse primers, and 200 ng genomic DNA. The PCR was conducted at 98°C for 3 min, followed by 32 cycles of 98°C for 1 min, varying annealing temperatures (as indicated in Table I) and 72°C for 10 sec, and 72°C for 5 min. All these 5′-UTR cDNAs were each inserted immediately upstream of the translation start codon of the FLUC gene in the dual luciferase vector pRF at the EcoRI and NdeI sites.

Table I. Oligonucleotide primers used in polymerase chain reaction for plasmids construction.

Table I.

Oligonucleotide primers used in polymerase chain reaction for plasmids construction.

Vector (nt)	Primer sequence, 5′-3′	Temperature, °C
pR-ATF2-F (31–299)	F1: GGAATTCCATATGGAAGCCTGTGGGAGCCC	50.0
	R1: CGGAATTCAAGTTGAATAACTTATCACATTC
pR-ATF2-F (51–299)	F2:GGAATTCCATATGGCCTTTAAAGTGCCGTTCAG	50.0
	R2: CGGAATTCAAGTTGAATAACTTATCACATTC
pR-ATF2-F (76–299)	F3: GGAATTCCATATGTCCTCCAGGGGTGCTTTGTA	50.0
	R3: CGGAATTCAAGTTGAATAACTTATCACATTC
pR-ATF2-F (141–299)	F4: GGAATTCCATATGACTAGTGACCTGGAAAGGGT	50.0
	R4: CGGAATTCAAGTTGAATAACTTATCACATTC
pR-ATF2-F (1–229)	F5: GGAATTCCATATGGTTGTCAGTCCGATCTCGC	52.0
	R5: CGGAATTCATTTACTCTGCTTCCAGGAATACC
pR-ATF2-F (1–159)	F6: GGAATTCCATATGGTTGTCAGTCCGATCTCGC	52.8
	R6: CGGAATTCCCCTTTCCAGGTCACTAGTTC
pR-ATF2-F (1–89)	F7: GGAATTCCATATGGTTGTCAGTCCGATCTCGCG	54.5
	R7: CGGAATTCGCACCCCTGGAGGAAAAGG

[i] F, forward; R, reverse; ATF2, activating transcription factor 2.

Cell culture and DNA transfection

The HEK293 cell line (Type Culture Collection of the Chinese Academy of Sciences, Shanghai, China) was cultured in Dulbecco's modified Eagle medium (Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA), while the Bel7402, HCT-8 and NIH-3T3 cell lines (Type Culture Collection of the Chinese Academy of Sciences) were cultured in RPMI 1640 medium (Gibco; Thermo Fisher Scientific, Inc.) with 10% (vol/vol) fetal bovine serum (Gibco; Thermo Fisher Scientific, Inc.), penicillin (100 U/ml) and streptomycin (100 µg/ml). All cells were kept at 37°C in a humidified atmosphere with 5% CO2. Transient transfection was performed using Lipofectamine 2000 (Invitrogen; Thermo Fisher Scientific, Inc.)according to the manufacturer's protocol. The cell media were replaced with complete culture media at 6 h post-transfection, and 24–48 h later, the cells were rinsed twice with phosphate-buffered saline, and cell extracts were then prepared using 5X Passive Lysis Buffer (Promega Corporation).

Dual luciferase assay

FLUC and RLUC activities were measured using the Dual-Luciferase Reporter Assay System (Promega Corporation) according to the manufacturer's protocol, with the exception that only 100 µl of each reagent was used. The signals were measured with a luminometer.

RNA isolation and reverse transcription (RT)-PCR

Total RNA was isolated from the cells using TRIzol reagent (Beyotime Institute of Biotechnology), and was reverse transcribed into cDNA using oligo(dT)18 primer (Takara Biotechnology Co., Ltd.) and PrimeScript Reverse Transcriptase (Takara Biotechnology Co., Ltd.). PCR was next performed using specific primers, which were designed according to the corresponding sequences of the ATF2 5′-UTR mRNA: ATF2F 5′-GCACGTAATGACAGTGTCATTGT-3′ (forward) and ATF2R 5′-ATGTGGGCTGTGCAGTTTGTG-3′ (reverse). The PCR was conducted in a 50-µl reaction mixture containing 2X PrimeSTAR Max Premix, 0.2 µM forward and reverse primers, and 250 ng total RNA. The PCR was conducted at 98°C for 3 min, followed by 32 cycles of 98°C for 1 min, 51.6°C for 15 sec and 72°C for 18 sec, and 72°C for 5 min. Upon electrophoresis on a 1.5% agarose gel, the PCR products were visualized with ethidium bromide staining under UV light. DNA bands were analyzed using ImageJ software (NIH, Bethesda, MD, USA).

