Background
Multiple-agent chemotherapy is the conventional therapy for patients with advanced stages of neuroblastoma (NB) and disseminated NB. However, drug resistance arises in the majority of stage IV and relapse NB disease, initially responding to chemotherapy [
1]. Classical multidrug resistance is attributed to the elevated expression of ATP-dependent drug-efflux pumps such as P-glycoprotein (Pgp) or multidrug resistance-associated protein (MRP). Both drug-efflux pumps are thought to decrease cellular accumulation of anti-cancer drugs and therefore limit the success of chemotherapy regimens.
However, recent observations suggest that the hypothesis of drug-efflux driven chemoresistance might not always hold true. Retrospective analysis of bladder cancer patients submitted to chemotherapy have revealed no correlation between tumor progression and Pgp modification [
2]. Overexpression of Pgp and MRP was also not correlated to chemoresistance and subsequent tumor recurrence and progression in sarcoma patients [
3]. In particular, the clinical significance of the expression of the multidrug resistance gene (MDR1) product Pgp in NB is still a matter of debate. Although frequent expression of functional Pgp has been found in patients with NB, no correlation has been seen between Pgp, disease stage and histopathological grading [
4]. Other studies have also failed to predict the correlation between MDR1 gene expression and clinical outcome for children with NB [
5,
6].
Recently, we developed multi-drug resistant NB in in vitro models and have demonstrated for the first time that an increased malignant phenotype in multidrug-resistant neuroblastoma cells is not mediated by up-regulated functional Pgp [
7]. Rather, chemotherapy might have a direct impact on the biological characteristics of tumors leading to increased malignancy and metastasis [
8]. Based on this, we hypothesized that chemoresistance itself might accelerate tumor progression and invasion.
To investigate the influence of chemotherapy on tumor invasion, we used an in vitro model of acquired drug resistance closely resembling progressive NB disease through long-term treatment of NB cell lines with vincristine- (VCR) or doxorubicin (DOX) to establish VCR and DOX-resistant tumor cell sublines (NB
VCR and NB
DOX). We additionally analyzed NB tumor cells with intrinsic multidrug resistance (MDR) phenotype (UKF-NB-4) [
9]. A transendothelial migration assay allowed the separate analysis of tumor cells which adhered to an endothelial cell monolayer and those which transmigrated beneath the endothelium. Since surface receptors are strongly involved in tumor invasion and data has indicated that changes in neural cell adhesion molecule (NCAM, CD56) expression play an essential part in the progression of NB, we investigated NCAM expression. This is of particular interest because the modulation of NCAM is a rate-limiting event in the metastatic dissemination of tumor cells [
10].
The data provide evidence that NB cells resistant to anticancer drugs acquire increased invasive capacity relative to non-resistant parental cells, and that enhanced invasion is caused by strong down-regulation of NCAM adhesion receptors.
Methods
Cell cultures and induction of drug resistance
The human neuroblastoma cell lines UKF-NB-2, UKF-NB-3 and UKF-NB-4 were established in our laboratory from bone marrow metastases. IMR-32 was derived from LGC Promochem, Wesel, Germany. The vincristine- (VCR) and doxorubicin-resistant (DOX) cell sublines were established by exposing parental UKF-NB-2, UKF-NB-3 [
8], or IMR-32 cells to increasing concentrations of the respective drug. Solutions of VCR (Sigma-Aldrich, Deisenhofen, Germany) and DOX (Farmitalia, Milan, Italy) were prepared in accordance to the manufacturer's instructions. The initial VCR and DOX concentrations were 0.2 ng/ml and 2 ng/ml medium, respectively. The resistant sublines were grown for more than 6 months in Iscove's modified Dulbecco's medium (IMDM; Gibco, Karlsruhe, Germany) supplemented with 10% fetal calf serum (FCS, Gibco) and 10 ng/ml VCR (UKF-NB-2
VCR, UKF-NB-3
VCR, IMR-32
VCR) or 20 ng/ml DOX (UKF-NB-2
DOX, UKF-NB-3
DOX, IMR-32
DOX). All doses were in the range of clinical plasma concentrations. Multidrug resistant parental UKF-NB-4 cells were exposed to 50 ng/ml VCR (UKF-NB-4
VCR) or 100 ng/ml DOX (UKF-NB-4
DOX). All cells were subcultured at 5-day intervals.
