Background
In the United States, renal cell carcinoma (RCC) is the seventh and ninth most common form of cancer in men and women, respectively, and a recent report estimates that in 2012, 40,250 men and 24,520 women will be diagnosed with, and 13,570 will die of, this disease [
1]. The therapeutic options for RCC have increased considerably since 2005, due to the availability of seven new agents [
2,
3] developed to interrupt the molecular pathways regulating tumor angiogenesis, cell proliferation, and survival. Treatments of metastatic RCC with these agents, which are inhibitors of vascular endothelial growth factor (VEGF) (bevacizumab), VEGF-receptors (VEGFR) (sorafenib, sunitinib, pazopanib, and axitinib), or mTOR (temsirolimus and everolimus), have a significantly improved survival, but remain palliative. Thus, a cure for metastatic RCC continues to be elusive, but is being pursued actively with various combination strategies. In this respect, it is noted that the time-honored, but not regulatory-approved, therapies with interferon-alpha (IFN-α) have had mixed results in RCC when used in combination with some of these agents. For example, IFN-α2b combined with sorafenib achieved an overall response rate of 33% in patients with metastatic disease [
4]; IFN-α2b combined with temsirolimus was not as effective as temsirolimus alone [
5]; and IFN-α combined with bevacizumab significantly increased progression-free survival and objective responses [
6]. One major challenge with IFN-α therapy, either alone or in combination, is the frequency with which IFN-α needs to be administered (6 to 10 ×10
6 U three times weekly). Another problem associated with IFN-α therapy was the adverse events, which include fatigue, fever, nausea, flu-like symptoms, and anorexia [
4,
6]. While pegylated IFN-α has allowed for less frequent dosing, many of the same toxic effects remain without appreciable improvement in patient outcome [
7,
8].
Inhibition of the mTOR kinase results in the reduction of regulatory proteins involved in the progression of cells from the G
1 to S-phase of their growth cycle [
9]. However, blocking mTOR activity with rapamycin (the prototype mTOR inhibitor) or rapamycin analogs inadvertently activates the Akt-signaling pathway [
9] through an IGF-1R-dependent mechanism [
10], which mitigates the anti-tumor effects of the mTOR inhibitors. Thus, the combination of an anti-IGF-IR antibody with mTOR inhibitors was shown to block the Akt-signaling pathway in rhabdomyosarcoma, breast, and prostate carcinomas, resulting in an additive increase in cell growth-inhibition [
9,
10].
IGF-1R-targeted therapy in RCC was implicated by an early finding of a greater than 10-fold reduction in tumor growth in mice bearing xenografts of human clear-cell RCC when administered with an antagonist to growth hormone-releasing hormone, which was attributed to a reduction of IGF-1 [
11]. Analysis of RCC tissue specimens showed the expression of both IGF-1 and IGF-IR in clear-cell-RCC, papillary-RCC, and chromophobe RCC [
12]. Overall, an association of IGF-1R expression and poor long-term patient survival was found, particularly among patients with high-grade tumors [
13]. Mutations in the von Hippel-Lindau (VHL) gene have been linked to hereditary kidney cancer and in 70% of non-hereditary clear-cell-RCC [
14]. It was shown that the wild type VHL encodes a 30-kDa protein that inhibits RCC metastasis and IGF-IR to form complexes with PKCδ, a protein kinase linked to cell proliferation and transformation [
15].
We have developed a humanized anti-IGF-1R antibody, hR1, which binds to IGF-1R without blocking binding of IGF-1 or IGF-2 to the receptor, yet effectively causes receptor down-regulation, and inhibits cell proliferation, colony formation, and cell invasion in a variety of cancer types, including breast, prostate, cervical, pancreatic, and rhabdomyosarcoma [
16]. Additionally, using the DOCK-AND–LOCK™ (DNL™) platform technology [
17,
18], a hexavalent form of hR1 (Hex-hR1) was engineered in which four hR1 Fabs were linked to hR1 IgG [
16]. Hex-hR1 and hR1 were found to have similar activity, although Hex-hR1 was more effective at down-regulating IGF-1R. Importantly, both hR1 and Hex-hR1 were able to significantly inhibit the anchorage-independent growth of two different RCC lines in soft-agar assays. When both hR1 and Hex-hR1 were combined with rapamycin treatment of mice bearing a human rhabdomyosarcoma, significant tumor growth inhibition was achieved in comparison to either agent used alone [
16].
