Background
Growth of a tumor can be significantly influenced by its interactions with the surrounding stromal tissue. Endothelial and immune system cells that invade the tumor affect its rate of proliferation. Chemokines can act to attract cells of the immune system to the site of tumor growth. Monokine induced by interferon-γ (Mig) [
1], also known as CXCL9, is a chemokine that attracts T-cells and natural killer (NK) cells [
2]. Mig also has angiostatic properties [
3]. Overexpression of Mig in tumors can lead to T-cell accumulation, vascular damage, and tumor regression [
4,
5].
Egr-1 is a zinc-finger transcription factor that is inducible by radiation [
6], serum [
7], shear stress [
8], and other stimuli in a variety of cell types, including tumor cells [
9,
10]. Previous studies have examined the effects of manipulating Egr-1 in tumors. Overexpression of Egr-1 delivered via adenovirus resulted in reduced tumor growth and diminished expression of angiogenic factors in a mouse model [
11]. However, reduction of Egr-1 levels through use of a DNAzyme also resulted in slower tumor growth [
12,
13]. In some of these studies it was difficult to clearly distinguish the effects of the delivered reagents on tumor versus stromal tissue.
We have previously shown that Egr-1 knockout mice exhibit a defect in arteriogenesis, as illustrated by their greatly reduced capacity to recover hind limb blood flow after femoral artery ligation [
14]. We speculated that the absence of Egr-1 in the stromal tissue of mice might have an effect on tumor growth, possibly due to dysregulation of angiogenic signalling. Our present work shows that growth of at least some tumors is slowed in Egr-1 deficient mice, but with no apparent effect on angiogenesis. Instead, Mig accumulates in the tumor, along with NK cells.
Discussion
Our work demonstrates that the growth of subcutaneous LLC1 tumors in Egr-1
-/- mice is impeded. This impediment correlates with overexpression of Mig in the tumor, a phenomenon that is not observed in B16F10 tumors, which do not exhibit slower growth in Egr-1
-/- mice. Mig has previously been shown to slow the growth of tumors in various models. In a mouse model of Burkitt's lymphoma, intra-tumoral injection of Mig protein results in partial necrosis of the tumor [
5]. Likewise, adenoviral delivery of the Mig gene shrinks non-small cell lung carcinomas [
16]. Walser, et al. [
4], injected mice with mammary adenocarcinoma cells overexpressing Mig and found that these cells formed smaller tumors than the parental cell line. Our antibody array analysis (figure
2) examined expression of several genes potentially regulated by Egr-1, including bFGF [
17], TNF-α [
18], IGF-II [
19], and M-CSF [
20], but there was no significant alteration in expression of these genes between groups.
CXCR3 serves as a receptor for Mig, as well as for related chemokines IP-10 (CXCL10) [
21] and I-TAC (CXCL11) [
22]. It is expressed on T-cells and NK cells. We were somewhat surprised that there was not a greater degree of T-cell infiltration in the tumors grown in Egr-1
-/- mice, but there may have been dysregulation of other chemokines that were not assayed on our antibody array, and these may have influenced the degree of lymphocyte invasion and activation. Also, our analysis looks at one time point, and we cannot exclude the possibility T-cells may be involved at earlier or later time points. While we cannot conclude from our data that NK cells were responsible for the slower tumor growth that we observed, others have implicated NK cells in Mig-mediated tumor inhibition [
23] and have shown that NK cells recruited by Mig impair metastasis [
4]. Also, Wald, et al. [
24] showed that growth of Lewis lung carcinoma tumors is impaired in an NK cell-dependent manner in response to IFN-γ, which stimulates production of Mig.
The connection between the lack of Egr-1 and overexpression of Mig is unclear. We are not aware of any literature suggesting that Egr-1 directly regulates Mig, or whether other Egr family members play a role in its expression. Mig is not produced in the tissue underlying the tumor, nor is it systemically higher in the knockout mice, which suggests that it is being produced in the tumor mass itself. Since the injected tumor cells are identical in the two types of animals, we hypothesized that Mig is produced from a host-derived cell that invades the tumor, and our colocalization experiment with a macrophage marker, CD68, confirms this. Previous studies have shown that monocyte/macrophages develop normally in Egr-1
-/- mice [
25], and respond to stimulus with lipopolysaccharide similarly to wild type monocytes [
26]. We were unable to detect any difference in the expression of Mig in monocytes from knockout mice, but we cannot exclude the possibility that macrophages exposed to the tumor environment may express Mig aberrantly.
We originally hypothesized that there might be a difference in blood vessel growth in the knockout mouse tumors, based on our previous work showing a defect in arteriogenesis in these animals [
14]. However, the antibody array revealed no differences in expression of common angiogenic growth factors like VEGF and bFGF. Mig is reported to have an angiostatic effect [
3], and disrupted blood vessel growth has been implicated as a factor in the mechanism for Mig-mediated tumor shrinkage in some studies [
5,
16]. But experiments with breast adenocarcinomas [
4] and lung carcinomas [
27] have failed to find changes in angiogenesis in Mig-treated tumors. The immunohistochemical staining we employed to measure vascular density did not detect any difference in vascularity, though we cannot rule out subtle effects on vessel growth. Given that Egr-1 can potentially regulate expression of hundreds of genes [
28], other factors may have compensated for any angiostatic effects of Mig in our model.
