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vol. 8
Original paper

Insulin, insulin-like growth factor 1 and insulin-like growth factor binding protein 3 serum concentrations in patients with adenomatous colon polyps

Adam Janiak
Piotr Oset
Renata Talar-Wojnarowska
Anna Kumor
Ewa Małecka-Panas

Prz Gastroenterol 2013; 8 (5): 308–314
Online publish date: 2013/10/28
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Incidence rates of colorectal cancer (CRC) in Poland are 30–35 cases/100 000/year and increase by 2.5% per year. Five-year survival rates in Poland are 25% and are among the lowest in the world [1]. Adenomatous polyps are the most common precancerous conditions of the large intestine; 70–90% of CRC arise on their background. Incidence rates of adenomatous polyps are estimated at 15% among women and 25% among men and these values increase with age [2]. The risk of malignant transformation depends on histopathological pattern, size and dysplasia grading of the adenoma [3, 4]. It is considered that the risk of development of cancer in adenomas measuring less than 5 mm is 1%, in those measuring 6–9 mm it is 5%, and in adenomas measuring more than 10 mm it is 20%. Median age at which adenomas arise is 50 years and it precedes the development of cancer by 7–10 years [2, 5].

In recent years, there has been growing concern about the influence of metabolic disorders on adenoma formation and the development of colorectal cancer. In a meta-analysis presented by Larson et al., which included 15 studies and over 2.5 million people, there was found a 30% increase in the risk of CRC among people who suffer from diabetes, regardless of gender and location of polyps [6]. Convincing evidence was found that hyperinsulinaemia might play an important role in pathogenesis of diabetes type 2, as well as in formation of adenomatous polyps and CRC [7]. Insulin stimulates proliferation of mucous membrane cells and CRC cells directly, as well as by the influence on concentration and bioavailability of insulin-like growth factor-1 (IGF-1). Insulin also stimulates directly in vitro mitogenesis of large intestine mucous membrane regular cells and angiogenesis of tumour vessels [8–11].

Interrelations and interactions of insulin and IGF are called the insulin-IGF axis. Elements that belong to the IGF axis are: three ligands (insulin, IGF-1, IGF-2), six receptors (insulin receptors IR (fetal) and IR (adult), IGF-1 receptor (IGF-1R), IGF-2R, IGF-1R/IR hybrid, and IGF-1R/IR hybrid) and over seven insulin-like growth factor-binding proteins (IGFBP1-7) [12].

Insulin-like growth factor-1 is a single-chain polypeptide, which consists of 70 amino acids 50% homologous in structure to proinsulin. The gene for IGF-1 is located on chromosome 12q22-q24.1. Regulation of IGF-1 synthesis takes place in the liver in response to stimulation by growth hormone (GH), which is produced in the pituitary gland. Meanwhile, IGF-1 reflexively inhibits growth hormone and insulin release. Insulin-like growth factor-1 exerts its biological activity on cells by binding with its specific receptor (insulin-like growth factor receptor-1 – IGF-R1), which is 70% homologous to the insulin receptor and has tyrosine kinase activity. Binding with the receptor, IGF-1 initiates many changes and by tyrosine kinase activation, and afterwards by 3-phosphatidylinositol and MAP kinase activation, it leads to inactivation of the BAD protein, which encourages apoptosis. Apart from inhibiting apoptosis, IGF-1 plays an important role in regulation of growth processes, proliferation and cell transformation. Insulin-like growth factor-1 can also induce vascular endothelial growth factor (VEGF) production, which positively influences the production of blood vessels and progression of tumour development [10]. In blood 90% of IGF-1 binds with the binding protein IGFBP-3 [8].

The protein that binds insulin-like growth factor-3 (insulin-like growth factor binding protein-3 – IGFBP-3) is a single-chain polypeptide, which consists of 264 amino acids. The gene for IGFBP-3 is located on chromosome 7p14-p12. This protein is produced mainly in the liver, but also by mesenchymal cells. Its production is influenced mainly by GH, but also by parathormone, insulin and cytokines, such as TNF- and interleukin-8. The IGFBP-3, binding with IGF-1, inhibits its activity and prolongs its half-life in serum. Not only does IGFBP-3 regulate IGF-1 bioavailability, but it also has an independent inhibitory effect on cell growth and increases proliferation and apoptosis of cells [8].

Although there has been conducted extensive research confirming the importance of insulin, IGF-1 and IGFBP-3 in the development of colorectal cancer, not much is known about their influence on early carcinogenesis of the large intestine.