This same DNL technology can be utilized to attach four molecules of IFN-α to hR1. It has already been demonstrated that by using this method with an anti-CD20 antibody, a significant improvement in therapeutic efficacy in mice bearing xenografts of human non-Hodgkin lymphoma is achieved when compared to either the parental antibody alone or peginterferon alfa-2a [
19]. By attaching the IFN-α2b to an antibody that targets the tumor, the therapeutic window of IFN-α should improve by concentrating IFN-α at the tumor, while at the same time decreasing the amount in the blood and normal tissues, where its toxicity manifests.
The known association of mTOR and IGF-IR signaling pathways, along with the correlation in IGF-1 and IGF-IR expression patterns in RCC, provide an attractive rationale for a combination therapy. Moreover, with current IFN-α treatments and the added benefit already observed in a rhabdomyosarcoma tumor model with an anti-IGF-IR antibody enhancing the therapeutic effects of mTOR inhibitors or to specifically target IFN-α to a tumor, there is the potential to provide a new combination therapy for metastatic RCC. We report here that a screening of eight different human RCC cell lines reveals that all eight express IGF-1R at varying levels. Sensitivity to IGF-1 stimulation and growth-inhibitory effects of hR1 or Hex-hR1 are related to this expression. The hR1-IFN-α2b DNL product, 1R-2b, was found to have activity similar to recombinant human IFN-α and could inhibit RCC growth with EC50-values in the picomolar range. Importantly, there is a strong synergistic effect when hR1, Hex-hR1, or 1R-2b is combined with the rapamycin analog, temsirolimus.
Methods
Cell lines, antibodies, and reagents
All cell lines were purchased from American Type Culture Collection, except CAL-54 and RH-30, which were obtained from the Deutsche Sammlung von Mikroorganismen und Zellkulturen. Humanized antibodies, including hR1, hA20 (anti-CD20), hRS7 (anti-Trop-2), and h225 (anti-epidermal growth factor receptor (EGFR)), were provided by Immunomedics. Recombinant human IGF-1 and murine anti-human IGF-1R MAb (MAB391) were obtained from R&D Systems. Phospho-specific antibodies and other primary antibodies were acquired from Cell Signaling or Santa Cruz Biotechnology. Horseradish peroxidase (HRP)-conjugated secondary antibody and One Solution Cell Proliferation assay (MTS) were obtained from Promega. FITC-conjugated secondary antibodies were from Jackson ImmunoResearch Laboratories. PhosphoSafe Extraction Reagent and RIPA buffer used for cell lysis were obtained from EMD Biosciences and Cell Signaling, respectively. Cell culture media, supplements, and bovine transferrin (holo form) were purchased from Invitrogen. Temsirolimus (Wyeth) was purchased from Florida Infusion. Recombinant human Interferon-α2a (rhIFN-α2a, Millipore), peginterferon alfa-2b (Schering) and peginterferon alfa-2a (Hoffmann-La Roche) were purchased. Protein Assay Dye Reagent Concentrate was from Bio-Rad. All other chemicals were purchased from Sigma.
Cell culture
RCC cell lines 769-P and 786-O were maintained in RPMI-1640 medium. For CAL-54, A-498, A-704 and ACHN, Eagle’s MEM medium was used, and for Caki-1 and Caki-2, McCoy’s 5a medium. All three media were supplemented with 10% heat-inactivated fetal bovine serum (FBS), 1% GlutaMax, 1% non-essential amino acids, and 1% sodium pyruvate. Cultures were maintained at 37°C in 5% CO2 and medium changed at least once weekly. Only cells with fewer than 50 passages were used for experiments.