Human endothelial cells (HUVEC) were isolated from human umbilical veins and harvested by enzymatic treatment with chymotrypsin. HUVEC were grown in Medium 199 (M199; Biozol, Munich, Germany), supplemented with 10% FCS, 10% pooled human serum, 20 μg/ml endothelial cell growth factor (Boehringer, Mannheim, Germany), 0.1% heparin, 100 ng/ml gentamycin and 20 mM HEPES-buffer (pH 7.4). Subcultures from passages 2–6 with intact morphology and proliferative capacity were selected for experimental use.
Monolayer invasion assay
Round cover slips were treated with 3-aminopropyl-triethoxy-silan (2%; Sigma, München, Germany) – acetone solution for 60 minutes (20°C) to allow firm adhesion of HUVEC and placed into six-well multiplates (Falcon Primaria; Becton Dickinson, Heidelberg, Germany). HUVEC subcultures were transferred to prepared multiplates in complete HUVEC-medium. When confluency was reached, 0.5 × 106 neuroblastoma cells/well were carefully added to the HUVEC monolayer for various time periods. Subsequently, non-adherent neuroblastoma cells were washed off using warmed (37°C) M199. The remaining cells were fixed with 1% glutaraldehyde. Bound tumor cells were counted in five different fields (5 × 0.25 mm2) using a phase contrast microscope (20 × objective) and the mean cellular adhesion rate was calculated.
To separately assess neuroblastoma cells which had penetrated the HUVEC monolayer, a reflection interference contrast microscope with a Ploem apparatus was used. The relevant theoretical evaluation of reflection contrast microscopy is given by Bereiter-Hahn et al. and Gingell and Todd [
11,
12]. The resulting images were visualized and amplified by a Proxitronic CCD-camera (Proxitronic, Bensheim, Germany). The number of penetrated neuroblastoma cells were then quantified using the image analyzing system ARGUS 20 (Hamamatsu, Hersching, Germany). To optimize the signal to noise ratio, online background subtraction and averaging of 8 images was performed, using the image processing system QUANTIMET Q520 (Cambridge Instruments, Bensheim). Cells that penetrated the HUVEC monolayer were counted in five different fields (5 × 0.25 mm
2, 20 × objective), and mean penetration rate was calculated.
Cell proliferation
Proliferative activity of NB cells and HUVEC was estimated by the PicoGreen assay as described elsewhere [
13]. Briefly, at several time points after plating the cells in six-well multiplates, culture medium was removed and cells were digested with papain (0.125 mg protein/ml) for 20 h at 60°C. Thereafter, the fluorescent dye PicoGreen (MoBiTec, Goettingen, Germany), which shows high specificity for dsDNA, was added (1:200 dilution) for 10 min at 20°C. Fluorescence intensity was determined using a computer-controlled fluorescence reader (Cytofluor 2300 plate scanner; Millipore, Eschborn, Germany) at λex = 485 nm and λem = 530 nm.
Plasmids and transfection
UKF-NB-4
VCR cells were transfected using the calcium phosphate co-precipitation method with full-length cDNA, encoding the human NCAM-140 kDa isoform inserted in sense of the eukaryotic expression vector pHβ-Apr-1-neo [
14]. Control cells were transfected with the expression vector alone. 0.5 × 10
6 NB were seeded in 25 cm
2 culture flasks, grown overnight, and transfected with 2 μg of DNA. After culturing for 16 h in complete medium, cells were washed twice with PBS without Ca
2+ and Mg
2+ and then incubated with fresh cell culture medium. Efficiency of NCAM transfection using pHβ-Apr1-neo was investigated fluorometrically by calcium phosphate co-precipitation of pHβ-Apr1-neo in combination with pEGFP-N1 vector (Clontech GmbH, Heidelberg, Germany) at a ratio of 1:1. pEGFP-N1 encodes a red-shifted variant of wild-type GFP which has been optimized for brighter fluorescence and higher expression in mammalian cells. Fluorescence analysis revealed a transfection rate of pHβ-Apr1-neo of 30%. Viability of the cells, which was controlled by trypan blue dye exclusion or by quantitative fluorescence analysis of propidium iodide uptake, was > 90%.
