Could recombinant insulin compounds contribute to adenocarcinoma progression by stimulating local angiogenesis?

Abstract

Aims/hypothesis

Negative effects on the progression of adenocarcinomas by hyperinsulinaemia and the insulin analogue glargine (A21Gly,B31Arg,B32Arg human insulin) have recently been suggested. Most actions of this insulin analogue have hitherto been explained by direct stimulation of growth potential of neoplastic cells and by its IGF-1 related properties. However, insulin-stimulated angiogenesis could be an additional factor involved in tumour progression and clinical outcomes associated with cancer.

Methods

Five types of human adenocarcinoma (breast, colon, pancreas, lung and kidney) were evaluated for the presence of insulin receptors (IRs) on angiogenic structures. In an in vitro angiogenesis assay, various commercially available insulin compounds were evaluated for their potential to increase capillary-like tube formation of human microvascular endothelial cells (hMVEC). Insulin compounds used were: human insulin, insulin lispro (B28Lys,B29Pro human insulin), insulin glargine and insulin detemir (B29Lys[e-tetradecanoyl],desB30 human insulin).

Results

Insulin receptors were found to be strongly expressed on the endothelium of microvessels in all evaluated adenocarcinomas, in addition to variable expression on tumour cells. Low or no detectable expression of IRs was seen on microvessels in extratumoral stroma. Incubation with commercially available insulin compounds increased capillary-like tube formation of hMVEC in vitro.

Conclusions/interpretation

Our results suggest that all tested insulin compounds may stimulate tumour growth by enhancing local angiogenesis. Future studies need to confirm the association between insulin therapy in type 2 diabetes and tumour progression.

Introduction

Recent retrospective studies suggest that patients with type 2 diabetes who use the insulin analogue insulin glargine (A21Gly,B31Arg,B32Arg human insulin) might have an increased risk of developing cancer. Hemkens et al. found a positive association between daily insulin dosage and the incidence of malignant neoplasms. Interestingly, this association was present for human insulin and insulin analogues such as glargine, lispro (B28Lys,B29Pro human insulin) and aspart (B28Asp human insulin). Moreover, after adjusting for insulin dose, they found a dose-dependently increased risk of cancer in patients treated with insulin glargine compared with patients treated with human insulin with an adjusted hazard ratio of 1.31 (95% CI 1.20–1.42) for a daily dose of 50 IU [1]. In another report, Jonasson et al. mentioned that patients taking insulin glargine had an almost twofold increased risk of breast cancer compared with patients using other types of insulin [2]. The SDRN Epidemiology Group observed a similarly increased risk, but attributed this to an allocation bias [3]. A study by Currie et al. showed no association between insulin analogues and cancer progression as compared with human insulin, but did show that patients using any kind of insulin had a higher risk of developing adenocarcinomas than those on metformin [4].

An important point to elucidate in this context is the pathophysiological mechanism through which insulin could be involved in tumour progression. In their editorial accompanying the above-mentioned articles, Smith and Gale [5] noted that it is surprising that these studies were able to detect differences in cancer rates after only a few years of insulin exposure, because cancer takes many years to develop. Supported by existing literature, they suggest that, if insulin does indeed influence cancer incidence, this is possibly due to stimulatory effects on pre-existing malignant foci rather than to de-novo carcinogenesis. Insulin is known to augment mitogenesis and proliferation of distinctive cell types and its effect can be mediated through insulin receptors (IRs), insulin like growth factor-1 (IGF-1) receptors (IGF-1Rs) or hybrid IR-IGF-1Rs. IRs and IGF-1Rs are frequently present on pre-existing tumour cells and this could give insulin a molecular pathway to contribute to tumour expansion [5]. However, we recently showed that IRs are also abundantly present on angiogenic structures in human atherosclerotic plaques suggesting a biological role of insulin on local angiogenesis [6]. Furthermore, it has been shown that insulin is involved in angiogenesis during wound healing [7]. We therefore hypothesised that such a mechanism might also be involved in tumour expansion and tumour growth.

We analysed whether IRs are expressed on angiogenic structures in adenocarcinomas. In addition, we evaluated the effect of commercially available human insulin and insulin analogues on capillary-like tube formation of human microvascular endothelial cells (hMVEC) in vitro.

Methods

Collection of specimens

Tissue was obtained from archival material of resection specimens in accordance with guidelines set out by the ‘Code for Proper Secondary Use of Human Tissue’ of the Dutch Federation of Biomedical Scientific Societies. Included were adenocarcinomas from breast (n = 15), colon (n = 15), pancreas (n = 15), lung (n = 15) and kidney (n = 15). As a control, we investigated peritumoural parenchyma of the included specimens, especially of those known to be insulin-sensitive (kidney and pancreas).