Generation of Hex-hR1 and 1R-2b by DNL
The preparation of Hex-hR1 has been described [
16]. 1R-2b was prepared as described for 20-2b [
19] by reacting C
H3-AD2-hR1-IgG, instead of C
H3-AD2-hA20-IgG, with IFN-α2b-DDD2. The molecular integrity and product purity of Hex-hR1 and 1R-2b were determined by size-exclusion high performance liquid chromatography (SE-HPLC) on a Beckman System Gold Model 116 with a BioSep-SEC-s3000 column (300 × 7.80 mm) of Phenomenex using 0.04 M PBS (pH 6.8) plus 1 mM EDTA as the mobile phase.
Surface IGF-1R expression by flow cytometry
Each sample was prepared in duplicate to contain 2×105 cells and 67 nM of a test antibody in a final volume of 200 μL. After incubation at 4°C for 45 min, samples were washed twice with PBS-1% BSA, followed by the addition of FITC-GAH IgG, (H + L), and a further incubation at 4°C for 45 min in the dark. Samples were washed twice with PBS-1% BSA, resuspended in 500 μL of PBS-buffered formalin, and analyzed on FACScan.
Cell proliferation assay
All cell incubations were performed at 37°C in a humidified 5% CO
2 incubator. Cells were detached with trypsin, washed three times with PBS to remove any trace of serum, and resuspended in a serum-free medium containing 10 μg/mL of bovine transferrin (SFM-Trf). Cells were seeded at 1×10
3 cells/50 μL/well and incubated overnight. On the following day each test article in SFM-Trf was 5-fold serially diluted from 400 nM to 0.001 nM and 50 μL of each concentration were added in triplicate to the wells, such that the final concentrations of the test article ranged from 200 nM to 0.0005 nM. Untreated control cells received only 50 μL of SFM-Trf. After incubation for 1 h, designated wells received 100 μL of each test article at the same concentration in SFM-Trf containing 50 ng/mL of IGF-1. Plates were then incubated for a period of time as indicated and cell viability assessed using the MTS assay as per the manufacturer’s protocol. Growth inhibition was measured as a percent of growth relative to untreated cells using Microsoft Excel and Prism GraphPad Software (v4.03; Advanced Graphics Software, Inc.). Combinatorial Index (CI) was calculated by median effect analysis [
20,
21] to determine synergism (CI < 0.9), additivity (1.1 > CI > 0.9), or antagonism (CI >1.1).
Immunoblot analysis
Unless otherwise stated, cells were starved in serum-free medium for 24 h, treated, and lysed at ice-cold temperature in a buffer as specified. Protein concentrations were determined by the Bio-Rad Protein Assay and samples (20 μg loaded in each lane) were separated on 4-20% Tris-Glycine gels, transferred to PDVF or nitrocellullose membranes, blocked with TBST buffer (50 mM Tris pH 8.0, 150 mM NaCl, 0.1% Tween 20) containing 5% nonfat milk, washed with TBST buffer, and incubated overnight at 4°C with primary antibodies. The membranes were then washed in TBST four times (once for 15 min and three more for 5 min each), incubated with HRP-conjugated secondary antibodies for 1 h at RT, washed in TBST buffer four times as described above, then detected with Super Signal West Dura Extended Duration Substrate (Thermo Scientific) according to the directions provided by the manufacturer. The immunoblot signals were visualized with a chemiluminescence system (Thermo Scientific). Digital images were processed by Carestream (Carestream Molecular Imaging).
Down-regulation of IGF-IR
Cells were seeded at 1×106 per well in a 6-well plate and cultured overnight for attachment. On the next day, the medium was replaced with fresh media containing a test article of interest at indicated concentrations and cells were further incubated as indicated. Treated cells were washed with cold PBS, scraped from the dishes, collected, and centrifuged at 4°C at 2,000 rpm for 5 min. Cells pellets were lysed for 10 min on ice in RIPA buffer or a buffer consisting of 25 mM Tris (pH 8), 150 mM NaCl, 1 mM EDTA, 1% Triton and 1 X Complete, EDTA-free Protease Inhibitor Cocktail (Roche Diagnostics). The lysates were clarified by centrifugation, assayed for protein concentration, and analyzed by immunoblotting.
