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Identification of membrane-type 1 matrix metalloproteinase tyrosine phosphorylation in association with neuroblastoma progression
© Nyalendo et al; licensee BioMed Central Ltd. 2009
Received: 17 April 2009
Accepted: 4 December 2009
Published: 4 December 2009
Neuroblastoma is a pediatric tumor of neural crest cells that is clinically characterized by its variable evolution, from spontaneous regression to malignancy. Despite many advances in neuroblastoma research, 60% of neuroblastoma, which are essentially metastatic cases, are associated with poor clinical outcome due to the lack of effectiveness of current therapeutic strategies. Membrane-type 1 matrix metalloproteinase (MT1-MMP, MMP-14), an enzyme involved in several steps in tumor progression, has previously been shown to be associated with poor clinical outcome for neuroblastoma. Based on our recent demonstration that MT1-MMP phosphorylation is involved in the growth of fibrosarcoma tumors, we examined the potential role of phosphorylated MT1-MMP in neuroblastoma progression.
Tyrosine phosphorylated MT1-MMP was immunostained on tissue microarray samples from 55 patients with neuroblastoma detected by mass screening (known to be predominantly associated with favourable outcome), and from 234 patients with standard diagnosed neuroblastoma. In addition, the effects of a non phosphorylable version of MT1-MMP on neuroblastoma cell migration and proliferation were investigated within three-dimensional collagen matrices.
Although there is no correlation between the extent of tyrosine phosphorylation of MT1-MMP (pMT1-MMP) and MYCN amplification or clinical stage, we observed greater phosphorylation of pMT1-MMP in standard neuroblastoma, while it is less evident in neuroblastoma from mass screening samples (P = 0.0006) or in neuroblastoma samples from patients younger than one year (P = 0.0002). In vitro experiments showed that overexpression of a non-phosphorylable version of MT1-MMP reduced MT1-MMP-mediated neuroblastoma cell migration and proliferation within a three-dimensional type I collagen matrix, suggesting a role for the phosphorylated enzyme in the invasive properties of neuroblastoma cells.
Overall, these results suggest that tyrosine phosphorylated MT1-MMP plays an important role in neuroblastoma progression and that its expression is preferentially observed in tumor specimens from neuroblastoma patients showing poor clinical outcome.
Neuroblastoma (NB) is the most common extracranial solid cancer in childhood, accounting for 15% of all cancer-related fatalities in children . NB is a neuroendocrine malignant tumor of the autonomic nervous system that arises from neural crest cells . NB shows heterogeneous pathological characteristics due to its variable sites of origin, diverse histopathologic appearance and biologic characteristics. This malignant tumor exhibits a broad spectrum of clinical features, including spontaneous regression without any treatment, maturation to a benign ganglioneuroma, or progression to metastasis leading to death. Numerous factors, such as patient's age at diagnostic, stage of disease, tumor histopathology and genetic abnormalities have all been shown to influence NB progression . Among them, the metastatic status (Stage 4) is a very strong prognosis factor indicating poor outcome. Survival of children older than one year with an advanced stage of NB is poor despite aggressive treatment, as opposed to the survival of children younger than one year . NB secretes catecholamine metabolites that are excreted in urine, offering a non-invasive diagnostic technique. This observation has led to the suggestion of screening for NB in infants using specific catecholamine markers. Large studies showed that mass screening did not appear to reduce neither the disease-related mortality nor the yearly numbers of aggressive NB [5–7]. Moreover, patients with mass screening-detected NB very rarely died from tumor progression . Although the mechanisms underlying NB progression have been under intense investigation, therapeutic advances have failed to significantly increase the survival rates of children with aggressive NB.
Matrix metalloproteinases (MMPs), a family of zinc-dependent endopeptidases that degrade extracellular matrix (ECM) components, play crucial roles in several processes underlying tumor progression, including cell attachment, cell migration, invasiveness, cell proliferation, apoptosis, and angiogenesis [9–12]. There are 23 different human MMPs described to date, some of which are secreted in the pericellular environment while others are associated with the cell membrane. Membrane-type 1 matrix metalloproteinase (MT1-MMP, MMP-14), the best characterized membrane-anchored MMP, plays essential roles in tumor cell migration and invasion by acting as a potent matrix-degrading protease that digests a broad spectrum of ECM proteins [13–15] as well as a number of cell surface-associated adhesion receptors [16, 17]. In particular, elegant studies have unequivocally shown that MT1-MMP-mediated pericellular proteolysis of the ECM is essential for tissue-invasive activity of tumor cells  as well as for tumor cell growth in an otherwise growth-restrictive three-dimensional (3-D) environment . Accordingly, MT1-MMP is overexpressed in many types of tumors, including breast, colon, head and neck , cervical , gastric  and lung  carcinomas, as well as in brain tumors . Moreover, MT1-MMP expression has been shown to correlate with unfavourable outcome in pediatric NB patients .