The aim of our study was to assess the IGF-1, IGFBP-3 and insulin concentrations in patients with adenomatous colon polyps and find the connection between their concentrations and location, dysplasia grading, histopathological pattern, size and number of adenomatous colon polyps.

Material and methods

Sixty patients were included in this study (25 women and 35 men), aged 30-77 years (average age 58.47 ±8.36), all of whom underwent colonoscopy with polypectomy, and adenomatous colon polyps were found in histopathological examination. The control group consisted of 30 patients (15 women and 15 men) with no positive findings on colonoscopy. In the group of patients with adenomas there were analyzed location and size of the polyp, dysplasia grading and histopathological pattern. There were no significant differences in age, sex and body mass index (BMI) between the study group and the control group.

All patients expressed written consent to participate in the study and were informed about its aim and progress. The protocol of the study was accepted by the Bioethics Committee at the Medical University of Lodz, agreement number RNN/44/04/KE.

Detected adenomatous colon polyps were removed endoscopically and submitted for histopathological examination in the Pathomorphology Department at the Medical University of Lodz. Adenomas of the large intestine located in the caecum, ascending colon and transverse colon were defined as proximal colon polyps, whereas those located in the descending colon, sigmoid colon and rectum were classified as distal colon polyps. The term advanced colorectal adenoma concerned polyps with diameter in excess of 1 cm and/or including villous pattern. In all patients a blood sample was taken into a test-tube with EDTA of capacity 9 mm. The serum, after producing a thrombus, was centrifuged, separated, frozen at –70°C and stored for further determination.

Insulin, IGF-1 and IGFBP-3 assessment was done in the Department of Laboratory Diagnostics of the Medical University of Lodz. There were used such tests as: DRG Insulin ELISA Kit, DRG IGF-1 ELISA Kit and DRG IGFBP-3 ELISA Kit by DRG Instruments GmbH (Germany). They are based on the so-called heterogeneous sandwich method and are carried out in solid phase. The first step is to incubate serum containing the investigated antigen in solid phase (coated pits) with addition of a conjugate made of mouse antibodies and biotin. A product of this reaction was a complex: solid phase-bound antibody-antigen-biotin marked antibody. After 30 min of incubation, the superfluous amount of unbound antibodies is removed by three-fold plate flushing. The next step requires addition of an enzyme (Streptavidin Peroxidase Enzyme Complex), which specifically binds with the biotin-antibodies complex, and is followed by adding enzyme substrate. This reaction produces a substance, the colour intensity of which is proportional to the amount of the antigen and is assessed by means of spectrophotometry.

Statistical analysis

Statistical analysis was carried out with Statistica 5.5PL, using the non-parametric Mann-Whitney U significance test for measurable subjects, the 2 (amended by Yates) test for the assessment of relations between qualitative subjects, and Pearson’s r correlation coefficient for the assessment of relations between measurable subjects. In all tests statistical significance was set at p < 0.05.


One hundred and nine adenomas were diagnosed altogether in the study group. A solitary adenoma was found in 36 patients, and the 24 remaining were diagnosed with 2 to 6 polyps. Multiple adenoma patients’ mean age was significantly higher than in the single polyp group (61.1 vs. 56.7 years, p < 0.05). In multiple adenoma patients the one staged the highest was chosen for further evaluation.

In 23 cases pathology revealed tubular, and in 37 tubulo-villous polyp structure. No villous adenomas were found in this study. In patients with tubular adenomas 22 had low-grade, and 1 had high-grade dysplasia. In the tubulo-villous adenoma group 32 had low-grade and 5 had high-grade dysplasia.

Statistically significantly higher incidence of distal colon adenomas (50 cases; 83.3%) than proximal ones (10; 16.7%) was observed (p < 0.01). In the proximal colon 5 tubular polyps were diagnosed, each of them with low-grade dysplasia, and 5 tubulo-villous ones including 3 with low and 2 with high-grade dysplasia. In the distal colon 18 tubular polyps were found, 17 with low and 1 with high-grade dysplasia. Also, 32 tubulo-villous polyps were found in that location, of which 28 had low-grade and 4 had high-grade dysplasia. However, no correlations between adenoma location and their pathological pattern and dysplasia grading were found.

Adenoma diameters ranged from 6 mm to 40 mm (mean: 13.35 ±7.11 mm). The mean diameter of tubulo-villous adenomas was 14.22 ±6.23 mm and was not significantly different from tubular adenoma size – 11.96 ±8.29 mm in diameter (p < 0.05). Thirty-nine adenomas (65%) of a diameter less than 15 mm (mean 9.21 ±1.85 mm) and 21 (35%) of more than 15 mm (mean diameter of 21.05 ±6.85 mm) were found. Statistical significance of a greater frequency of high-grade dysplasia occurrence in large adenomas (mean 22 ±6 mm) as compared to small ones (mean diameter of 12.4 ±6.6 mm) was established, which is illustrated in Figure 1.

