Background
Cervical cancer is the second largest cause of cancer mortality in women worldwide with more than 270,000 deaths per year [
1]. Current therapies for the treatment of advanced cervical cancer involve the use of cisplatin, often in combination with radiotherapy [
2]. Cisplatin is believed to act via the formation of inter- and intrastrand cross-links in DNA, culminating in the initiation of cell death via caspases [
3]. Unfortunately, the current cisplatin-based treatment for cervical cancer does not lead to a high disease-free survival rate in patients with bulky or locally-advanced disease. To develop new potentially therapeutic treatments for cancers, two strategies have been developed. The first strategy uses an approach to identify potential mechanisms of resistance to cancer therapy, and to overcome these resistance phenotypes using specific resistance modulators [
4]. The second strategy seeks to correlate biological features with genetic alterations in cancer cell [
5]. Although some progress has been achieved in the past three decades, much more efforts are still needed to resolve cisplatin-resistance of cervical cancer.
NDRG2, a member of N-Myc downstream regulated gene (NDRG) family, was first cloned in our laboratory in 1999 (GenBank accession no. AF159092). NDRG gene family represents a new class of Myc-repressed genes which also consist of NDRG1, NDRG3 and NDRG4 [
6]. The NDRGs share 57-65% amino acid identity and are highly conserved in plants, invertebrates and mammals, suggesting that this gene family may have important cellular functions. Although NDRG2 has been implicated in cellular stress [
6], it’s physiological function still remains unclear. Interestingly, NDRG2 has been found to be deregulated in many kinds of human malignant tumors [
7‐
17]. We previously reported that NDRG2 could be up-regulated by hypoxia and radiation and could promote radioresistance of human cervical cancer Hela cells [
18]. In another study, we found adriamycin enhanced NDRG2 expression in several tumor cell lines [
19]. This led us to further explore whether NDRG2 has a role in regulation of cisplatin-sensitivity of cervical cancer cells.
Methods
Cell culture
The human cervical cancer cell line Hela was obtained from the American Type Culture Collection (Manassas, VA) and maintained as a monolayer in Dulbecco’s modified Eagle’s medium (Invitrogen, Carlsbad, CA) supplemented with 10% fetal bovine serum (Sijiqing Biological Engineering Materials Co., Hangzhou, China) at 37°C in the presence of 5% CO2-balanced air.
Constructs and transfection
The recombinant pSilencer 3.1 (Ambion, Austin, TX) constructs expressing a scramble control small interference RNA (siRNA) or siRNA specific to NDRG2 have been described previously [
20]. All construct sequences were directly confirmed by DNA sequencing. Hela cells were transfected with the corresponding constructs using Lipofectamine
TM 2000 (Invitrogen, Carlsbad, CA) according to the manufacturer’s instruction.
RT-PCR
Total RNA was extracted from Hela cells using Trizol reagent according to instructions provided by the manufacturer (Invitrogen, Carlsbad, CA). cDNAs were obtained by reverse transcription using Revert Aid First Strand cDNA Synthesis Kit (Fermentas, Shenzhen, Guangzhou, China) with 2 μg of total RNA. The RT-PCR exponential phase was determined on 25–30 cycles to allow semi-quantitative comparisons among cDNAs developed from identical reactions. Each PCR involved a 94°C, 5 min initial denaturation step followed by 35 cycles (for NDRG2) at 94°C for 30 s, 52°C for 40 s, and 72°C for 40 s, 20 cycles (for β-actin) at 94°C for 30 s, 55°C for 10 s, and 72°C for 30 s, 25 cycles (for Bcl-2) at 94°C for 30 s, 62°C for 30 s, and 72°C for 30 s, then 72°C, 10 min extension step. Oligonucleotide primer sequences for NDRG2 [
20], Bcl-2 [
21] and β-actin [
21] have been described previously. The PCR products were separated by electrophoresis on 1.5% agarose gels.
Real-time PCR
NDRG2 and Bcl-2 mRNA expression levels were evaluated by real-time PCR using the ABI PRISM 5700 sequence detection system (Applied Biosystems, Foster City, CA). Primers for NDRG2 have been described previously [
12]. The primer sequences for Bcl-2 were: 5'-GGTGAACTGGGGGAGGATTGT-3' for the forward primer, and 5'-CTTCAGAGACAGCCAGGAGAA-3' for the reverse primer. Fluorescent data were converted into cycle threshold measurements using the SDS system software and exported to Microsoft Excel. Fold expression changes relative to Hela cells were calculated with the ΔΔCT method [
22] using ARF1 (ADP-ribosylation factor 1) as the reference transcript [
12].