Detection of IGF-1R/IR hybrid
Cells grown in T150 flasks were washed twice with ice-cold PBS and scraped by adding ice-cold lysis buffer. Lysates were centrifuged for 15 min at 13,000 × g at 4°C. Supernatants were assayed for protein content using the BCA assay kit. Aliquots of 500 μg of total protein in equal amount of lysis buffer were pre-cleared with protein A beads (Cell Signal Technology) for 2 h. The pre-cleared lysate was incubated overnight at 4°C with anti-IGF1R antibody (MAB391,1:100, Santa Cruz Biotechnology). Samples were then incubated with 40 μL of protein A beads for 2 h. The beads were washed four times with lysis buffer and collected by centrifugation. Beads were resuspended in 2× sample buffer and boiled for 5 min. A 20-μL aliquot of the supernatant was subjected to gel electrophoresis and Western blotting with an anti-insulin receptor-β antibody (anti-IR-β) to detect heterodimers. As a control for the presence of IGF-1R in the immunoprecipitated samples, the blots were also probed with an anti-IGF-1Rβ antibody. IR-β levels were assessed by running 25 βg from the same lysates used for immunoprecipitation and probed with anti-IR-β antibody. Loading control was β-actin.
Determination of IFN activity
Two different assays were utilized to determine the specific activity of 1R-2b. The first used the luciferase reporter gene assay (iLite kit; PBL InterferonSource) following manufacture’s instructions in which rhIFN-α2a was used as a standard for activity. A second measure of activity tested the ability of IFN-α2a to mediate the phosphorylation of STAT1, AKT or ERK1/2 in ACHN cells. Briefly, cells (5 × 105 per well) were grown in 10% FBS medium in 6-well plates overnight for attachment. Medium was changed and interferon (rhIFN-α2a or 1R-2b) was added at the indicated concentrations. At indicated times, cell lysates were prepared and resolved by SDS-PAGE, transferred to nitrocellulose membranes and probed with appropriate anti-phospho antibodies (p-STAT1, p-ERK1/2, p-AKT) or anti-NUB1. Loading controls utilized antibodies to unphosphorylated proteins (STAT1, ERK1/2, AKT) or to β–actin (NUB1).
Statistical analysis
Results are shown as means ± standard deviations. Statistical differences between two values were determined by Student’s t-test. A value of P < 0.05 was considered statistically significant.
Discussion
Among kidney cancer types, approximately 90% are RCC, in which clear-cell-RCC comprises approximately 75% of all cases, and papillary RCC makes up an additional 15%. Patients present with metastatic disease 30% of the time. Unfortunately, patients with metastatic RCC have a poor prognosis, since it has remained resistant to both radiotherapy and chemotherapy [
14].
Current treatments for metastatic RCC include IFN-α [
7,
8,
26], RTK inhibitors, for example, sorafenib, sunitinib, and temsirolimus [
4,
5,
27], and anti-VEGF receptor antibodies, such as bevacizumab [
6]. These agents have been tested alone and in combinations, with some improvement in clinical outcomes.
Another approach focuses on IGF-IR as a potential therapeutic target [
11‐
13,
15]. There is evidence of an autocrine-paracrine loop in RCC growth [
12], and that the expression of IGF-IR and one of its ligands, IGF-1, has a positive association with poor survival of patients with high-grade tumors [
13]. By blocking IGF-IR signaling, it was shown pre-clinically that RCC growth could be reduced significantly [
11] and cell invasiveness inhibited [
15]. We have demonstrated that hR1 binds to multiple tumor types, including RCC [
16]. Additionally, a hexavalent form of hR1 (Hex-hR1) was created by the DNL™ -platform technology. DNL explores a pair of distinct protein domains involved in the natural association between cAMP-dependent protein kinase (PKA) and A-kinase anchoring proteins (AKAPs), which can serve as linkers for site-specific conjugation of an immunoglobulin to either two dimers of IFN-α2b or four Fab fragments of an immunoglobulin, resulting in a hexavalent antibody [
17‐
19]. Recently, in a variety of solid tumor lines, including breast, colon, and prostate, both hR1 and Hex-hR1 were shown to cause receptor down-regulation, inhibiting cell growth and invasiveness. It was noted that Hex-hR1 was much more effective at receptor down-regulation than the parental hR1. Additionally, they could both inhibit colony formation and growth in soft-agar of two human RCC cell lines [
16]. In the present study, hR1 and Hex-hR1 were likewise very effective at mediating down-regulation of IGF-1R in RCC. Also, as was noted in other solid tumor lines, Hex-hR1 was more effective than hR1 at mediating receptor down-regulation at picomolar concentrations, suggesting that it may be a more potent anti-tumor agent than its parental hR1 antibody.