Western blotting

Whole-cell proteins were obtained using radioimmunoprecipitation assay buffer containing 1 mM phenylmethane sulfonyl fluoride. The same quantity of total protein was loaded onto each lane of the gel, and the proteins were electrophoresed on 8% polyacrylamide gels containing 0.1% sodium dodecyl sulfate. The resolved proteins were semi-dry transferred to a polyvinylidene fluoride membrane. The membrane was blocked with 0.5% bovine serum albumin (Beyotime Institute of Biotechnology) at room temperature for ~3 h, prior to be incubated with the corresponding primary antibodies [anti-ATF2 (1:5,000; ab32061; Abcam, Cambridge, MA, USA) or anti-β-actin (1:1,000; AA128; Beyotime Institute of Biotechnology), which was used as an internal reference] at room temperature for 2 h. Next, the membrane was incubated with the secondary antibody Goat Anti-Rabbit HRP (IgG H&L) (1:3,000; ab6721; Abcam) at room temperature for 1.5–2.0 h. Finally, the antigen-antibody complexes were visualized by enhanced chemiluminescence (Thermo Fisher Scientific, Inc.).

Statistical analysis

Each experiment was performed ≥3 times. All experimental data were analyzed using GraphPad Prism 5.0 (GraphPad Software, Inc., La Jolla, CA, USA) and presented as mean values ± standard error of the mean. Statistical analysis was performed using the Student's t-test. P<0.05 was considered to indicate a statistically significant difference.

Results

Protein expression of ATF2 is induced at the translational level following treatment with chemotherapeutic drugs in Bel7402 cells

ATF2 exhibited very low expression in Bel7402 cells (Fig. 1A). Notably, when Bel7402 cells were treated with increasing concentrations (0.01, 0.2 and 0.4 µg/ml) of two chemotherapeutic drugs (ADM and PTX), ATF2 protein expression was induced following treatment with ADM and PTX (Fig. 1A) in a dose-dependent manner. To demonstrate whether the ATF2 induction changed with the exposure time to the drugs, ATF2 protein expression was detected at various times following 0.4-µg/ml ADM and PTX treatment for 2, 4, 8, 12 and 24 h. Fig. 1B reveals that ATF2 protein expression is increased in a time-dependent manner following treatment with ADM and PTX. Next, the mechanism by which these drugs increased the levels of ATF2 in Bel7402 cells was examined. Treatment of Bel7402 cells with either ADM or PTX did not result in any significant change (P=0.552) in ATF2 mRNA levels (Fig. 1C), indicating that ADM/PTX-induced ATF2 expression occurs at the translational level.

Figure 1. Induction of ATF2 translation by PTX and ADR in cancer cells. (A) Dose- and (B) time-dependent induction of ATF2 protein expression in Bel7402 cells treated with ADM and PTX. Bel7402 cells were treated with 0.4 µg/ml ADM and PTX for different times, or with ADM and PTX for 24 h at different doses, as indicated, and protein expression was examined by western blotting. (C) The messenger RNA expression levels of ATF2 upon treatment with or without increasing concentrations (0.01, 0.2 and 0.4 µg/ml) of ADM and PTX in Bel7402 cells were determined by reverse transcription-polymerase chain reaction. ATF2, activating transcription factor 2; ADR, adriamycin; PTX, paclitaxel.

