Decreased expression of the mannose 6- phosphate/insulin-like growth factor-II receptor promotes growth of human breast cancer cells
© Chen et al; licensee BioMed Central Ltd. 2002
Received: 14 April 2002
Accepted: 30 July 2002
Published: 30 July 2002
Loss or mutation of the mannose 6-phosphate/insulin-like growth factor-II receptor (M6P/IGF2R) has been found in breast cancer. However, whether or not decreased levels of functional M6P/IGF2R directly contribute to the process of carcinogenesis needs to be further verified by functional studies.
In this study, using viral and ribozyme strategies we reduced the expression of M6P/IGF2R in human breast cancer cells and then examined the effect on growth and apoptosis of these cells.
Our results showed that infection of MCF-7 cells with the adenovirus carrying a ribozyme targeted against the M6P/IGF2R mRNA dramatically reduced the level of transcripts and the functional activity of M6P/IGF2R in these cells. Accordingly, cells treated with the ribozyme exhibited a higher growth rate and a lower apoptotic index than control cells (infected with a control vector). Furthermore, decreased expression of M6P/IGF2R enhanced IGF-II-induced proliferation and reduced cell susceptibility to TNF-induced apoptosis.
These results suggest that M6P/IGF2R functions as a growth suppressor and its loss or mutation may contribute to development and progression of cancer. This study also demonstrates that adenoviral delivery of the ribozyme provides a useful tool for investigating the role of M6P/IGF2R in regulation of cell growth.
With one million new cases each year, breast cancer is the most common cancer among women and is the leading cause of death in women 30 to 70 years of age in the world. Breast cancer results from genetic and environmental factors including diet, radiation and hormones [1–5]. The molecular events involved in breast carcinogenesis, however, remain to be elucidated.
Numerous studies have shown that polypeptide growth factors such as insulin-like growth factors (IGFs) are mitogens for breast cancer cells [6–9]. The IGF-I and IGF-II signal through a common tyrosine kinase receptor, the insulin-like growth factor 1 receptor (IGF1R), and have mitogenic and cell survival actions that may promote tumor development. Modulation of this mitogenic pathway occurs in part via the M6P/IGF2R, which functions in the internalization and degradation of IGF-II . M6P/IGF2R is also important in activation of TGF-β, a potent growth inhibitor for most cell types, and in binding, transport and activation of lysosomal enzymes, such as cathepsins [12, 13]. It has been shown that M6P/IGF2R expression is significantly reduced in both rat and human hepatocellular carcinomas . Loss of hetorozygosity (LOH) at the M6P/IGF2 receptor gene locus on 6q26-27 coupled with somatic point mutations in the remaining allele has recently been demonstrated in liver and breast cancers [15–23]. In addition, somatic mutations of the M6P/IGF2R gene were also found in prostate cancer, lung carcinoma, and genetically unstable cancers of the endometrium, brain, stomach and colorectum [24–29]. The findings of LOH and mutations of M6P/IGF2R in a wide variety of tumor types have led to the proposition that the M6P/IGF2R is a tumor suppressor gene. In addition to genetic data, a tumor suppressor gene candidate has to meet functional criteria. The functional characteristics of a tumor suppressor gene have not been well established for M6P/IGF2R. Thus, further studies that address the relationship between the functional M6P/IGF2R level and cell growth activity are needed.
To verify whether decreased levels of functional M6P/IGF2R can provide a growth advantage for cancer cells, we used viral and ribozyme strategies to reduce the expression of M6P/IGF2R in human breast cancer cells and then examined the effect on growth and apoptosis of these cells.
Construction of a recombinant adenoviral vector containing the M6P/IGF2R-ribozyme
A 49 bp M6P/IGF2R ribozyme oligonucleotide, 5'-GAATTCTCCACACTGATGAGCCGCTTCGGCGGCGAAACATTCAACGCGT-3' and the corresponding reverse complementary strand were synthesized. The fragments were subcloned into pRz951 to produce a plasmid (designated as pRz-IGF2R) containing a ribozyme targeted against the M6P/IGF2R. For construction of the recombinant adenovirus containing the M6P/IGF2R-ribozyme (pAd-GFP/Rz-IGF2R), the segments containing the ribozymes were amplified by PCR and cloned into a pAdTrack-CMV vector and then recombined homologously with an adenoviral backbone pAdEasy 1 vector to generate pAd-GFP/Rz-IGF2R, following the protocol described by He et al . The pAd-GFP/Rz-IGF2R carries both the Rz-IGF2R and GFP (as reporter) genes, each under the control of separate cytomegalovirus (CMV) promoters. Another viral vector, pAd-GFP, which carries the GFP gene only under the control of the CMV promoter, was generated and used as a control vector. The adenoviral vector DNA were linerized with Pac I and transfected into the replication-permissive 293 cells (E1A transcomplementing cell line) using Lipofectamine (Life Technologies) to produce E1-deleted, replication-defective recombinant adenovirus as described previously . Large-scale amplification of the recombinant adenovirus in 293 cells was followed by purification using a discontinuous CsCl gradient. The constructs were confirmed by enzymatic digestion and DNA sequencing.