In human breast cancer, of 41 different cell lines tested, only 7 were sensitive to the growth-inhibitory effects of an anti-IGF-1R antibody [
23]. Two of the main factors cited as predictive for anti-IGF-1R treatment were expression of IGF-1R and growth-stimulatory effects of IGF-1. In addition, the presence of IGR-1R and IR-β heterodimers in hepatic and gastric cell lines has been linked to sensitivity to anti-IGF-1R antibodies [
22]. A panel of eight different human RCC cell lines was screened by FACS with hR1 for surface expression of IGF-1R and by Western blotting for IGF-1R/IR-β hybrid receptors. While all eight expressed IGF-1R, this expression varied between the cell lines, from a high in Caki-2 to a low in A-498. Conversely, only three of the RCC lines expressed the IGF-1R/IR-β heterodimer (A704, Caki-1 and CAL-54). We found that, like the breast cancer lines, RCC lines varied in their sensitivity to IGF-1 stimulation. Except for ACHN, which had IGF-1R expression similar to Caki-2, the other cell lines tested fell in the order of the higher the IGF-1R expression, the greater the effect of IGF-1 stimulation. Expression of the IGF-1R/IR-β hybrid receptor did not correlate with increased sensitivity to IGF-1 stimulation. For example, A-704, which has the heterodimer, had a lower response to IGF-1 than did Caki-2, which did not demonstrate the presence of the hybrid receptor despite expressing both IGF-1R and IR-β. To further test whether this stimulation by IGF-1 translated to growth-inhibitory effects of an anti-IGF-1R treatment, cell lines that were very sensitive (Caki-2), moderately sensitive (786-O), and with low sensitivity (ACHN) to IGF-1 treatment were incubated with hR1 or Hex-hR1 in the presence of IGF-1. As predicted by the stimulation experiment, both Caki-2 and 786-O demonstrated greater growth-inhibition by hR1 than did ACHN. Interestingly, Caki-2 also had the lowest EGFR expression and ACHN one of the highest. Over-expression of EGFR relative to normal kidney tissue has been documented in patient RCC samples, and is thought to be associated with the transformation of normal renal tissue to malignancy [
28]. Additionally, it is known that both the IGF-1R and EGFR signaling pathways overlap, and both make use of phosphatidylinositol-3 kinase (PI3-K) and growth factor receptor bound protein 2 (Grb2) signaling pathways [
29]. It is possible that in cell lines with high EGFR surface expression relative to IGF-1R, there may be less reliance on IGF-1 and therefore less sensitivity to the stimulatory effects of IGF-1. This was noted in hepatocellular carcinoma lines, in which resistance to anti-IGF-1R treatment was associated with increased signaling through EGFR pathways, and that this resistance was overcome by targeting both IGF-1R and EGFR [
30]. It should be noted that the rhabdomyosarcoma line, RH-30, has the same surface expression of IGF-1R and EGFR when examined by FACS (data not shown). This same cell line was extremely sensitive to IGF-1, with growth-stimulation more than 10-fold above cells grown in SFM. We have demonstrated previously that this same cell line was inhibited in cell migration assays by hR1 and could be inhibited in its growth
in vivo by both hR1 and Hex-hR1 [
16]. These data suggest that EGFR expression levels relative to IGF-1R also may be predictive of sensitivity of RCC to monotherapy with an anti-IGF-1R antibody, and that targeting both IGF-1R and EGFR would be a rational approach in RCC.
