Background
Hypoxia is a fundamental micro-environmental component of solid tumour tissue which is associated with resistance to therapy, poor survival and a malignant phenotype [
1]. Hypoxia induces stabilisation of the Hypoxia-Inducible Factor transcription factors, HIF-1 and HIF-2, which direct responses central to survival and expansion of the malignant cell population.
HIF comprises a hypoxia-inducible alpha subunit and a constitutively expressed beta subunit. Regulation of the active transcription factor occurs via enzymatic control of the abundance and activity of HIF
α subunits. Under normoxia HIFα is post-translationally hydroxylated by the prolyl hydroxylase domain enzymes, targeting it for proteasomal degradation [
2,
3]. These enzymes are absolutely dependent on O
2 and limitation of activity under hypoxia allows stabilisation of HIFα. Binding of the active complex to the hypoxia-response element (HRE) of target genes results in activation of pathways regulating processes such as angiogenesis, apoptosis and metabolic adaptation [
4].
HIF over-expression is an independent prognostic factor in many carcinomas [
5], although limited data is available in primary bone sarcomas. Nuclear over-expression of HIF-1α has been reported in approximately 60% of clinical osteosarcomas where it correlates with disease grade, stage, recurrence and survival [
6‐
8]. In Ewing's sarcoma the presence of tumour cell-lined blood lakes correlates with clinical outcome. Cells surrounding these lakes also express HIF-1α and the hypoxia marker pimonidazole [
9]. Expression of both HIF-1α and HIF-2α has been reported in chondrosarcoma [
10] and giant cell tumour of bone [
11], HIF-1α expression correlating with reduced disease-free survival in chondrosarcoma. Levels of serum VEGF, a HIF target gene, are significantly higher in Ewing's patients than healthy controls [
12] and are an independent prognostic factor for survival [
13]. In osteosarcoma VEGF levels were higher in the tumour and serum of patients who subsequently relapsed, tumour VEGF being predictive of pulmonary metastasis and poor prognosis [
14,
15]. In Ewing's sarcoma the presence of necrotic, non-perfused and presumably hypoxic tumour areas correlates with survival and frequency of metastatic spread [
16‐
18].
This data implies that hypoxia and/or HIF contribute substantially to the pathobiology of primary bone sarcomas. Hypoxia induces expression of HIF-1α and VEGF in the osteosarcoma cell lines Saos2, 143B, U2-OS and MG-63 [
11,
19‐
21], with MG-63 also expressing HIF-2α [
11,
22]. The Ewing's sarcoma cell lines A673, SK-ES-1, SK-N-MC and TC-71 also demonstrate hypoxic induction of HIF-1α and downstream genes [
23‐
25]. Despite such evidence for hypoxic activation of the HIF transcriptional cascade in osteosarcoma and Ewing's sarcoma cells, little is known regarding the effect of either HIF-1α or HIF-2α on the hypoxic phenotype of these cells. We have therefore analysed characteristics of the induction of HIF-1α, HIF-2α and HIF target genes in a panel of osteosarcoma and Ewing's sarcoma cell lines and investigated effects of isoform-specific HIF siRNA on the hypoxic phenotype of these cells.
Methods
Reagents
Tissue culture reagents were from Lonza (Wokingham, UK), except FBS (Invitrogen, Paisley, UK). Unless otherwise stated, reagents were from Sigma (Poole, UK). This study was approved by the Oxford Clinical Research Ethics Committee (C01.071).
Immunohistochemistry
A tissue array comprising 47 Ewing's sarcomas was constructed at the University of Dusseldorf. Additional sections were from the Nuffield Orthopaedic Centre. Formalin fixed sections were stained for HIF-1α (BD Biosciences, Oxford, UK), HIF-2α (EP190b, Abcam, Cambridge, UK), Glut-1 (Abcam) and cleaved caspase 3 (Cell Signalling Technology, Danvers, USA). Staining was visualized with the EnVision™ Peroxidase/DAB Rabbit/Mouse detection kit (Dako, Ely, UK). Image acquisition was performed using an Olympus BX40 microscope with 20× or 40× objective, Olympus DP70 camera and CellF. Tumours were considered positive for an antigen when ≥ 3 positive cells/field of view were observed at 20× magnification.
Cell culture
Cell lines were obtained from the EuroBoNeT cell line biobank, comprising recently characterised bone tumour cell lines [
26], and maintained in culture for < 30 passages. All cell lines were maintained in RPMI (except TC-71; IMDM) with 10% FBS, L-glutamine (2 mM), penicillin (50 IU/ml) and streptomycin sulphate (50 μg/ml) in a humidified atmosphere at 37°C (5% CO
2 in air). Hypoxic exposures were performed in 0.1% O
2, 5% CO
2, balance N
2 in a MiniGalaxy incubator (RS Biotech, Irvine, UK). Low glucose conditions were achieved using RPMI media without glucose, supplemented as for normal media, under normoxic conditions.