For detection of microRNAs (miRNA), stem-loop reverse transcription followed by real-time PCR analysis was performed as previously described [
21]. The primers used for stem-loop RT-PCR for Let-7a [
23], miR-15b [
21] and miR-16 [
21] have been reported elsewhere. The relative amount of each miRNA was normalized to U6 snRNA. The fold-change for each miRNA relative to the Hela cells was calculated using ΔΔCT method [
22]. PCR was performed in triplicate.
Western blot analysis
Hela cells and their variants were solubilized in lysis buffer containing 20 mM Tris, pH 7.4, 150 mM NaCl, 1% Triton X-100, 5 mM EDTA, 10 μg/ml leupeptin, 10 μg/ml aprotinin, 1 mM phenylmethylsulfonyl fluoride. Fifty micrograms of cell lysate was resolved by SDS-PAGE and transferred to nitrocellulose membranes (0.22 μm, Millipore, Bedford, MA). The blots were probed with antibodies (from Santa Cruz Biotechnology, Santa Cruz, CA, unless otherwise indicated) against NDRG2, NDRG1, Bcl-2, Bax, P-glycoprotein, multidrug resistance protein, caspase-3 (Cell Signaling Technology, Danvers, MA) or caspase-9 (Cell Signaling Technology), followed by incubation in a species-matched horseradish peroxidase (HRP)-conjugated secondary antibody. The blots were developed with a chemiluminescence substrate solution (Pierce, Rockford, IL) and exposed to X-ray film. Equal loading of all lanes was confirmed by reprobing the membranes with anti-β-actin antibody (Sigma, St. Louis, MO).
Cytotoxicity assay
The effect of cisplatin on growth of Hela and its variants was determined by 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) assay as previously described [
24]. Briefly, 2000 cells were plated into 96-well plates in 200 μl aliquots and allowed to adhere overnight before cisplatin (Qilu Pharmaceutical Co Ltd, Jinan, Shandong, China) was added. The final concentrations of cisplatin were as 0.01, 0.1, 1, 10 and 100 times of human peak plasma concentration of cisplatin (2 μg/ml) [
24], respectively. After incubation with cisplatin at 37°C for 72 h, 20 μl aliquots of an MTT solution (5 mg/ml) were added to each well and plates were incubated for an additional 4 h at 37°C. The media was then removed and replaced with 150 μl of 100% DMSO to dissolve the formazan crystals with agitation for 5–10 min on a shaker. The absorbance was measured at 490 nm using a multiwell scanning spectrophotometer (Molecular Devices, Sunnyvale, CA). Cell viability was expressed as A490 percentage of untreated cells. The IC
50 values were determined from a plot of cell viability using probit module of SPSS software (version 10.0; SPSS, Chicago, IL). Three replicates were performed for each experimental condition.
Cells were seeded on six-well tissue culture plates with 500 cells per well and incubated in complete medium with or without cisplatin (2, 5, 10 μg/ml). After 12 days of culture, colonies of surviving cells were counted and the cloning efficiency was calculated in comparison to seeded cells.
Detection of apoptosis
Hela cells and their variants were treated with cisplatin at desired concentration for 24 h. The apoptotic cells were stained with fluorescein isothio-cyanate (FITC)-labeled annexin V (Roche Applied Science, Basel, Switzerland) and propidium iodide (PI) as previously described [
18]. Apoptotic cells were measured using a Becton Dickinson fluorescence-activated cell sorter (FACS) apparatus.
Statistical analysis
Data are expressed as mean ± SD. Statistical analyses were performed with the SPSS software (version 10.0; SPSS, Chicago, IL) by using one-way ANOVA followed by the t-test for independent groups. A p level of < 0.05 was considered statistically significant.
Discussion
Platinum-based drugs, and in particular cisplatin, are widely used for the treatment of many kinds of solid malignancies, including cervical cancer [
2]. Cisplatin often leads to an initial therapeutic success associated with partial responses or disease stabilization. However, some patients developed resistance to cisplatin before and even after exposing to this chemotherapeutic agent. It is widely accepted that the high incidence of chemoresistance is the main reason for cisplatin treatment failure. Although the pre-target, on-target, post-target and off-target mechanisms of cisplatin-resistance have been proposed recently [
25], the molecular mechanisms underlying cisplatin-resistance are still far from understood.
In the present study, we provide evidence that NDRG2 is involved in the regulation of cisplatin-resistance of cervical cancer cells. Firstly, it was shown that cisplatin treatment induced up-regulation of NDRG2 in a time-dependent manner. Secondly, knock-down of NDRG2 by siRNA increased the suppressive effects of cisplatin on colony-forming ability of Hela cells. Thirdly, inhibition of NDRG2 significantly lowered the IC50 values of cisplatin for Hela cells, indicating down-regulation of NDRG2 increased the sensitivity of Hela cells to cisplatin. Finally, down-regulation of NDRG2 resulted in decreased expression level of Bcl-2, one of important regulators of apoptosis and drug resistance.