Immunohistochemical analysis

All specimens were routinely fixed in buffered formalin and embedded in paraffin. After heat-induced epitope retrieval in Tris-EDTA pH 9.0 (20 min at 98°C), anti-IR β-subunit antibody (1 μg/ml, 60 min, room temperature; Millipore/Chemicon, Temecula, CA, USA) and anti-IGF1-R α-subunit antibody (0.5 μg/ml, 60 min, room temperature; Millipore/Chemicon) were immunostained using a three-step polymer detection system (ImmunoLogic, Duiven, the Netherlands). Horseradish-peroxidase activity was visualised in brown with diaminobenzidine (DAB+; Dako, Glostrup, Denmark). Negative controls consisted of concentration-matched isotype controls (Dako).

Expression of IRs on endothelial and epithelial cells within adenocarcinoma and in surrounding tissue was assessed using a semi-quantitative score: 0 = no IR expression, 1 = minimal IR expression, 2 = moderate IR expression, 3 = strong IR expression.

Immuno double-staining combining anti-IR antibody in red (Vector Red; Vector Laboratories, Burlingame, CA, USA) and anti-CD31 (Dako) antibody in blue (Vector Blue) was performed with the sequential double alkaline phosphatase method [8].

Spectral imaging

Analysis of double staining slides was performed with spectral imaging using a multispectral imaging system (Nuance VIS-FL; Cambridge Research Instrumentation, Woburn, MA, USA). Data sets were acquired from 420–72 nm at 20 nm intervals. Spectral library of single-Vector Red and single-Vector Blue was used to unmix the double staining into the individual components. Using Nuance software version 2.8 (Cambridge Research Instrumentation), an exclusive image of IR/CD31 co-localisation as well as fluorescent-like pseudo-coloured images were created [9].

In vitro angiogenesis

Individual human foreskin MVEC (hMVEC), obtained from three different donors, were confluently seeded in M199 supplemented with 10% (vol./vol.) heat-inactivated human serum and 10% (vol./vol.) newborn calf serum on a three-dimensional fibrin matrix, prepared with 2 mg/ml fibrinogen (Calbiochem, La Jolla, CA, USA) and 0.1 U/ml thrombin (Organon, Boxtel, the Netherlands), as previously described [10]. To study the effect of different insulin compounds and IGF-1 on capillary-like tube formation, hMVEC were stimulated with 10 ng/ml basic fibroblast growth factor (bFGF) (Peprotech, London, UK) and 10 ng/ml TNF-α (Sigma Aldrich, St Louis, MO, USA) in absence or presence of 1 × 10⁻⁹, 1 × 10⁻⁸ or 1 × 10⁻⁶ mol/l of human insulin (actrapid), short-acting insulin analogue (insulin lispro), long-acting insulin analogues (insulin detemir [B29Lys(e-tetradecanoyl),desB30 human insulin], insulin glargine) or IGF-1 (GroPep, Adelaide, Australia) in triplicate or quadruplicate. Medium was refreshed every other day. After 7 to 12 days of incubation, the formation of tubular structures was analysed by phase contrast microscopy and quantified with Optimas image analysis software (Media Cybernetics, Bethesda, MD, USA). The use of hMVEC was approved by the ethical committee of the VU University Medical Centre, Amsterdam, the Netherlands.

Statistical analysis

Semi-quantitative expression data were compared by means of the Wilcoxon matched-pairs signed-ranks test. Results from the in vitro angiogenesis experiments were combined and are presented as mean ± SEM. Statistical differences were determined by a paired t test, using Prism 4 (GraphPad, San Diego, CA, USA). p < 0.05 was considered to be statistically significant.

Results

Presence of insulin receptors (immunohistochemical evaluation)

The endothelium of microvessels in the tumour stroma of all examined tumour types was consistently and strongly positive for the IR, with much reduced or absent staining in the microvasculature of surrounding non-tumour stroma and parenchymal tissue, including that of insulin-sensitive tissues (kidney and pancreas; Fig. 1). The endothelial nature of this staining pattern was confirmed by double immunohistochemistry for the IR and CD31, aided by spectral imaging analysis. In addition, all tumour types showed variably cytoplasmic and/or membranous staining on epithelial cells for the IR, ranging from none to strong expression.

Fig. 1.

Immunohistochemical staining for the insulin receptor in colon (a), breast (b) and renal (c) adenocarcinoma (magnification ×400). Tumour cells are variably positive (*), whereas neovessels in the tumour stroma are invariably strongly positive (arrows). Double-staining (magnification ×200) demonstrates colocalisation (purple, arrows) for the IR (red) and CD31 (blue) in neovessels in the tumour stroma in breast (d) and kidney carcinoma (g), which was confirmed by spectral imaging analysis for breast (e, f) and kidney (h, i) carcinoma respectively, with colocalisation in magenta/yellow. d, g Endothelial cells in the surrounding non-tumour stroma show no or very little IR staining (*) compared with endothelial cells in the tumour stroma (**)

Staining intensity was scored semi-quantitatively, showing a clear significant increased staining in tumour microvessels as compared with microvessels in non-tumour stroma for all tumour types. The pattern for epithelial staining was more complex and revealed more intensive staining in the parenchyma for most tumour types compared with the neoplastic epithelium (Fig. 2). Staining for IGF-1R was weak on endothelial cells, with no differences between tumour and non-tumour tissue (data not shown).