A statistically significant rise in occurrence of multiple polyps was noted in patients in whom at least one adenoma was greater than 15 mm in diameter. There were no correlations between adenoma size, sex, age and patient BMI.

There were no differences between insulin serum concentrations in adenoma and control groups. Moreover, we found no correlation between insulin serum level and pathology pattern, dysplasia grade, size and adenoma localization (Table I).

However, a greater IGF-1 serum concentration was observed in the adenoma group (120 ±33.3 ng/ml) as compared to the control group (103.4 ±44.91 ng/ml), p < 0.05 (Table II). Mean IGF-1 serum concentration in patients with proximal adenomas was also higher than in those with distal ones (p < 0.05; Table I).

Mean IGF-1 serum levels showed no difference between tubular and tubulo-villous adenoma groups. Also there were no differences between IGF-1 serum levels in patients who had non-matching pathology patterns, dysplasia levels, sizes, and localizations of adenomas. We found a statistically significant difference between IGFBP-3 serum levels in the adenoma (2808 ±884.89 ng/ ml) and the control group (2260 ±583.67 ng/ml), p < 0.05 (Figure 3). There were no dissimilarities between IGFBP-3 serum levels in patients who had different pathology patterns, dysplasia levels, sizes, and localizations of adenomas.


The increase in colorectal carcinoma (CC) occurrence in Poland and worldwide as well as the high mortality rate due to this disease stimulates multiple analyses of this phenomenon. Colorectal carcinoma morbidity affects particularly developed countries as an effect of the so-called “western lifestyle”. Epidemiological data presented by McKeown-Eyssen indicate that increased serum levels of triglycerides and/or glucose as well as increasing colorectal carcinoma incidence may be affected by common factors arising from specific lifestyle and diet. The mechanism that encourages CC incidence in patients with increased serum triglycerides and glucose may be the increased concentration of bile acids in faeces. A rise in serum glucose levels stimulates insulin production, which in turn increases triglyceride levels secondary to hyperinsulinaemia and insulin resistance [13].

Metabolic disorders are thought to be supportive in colorectal adenoma formation, which appears to be the most frequent pre-cancerous condition of this organ. In a Polish multicenter screening study comprising 43042 colonoscopies carried out in patients aged 50 to 65, Reguła et al. revealed adenomas in 5623 (13.1%) patients. There were 3374 (80.27%) tubular, 998 (17.76%) tubulo-villous, and 111 (1.97%) villous adenomas [2].

On the other hand, Rickert et al. investigated the occurrence of adenomas in 518 autopsies. Adenomas were found in 243 (46%) corpses, including 94.685 tubular, 2.43% tubulo-villous, and 2.89% carcinomas. Similarly to our study, there were no villous adenomas revealed. Mean tubular adenoma diameter was 5.8 mm, and tubulo-villous was 19.0 mm. In this study 66.5% of tubular and 62.5% of tubulo-villous adenomas were located in the proximal colon, and respectively 33.5% and 37.5% of them distally [3]. Differences between Rickert’s and our study regarding the incidence of tubular and tubulo-villous polyps and their localization may be explained by variable adenoma size and age heterogeneity of study groups.

In our study there were no differences in insulin levels between adenoma and control groups. The relationship between insulin level and colorectal adenoma and cancer formation is widely discussed. As in this study, Schoen et al. did not find any differences in fasting insulin levels between adenoma and non-adenoma patients [14]. Also Palmquist et al., as well as Saydah, did not confirm any relations between colorectal carcinogenesis and fasting serum insulin levels [15, 16].

However, Keku et al. observed an increased fasting insulin concentration, which was linked, especially in women, to colorectal adenoma risk increase. Apoptosis in normal mucosa was also assessed in this study, based upon morphological features such as cell shrinkage, chromatin condensation, and apoptotic body formation. A decrease in apoptosis intensity was also observed in patients with increased fasting insulin levels [17].

Flood et al. observed a 50% increase in recurrent adenoma occurrence in the 4th year of the Polyp Prevention Trial in patients with high fasting levels of insulin and glucose. A 2.43-fold increase of advanced adenoma incidence was observed in patients with fasting glucose levels higher than 99 mg% [18]. In contrast, Miscigan et al. observed a decrease in adenoma recurrence risk in 153 patients with high fasting levels of insulin [19].