ATF2 5′-UTR-mediated IRE in mammalian cultured cell lines

Since by searching the ATF2 gene in the human genome database (http://www.ncbi.nlm.nih.gov/nuccore/NM_001880.3) it was observed that the ATF2 5′-UTR is generally long (ATF2, 299 nt) and rich in GC, the possibility that the ATF2 5′-UTR contains an IRES that could regulate ATF2 protein synthesis following treatment with chemotherapeutic drugs was examined. To evaluate whether ATF2 translation was initiated from an IRE, the ATF2 5′-UTR was inserted between the two cistrons of a bicistronic vector, in which the first cistron encodes the RLUC gene and the second cistron encodes the FLUC gene (Fig. 2A). The first cistron is proximal to the mRNA's cap structure, and therefore, is expected to be translated by the conventional cap-dependent translation mode. The second cistron is distal from the cap site; therefore, it is expected to undergo translation only upon insertion of an IRES element between the two cistrons (27). The bicistronic vectors pR-ATF2-F were transfected into HEK293 Bel7402 and HCT-8 human cells, and into murine NIH-3T3 cells. The pR-XIAP-F and pR-NRF-F vectors, which contain the well-characterized cellular XIAP and NRF IRES, were transfected as positive controls, while pRF was used as a negative control. The RL and FL activities were determined as aforementioned described. The IRES activity was calculated as the ratio of FLUC to RLUC normalized to that of pRF-transfected cells. As indicated in Fig. 2B, the ATF2 IRES was observed to be active in the HEK293, Bel7402 and HCT-8 cell lines, but not in the NIH-3T3 cell line. The ATF2 IRES activity was different in each cell line, being high in Bel7402 and HEK293 cells (~5-fold higher than the XIAP IRES activity). These results suggest that a putative IRES element was present in the 5′-UTR of the ATF2 mRNA. The difference in the levels of IRES activity observed in these cell lines is probably due to intrinsic differences between these cell types.

Figure 2. Identification of the IRES activity in the ATF2 5′-UTR. (A) The plasmids pRAF, pRXF, pRNF and pRF were transfected into the cell lines HEK293, Bel7402, HCT-8 and NIH-3T3. The IRES activity was expressed as the ratio of downstream cistron expression to upstream cistron expression (FL/RL). The error bars indicate the SD determined from ≥3 independent experiments performed in triplicate. (B) Schematic representation of the expression cassette of the dual-luciferase bicistronic constructs pRF, pRAF, pRXF and pRNF. (C) The translation of the second cistron is not due to reinitiation or aberrant messenger RNA species. To test the cryptic promoter activity in the ATF2 5′-UTR, the sequence was cloned upstream of the FL reporter, and the SV40 promoter was removed. The empty vector was used as a negative control. The plasmids were transfected into Bel7402 cells. The RL and FL activities were measured after 24 h. The error bars indicate the SD determined from ≥3 independent experiments performed in triplicate. (D) Schematic representation of the expression cassette of the dual-luciferase bicistronic constructs pRF and pRAF in which the promoter was deleted. RL, Renilla luciferase; FL, firefly luciferase; SV, simian virus; ATF2, activating transcription factor 2; NRF, nuclear respiratory factor; XIAP, X-linked inhibitor of apoptosis protein; IRES, internal ribosome entry segment; UTR, untranslated region; SD, standard deviation.

Internal initiation of translation mediated by the ATF2 5′-UTR is not due to cryptic promoter activity

To exclude the possibility that the expression of the second cistron in these two bicistronic mRNAs could be derived from monocistronic RNAs due to the presence of a cryptic promoter in the 5′-UTR, pR-ATF2-F-basic plasmids were generated, in which the ATF2 5′-UTR was inserted in the promoterless pRF-basic vector upstream of the RLUC coding sequence. The HEK293 and Bel7402 cell lines were each transfected with the pRF plasmid (a vector containing the SV40 early promoter and serving as a positive control), the promoterless pRF-basic plasmid and the pR-ATF2-F-basic plasmid. Luciferase activities were measured as aforementioned described. Fig. 2C indicates that the FLUC activity measured in pR-ATF2-F-basic-transfected cells is comparable to that measured in cells transfected with the pRF-basic plasmid, and is ~350-fold lower than the activity produced by pR-ATF2-F. This result clearly illustrated that the ATF2 5′-UTR was devoid of promoter activity.