While hR1 had modest effects at inhibiting cell growth, Hex-hR1 had a greater effect on RCC, even on the resistant ACHN cell line. This could be linked to the observation that the hexavalent form of hR1 is more effective at mediating down-regulation of IGF-1R than the parental hR1. Interestingly, MAB391, whose mechanisms of action include blocking IGF-1 from binding to IGF-1R as well as down-regulation of IGF-1R [
24], also was as effective as Hex-hR1 at inhibiting cell growth. However, it is noted that excess IGF-1 could reverse the IGF-1-mediated signaling events blocked by MAB391 [
24].
It has been observed that in cancer cells treated with rapamycin, a negative feedback resulted in which p-AKT levels increased in the cells [
9,
10]. Even under serum-free conditions, when IGF-1 was added to cultures, rapamycin-induced growth-inhibition was reversed and cell proliferation resumed at untreated levels [
9]. One way this feedback was prevented was to treat cells with anti-IGF-1R antibodies. When rapamycin treatment was combined with anti-IGF-1R antibodies, an additive effect was achieved [
9,
10]. Consistent with these findings and using a similar system with RCC, cells treated with hR1 or Hex-hR1 plus temsirolimus resulted in a synergistic growth-inhibitory effect. A higher degree of growth-inhibition was achieved with Hex-hR1 when combined with temsirolimus, in which a greater than 130-fold improvement in the IC
50 of temsiroliumus could be attained under these conditions. Such a combination had previously been tested
in vivo in which hR1 and Hex-hR1 could significantly inhibit the growth of a rhabdomyosarcoma when each was used with rapamycin [
16]. These combinations demonstrated more efficacy than when any of the three agents were used alone, and provide the rationale for such a combination in RCC.
As noted previously, efforts have also been made to use cytokine therapy, in particular IFN-α, either alone or with other treatment modalities to improve patient outcomes [
4‐
8]. However, one of the limitations of systemic treatment with IFN-α is the adverse events associated with the therapy [
4,
6‐
8]. We have previously used the DNL method to incorporate four molecules of IFN-α into veltuzumab, an anti-CD20 antibody currently in clinical development, and shown that the resulting 20-2b had greatly improved pharmacokinetics (PK) when compared to pegylated IFN-α. We also showed that the tumor targeting ability of 20-2b allowed for a low therapeutic dose to be administered in lymphoma models [
19], suggesting a high therapeutic window for this immunocytokine. In the present study, we explored the potential of 1R-2b, a new DNL-based immunocytokine comprising hR1 IgG and four IFN-α molecules, for use against RCC. 1R-2b had a specific activity similar to peginterferon alfa-2b and superior to peginterferon alfa-2a. When compared to IFN-α, 1R-2b had the same ability to mediate phosphorylation of STAT1, AKT and ERK1/2 at comparable concentrations. Additionally, 1R-2b could inhibit the growth of two different RCC lines in a similar manner as free IFN-α, indicating that the IFN-α on 1R-2b is fully functional.
