AIMS To study changes in the expression of insulin-like growth factors (IGFs) and their receptors, as well as production of the IGF-I and IGF-II polypeptides, in adenocarcinoma of the colon.
METHODS Malignant tissue obtained at operation was used. Total RNA was extracted and specific IGF-I and IGF-II and their receptor mRNAs were measured by a solution hybridisation RNase protection assay. IGF-I and IGF-II polypeptides were measured by specific immunoassays.
RESULTS All normal tissues expressed IGF-II, IGF-I receptor, and IGF-II/mannose-6-phosphate (Man-6-P) receptor. IGF-I mRNA could not be detected but the polypeptide was present in small but equal amounts in normal and malignant tissue. IGF-II was expressed 40 times more abundantly in colonic tumours than in adjacent normal tissue and the concentration of the corresponding polypeptide was twice as high in the malignant tissue. IGF-I receptor expression was increased by a factor of 2.5 and IGF-II/Man-6-P receptor by a factor of 4.
CONCLUSIONS This study confirms that in adenocarcinoma of the human colon there is increased expression of IGF-I receptor and IGF-II. Furthermore, IGF-II/Man-6-P receptor message is increased and the increase in IGF-II message is accompanied by a doubling of the IGF-II protein in the tumour tissue compared with the adjacent normal tissue. These findings suggest that the IGF-II/Man-6-P receptor may also be involved in development of adenocarcinoma of the colon. There is rapidly accumulating evidence implicating the IGF system in the development of malignancy of the large bowel.
- insulin-like growth factors
- insulin-like growth factor
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Cancer of the colon is one of the most common types of cancer in humans. So far, it has not been possible to devise effective medical treatment against it. As intestinal growth throughout life is under the control of various growth factors, an understanding of their possible role in this neoplasm may be essential to planning effective treatment. These growth factors are both endocrine products and locally produced peptides with paracrine and autocrine effects. The factors known to stimulate intestinal growth include epidermal growth factor, gastrin, cholecystokinin, insulin-like growth factors I and II (IGF-I and -II), growth hormone, enteroglucagon, neurotensin, and peptide YY.1 ,2
IGF-I and -II play an important role in the growth, normal and abnormal, of many tissues in the human body. In order to exert their effect they bind to specific cell surface receptors. Furthermore, the IGFs are bound in the serum to one of six binding proteins. Biological functions attributed to these binding proteins include regulation of the stability and clearance of the IGFs, acting as shuttles for IGF transport, and modulating IGF action at the cellular level.3
IGFs are expressed in the normal intestine in both the fetus and the adult.4 After intestinal resection in the experimental animal, IGF-II receptors are increased in the villous and crypt regions of the jejunum and ileum at 12 hours, providing circumstantial evidence for the role of IGF-II during phases of regeneration of the intestine.5 Recent work has suggested that IGF-II also plays a role in human colorectal cancer. A certain proportion of colorectal cancers contain increased IGF-II message,4 ,6and adenocarcinoma cell lines also produce IGF-II protein.7 ,8 IGF-I receptor is increased in several colon cancer cell lines and in colorectal cancer tissue obtained at operation.9 ,10 The IGF-II/Man-6-P receptor has been found in malignant colorectal cell lines,10 ,11 but it has not so far been shown that the expression of this receptor is higher in colorectal cancer than in normal colonic tissue. Nor has it been shown that IGF-II protein is increased in colorectal cancer. We studied the expression of IGF-I and -II and their two receptors in tissue obtained at operation for resection of adenocarcinoma of the colon. Furthermore, we measured IGF-I and IGF-II polypeptide in cancerous and normal adjacent bowel.
GROUPS OF INDIVIDUALS
IGF gene expression was studied in six patients with carcinoma of the colon, two men and four women, whose ages ranged from 46 to 82 years. In three, the carcinoma was in the sigmoid colon, in two near the splenic flexure, and in one in the ascending colon near the hepatic flexure. Two patients had metastases in the liver: a 46 year old woman had a mucinous adenocarcinoma near the hepatic flexure; a 56 year old man had a moderately differentiated adenocarcinoma in the sigmoid.
In addition, IGF gene expression was studied in biopsy specimens from three patients with malignant polyps and in ten normal biopsy samples obtained from individuals undergoing colonoscopy for diagnostic purposes.
In another group of 10 patients, carcinomatous and normal adjacent tissue obtained at operation was kept for estimation of IGF-I and IGF-II protein.
PREPARATION OF TISSUES
Tissues were obtained during resection of the bowel for adenocarcinoma. Tumour tissue and normal tissue adjacent to the tumour were removed and thoroughly rinsed in isotonic saline to avoid contamination by serum. These were placed on ice within a few minutes of removal, and appropriate tissues were selected by the pathologist and placed in RPMI 1640. Ulcerated and necrotic areas were avoided. Within 15 minutes of removal, the tissues were rapidly frozen in liquid nitrogen and subsequently preserved at −70°C until used for preparation of total RNA. Tissues from normal healthy individuals and from patients with malignant polyps were obtained during routine colonoscopy of persons at risk for colorectal tumour. The remainder of the tissue was placed in formalin and underwent formal histological evaluation and staging by Dukes’ classification.