Transcription and cleavage reaction of the ribozyme in vitro
Plasmids containing the ribozyme or the substrate (either 45 bp of M6P/IGF2R mRNA or an unmatched sequence 5'-ATATTGTCCAGTGC-3') were linearized with Mlu I. All transcripts were generated with T7 RNA polymerase (Promega). Substrate transcripts were labeled by incorporation of [32P]UTP (10 μCi/ml; Nen Life Science Products, Inc.). Specific activity of the [32P]UTP and the base composition of each substrate molecule were used to calculate substrate concentration. Ribozyme transcripts were quantified spectrophotometrically. Cleavage reactions contained 30 nM substrate RNA, increasing amounts (60 nM) of ribozyme, 20 mM MgCl2 and 20 mM Tris-HCl (pH 8.0), 1 μl DTT, and 1 μl RNA inhibitor in a final volume of 10 μl. Cleavage reactions were incubated at 37°C for 2 hrs. Reactions were stopped by addition of loading buffer: 80% formamide, 10 mM Na2EDTA (pH 8.0), and 1 mg/ml each bromophenol blue and xylene cyanol. Cleavage products were analyzed on 15% polyacrylamide and 8 M urea denaturing gels. NIH Imager was used to quantitate product and substrate fragments.
Cell cultures and infection with Ad-GFP/IGF2R-Rz and Ad-GFP
MCF-7 cells were cultured in DMEM medium containing 10% FBS at 37°C in a tissue culture incubator with 5% CO2 and 98% relative humidity. Cells were used for experiments after 2–3 days in culture. Viral infections were carried out by adding viral particles at various concentrations (usually, 2 × 108 virus particles/ml) to culture medium containing 2% FBS. Initially, optimal viral concentration was determined by using Ad-GFP to achieve an optimal balance of high gene expression and low viral titer to minimize cytotoxicity. After 24 hrs of incubation, the infection medium was replaced with normal (10% FBS) culture medium. For treatment with IGF-II, cells were incubated with 50 ng/ml IGF-II after infection with Ad-GFP/IGF2R-Rz or Ad-GFP. Seventy two hrs post infection, cells were used for analysis of M6P/IGF2R gene expression and its effect on cell growth.
Analysis of M6P/IGF2R gene expression in MCF-7 cells
The M6P/IGF2R transcripts were determined by RT-PCR using the GeneAmp EZ rTt RNA PCR kit (Roche). Total RNA was extracted from cultured cells using an RNA isolation kit (Qiagen), according to the manufacturer's protocol. M6P/IGF2R transcripts were amplified using primers 5'-GACAGGCTTGTCCTGAGTTA-3' and 5'-TTCTGCTCTGGTTCTGCATG 3', specific to the M6P/IGF2R receptor. Each RT-PCR assay was performed in triplicate. Primers specific for human β-actin cDNA were added to a parallel reaction to standardize for variations in PCR between samples. PCR products were resolved on a 1.0 % agarose gel, visualized under UV light and quantitated using NIH Imager.
Measurement of 125I -IGF-II internalization
Cells were incubated at 37°C for 2 hrs in serum-free DMEM containing 125I-labeled IGF-II (0.5 ng/ml) with or without excess unlabeled IGF-II (2 μg/ml). Following the incubation, the cells were washed three times with ice-cold PBS, and cell-associated radioactivity was determined by a γ-counter. Specific internalized 125I-IGF-II was calculated by subtracting the counts of samples with excessive unlabeled IGF-II from that without unlabeled IGF-II, and normalized to protein content.
