- Research article
- Open Access
- Open Peer Review
Expression of NDRG2 is down-regulated in high-risk adenomas and colorectal carcinoma
© Lorentzen et al; licensee BioMed Central Ltd. 2007
- Received: 18 June 2007
- Accepted: 12 October 2007
- Published: 12 October 2007
It has recently been shown that NDRG2 mRNA is down-regulated or undetectable in several human cancers and cancer cell-lines. Although the function of NDRG2 is unknown, high NDRG2 expression correlates with improved prognosis in high-grade gliomas. The aim of this study has been to examine NDRG2 mRNA expression in colon cancer. By examining affected and normal tissue from individuals with colorectal adenomas and carcinomas, as well as in healthy individuals, we aim to determine whether and at which stages NDRG2 down-regulation occurs during colonic carcinogenesis.
Using quantitative RT-PCR, we have determined the mRNA levels for NDRG2 in low-risk (n = 15) and high-risk adenomas (n = 57), colorectal carcinomas (n = 50) and corresponding normal tissue, as well as control tissue from healthy individuals (n = 15). NDRG2 levels were normalised to β-actin.
NDRG2 mRNA levels were lower in colorectal carcinomas compared to normal tissue from the control group (p < 0.001). When comparing adenomas/carcinomas with adjacent normal tissue from the same individual, NDRG2 expression levels were significantly reduced in both high-risk adenoma (p < 0.001) and in colorectal carcinoma (p < 0.001). There was a trend for NDRG2 levels to decrease with increasing Dukes' stage (p < 0.05).
Our results demonstrate that expression of NDRG2 is down-regulated at a late stage during colorectal carcinogensis. Future studies are needed to address whether NDRG2 down-regulation is a cause or consequence of the progression of colorectal adenomas to carcinoma.
- Colorectal Carcinoma
- Colorectal Adenoma
- Flexible Sigmoidoscopy
N-myc Downstream Regulated Gene 2 (NDRG2) is a member of a recently identified gene family which has been implicated in human nervous system disorders and cancer . Although the four members of this family contain a putative α/β-hydrolase fold, it is unclear whether or not they have enzymatic activity . NDRG1 was first identified as a gene under negative regulation by N-myc in early mouse development . NDRG2 was identified through sequence homology and is implicated in cell growth, differentiation and neurodegeneration [4–7]. Recently, it has been shown that expression of NDRG2 is transcriptionally repressed by c-Myc .
Several studies have suggested that NDRG2 mRNA is down-regulated or undetectable in a number of human cancers and cancer cell-lines [4, 9–11]. Semiquantitative RT-PCR was used to demonstrate that NDRG2 expression levels were reduced in squamous cell carcinoma, pancreatic cancer and glioblastoma compared to normal tissue [4, 9, 11]. NDRG2 expression levels in gliomas and meningiomas were significantly attenuated in high-grade compared to low-grade tumors [4, 10]. In meningiomas, higher expression of NDRG2 mRNA correlated with clinically less aggressive tumors . Furthermore, NDRG2 was identified as a gene whose expression in high-grade gliomas was positively correlated with survival . Forced NDRG2 overexpression in a human glioblastoma cell-line markedly inhibited cell proliferation . These findings implicate NDRG2 as a possible tumor suppressor gene.
Prompted by the finding that NDRG2 expression correlates inversely with tumor grade in various cancers, we set out to analyse NDRG2 mRNA expression during colorectal carcinogenesis in humans.
Characteristics of cases and healthy persons in this study.
n = 15
n = 15
n = 57
n = 50
Mean age 2 (SD)
Cancer Profiling Array (CPA)
The Cancer Profiling Array II (Clontech) was hybridised with 50 ng of radioactively labelled NDRG2 probe according to the manufacturer's instructions. The 460 bp NDRG2 probe was generated by PCR using the primers 5'CTCACTCTGTGGAGACACCAT3' and 5'GGGTGATATCACCTCCACGCT3'. The hybridised array was exposed to a phosphorimaging screen for 24 hours and the intensity of each spot was quantified using ImageQuant (Molecular Dynamics). The CPA consists of paired cDNA samples generated from the total RNA of normal and tumor tissue. Because the array is normalised for several housekeeping genes, quantification of the hybridisation signal provides an estimate of relative transcript abundance.