This growth-inhibitory effect by IFN-α has been demonstrated previously in several human RCC lines, including ACHN and 786-O [
25]. One main mechanism of action of IFN-α described in these RCC lines is the up-regulation of the NEDD8 ultimate buster I (NUBI) protein. There is a positive correlation in NUBI up-regulation and cell growth inhibition in RCC [
25]. NEDD8 is an ubiquitin-like molecule that covalently binds to several different proteins including the VHL protein (pVHL) [
31]. Normally, pVHL targets proteins in the hypoxia-inducible factor (HIF)-α family for ubiquitination and subsequent destruction. Defects in this gene, as in many RCC tumors, result in the accumulation of HIF proteins which in turn activate other growth factor genes that promote angiogenesis and cell proliferation associated with RCC [
32]. NEDD8 covalently binds to pVHL and modifies it to allow for the proper assembly of the fibronectin matrix, but failure to bind does not affect the ability of pVHL to ubiquinate HIF [
31]. In pVHL mutants, failure of fibronectin assembly is associated with an undifferentiated phenotype in RCC [
33]. RCC cells treated with IFN-α exhibit an up-regulation in cyclin E and p27 and the down-regulation of NEDD8, which results in the accumulation of cells in S-phase and induction of apoptosis. It is thought that the NEDD8 conjugation system plays a role in the ubiquitination of p27 and cyclin E such that NUBI-mediated degradation of NEDD8 induces growth arrest and apoptosis of RCC [
25]. When ACHN and 786-O were exposed to 1R-2b, there was a greater than 2-fold increase in NUB1 expression. However, while rhIFN-α2a had a similar effect in 786–0, in ACHN 1R-2b mediated a higher increase in expression levels than what was observed with rhIFN-α2a. Likewise, similar to what was reported previously [
25], a correlation between NUB1 expression and growth inhibition was observed with 1R-2b in ACHN, in that 1R-2b resulted in a significantly greater degree of growth inhibition when compared to rhIFN-α2a.
Inhibition of mTOR likewise affects the cell cycle, with a down-regulation of cyclin D and the inability to progress from G
1 to S-phase [
5]. There is also evidence that Type I IFNs, such as IFN-α, may have parallel AKT/mTOR signaling pathways that promote growth-inhibitory signals [
34], and that by blocking mTOR it may antagonize the effect of IFN-α treatment. To determine if this action by IFN-α would have an added or antagonistic effect when combined with the mTOR inhibitor, temsirolimus, RCC cells were incubated with both temsirolimus and 1R-2b. This combination proved to be very potent, with a synergistic effect observed at a 1R-2b concentration as low as 2.6 nM. These data indicate that even if IFN-α used the mTOR pathway in parallel to inhibit cell growth in RCC, it must play only a minor role, because blocking such activity by temsirolimus did not blunt the effect of 1R-2b, and actually worked in synergy with it to inhibit cell growth. Given the improved PK profile of the MAb-2b construct in comparison to PEGylated-IFN-α [
19] and its added ability to potentially target the IFN to the tumor, 1R-2b should have the ability to be active clinically at doses substantially lower than currently administered IFN-α. Moreover, this synergistic effect, when combined with temsirolimus, provides the rationale for clinical use of 1R-2b to mitigate the dose-limiting toxicity associated with systemic administration of IFN-α when used in concert with RTK inhibitors.
In summary, monotherapy with mTOR inhibitors has met with only modest effects clinically due mainly to the ability of some cancer cells to use signaling pathways upstream and parallel to mTOR to overcome this inhibition [
35]. Two such upstream pathways originate with IGF-1R, which will activate Akt and Ras when bound by its ligand [
36]. It has been demonstrated that depletion of RCC cells of IGF-1R with small interfering RNA (siRNA) enhanced the sensitivity of these cells to the inhibitory effects of rapamycin [
37]. Here we show that this same effect in RCC can be accomplished with hR1 and Hex-hR1. We believe that by using hR1 or Hex-hR1 to down-regulate IGF-1R in combination with temsirolimus, multiple proliferation pathways are blocked, leaving RCC little chance to bypass them and escape death. In a similar fashion, 1R-2b may affect a cell’s ability to progress through a normal cell cycle by the accumulation of cyclin E and p27, resulting in arrest at the S-phase [
25]. Inhibition of mTOR also will block a normal progression through the cell cycle by the down-regulation of cyclin D [
5]. Again, by combining 1R-2b with temsirolimus, two different pathways that lead to normal progression through the cell cycle may be affected, resulting in cell cycle arrest and inhibition of cell growth.
Authors’ contributions
Conceived and designed the experiments: TMC, DMG, CHC. Performed the experiments: PT, RA. Analyzed the data: TMC, CHC, PT, RA. Contributed reagents/materials: CHC. Wrote and revised the paper: TMC, DMG, CHC. Provided financial support: DMG. All authors read and approved the final manuscript.