Mapping the ATF2 IRES

To further identify the core regions that promote the internal initiation of translation, serial truncations of the ATF2 5′ leader sequence were created (Fig. 3A). Subsequently, the activities of the inserted sequences were assayed as aforementioned described. The ability of these truncated sequences to promote the translation of the mRNA was also compared with that of pRF. Deletions of 30 nt of the 5′ end of ATF2 resulted in a marked decrease in IRES activity, and further deletion of 52, 75 and 142 nt of the 5′ end of ATF2 led to a similar reduction. Notably, at the 3′ end of ATF2, deletion of 70, 140 and 210 nt did not produce a significant decrease (P=0.148), since the IRES activity remained almost the same as that of the full-length ATF2 5′-UTR (Fig. 3B). These data indicated that the 5′ end of ATF2 is important for positioning the IRES in context with the translational start site, and the core IRES region of ATF2 contains 30 bases and resided between nt −299 and −269. The results were the same when different cells were transfected. These results demonstrated that the full length of the ATF2 5′-UTR contributes to its maximal IRES activity, and the 5′ 30 nt of the ATF2 5′ leader region are essential for its IRES activity.

Figure 3. Mapping the ATF2 internal ribosome entry segment. (A) Schematic representation of bicistronic pRF constructs containing a series of 5′-3′- or 3′-5′-deleted ATF2 5′-untranslated region fragments. (B) HEK293 and Bel7402 cells were transfected with each indicated plasmid. After 24 h, the luciferase activities were tested. Data represent the mean ± standard deviation of FL vs. RL activity in ≥3 independent experiments. RL, Renilla luciferase; FL, firefly luciferase; SV, simian virus; ATF2, activating transcription factor 2.

Induction of ATF2 IRES activity under cellular stress conditions

It has been reported that, for certain mRNAs, IRES-mediated initiation of protein translation is activated during conditions such as cellular stress and apoptosis (28). In the present study, ATF2 protein expression in Bel7402 cells was induced under treatment with ADM and PTX (Fig. 1). To investigate whether the ATF2 IRES activity is also affected by cellular stress, the ATF2 activity was examined in Bel7402 cells treated with two chemotherapeutic drugs (ADM and PTX), which induce a stress condition in cells. Gene transfections and reporter assays were performed to determine if ADM and PTX induced ATF2 IRES activity. Bel7402 cells were transfected with the pRF plasmid, containing the full-length fragment of the ATF2 5′-UTR sequence, and then treated with ADM and PTX. It was observed that the FLUC activity in transfected cells treated with ADM and PTX was higher than that of untreated cells (Fig. 4). Furthermore, RT-PCR analyses of mRNA expression of FLUC were performed in cells transfected with pRL-ATF2-FL following treatment with ADM and PTX. It was observed that FLUC mRNA expression was not altered by drugs-induced cellular stress (Fig. 5), suggesting that ADM and PTX induced ATF2 IRES activity.

Figure 4. Transfection and reporter assay for the effect of ADM and PTX on ATF2 internal ribosome entry segment activity. (A and B) Bel7402 cells were transfected with the pRL-ATF2-FL plasmid and treated with or without increasing concentrations (0.01, 0.2 and 0.4 µg/ml) of (A) ADM and (B) PTX. Data are represented as the mean ± standard deviation of RL and FL activities in ≥3 independent experiments. RL, Renilla luciferase; FL, firefly luciferase; ATF2, activating transcription factor 2; ADR, adriamycin; PTX, paclitaxel.

Figure 5. RLUC and FLUC mRNA expression levels are not affected by ADM or PTX treatment. (A and B) Bel7402 cells were transfected with the pRL-ATF2-FL plasmid and treated with or without increasing concentrations (0.01, 0.2 and 0.4 µg/ml) of PTX. The mRNA expression levels of (A) RLUC and (B) FLUC were determined by RT-PCR. (C and D) Bel7402 cells were transfected with the pRL-ATF2-FL plasmid and treated with or without increasing concentrations (0.01, 0.2 and 0.4 µg/ml) of ADM. The mRNA expression levels of (C) RLUC and (D) FLUC were determined by RT-PCR. RLUC, Renilla luciferase; FLUC, firefly luciferase; ATF2, activating transcription factor 2; ADR, adriamycin; PTX, paclitaxel; mRNA, messenger RNA; RT-PCR, reverse transcription-polymerase chain reaction.