This project was approved by the ethical committee of the Shaare Zedek Hospital, and written permission was obtained for removal of the biopsy material.
GENE EXPRESSION OF IGF-I, IGF-I RECEPTOR, IGF-II, AND IGF-II RECEPTOR
Tissue mRNA for IGF-I, IGF-II, and their receptors was analysed by an RNase protection assay as follows. Total RNA was prepared from the tissues by the method of Chomczynski and Sacchi12 and quantified by measuring absorbance at 260 nm. The integrity of the RNA and the accuracy of the spectrophotometric determinations were assessed by visual inspection of the ethidium bromide stained 28S and 18S ribosomal RNA bands after agarose gel electrophoresis. The IGF-I, IGF-II, IGF-I receptor, and IGF-II/Man-6-P receptor riboprobes were a gift from Dr Derek LeRoith, NIH, Bethesda, MD, USA.
The riboprobe for human IGF-I was a 442 bpPstI/RsaI fragment of a human IGF-I cDNA subcloned into plasmid vector pGEM-3. When this construct was linearised withHindIII, a protected band of 420 bases was obtained.13 The riboprobe for human IGF-II was a 556 bpPstI/AccI fragment of human IGF-II cDNA subcloned into plasmid vector pGEM-3. For generation of antisense RNAs, this construct was linearised withHindIII, and, using T7 RNA polymerase, a 603 base transcript containing 251 bases of the 5’ untranslated region and 283 bases of the coding region was generated.14 The riboprobe for human IGF-I receptor was a 379 bpEcoRI/XhoI fragment coding for part of the α-subunit of the human IGF-I receptor subcloned into plasmid vector pGEM-3. After linearisation of this construct with HindIII, an antisense riboprobe was generated with T7 RNA polymerase. The final riboprobe contained 32 bases of pGEM-3 plasmid sequence and 379 bases complementary to IGF-I receptor mRNA.15 A human IGF-II/Man-6-P receptor riboprobe was generated by subcloning a 500 bpEcoRI/HindIII fragment of the corresponding cDNA into pGEM-2. After linearisation of this construct with EcoRI, an antisense riboprobe containing 250 bases complementary to IGF-II/Man-6-P receptor mRNA and 10 bases of pGEM-2 sequence was generated with T7 RNA polymerase.13
Solution hybridisation RNase protection assays were performed as follows. A 20 μg sample of total RNA was hybridised with 1 × 106 dpm 32P-labelled antisense RNA probes. The hybridisation was carried out at 45°C for 16 hours in a buffer containing 80% formamide. After hybridisation, RNA samples were digested with RNase A, and T1 and the protected hybrids were extracted with phenol/chloroform, ethanol precipitated, and electrophoresed on 8% polyacrylamide/8 M urea denaturing gel. Multiple autoradiograms from each gel were scanned by a densitometer connected to an Apple Macintosh computer.
TISSUE IGF-I AND -II EXTRACTION AND IMMUNOASSAYS
For the extraction of IGF-I, about 100 mg tissue was homogenised on ice in 1 mol/l acetic acid (5 mg/g tissue) with an UltraTurrax TD 25 and further disrupted using a Potter Elvehjelm homogeniser.16 ,17 The tissues were extracted twice and after lyophilization were redissolved in 40 mmol/l phosphate buffer (pH 8). IGF-II was extracted by homogenising about 100 mg tissue on ice in 3.3 mol/l formic acid/0.5% Tween 20 (5 ml/g tissue) and centrifuged at 40 000 g for 10 minutes at 4°C.18 A 150 μl aliquot of the supernatant was transferred into a second set of tubes and placed in a water bath at 90°C for 30 minutes. The tubes were removed and 350 μl reagent grade acetone was added; the resulting mixture was vortex-mixed and centrifuged at 3000 g. The supernatants were lyophilized and redissolved in 40 mmol/l phosphate buffer (pH 8). A linear relation was found between biosynthetic IGF-I and IGF-II and the tissue IGF-I and IGF-II immunoreactivity at multiple concentrations, indicating antigen similarity and absence of interference from proteins and receptors in the extracts. Tissue extracts were kept at −20°C until tissue IGF-I and IGF-II were measured in duplicate in diluted extracts by a non-competitive time-resolved immunofluorimetric assay as previously described.19 IGF-I and IGF-II cross reactivity were less than 0.0002%, and the detection limits were 2.5 ng/l and 10 ng/l for the IGF-I and IGF-II assays respectively. The intra-assay coefficient of variance for the IGF-I and -II method was less than 5% and the interassay coefficient less than 10%.