Evaluation of NCAM surface expression
Neuroblastoma cells were disaggregated mechanically, washed in blocking solution (PBS, 0.5% BSA) and then incubated for 60 min at 4°C with FITC-conjugated monoclonal antibody anti-CD56 which detects the NCAM 120, 140 and 180 kDa isoform (clone 16.2). NCAM expression of NB cells was then measured using a FACscan (Becton Dickinson; FL-1H (log) channel histogram analysis; 1 × 104 cells/scan) and expressed as mean fluorescence units (MFU). A mouse IgG1-FITC was used as the isotype control.
To explore NCAM localization, tumor cells were transferred to round cover slips which were placed in a 24 well multiplate. Upon reaching confluency, cell cultures were washed two times with PBS (with Ca2+ and Mg2+) and then fixed in cold (-20°C) methanol/acetone (60/40 v/v). Subsequently, cells were washed again with PBS (without Ca2+ and Mg2+), and afterwards once with blocking buffer (0.5% BSA in PBS without Ca2+ and Mg2+). After removing the washing buffer, cells were incubated for 60 min with FITC-conjugated anti-NCAM monoclonal antibody. To prevent photobleaching of the fluorescent dye, cover glasses with stained cells were taken out of the wells and the residual liquid was removed. The cells were then embedded in an antifade reagent/mounting medium mixture (ProLong™ Antifade Kit, MoBiTec, Göttingen, Germany) and mounted on slides. The slides were viewed using a confocal laser scanning microscope (LSM 10; Zeiss, Jena, Germany) with a plan-neofluar × 100/1.3 oil immersion objective.
Western blot analysis
Total NCAM content in neuroblastoma cells was evaluated by Western blot analysis: cell lysates were applied to a 7 % polyacrylamide gel and electrophoresed for 90 min at 60 V. The protein was then transferred to nitrocellulose membranes. After blocking, the membranes were incubated overnight with the anti-NCAM-antibody (dilution 1:1000). HRP-conjugated goat-anti-mouse IgG (Upstate Biotechnology, Lake Placid, NY, USA; dilution 1:5000) served as the secondary antibody. The membrane was briefly incubated with ECL detection reagent (ECL™, Amersham) to visualize the proteins and exposed to an x-ray-film (Hyperfilm™ EC™, Amersham).
Reverse transcription/polymerase chain reaction (RT/PCR)
Total RNA was extracted and purified with Trizol reagent according to the manufacturer's instructions and treated with RNase-free DNase. The NCAM primer sequences were as follows: for NCAM-180 (AccNo AK056258): 5'CGAGGCTGCCTCCGTCAGCACC 3' and 5'CCGGATCCATCATGCTTTGCTCTCG 3'; for NCAM-140 (AccNo U63041): 5'GAACCTGATCAAGCAGGATGACGG 3' and 5'CCGGATCCATCATGCTTTGCTCTCG 3' [
15]. Internal controls for the RT-PCR reaction was performed by running parallel reaction mixtures with the housekeeping gene GAPDH: 5'ATCTTCCAGGAGCGAGATCC 3' and 5'ACCACTGACACGTTGGCAGT 3'. RNA (1–10 μg) was reverse transcribed and the resulting cDNA directly added to the polymerase chain reaction. Amplification reactions (20 μl) were performed in the presence of 1/10 (2 μl) of the cDNA reaction, with an initial incubation step at 94°C for 1 min. Cycling conditions consisted of denaturation at 94°C for 1 min, annealing at 55°C for 1 min, and extension at 72°C for 1 min over a total of 30 cycles. The reaction was completed by another incubation step at 72°C for 10 min. The PCR products were subjected to electrophoresis in 2% agarose gel and visualized by ethidium bromide.
Statistics
All experiments were performed 3–6 times. Statistical significance was investigated by the Wilcoxon–Mann-Whitney-U-test. Differences were considered statistically significant at a p value less than 0.05.