Both over- and under-expression of Egr-1 can impede tumor growth. In a mouse fibrosarcoma model, anti-tumor and anti-angiogenesis effects were observed in response to injection of an adenovirus encoding Egr-1 [
11], but the gene was delivered to both tumor and stroma. Other researchers have shown that reducing Egr-1 expression in human breast cancer cells can dampen their growth and invasiveness [
12]. Fahmy, et al. [
13] used DNAzymes to block expression of murine Egr-1 in nude mice injected with the human breast cancer cell line MCF-7. They found a reduced rate of tumor growth, which they attributed to inhibition of angiogenesis. But since this experiment was performed in athymic nude mice, the role of the immune system is uncertain. Another study examined tumor development in mice genetically predisposed to prostate cancer that had been crossed with Egr-1
-/- mice. This study showed a decreased progression of the tumor from carcinoma in situ to invasive carcinoma, though initial growth rate and vascularity were unaffected [
29]. Again, both tumor and stroma lacked Egr-1, making it difficult to assess the contribution of these two compartments. Our work stands apart from these previous efforts in that we have looked at the effect of eliminating Egr-1 in the stroma alone using an immunocompetent animal. Doing so has allowed us to uncover a previously undescribed involvement of Egr-1 in Mig regulation and natural killer biology.
A limitation of our study is that our work does not tell us whether Mig is the primary causative agent involved in the reduction of tumor growth seen in the knockout mice. The fact that the B16F10 tumors do not overexpress Mig and also do not exhibit growth inhibition suggests that Mig might be playing a role. The reason for the lack of Mig expression in the B16F10 melanomas is unclear, but we note that the antibody array shows a dramatic difference between the two types of tumors in the expression of monocyte chemoattractant protein-1 (MCP-1). In both wild type and knockout mice, MCP-1 is absent in the melanomas but is so abundant in the LLC1 tumors that it saturates the array. We speculate that the lack of MCP-1 may affect monocyte activity in the B16F10 tumors, and hence Mig expression, but we cannot exclude other potential differences between the two types of tumors.
Methods
Mice and tumor model
Egr-1 knockout mice were obtained from Taconic and maintained on a C57Bl/6 background. Wild type C57Bl/6 mice were used as negative controls. All procedures were approved by the Stony Brook University Institutional Animal Care and Use Committee. Lewis lung carcinoma cells (LLC1) were obtained from ATCC (#CRL-1642) as were B16F10 melanoma cells (#CRL-6475). Both cell lines were maintained in Dulbecco's modified Eagle's medium with 10% fetal bovine serum. One million cells were injected subcutaneously in the flank in a volume of 50 μl of saline. Cells were filtered through a 70 μm filter prior to injection to remove any clumps.
Flow cytometry
Tumors were excised after 11–12 days of growth, weighed, and digested in 470 units/ml collagenase II and 167 μg/ml hyaluronidase in RPMI medium at 37° for 25 minutes. Single cell suspensions were obtained by trituration and the cells were labelled with antibodies against CD3 (eBioscience, phycoerythrin-labelled), NK1.1 (eBioscience, allophycocyanin-labelled) and CD45 (BioLegend, PerCP-labelled) as described in the text. In some cases, cells were also labelled with anti-CD11b antibodies (BioLegend, Alexa Fluor 488-labelled). After fixation with 10% formalin, cells were analyzed on a FACS Calibur (Becton, Dickinson). Blood cells were similarly measured in whole blood obtained via cardiac puncture from tumor-bearing mice at the time of euthanasia. Blood was cleared of erythrocytes by lysis in ACK lysing buffer (BioWhittaker).
Expression assays
Lysates were made from powdered frozen tumors and were subjected to analysis on a RayBiotech Mouse Angiogenesis Antibody Array I using the manufacturer's reagents and protocols. Mig levels were measured using a BD Cytometric Bead Array (Becton, Dickinson) on tumor lysates and on serum collected from tumor-bearing mice at the time of euthanasia. Protein in the lysates was measured using the DC protein assay (Bio-Rad).
Monocyte culture
Mouse spleens were crushed and forced through a 70 μm nylon filter and erythrocytes were lysed with ACK lysing buffer. The resulting cells were labelled with anti-CD11b antibodies (BioLegend, Alexa 488-labelled) and anti-Ly6c antibodies (Southern Biotech, phycoerythrin-labelled). Monocytes were sorted on a FACS Aria (Becton, Dickinson) and cultured in RPMI. IFN-γ was obtained from RayBiotech.
Immunohistochemistry
Tumors were frozen in optimal cutting temperature (OCT) medium, sectioned, fixed in methacarn, and stained using Alexa 488-labelled anti-CD68 (Serotec) and biotinylated anti-Mig (R&D Systems). The Mig staining was achieved using a tyramide staining kit (Invitrogen). Endothelial cells were stained on frozen sections using biotinylated anti-CD31 (eBioscience) and tyramide staining. Endothelial cell counting was performed by a blinded observer as described [
15].
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
GC assisted with labeling of cells for flow cytometry and harvesting tumors. CB contributed to the intellectual development of the work and to feasibility studies. GP performed the laboratory and animal work, developed the idea for the project, and wrote the manuscript.