IGF-II/Man-6-P receptor gene expression in biopsy specimens from healthy individuals was similar to that in biopsy specimens from normal tissue adjacent to adenocarcinoma. However, it was five times higher in the malignant tissue. In malignant polyps, IGF-II expression was about twice as high (fig 1A, B). The integrity of the RNA used in the RNase protection assay was assessed by visual inspection of ethidium bromide stained 28S and 18S ribosomal bands of 10 μg aliquots in agarose gel (fig 1C). The two patients with liver metastases had 2.4 and 4 times higher IGF-II/Man-6-P receptor gene expression than patients of Dukes’ classification A (data not shown).
Expression of IGF-II was about 40 times higher in malignant tissue than in tissue adjacent to the tumour (fig 2).
Expression of IGF-I receptor was 2.5 times higher in the malignant tissue than in tissue adjacent to the tumour (fig 3).
We did not find IGF-I mRNA in healthy or malignant colonic tissue (data not shown).
The amount of IGF-I and IGF-II protein was measured in adenocarcinoma of the colon and in normal adjacent tissue in another group, comprising ten patients. IGF-I was present in equal but small amounts in healthy and malignant tissue (2.3 (1.3) and 2.3 (1.9) ng/g tissue respectively; mean (SD)). IGF-II, however, was twice as abundant in the malignant tissue (31.2 (11.8) v 16 (3.1) ng/g tissue; p<0.05). The levels of tissue IGF-I and -II amounted to about 3–5% of circulating levels (data not shown).
IGF-II RECEPTOR mRNA IN COLONIC TISSUE
Our results show that colonic tissue from healthy subjects expresses IGF-II/Man-6-P receptor mRNA, suggesting that the receptor is a physiological constituent of healthy colonic tissue in adults.
In our series, all six patients with carcinoma of the colon and the three with carcinomatous polyps had increased expression of IGF-II/Man-6-P receptor mRNA compared with the 10 control individuals. IGF-II/Man-6-P receptor has previously been shown to be present in malignant colorectal cancer cell lines,9 ,10 but this is the first demonstration that it exists in normal colonic tissue and that its expression is higher in colorectal tumour tissue than normal colonic mucosa. Although our numbers are not sufficiently large to allow a correlation of the clinical state and gene expression, it is of interest that the two patients with metastases in the liver had exceptionally high expression compared with other patients with colorectal cancer of a lower grade of invasiveness.
In experimental studies in rats, the IGF-II/Man-6-P receptor was found to be localised along the whole intestine. It was more densely represented in the distal small intestine and colon than in the jejunum.20 The receptor was more abundant in the crypts, a region engaged in proliferation of enterocytes, than in the villus. At 12 hours after resection of the intestine in rats, a significant increase in immunoreactive IGF-II/Man-6-P receptor was found in the villus and crypt regions of the jejunum and ileum, and this increase was maintained for 48 hours.4 These observations suggest at first sight that the IGF-II/Man-6-P receptor has a proliferative effect in enterocytes. This, however, seems unlikely as the IGF-II/Man-6-P receptor, unlike the IGF-I receptor, does not possess an intracellular tyrosine kinase activating domain.21 Rather, this receptor appears to be similar to the receptor for proteins bearing Man-6-P, a post-translational modification that functions as a key signal for intracellular targeting of hydrolases, and possibly other proteins, to lysosomes. It is for this reason that the IGF-II/Man-6-P receptor is believed not to subserve a mitogenic function. Indeed, there is overwhelming evidence in the literature indicating that it is the IGF-I receptors that mediate the mitogenic effects of IGF-II.10 ,22 Although we found the IGF-II/Man-6-P receptor expression to be upgraded in colorectal cancer, we could not prove that it contributes to the development of the tumour. In contrast, in carcinoma of the breast and liver, the IGF-II/Man-6-P receptor has recently been implicated as a putative tumour suppressor gene. In these tissues, loss of heterozygosity for this gene was shown in 30% and 70% of tumours respectively. In addition, point mutations were found in the remaining alleles.23-25 In contrast, in colorectal cancer we found that the IGF-II receptor message was overexpressed fivefold and the IGF-II message by a factor of 40.
IGF-I RECEPTOR mRNA IN COLONIC TISSUE
Like others,9 we found that IGF-I receptor mRNA was also increased in the malignant tissue. Increased amounts of IGF-I receptor at the functional binding protein level have previously been described in several adenocarcinomata.9 The IGF-I receptor has been shown also to bind a substantial amount of the IGF-II and to mediate its effects in stimulating proliferation of cells.10 ,22 Expression of IGF-I receptor is also upgraded in states of malnutrition,26 in tissue repair,27 and in numerous malignancies.7 ,28
IGF-I mRNA AND IGF-I PROTEIN IN COLONIC TISSUE
Like other investigators, we did not find any IGF-I mRNA in healthy or malignant human colonic tissue.3 Tricoliet al 4 on the other hand did find a 3–5-fold increase in IGF-I mRNA in 20% of tumours. Although rare in epithelial tumours, increased IGF-I expression is, however, a very common occurrence in ovarian cancers.29 We found small amounts of IGF-I protein in the tissues and these were the same in normal adjacent tissue and in the tumour.