Ma et al. showed that increased insulin and C-peptide levels may predict higher risk of colorectal carcinoma in males, regardless of BMI and other insulin resistance indicators [20], which was confirmed in an experimental model. Tran et al. showed in an animal model that hyperinsulinaemia is responsible for the increase of large intestine colonic mucosal cells, administering glucose, insulin and Intralipid. Hyperinsulinaemia levels were parallel to those in insulin resistance. The authors suggest that it is hyperinsulinaemia, and not insulin resistance, that is responsible for increased CRC risk [21].

In our study we revealed increased IGF-1 serum levels in patients with adenomatous colonic polyps. Moreover, we observed significantly higher IGF-1 serum concentrations in patients with proximal colon compared to distal localization. Similarly, Giovannucchi et al. disclosed the relationship between increased IGF-1 serum levels and increased risk of advanced adenomas in the Nurses’ Health Study. No correlation was noted in the case of tubular adenomas and small ones, with a diameter less than 1 cm [22].

The majority of authors confirm the relationship between IGF-1 serum level increase and colonic adenoma risk [14, 23–25] as well as colorectal cancer [26–29]. Jenkins et al. described acromegaly patients in whom 2 colonoscopies were performed. During the first examination there were colorectal polyps diagnosed and removed in 66 of them. On control examination, carried out at a mean of 32.7 months after the previous exploration, adenomas were re-diagnosed in 14%, and in 27% hyperplastic polyps were found. Patients in whom investigators found polyps on second examination had increased levels of serum IGF-1 [23]. On the other hand, Renehan et al. described equal IGF-1 serum levels in small adenoma and non-adenoma patients. At the same time, IGF-1 serum levels were higher in the advanced adenoma group as compared to adenoma-free individuals [24].

Primarily acromegaly patients in whom there were increased levels of growth hormone as well as IGF-1 were focused upon with regard to IGF-1 levels [30]. It is widely known that in colorectal carcinoma increased expression of IGF-1R receptor is observed, and its blockage by means of monoclonal antibodies suppresses proliferation [31, 32]. In other studies the relationship between serum IGF-1 levels and CRC development in patients without previously diagnosed metabolic disorders were investigated. In a prospective study by Ma et al., carried out on 22 071 healthy males aged 40–84, the authors concluded that a rise in serum levels of IGF-1 was associated with increased CRC risk [26]. Similar results were obtained in Greek and Swedish studies [27, 28].

On the other hand, Teramukai et al. observed no increase of IGF-1 serum concentration in patients with CRC as compared to the control group, in the case of both advanced and non-advanced adenomas [33]. Similarly, Keku et al. did not find any correlations between serum IGF-1 levels and colorectal adenoma incidence and colonic mucosal apoptosis intensification [17].

Also studies describing the role of IGFBP-3 in colonic carcinogenesis are non-coherent. Parallel to our results, Schoen et al. revealed higher serum IGFBP-3 concentrations in patients with advanced colorectal adenomas than in the control group [14]. Some authors observed no statistically significant differences in IGFBP-3 between adenoma and non-adenoma patients regardless of the level of advancement [17, 25, 33]. On the other hand, Renehan et al. described similar IGFBP-3 levels in non-advanced adenoma and non-adenoma patients. Yet in the advanced adenoma group IGFBP-3 serum levels were statistically lower than in the control group [24]. Similarly, low serum levels of IGFBP-3 were linked to increased risk of adenomas larger than 1 cm in diameter or villous, and not in smaller ones, as described in outcomes of the Nurses’ Health Study [22].

The relationship between serum level of IGFBP-3 and CRC risk remains unclear. In a prospective study, Ma et al. revealed that decreased IGFBP-3 serum levels were linked to an increased CRC risk [26]. Palmquist et al. observed increased risk of CRC that accompanied increase in serum IGFBP-3 levels. At the same time, they noted a unique trend towards decrease of CRC risk in patients with high levels of IGFBP-3, although they did not confirm it in statistical analysis [27]. The results mentioned above indicate a burning need of further large cohort studies on the role of IGFBP-3 in CRC.

Summing up, the obtained results suggest the association of IGF-1 and IGFBP-3 levels with the development of CRC. IGF-1 seems to especially affect malignant transformation in the proximal colon. Increased serum levels of these proteins were not however related either to polyp size or to dysplasia level or histopathological pattern. Undoubtedly, the observed abnormalities require further studies which may reveal mechanisms of concentration increase as well as the role of IGF-1 and IGFBP-3 in colonic carcinogenesis.


The work was supported by the Polish Society for the Prevention of Digestive Tract Neoplasms.


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Received: 7. 12.2012

Accepted: 19.03.2013
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