Western blotting
Cells were homogenized in lysis buffer (6.2 M urea, 10% glycerol, 5 M DTT, 1% SDS, protease inhibitors). Whole cell extract was separated by 8% SDS-PAGE and transferred to PVDF membrane. Primary antibodies were against HIF-1α, HIF-2α, Glut-1, Ki-67 (MIB-1, Dako) and β-tubulin. Immuno-reactivity was visualised with HRP-linked goat serum and chemiluminescence. Densitometric quantification of Ki-67, normalised to β-tubulin, was performed on scanned blots using ImageJ.
Luciferase assay
Cells at 60% confluence were transfected with a PGK-HRE-firefly luciferase reporter construct and the control pHRG-TK renilla luciferase plasmid (Promega, Southampton, UK) using Lipofectamine 2000 (Invitrogen). 24 h post-transfection cells were exposed to experimental conditions then lysed in Passive Lysis Buffer. Firefly and renilla luciferase were assayed using the Dual-Luciferase Reporter Assay System (Promega), with firefly luciferase values normalized to the renilla transfection control.
ELISA
Secretion of VEGF and TGFα was measured using the Human VEGF DuoSet and Quantikine Human TGFα Immunoassay (R&D Systems, Abingdon, UK) respectively.
Cell number, proliferation and apoptosis
Cellular apoptosis was assessed using the Apo-One Homogeneous Caspase-3/7 Assay (Promega), with apoptosis levels normalised to total cell number (CellTiter 96 Aqueous One Solution Cell Proliferation Assay, Promega). For quantification of mitotic index cells were fixed in formalin, stained for H&E and the number of mitotic figures was expressed as a percentage of total cell number in 4 random fields of view.
siRNA transfection
Small interfering RNA (siRNA) sequences against HIF-1
α (H1), HIF-2
α (H2) and HIF-1
α scrambled control (scr) were as described [
27] and obtained pre-annealed from Eurogentec. Cells at 40% confluence were transfected with 50 nM siRNA duplex using Lipofectamine 2000. Duplexes were removed after 24 h and cells treated as required.
Scratch migration assay
A scratch was made through cells at 90% confluence using a 20 ul pipette tip. Specific points of the scratch were photographed before and after exposure to experimental conditions. Wound width was measured in CellF and migration expressed as fraction wound closure.
Statistical significance
Results are expressed as mean ± SD of at least three independent experiments. Statistical analysis comprised one-way ANOVA using Bonferroni's multiple comparison as a post-hoc test, with results considered significant at p < 0.05.
Discussion
These results provide the first detailed description of HIF induction by micro-environmental conditions relevant to primary bone tumours in Ewing's sarcoma and osteosarcoma. We have described phenotypic effects of these conditions, outlining the HIF dependence of these phenotypes and differences between the two tumour types regarding these responses.
Work in many cell types describes HIF-1α as constitutively hypoxia-regulated and HIF-2α as more cell type specific, its transcriptional activation being influenced by micro-environmental conditions other than hypoxia [
30,
31]. Despite both isoforms sharing an identical core binding motif, the majority of HIF-regulated hypoxia-inducible genes are induced by HIF-1α alone or by a combination of both HIF-1α and HIF-2α [
27,
31‐
33]. Our results in ES cells reflect this, with HIF-regulated expression of VEGF, Glut-1 and PGK (the luciferase assay HRE) being mediated solely by HIF-1α. Also in accordance with previous results [
32,
34], inducible HIF-2α stimulated expression of HIF-2-specific genes, e.g. TGFα, suggesting that HIF-2α is functional in ES cells but that its effects are normally masked by HIF-1α to regulate the majority of HIF-dependent genes. In contrast, gene expression in OS cells was regulated by both HIF isoforms. Indeed, the observed shift towards relative transcriptional domination of HIF-2α places OS cells in a small group, including 786-0 renal cancer cells and the MDA-MB-435 melanoma cell line [
27,
28], displaying preferential utilisation of HIF-2α.
Hypoglycaemic induction of HIF-2α is the second transcriptional feature distinguishing ES and OS cell lines. Reports of HIF pathway induction under low glucose conditions suggest a specific role for HIF-2α, for example in neuroblastoma cell lines [
35]. Similarly, embryonic stem cells and pancreatic cancer cells under hypoglycaemia induced HIF target gene expression in a manner dependent on the HIFα dimerisation partner ARNT [
36], but independent of HIF-1α [
37]. Our results in ES cell lines also suggest a dominant role for HIF-2α in regulation of the HIF response to hypoglycaemia. Hypoxic stabilisation of HIF-1α is dependent on the presence of glucose [
38], which regulates translation via effects on the mTOR/Akt pathway [
39,
40]. The lack of a HIF transcriptional response to low glucose in OS cells may represent a differential sensitivity to glucose deprivation. This could be a consequence of the high levels of PAS
+ glycogen present in ES cells [
41] that might provide sufficient intracellular available glucose for translation of HIF under hypoglycaemic conditions.