NDRG2, similar to NDRG1, has been proposed to be involved in cell stress [
6]. Previous studies demonstrated that NDGR2 expression in cancer cell lines could be enhanced by adriamycin [
19], hypoxia [
20] and radiation [
18], and that NDRG2 was implicated in regulation of adriamycin-induced apoptosis [
19] and radioresistance [
18]. All those data support a role of NDRG2 in cell stress. It is well-characterized that the mode of action of cisplatin involves the DNA-damage response and mitochondrial apoptosis [
26,
27]. From this view, it is reasonable that NDRG2 can be induced by cisplatin. In line with previous reports, the present study indicates modulation of NDRG2 expression occurs at transcriptional level. Although NDRG2 transcription can be suppressed by Myc [
28], several binding sites for hypoxia-inducible factor 1 (HIF-1) have been found in the promoter region of NDRG2 gene and HIF-1 is responsible for NDRG2 up-regulation induced by hypoxia and radiation [
18,
20]. It has been reported that HIF-1 can be activated by vincristine in gastric cancer cells under normoxic condition [
29]. Cisplatin, as a chemotherapeutic drug like adriamycin and vincristine, might induce NDRG2 expression through activation of HIF-1. However, this speculation needs to be validated in future study.
It is well known that Bcl-2 and Bax play critical roles in mitochondria apoptosis. As discussed in a recently published review [
25], there are increasing evidences that overexpression of Bcl-2 confers multidrug resistance and that clinical data have linked Bcl-2 expression level with cisplatin resistance and recurrent disease. The present study revealed that suppression of NDRG2 significantly inhibited Bcl-2 expression, which depictes how does NDRG2 influence cisplatin-induced apoptosis of Hela cells. Interestingly, NDRG2 regulates Bcl-2 expression at post-transcriptional level. It has been well defined that Bcl-2 can be targeted and regulated by microRNAs such as miR-15b and miR-16 in gastric cancer cells [
21]. These microRNAs bind to the 3’ untranslational region of Bcl-2 mRNA and inhibit translation of Bcl-2 protein without changing mRNA level. Similarly, the present study indicated that down-regulation of NDRG2 resulted in increased level of miR-15b and miR-16, which might in turn reduce Bcl-2 protein expression. However, the study does not exclude the possibility that NDRG2 influences stabilization of Bcl-2 protein.
It has been well documented that hypoxia- and radiation-induced NDRG2 promotes resistance of Hela cells to radiation [
18]. The present study demonstrated that cisplatin-induced NDRG2 increases chemoresistance of Hela cells. Considering cisplatin is often used in combination with radiotherapy for advanced cervical cancer [
2], NDRG2 may represent a key regulator of therapy-resistance in cervical cancer cells. It should be noted that NDRG2 has been proposed as a potential tumor suppressor. An increasing number of reports showed that the level of NDRG2 was reduced in many kinds of malignant tumor comparing to the normal counterpart and that NDRG2 level was an independent prognostic factor for cancer patients [
7‐
17]. It was also reported that restoration of NDRG2 could inhibit proliferation of cancer cells [
6]. Recently, the crystal structure of human NDRG2 protein was resolved and NDRG2 was proposed to suppress TCF/β-catenin signaling in the tumorigenesis of human colorectal cancer via a molecular interaction [
30]. Moreover, a role for NDRG2 in the oncogenic properties of renal cell carcinoma has been suggested [
31]. However, these data cannot exclude the possibility of NDRG2 to promote drug and radiation resistance. We proposed NDRG2 as a multifunctional protein. As a tumor suppressor, NDRG2 is inhibited to facilitate tumor development in the process of tumorigenesis. As a resistance regulator, NDRG2 may be re-activated or up-regulated to promote cancer cell survival during or after chemotherapy/radiotherapy. In an early study, it was shown inhibition of NDRG2 resulted in slightly increased proliferation and cisplatin resistance as well as decreased Fas expression and Fas-mediated cell death in gastric cancer cells [
9]. The discrepancy of NDRG2 in cisplatin resistance in cervical cancer and gastric cancer cells may due to tissue specificity. However, our speculation needs supporting data from further studies. It will be helpful to validate the role of NDRG2 in cisplatin resistance in multiple cell lines other than Hela and to explore the clinical relevance of NDRG2 to cisplatin resistance in patients with cervical cancer.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
JL, LY, JZ, JZ, YC, KL, YL and YL performed experiments and summarized the data; JL, YL and GG designed experiments; JL, LY, YL and GG wrote the paper; all authors have read and approved the final manuscript.