Discussion
Intrinsic or acquired resistance to anticancer agents is a major obstacle to the success of chemotherapy. In the present work, we compared the invasive properties of drug sensitive NB with their drug-resistant sublines, as well as intrinsically resistant NB which were further treated with VCR or DOX. The selection of the various tumor sublines mimicked the severe problems arising in patients during chemotherapy. Based on our model, we demonstrate that drug resistant cancer cells develop an increased malignant phenotype, in part due to enhanced adhesion and transendothelial penetration, accompanied by a significant down-regulation of the adhesion receptor NCAM.
Our findings might explain the paradoxical situation that tumors sometimes become progressively more malignant during the course of chemotherapeutic treatment. Slotman et al. found an increased incidence of hematogenous metastases with induction chemotherapy for patients with advanced head-and-neck squamous carcinomas, compared to patients receiving only surgery and radiotherapy. They also found an increase in metastases at sites other than the usual pulmonary site [
16]. Stefani and coworkers reported that the use of hydroxyurea in combination with radiotherapy for the treatment of head and-neck cancer yielded no benefit in terms of response rate or survival, but rather increased the incidence of distant metastases from 8% to 23% [
17]. The administration of a single drug dose may be sufficient to induce spontaneous metastasis [
18].
Two reports have been published recently which underline our observations and suggest that drug resistance in melanoma and carcinoma cells may confer to a more invasive phenotype [
19,
20]. Nevertheless, it is still hypothesized that resistance to cytotoxic agents and invasive potential is associated with the over-expression of Pgp drug transporters [
19,
21]. Notably, increased Pgp expression was found in metastatic NB cells from bone marrow samples, as compared to non-metastatic NB [
22]. Previous experiments on UKF-NB-2 and UKF-NB-3 cells also revealed high amounts of functionally active Pgp in both DOX and VCR resistant sublines. However, expression of Pgp was 3.5-fold higher in UKF-NB-2
DOX when compared to UKF-NB-2
VCR cells, and therefore does not correlate to the changes seen with respect to cell adhesion and transendothelial penetration (UKF-NB-2
DOX < UKF-NB-2
VCR). Furthermore, pharmacological blockage of Pgp in resistant UKF-NB-2 and UKF-NB-3 cell lines restored chemosensitivity, but had no effect on colony formation and cell survival under serum free conditions [
7,
8].
Therefore, up-regulation of Pgp itself probably does not play a leading role in increasing NB malignant biology. However, concomitant deregulation of other pathways may result in increased metastatic potential, thus leading to a poorer prognosis of advanced forms of NB disease. In our cell culture model, modulation of NCAM seems to be the major parameter responsible for altered cell adhesion and penetration. This assumption is based on three observations: 1. Enhanced tumor binding and transmigration of drug resistant cell populations only occured when NCAM receptor expression was reduced. 2. NCAM loss strongly correlated with the elevation of adhesion and penetration capacity, and 3. Transfection of UKF-NB-4
VCR cells with NCAM cDNA up-regulated the NCAM expression level and diminished the interaction events between tumor and endothelial cells. In good accordance to the present data, we recently demonstrated an inverse correlation between NCAM expression and NB cell adhesion, assessed on 11 NB cell lines. In particular, transfection with a cDNA encoding the human NCAM-140 kD isoform enhanced NCAM expression and diminished initial NB cell adhesion, treatment with NCAM antisense oligonucleotides reduced NCAM surface level and induced up-regulation of NB cell adhesion to endothelium [
10].
Several studies have demonstrated the important role of NCAM in tumor migration and metastasis, with an inverse relationship between migratory potential of the cells and NCAM expression. In primitive neuroectodermal tumor cells, an increase in NCAM was paralleled by a significant reduction in cellular motility and adhesion capacity [
23,
24]. In a rat model, NCAM-transfected glioma tumor cells became less invasive and destructive than control cells with a low NCAM expression level [
25]. Diminished expression of NCAM was also associated with clinically aggressive colon cancers [
26‐
28], and dissemination of pancreatic beta tumor cells [
29,
30]. Tezel et al. suggested that NCAM expression in tubular adenocarcinoma of the pancreas has a significant impact on overall patient survival [
31]. It is currently assumed that NCAM, in its function as a homophilic receptor, stabilizes the primary tumor or tumor cell aggregates, while circulating in the blood vessels. Reduction of the NCAM expression level might lead to a reduction in cell-cell binding forces, and hence to the release of tumors as single cells. The less NCAM, the more metastatic cells leave the tumor mass, and the more penetration events can take place [
10]. Consequently, NCAM loss observed in DOX and VCR resistant NB tumor cells allows more cells to transmigrate the endothelial blood barrier and extravasate into surrounding tissue. In line with this, establishment of DOX or VCR resistant human glioma cells was accompanied by NCAM reduction and a concomitant down-regulation of adhesiveness [
32]. Analyses of tumor samples from relapsed patients have to be carried out to strenghthen the relevance of the in vitro findings.