Beta-glucuronidase binding assay
Binding of β-glucuronidase was assayed as described previously [31, 32]. Briefly, cells were permeabilized with 0.25% saponin in 50 mM Hepes (pH 7.0), 150 mM NaCl, 5 mM β-glycerophosphate, 0.5% human serum albumin, and 10 mM mannose-6-phosphate (M6P) for 30 minutes on ice. The cells were washed three times with ice-cold PBS containing 0.05% saponin. They were incubated with 20,000 units/ml β-glucuronidase from bovine liver (Sigma) in 50 mM Hepes (pH 7.5) containing 150 mM NaCl, 5 mM β-glycerophosphate, 0.5% human serum albumin, 0.5% saponin with or without 10 mM M6P overnight on ice. Cells were washed five times with ice-cold PBS containing 0.05% saponin and sonicated in 100 mM sodium acetate (pH 4.6). The protein concentration of solubilized cell extract was measured and enzyme activity was assayed as follows: for each reaction 50 μl cell extract were added to 500 μl of 100 mM sodium acetate (pH 4.0) containing 1 mM paranitrophenyl (PNP)-β-glucuronide (Sigma) as substrate. After an incubation period of 3 hours at 37°C, 500 μl 1 M Na2CO3 were added to each reaction and the absorbance was measured at 400 nm. Experimental values were compared to a standard curve that was constructed using 1–100 nM solutions of PNP (Sigma) in 500 μl 100 mM sodium acetate and 500 μl 1 M Na2CO3. Specific activity was calculated as nM of PNP produced/hour/mg of protein.
Beta-glucuronidase endocytosis assay
Beta-glucuronidase endocytosis assay was carried out as described previously . Briefly, confluent cell cultures were washed twice with pre-warmed serum-free DMEM followed by incubation with DMEM containing 5 mg/ml human serum albumin and 10 mM M6P for 20 minutes. Following incubation cells were washed 3 times with pre-warmed DMEM. Cells were then incubated in DMEM containing 5 mg/ml human serum albumin alone or 4000 units β-glucuronidase with or without 10 mM M6P for 2 hours at 37°C. Following the incubation, the cells were washed 5 times with ice-cold PBS and subjected to enzyme activity assay as described above.
Cell proliferation assay (MTT assay and cell counting)
MCF-7 cells were grown in culture plates (tissue culture grade, 12 wells, flat bottom) in a final volume of 1 ml serum-containing culture medium per well, in a humidified atmosphere at 37°C and 5% CO2 for 3 days. After infection with Ad-GFP/IGF2R-Rz or Ad-GFP, cells were incubated with or without 50 ng/ml IGF-II for 4 days. 100 μl MTT labelling reagent were added to each well and incubated for 4 hrs, followed by addition of 1 ml solubilization solution into each well. The cells were incubated at 37°C overnight. Spectrophotometrical absorbency of the samples was measured using an UV-visible Recording Spectrophotometer with wavelength of 550–690 nm. In addition, the total number of viable cells in each treatment group was counted by a trypan blue exclusion method using a hemocytometer.
Analysis of cell apoptosis
MCF-7 cells were infected with Ad-GFP or Ad-GFP/Rz-IGF2R. Seventy two hrs post infection, cells were treated with TNF (0.1 ng/ml) for 24 hrs. Apoptotic cells were identified by Hoechst staining using the Vybrant™ Apoptosis Kit #5 (Molecular Probes) according to the manufacturer's protocol. In addition, after infection with Ad-GFP or Ad-GFP/Rz-IGF2R and treatment with TNF, cell viability was assessed using the MTT assay Kit (Roche Molecular Biochemicals) and cell apoptosis was determined using the Cell Death Detection ELISA Kit assay (Roche Molecular Biochemicals) according to the manufacturer's protocol.
Students's t-test was used to evaluate the difference between two values. Each experiment was repeated at least three times. Statistical significance was accepted at the level of p < 0.05.
Cleavage reaction of the ribozyme in vitro
Expression of the M6P/IGF2R-ribozyme in cultured MCF-7 cells
Ribozyme treatment reduces M6P/IGF2R expression in MCF-7 cells
Effect of ribozyme expression on the functional activity of M6P/IGF2R
Effects of M6P/IGF2R-ribozyme expression on proliferation of MCF-7 cells
Effect of M6P/IGF2R-ribozyme expression on apoptosis of MCF-7 cells
A growing body of genetic evidence suggests that the M6P/IGF2 receptor is involved in carcinogenesis [15–29]. However, direct evidence of a growth-regulatory activity for M6P/IGF2R is lacking. In this study, using ribozyme technology, we demonstrate an association of decreased expression and function of the M6P/IGF2R with increased cell proliferation and decreased susceptibility to TNF-induced apoptosis in human breast cancer MCF-7 cells. Expression of the ribozyme targeted against the M6P/IGF2 receptor in MCF-7 cells resulted in down-regulation of M6P/IGF2R expression, as measured by RT-PCR, and M6P/IGF2R function, indicated by a decrease in internalization of 125I-IGF-II, and β-glucuronidase binding and endocytosis. Although we have not ruled out a RNAi effect in cells, the observed effects are likely the consequence of the specific cleavage of IGF2R mRNA by the ribozyme we used.