In addition to its important matrix-degrading activity, MT1-MMP contains a short cytoplasmic sequence that is involved in regulation of the enzyme activity  as well as in the activation of signal transduction processes [27, 28]. Previous work from our laboratory has also shown that MT1-MMP is phosphorylated on its unique cytoplasmic tyrosine residue and that this phosphorylation also participates in tumor cell migration and invasion [29, 30]. We have also shown that impaired tyrosine phosphorylation of MT1-MMP markedly reduced the tumorigenic properties of the highly invasive HT-1080 fibrosarcoma, leading to a complete inhibition of tumor growth in nude mice .
The aim of the present study is to investigate the role of tyrosine phosphorylated MT1-MMP (pMT1-MMP) in NB progression and its relation to clinical outcome. We report herein that tyrosine phosphorylation of the enzyme plays an important role in NB cell migration and proliferation within 3D collagen matrix in vitro. Furthermore, expression of pMT1-MMP correlated with some clinical features, patient age at diagnosis and mass screening versus standard NB, which are associated with poor prognosis in NB pediatric patients.
Clinical features of 289 patients with NB diagnosis
Median (range) in months
< 1 year
> 5 years
< 10 copies
> 10 copies
Tissue Microarray (TMA) construction
On average, 4 tissue cylinders of 0.6 mm diameter were obtained and were transferred into a recipient paraffin block using a manual tissue arrayer (Alphelys, Plaisir, France). Mass screening NB samples consisted of 55 primary tumors and 21 metastases (15 lymph nodes and 6 hepatic metastases). TMA blocks of standard NB contained 234 primary tumors and 78 metastases (68 lymph nodes, 8 hepatic and 2 cutaneous metastases) and 56 paired control normal tissues (40 adrenal glands and 16 sympathetic ganglia).
Five-μm sections of TMA blocks were cut and deparaffinized, treated with 1% H2O2 and submitted to antigen retrieval by microwave oven treatment for 15 min in citrate buffer. Immunohistochemical staining was performed on these sections using pMT1-MMP polyclonal antibodies (1/100, 1 hour at room temperature [29, 31]). Samples were then incubated with biotinylated immunoglobulin (LSAB II, DAKO, Glostrup, Denmark) at room temperature for 30 min followed by avidin-biotin peroxidase complexes for 30 min. Rabbit IgG was used as a negative control. Three-amino-9-ethylcarbazol was used as the chromogen and haematoxylin as the nuclear counterstain. TMA sections were treated in one set of immunostaining. Two pathologists, blinded from clinical data, independently evaluated immunostaining under a light microscope at a magnification of 400×. Immunostaining scores were established by a semi-quantitative optical analysis of samples containing more than 10 neuroblasts assessing the percentage of positive cells in each sample: 0 = all cells negative, 1+ = 1 to 25% of positive cells, 2+ = 26 to 50% of positive cells, 3+ = 51 to 75% of positive cells and 4+ more than 76% of positive cells. Inter-observer agreement was calculated by the kappa coefficient. The observed agreement between the two pathologists was Kappa = 0.61, 95% CI = [0.58-0.64], P < 0.0001.
The univariate relationship between immunohistochemical expression of pMT1-MMP and biological and clinical data (standard and mass screening NB, control samples, primary tumors, metastasis, stage 1 and stage 4 and patient under one year, MYCN amplification) was investigated by Student's t-test. Kaplan-Meier analysis was used to estimate cancer-specific survival and the groups were compared with the log-rank test. All analyses were performed with Graphpad Prism software. P < 0.05 was considered statistically significant.
Cell lines and transfection
NB-10 cells were from St Jude Children's Research Hospital (Memphis, TN, USA) and were a gift from Dr. Daniel Sinnett (CHU Sainte-Justine, Montreal). SK-N-SH cells were obtained from the American Type Culture Collection. Cells were cultured at 37°C in a humidified atmosphere composed of 95% air and 5% CO2 and were grown in Eagle's minimum essential medium (EMEM) supplemented with 1 mM sodium pyruvate and 10% fetal bovine serum (FBS). The cDNAs encoding the full-length human MT1-MMP (MT1 WT) and its cytoplasmic mutant (MT1 Y573F) have been previously described . NB-10 and SK-N-SH neuroblastoma cells were transiently transfected using the FuGENE HD transfection reagent (Roche Applied Science) according to the manufacturer's instructions.
The procedures used were described previously . Briefly, equal amounts of protein from cell lysates were solubilized in Laemmli sample buffer, boiled for 5 min, separated by SDS-PAGE, transferred onto PVDF membranes and immunodetected with antibodies against MT1-MMP (MAB3328, Chemicon International) or GAPDH (Santa Cruz Biothechnology, CA, USA). For phosphorylated MT1-MMP assessment, cell lysates were immunoprecipitated with MT1-MMP antibodies (MAB3328) prior to Western blot procedure and immunodetection with pMT1-MMP polyclonal antibodies .