Fig. 2.

Mean score of semi-quantitative insulin receptor expression on (a) endothelial cells and (b) epithelial cells in tumour (T) versus surrounding parenchyma (P). Scores: 0 = no, 1 = minimal, 2 = moderate, 3 = strong IR expression. n = 15 for each tumour type; **p < 0.01, ***p < 0.001 and ^† p = 0.02 compared with T

Capillary-like tube formation (in vitro experiments)

Figure 3 shows the combined results of five to eight in vitro experiments, in which the effect of insulin compounds on capillary-like tube formation of hMVEC in 3D fibrin matrices was assessed. Compared with stimulation with bFGF and TNF-α alone (control), addition of distinctive insulin compounds (1 × 10⁻⁹, 1 × 10⁻⁸ and 1 × 10⁻⁶ mol/l) to the incubation medium led to significant increased capillary-like tube formation of hMVEC. The extent of capillary-like tube formation varied between compounds, ranging from a 1.6- to 2.3-fold increase compared with control. Stimulation with IGF-1 (1 × 10⁻⁹, 1 × 10⁻⁸ and 1 × 10⁻⁶ mol/l) gave a similar increase in capillary-like tube formation (data not shown).

Fig. 3.

Increased capillary-like tube formation by hMVEC after stimulation with different insulin compounds. Black bar, control; light grey bars, human insulin; mid-grey bars, insulin lispro; dark grey bars, insulin detemir; white bars, insulin glargine. All human insulin compounds enhanced, to varying degrees, capillary-like tube formation compared with stimulation with bFGF/TNF-α alone. Each experiment was done in triplicate or quadruplicate. n = 5 for 1 × 10⁻⁹ mol/l, n = 8 for 1 × 10⁻⁸ mol/l and 1 × 10⁻⁶ mol/l insulin; *p < 0.05 and **p < 0.01 compared with control

Discussion

This study suggests that distinctive insulin compounds (exceeding a certain daily dose) could contribute to tumour growth by enhancing local angiogenesis, possibly parallel to the established direct mitogenic and proliferative effects of insulin on tumours [5].

Our observations showed that common adenocarcinomas, which frequently afflict patients with type 2 diabetes, contain large numbers of neovessels and that these vessels abundantly express IRs, independent of tumour type. This indicates that local expression of IR on neovessels is a rather general phenomenon in the process of tumour angiogenesis and that high volumes of exogenous insulin could have side effects. Stimulation of these receptors with insulin could promote angiogenesis and subsequent tumour progression. It should be noted that tumours can have high expression of hybrid receptors and particularly of the IR-A isotype, which is not readily detectable with currently available antibodies. Therefore, the IR expression detected may be an underestimate.

The effect of insulin on angiogenesis has been observed before. Liu et al. [7] recently reported that insulin stimulates hMVEC migration and two-dimensional Matrigel tube formation exclusively through the IR. Our in vitro experiments showed that not only the long-acting insulin analogue glargine enhances capillary-like tube formation, but also all other evaluated insulin compounds. Hence, insulin glargine is not an exclusive candidate for an assumed relationship between increased tumour growth and insulin use in patients with type 2 diabetes.

It is likely that the added insulin at high concentrations may act via both IRs and IGF-1Rs. This might be the case for insulin concentrations of 1 × 10⁻⁶ and 1 × 10⁻⁸, but not for 1 × 10⁻⁹ mol/l. Moreover, differences in capillary-like tube formation between insulin detemir and insulin glargine were not found. It is known that insulin glargine has a much higher affinity for the IGF-1R compared with insulin detemir [11]. Therefore, involvement of the IGF-1R becomes less probable. Furthermore, since we found increased IR expression and no increased IGF-1R expression on microvessels within adenocarcinomas, we assume that in vivo the insulin × IR interactions are likely to be of paramount importance for insulin-mediated angiogenic effects in adenocarcinomas.

We would have preferred to use human tumour-derived endothelial cells, instead of foreskin-derived hMVEC for our in vitro experiments. However, to our knowledge, no published reports describe the isolation and long-term culturing of endothelial cells from human tumour tissue. Since endothelial cells within tumour tissue are of benign origin and adenocarcinomas normally contain much fibrin, we consider our in vitro angiogenesis assay, which looks at tube formation of benign hMVEC into a three-dimensional fibrin matrix, to be appropriate.

In short, the current results suggest that insulin and insulin analogues play a biological role in tumour growth by stimulating local IRs with a subsequent increase in angiogenesis. Without any doubt, additional prospective studies will be required in order to confirm a possible relationship between insulin therapy and tumour progression either by direct effects of insulin on tumour growth or stimulation of local angiogenesis.

Abbreviations

3D

Three-dimensional

bFGF

Basic fibroblast growth factor

hMVEC

Human microvascular endothelial cells

IGF-1R

IGF-1 receptor

IR

Insulin receptor