Recently, it has been documented that the loss of NCAM function causes the formation of lymph node metastasis in pancreatic beta cell carcinogenesis via vascular endothelial growth factor -C and -D-mediated lymphangiogenesis [
33]. In a previous work, loss of NCAM resulted in a failure to activate beta1 integrins via fibroblast growth factor receptor signalling [
29]. Both findings implicate that NCAM, beside its role as an aggregation stabilizer, may also act in terms of a "metastasis suppressor protein", controlling proteins and genes that specifically inhibit the ability of tumor cells from forming metastases [
34].
Our hypothesis of drug evoked alterations of NB tumor cell binding and transvasation also appears to be applicable to tumor cells with intrinsic drug resistance. UKF–NB-4 cells with a multidrug resistant phenotype retained the potential to become even more aggressive when treated with DOX or VCR. From a clinical viewpoint, chemotherapy of NB might induce adverse effects concerning tumor biology. In fact, single chemotherapy may amplify the process of tumor progression if drug-resistant tumor subclones are present in the initial tumor burden.
The finding that extended drug exposure contributes to distinct modifications of adhesion receptors and invasive potential of single cancer cells, independent of Pgp over-expression, may be a signal to re-assess current therapeutic protocols. In fact, the use of escalating doses of cyclophosphamide and prolonging conventional chemotherapy with the same drugs has failed to improve the metastasis complete response rate in NB patients [
35]. Since initial pharmacological attempts to inhibit drug efflux and increase intracellular drug concentrations have not provided the desired clinical benefit in relapsed or resistant paediatric cancers [
36], the consequences of drug resistance might preferably be treated by agents which reverse cellular adhesion. In this context, the branched-chain fatty acid valproate has been demonstrated to inhibit tumor cell motility and adhesion by up-regulating NCAM [
37,
38]. The same is true for the differentiation inducing compound trichostatin A [
39]. A significant increase of NCAM expression level accompanied by blocking cellular adhesion has also been observed when neuroblastoma cells were treated with retinoic acid [
40,
41]. The introduction of differentiation inducing drugs may therefore advance the treatment of relapsed tumors. Currently, several studies dealing with this issue are underway.
It is important to note that extended drug exposure evoked different responses in the in vitro system described here. Although drug resistance was established in all tumor sublines, VCR resistance led to increased attachment of UKF-NB-2, UKF-NB-3 or UKF-NB-4 cell lines, but not of IMR-32, whereas DOX resistance induced marked elevation of IMR-32 attachment but had no influence on UKF-NB-3 adhesion. Alterations in the NCAM expression level followed the same pattern. Therefore, modifications of the invasive program cannot be expected in every case where drug resistance in tumor cells develops. VCR or DOX resistance might convert NCAM triggered cell adhesion in some but not in all tumor subpopulations, or in some but not in all tumor patients where chemotherapy has failed. It is still unknown how drug resistant tumor cells are selected to became "responders", i.e. increase their invasive activity. However, if our hypothesis holds true, a critical selection of those "responding" patients should be carried out who might be predestined for innovative antitumoral, adhesion blocking strategies.
Competing interests
The author(s) declare that they have no competing interests.
Authors' contributions
RAB performed adhesion and penetration studies and drafted the manuscript. FHD carried out flow cytometry, confocal microscopy and RT-PCR. MM performed analysis of IC50 values. CH and EV performed western blotting. DJ participated in the conception and design of the study. RK contributed to the manuscript design, data analysis and finalisation. HWD and JC participated in the conception and design of the study and its coordination. All authors read and approved the final manuscript.