Phenotypic effects of prolonged exposure to hypoxia and low glucose were similar in both cell types. Hypoxia did not affect cell number, despite evidence of increased apoptosis. Hypoglycaemia produced a ≥ 45% reduction in cell number, predominantly due to reduced cellular proliferation. The only previous reports on apoptosis in ES cell lines described A673 as resistant [
23] and SK-N-MC as sensitive [
42] to hypoxia-induced apoptosis. Our results for A673 and SK-N-MC show a 2 to 3-fold increase in apoptosis after 72 h at 0.1% O
2, longer exposure to more severe hypoxia potentially explaining the increased apoptosis in A673. Hypoxia-induced apoptosis of OS cells has not previously been reported, but was generally 2-fold greater than that in ES cell lines. There is considerably less data regarding hypoglycaemia-induced apoptosis [
43], suggesting that this is potentially a cell type-specific response which was largely absent from either ES or OS cell lines.
It is intriguing that both ES and OS cells were sensitive to hypoxia-induced apoptosis but that HIF siRNA had no effect on the apoptotic phenotype. In the majority of cells, hypoxia-induced apoptosis is mediated by HIF-1α [
23,
44,
45]. However there is an increasing literature suggesting that, in some cell types, apoptosis induced by severe hypoxia is HIF-1α-independent [
46,
47]. However, in ES
in vivo expression of HIF-1α and cleaved caspase 3 localised to areas adjacent to necrotic, and presumably hypoxic, tissue and HIF-1α has been correlated with the percentage of dead cells in OS tumours [
6]., This suggests some
in vivo relationship between HIF and apoptosis which we have been unable to dissect in the
in vitro situation.
The first phenotypic difference between ES and OS cell lines was the effect of HIF siRNA on hypoxic proliferation. Although overall proliferation rates were similar in normoxia and hypoxia in both cell types, HIF-1α siRNA enhanced proliferation 2 to 3-fold in ES cells whereas in 2/3 OS cell lines both HIF-1α and HIF-2α siRNA inhibited hypoxic proliferation. It is not uncommon for HIF-1α and HIF-2α to exert opposing phenotypic effects in different cell lines. For example, HIF-2α is necessary to maintain tumour growth in RCC4 renal carcinoma cells [
48], potentially via regulation of the cell cycle regulatory proteins TGFα and cyclin D1. It may also specifically promote proliferation by enhancing activity of the c-Myc oncoprotein [
49], in contrast to inhibition of cell cycle progression by HIF-1α counteracting c-Myc transcriptional activity [
50]. Conversely, in SW480 colon cancer cells, HIF-1α siRNA inhibits proliferation whereas HIF-2α siRNA increases anchorage independent growth [
51].
The second phenotypic difference between the two cell types encompassed hypoxic migration, which was inhibited in ES cells and maintained or increased in OS cell lines. In both cell types, however, HIF-2α siRNA stimulated hypoxic migration, suggesting an effect of HIF-2α to inhibit cell migration under hypoxia. There are many reports demonstrating migration to be dependent on either HIF-1α and/or HIF-2α in different cell types [
27,
51,
52], again demonstrating the ability of HIF-1α and HIF-2α to exert distinct phenotypic effects in different cell lines.
This data implicates hypoxia as the primary micro-environmental stimulus inducing expression of HIF and downstream genes in both ES and OS cells in culture. However, phenotypic results in both cell types suggest that hypoxia does not significantly increase either cell number or migration and, in addition, enhances tumour cell apoptosis. This does not correlate with clinical reports that hypoxia [
9,
16‐
18] and/or HIF-1α [
6‐
8] are predictive of poor outcome in these tumours. This may be due to antagonistic effects of genes downstream of HIF, which cancel each other out when manipulating the whole pathway
in vitro. For example, VEGF blockade decelerates the growth of experimental osteosarcoma [
53] and Ewing's sarcoma [
54], demonstrating the viablility of specific targeting of HIF downstream genes. Despite being currently unable to dissect specific mechanisms by which HIF promotes ES and OS progression
in vivo, we have identified features of the HIF pathway which distinguish the two cell types. This provides a solid platform from which to advance our understanding of the role of hypoxia and HIF in the biology of primary bone sarcomas.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
HJK designed the study, performed the experimental work and wrote the manuscript. KLS constructed the ES tissue microarray. UD collected samples and patient information for the tissue microarray. NAA conceived the study, contributed to the study design and writing of the manuscript and provided additional ES tissue sections. All authors read and approved the final manuscript.