IGF-II mRNA AND IGF-II PROTEIN IN COLONIC TISSUE
IGF-II mRNA levels were elevated in all the malignant colonic tissues investigated by us. Expression of IGF-II mRNA in tissue adjacent to the tumour was normal. These findings are compatible with previous reports. Lambert et al 6 analysed 21 human colorectal tumours and found overexpression of IGF-II in six (30%). Overexpression was moderate (2–15-fold) or marked (200–800-fold). It did not correlate with the site or stage of the tumour nor with the age or sex of the patient. In one of their patients a structural alteration of the IGF-II gene was found. Tricoli et al 4 studied IGF-II gene expression in 20 colorectal tumours and found 10–50-fold increase in 30–40%. They did find a correlation with Dukes’ classification of the tumour. Of special interest was the finding that there was no increased expression of epidermal growth factor or transforming growth factor α. This finding emphasises the unique importance of the IGFs in colorectal cancer. The malignant potential of IGF-II in mammary cancer was recently shown in transgenic mice overexpressing IGF-II30 and in the CaCo2 colon carcinoma cell line.31 In human colorectal cancer cell lines it has been shown that IGF-II mRNA expression is associated with production of IGF-II protein.7 ,8 As no control cell lines were available, it could not be established if the production of IGF-II was increased above normal. We showed a twofold increase in IGF-II protein in malignant tissue. Unfortunately, tissues from different patients were used for the determinations of IGF-II peptide and IGF-II mRNA, but we do not believe that this significantly affects our data. IGF-II peptide was raised by a factor of 2 in ten specimens of carcinoma when compared with control tissue, with a very small standard deviation. It is therefore highly unlikely that had we measured the original six patients we would have obtained significantly different results. On the other hand, the 40-fold increase in the IGF-II mRNA, which we found in carcinomatous tissue, is in accordance with data obtained by other investigators.4 ,6 This study does not establish whether the increase in IGF-II protein in the tumour was related to increased local production or increased entrapment by the IGF-I or the IGF-II/Man-6-P receptor or to both these mechanisms. Although the concentrations of IGF-I and -II in both normal and malignant tissue were low compared with circulating levels (3–5%), it seems unlikely that the increase in tumour IGF-II was due to contamination with serum IGF, as no increase in tumour IGF-I was seen. In the COLO 205 cell line, the addition of IGF-I receptor antibody or antibody to IGF-II significantly depressed growth. It was concluded that IGF-II secreted by these cells could stimulate cell growth in an autocrine fashion through IGF-I receptors.10 ,22
Some colorectal cancers have a genetic instability characterised by alterations within simple repeated nucleotide sequences termed microsatellites.32 Such instability is characteristically seen in the hereditary non-polyposis colorectal cancer syndrome, but is also found in 15% of sporadic colorectal cancers.33 In a recent study of colorectal cancer patients with microsatellite instability, 60% also showed hypermethylation of the IGF-II gene.34 This suggests that in this subset of patients, overexpression of the IGF-II gene may not be essential for development of colorectal cancer.
This study confirms that colorectal cancer is associated with increased expression of genes belonging to the IGF system. The rise in IGF-II/Man-6-P receptor message in colorectal tumour tissue shown here has not previously been reported; however, its relevance to the initiation or maintenance of the tumour remains to be established. We have also shown that, in parallel with the increased expression of IGF-II, IGF-I receptor, and IGF-II/Man-6-P receptor in adenocarcinoma of the colon, there is increased IGF-II protein in the malignant tissues while IGF-I protein remains unchanged. It is suggested that IGF-II may play an important role in the development of this tumour in most patients.
This work was supported by the Miriam Coven-Fish Foundation, by a grant from the Shaare Zedek Hospital, by the Chief Scientist, the Ministry of Health of Israel, the Danish Medical Research Council (grant no 700592), the Novo Foundation, The Nordic Insulin Foundation, the Aage Louis Petersen Foundation, the Institue of Experimental Research, University of Aarhus, Denmark, and the Aarhus University-Novo Nordisk Center for Research in Growth and Regeneration (Danish Medical Research Council; grant no 9600822). We wish to thank the staff of the Institute of Gastroenterology, the Institute of Pathology, and the Department of Surgery of the Shaare Zedek Hospital for help in obtaining the specimens.
- insulin-like growth factor
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