MTT analysis and viable cell counts showed that ribozyme-mediated down-regulation of M6P/IGF2R also resulted in increased cell proliferation. Noticeably, the effect of ribozyme expression on cell growth was more apparent in the presence of IGF-II. This result suggests that the proliferative effect of M6P/IGF2R down-regulation is likely the result of unchecked IGF-II stimulation. Because the M6P/IGF2R is believed to sequester and degrade IGF-II , a decrease in M6P/IGF2R could result in decreased degradation and hence increased bioavailability of IGF-II to the IGF-I receptor, which mediates the growth-promoting effect of IGF-II. Supporting evidence for the involvement of IGF-II in the proliferative effect resulting from loss of M6P/IGF2R function comes from studies of M6P/IGF2R knock-out mice. M6P/IGF2R-null mice display global hyperplasia that coincides with elevated levels of IGF-II. Most importantly, however, the lethal nature of an M6P/IGF2R-null phenotype is reversed in an IGF-II-null background . Although we did not measure extracellular levels of IGF-II, our results show that ribozyme-mediated down-regulation of M6P/IGF2R leads to a decrease in IGF-II internalization, supporting the above possibility.
Our results also showed that M6P/IGF2R down-regulation resulted in decreased sensitivity of MCF-7 cells to TNF-induced apoptosis. Although we do not rule out the potential contribution of the IGF-II pathway to this effect, we would like to consider other potential M6P/IGF2R-dependent mechanisms, such as lysosomal proteases and TGF-β signaling, that may directly affect cell sensitivity to apoptosis. Recent evidence suggests that lysosomal enzymes, such as cathepsins B and D contribute to TNF-induced apoptosis in vitro[35–38] and in vivo. The M6P/IGF2 receptor has been shown to be involved in binding, transport and activation of lysosomal enzymes, including cathepsins [12, 13]. Therefore, it is possible that down-regulation of the M6P/IGF2R results in improper trafficking and activation of cathepsins. This, in turn would eliminate the apoptotic cascades triggered by these enzymes under TNF stimulation and result in decreased sensitivity of MCF-7 cells to apoptosis.
It has also been shown that TNF stimulation involves the activation of TGF-β [40–42], a potent growth inhibitor for many cell types and a ligand of M6P/IGF2R. In fact, activation of TGF-β requires the binding of latent TGF-β to the M6P/IGF2 receptor . Therefore, down-regulation of M6P/IGF2R expression could also lead to a decreased bioavailability of activated TGF-β, thereby decreasing the sensitivity of MCF-7 cells to the TGF-β apoptotic pathway. A detailed mechanism of the observed effect is currently under investigation.
Our findings that ribozyme-mediated decrease in expression and functional activity of the M6P/IGF2R result in a growth advantage for MCF-7 cells indicate that this receptor acts as a negative regulator of cell growth. This is consistent with previous observations that M6P/IGF2R knockout mice displayed generalized increased growth and cardiomygaly (resulting from cardiac myocyte hyperplasia) , and that antisense-mediated reduction of M6P/IGF2R expression enhances tumorigenicity in JEG-3 cells . Thus, loss or mutation of M6P/IGF2R may contribute to development and progression of tumors via different pathways: by increasing the mitogenic activity of IGF-II and decreasing the apoptotic signaling of TGF-β and lysosomal proteases. Further studies using various cell types or using animals are needed to address this issue. Ribozyme technology, as we show here, is a useful tool for these studies.
adenovirus carrying GFP gene
adenovirus carrying both ribozyme against M6P/IGF2R and GFP gene
green fluorescent protein
insulin-like growth factor II
mannose 6-phosphate/insulin-like growth factor II receptor
ribozyme, TGF-β transforming growth factor beta.
We thank Dr. Alexander Leaf and Dr. Dennis Ausiello for their support and encouragement. We are grateful to Zhao B. Kang for his technical assistance. This work was supported by a grant from the NIH (CA79553 to JXK).
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