Cell Migration Assay
Migration assays were performed on transwells pre-coated with 10 μg/ml type I collagen. Transwells were assembled into 24-well plates and the lower chambers were filled with EMEM containing 10% FBS. Transfected cells were harvested, resuspended in 100 μl of fresh serum-free EMEM at a density of 5 × 105 cells/ml, and inoculated into the upper chamber of each transwell. The plates were then placed at 37°C in 5% CO2, 95% air for 3 h, and cells that had migrated were quantified using computer-assisted imaging (Northern Eclipse 6.0; Empix Imaging, Mississauga, ON, Canada). Statistical analyses were performed by one-way analysis of variance (ANOVA) followed by Bonferroni post-tests using GraphPad Prism software. P < 0.05 was considered statistically significant.
3D cell proliferation
Type I collagen was extracted from rat tail and resuspended at 2.7 mg/ml in acetic acid. Cells were mixed with 10× EMEM, 0.17N NaOH and 2.7 mg/ml type I collagen. The mixture was allowed to gel for 45 min at 37°C and EMEM containing 10% FBS was added atop. Collagen gels were dissolved with 2 mg/ml bacterial collagenase (Sigma, Burlington, ON, Canada) and viable cells were counted by trypan blue exclusion using a hemacytometer. Statistical analyses were performed by one-way ANOVA followed by Bonferroni post-tests using GraphPad Prism software. P < 0.05 was considered statistically significant.
Fluorescence and Confocal Microscopy
NB-10 cells were seeded on 10 μg/ml type I collagen-coated cover-slips, serum-starved overnight and stimulated with serum for 15 min. Cells were then fixed with 3.7% formaldehyde for 15 min, incubated for 5 min with 20 μM Hoechst (Sigma) for nuclei staining, permeabilized with 0.2% Triton X-100 for 5 min and blocked (1% BSA in Tris Buffered Saline containing 0.1% Tween 20) for 30 min. Samples were then incubated with FITC-conjugated phalloidin (for actin staining) for 30 min, and stained with specific primary antibodies against pMT1-MMP  for 30 min, followed by a 30 minute incubation with rhodamine-conjugated secondary antibodies (Molecular Probes - Invitrogen, Burlington, ON, Canada). Samples were covered with Immuno-Fluor Mounting Medium (MP Biomedicals, Solon, OH, USA). Fluorescence was visualized and photographed using a Zeiss LSM 510 Meta confocal microscope.
Results and Discussion
Phosphorylation of MT1-MMP in NB specimens
NB is characterized by its variable evolution that allows separation of these tumors into two major groups. Tumors in the first group are relatively benign, localized, well-differentiated and are successfully treated by surgery alone, or they sometimes regress spontaneously. Tumors in the second group (60% of all NB) are invasive and metastatic, and are usually associated with poor clinical outcome in spite of intensive treatment . Tumors detected by mass screening are usually part of the first group and are associated with good clinical outcome. Notwithstanding many advances in the identification of the molecular factors associated with the poor clinical income of NB, including amplified expression of the MYCN oncogene, deletion of 1p or 11q , lack of CD44 expression  as well as expression of neurotrophin receptors , the molecular mechanisms responsible for the progression/regression evolution of NB are poorly understood.
Relationship between pMT1-MMP and clinicopathologic parameters
Univariate analysis of pMT1-MMP expression in clinicopathologic features
Type of samples
Normal control samples
Tumor from primary site
Tumor from metastasis
< 1 year
> 1 year
A non phosphorylable mutant of MT1-MMP inhibits MT1-MMP-mediated tumorigenic properties of NB in vitro
These results suggest that phosphorylated MT1-MMP may play an important role in the MT1-MMP-mediated pro-migratory and pro-invasive properties of NB in vitro.
Overall, the findings reported in this study show that reduction of the tyrosine phosphorylation of MT1-MMP reduced the MT1-MMP-mediated tumorigenic properties of NB cells in vitro, and that pMT1-MMP is preferentially expressed in tumor specimens from standard NB and in patients older than one year, two clinical features associated with poor outcome in NB patients. In addition, our previous findings suggest that phosphorylation of MT1-MMP is observed under tumorigenic rather than normal conditions . Therefore, phosphorylation of MT1-MMP could represent the ''molecular switch" in NB cells responsible for the evolution from benign to malignant tumor. The identification of pMT1-MMP as an important player in the process of NB progression could be useful for the development of new therapeutic strategies for NB patients who cannot be cured with current therapeutic approaches.
RB and DG hold a grant from the Canadian Institutes for Health Research (Grant number MOP62918). CN hold a doctoral scholarship from the Canadian Natural Sciences and Engineering Research Council.
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