Discussion

The transcription factor ATF2 is a nuclear target of stress-activated protein kinases such as p38, which are activated by various extracellular stresses (29,30). Previous studies demonstrated that the stimulation of ATF2 mainly occurs by post-translational modification of protein subunits and changes in binding efficiency (31,32). However, the regulation at the translational level of ATF2 is poorly understood. To the best of our knowledge, the present study provided the first evidence of IRES-mediated translation of the ATF2 5′-UTR by using bicistronic Renilla firefly luciferase assays. The present study has revealed that the ATF2 IRES has various IRES activities in different cell types. The differences in ATF2 IRES activity between the different cells lines examined in the current study may be due to the levels of expression of IRES-transactivating factors (ITAFs) required for its function, which are probably different in these cells (33).

By performing deletion mapping, the core IRES region of the ATF2 mRNA was identified to be located between nt −299 and −269 of the ATF2 5′-UTR. In certain cases, a specific and stable RNA structure is necessary for IRES activity (34). For example, a module with a 9-nt motif in the Gtx mRNA, a novel murine homeobox gene which in adult animals is specifically expressed within glial cells of the central nervous system, including the forebrain, and in germ cells of the testis (35), recruits the 40S ribosomal subunit by base pairing to the 18S ribosomal RNA (rRNA) and initiates the internal translation (36), and in c-Myc mRNA, there are two 14-nt segments that can recruit the 43S preinitiation complex and activate the internal translation initiation (37). In line with these observations, our data lead to the postulation that the 30-nt short fragment of the ATF2 IRES is crucial for recruiting a ribosome and enhancing the initiation of translation, and this core IRES region of ATF2 may affect the translation efficiency through mRNA-rRNA interactions of these complementary regions. To gain more insight into the mechanism, further investigation is warranted to study the differences in the ability of recruiting a ribosome by the full-length ATF2 5′-UTR or the minimal ATF2 IRES region.

An important finding of the present study is that IRES-regulated ATF2 translation is activated upon the treatment of Bel7402 cells with two chemotherapeutic drugs, ADM and PTX. The difference in the ability to stimulate the expression of ATF2 protein may due to the treatment capability of these two drugs; perhaps the Bel7402 cells used in the present study have a greater ability to evade death during ADM therapy compared with PTX therpay. The expression and tissue distribution of ITAFs can change during cellular stress, and thus regulate IRES activity (38,39). To understand the mechanism of initiation of translation of the ATF2 IRES, it will be necessary to perform further experiments in order to identify the ITAFs that regulate the IRES activity and to clarify the functional association between each of these proteins.

It has been reported that c-Jun/ATF2 heterodimers can mediate a response to certain stress signals (31). Transcriptional activation domains and the target genes of c-Jun/ATF2 heterodimers, which are implicated in growth control, include c-Jun itself, cyclin D1 and cyclin A (3). Notably, an IRES has been demonstrated to be involved in the translation of the mRNA of several ATF2 targets, including c-Jun and cyclin D1 (40,41). This implies that IRES are very important in reposes to stress, and it would be relevant to investigate the ITAFs required for these IRES.

In the present study, it has been demonstrated that ATF2 5′-UTR harbors an IRES element localized between nt −299 and nt −269 upstream of the start codon, which would provide insights into the structure-function association of ATF2 in IRES-mediated translation. In addition, both ATF2 protein expression and IRES activity were increased in Bel7402 cells following treatment with the cellular stress-inducing chemotherapeutic drugs PTX and ADM, indicating the significant role of ATF2 IRES response to cellular stress in human hepatoma cells.

Acknowledgements

The present study was supported by the National Natural Science Foundation of China (Beijing, China; grant no. 81101667) and the Natural Science Foundation of Jiangsu Province (Nanjing, China; grant no. BK2009071).

References