Total RNA was purified from tissue as recommended by the manufacturers using an e.z.n.a. Gel Extraction kit (Omega Biotek). The tissue had been snap-frozen in liquid N2 and stored at -80°C before RNA purification. RNA purification included a DNAse treatment. The cDNA synthesis was performed on approximately 200 ng RNA per 10 μl using the High Capacity cDNA Reverse Transcription kit (Applied Biosystems, Nærum, Denmark). Quantitative RT-PCR was performed on an ABI7500 sequence detection system (Applied Biosystems) in Universal Mastermix (Applied Biosystems) using 220 nM probe and 700 nM primers for NDRG2. NDRG2 primers were NDRG2F: 5'CGATCCTTACCTACCACGATGTG3' and NDRG2R: 5'GCATGTCCTCGAACTGAAACAGT3' and the probe was 5'FAM-CTCAACTATAAATCTTGCTTCC-MGB-NFQ-3'. Primers were designed using Primer Express v3.0 Software and obtained from DNA Technology A/S. Primers were designed within different exons and with a probe covering the exon-exon border to prevent amplification of genomic DNA. The probe recognises all splice forms of NDRG2. β-actin primers and probe were obtained from Applied Biosystems. In a validation experiment using a control sample, a dilution series was produced and assayed for NDRG2 and β-actin expression as described in the comparative Ct method . When Ct values were plotted against log dilution it was shown that the assays are quantitative over a range of 128-fold dilution for both NDRG2 and β-actin and that the PCR reactions have similar efficiencies provided that a threshold of 0.2 is used for β-actin, while the threshold was 0.07 for NDRG2. The threshold is a fixed fluorescence signal above the baseline. The Ct value of a sample is determined as the fractional cycle number when the sample's fluorescence signal exceeds the threshold. The threshold is thus assay-specific, determined in the validation experiment and depends on the background of the individual assay.
NDRG2 and β-actin mRNAs were quantified separately in triplicates. The average standard deviations on triplicates were 15% and 11% for NDRG2 and β-actin respectively. The standard deviation on repeated measurements of the same sample (internal control) in separate experiments was 16% for NDRG2, indicating the day-to-day variation of the assay. Negative controls (where the RNA was not converted into cDNA) and positive controls were included in all sets. Two independent PCR reactions of 28 samples (5%) yielded a correlation coefficient of 0.95, indicating a high reproducibility of the assay.
GraphPad Prism 4 was used for the statistic calculations. The data were not adjusted for sex since the incidence ratio of colorectal cancer between genders (Male: 1128 and female: 1217 new cases in 2004) is 1:1 in Norway . P values < 0.05 were considered significant for all statistical tests.
Expression of NDRG2 mRNA in colonic adenomas and carcinomas
Expression analysis of NDRG2 in colon cancer using a Cancer Profiling Array.
Mean values of normalised levels of NDRG2 mRNA in normal and affected colonic tissues.
mRNA level in normal tissue Mean (SD)
mRNA level in adenomas/carcinomas Mean (SD)
Carcinoma Normal (distant)
< 0.001 c
Carcinoma Normal (adjacent)
< 0.001 d
Further analysis of the different groups of affected tissue using a paired two-tailed t-test showed that the level of NDRG2 in individuals with low-risk adenoma did not show any significant difference between normal and neoplastic tissue. However, a comparison of normal and high-risk adenoma from the same individual showed a highly statistically significant reduction (p < 0.001) in NDRG2 level. Finally, comparing the level of NDRG2 mRNA in normal tissue far (normal distant) and close (normal adjacent) to that of the tumor in the surgical specimens of CRC patients showed a statistically significant difference (p < 0.001) in both cases (Table 3).
Mean values of normalised levels of NDRG2 mRNA in adenomas1.
mRNA level in normal tissue Mean (SD)
mRNA level in adenomas Mean (SD)
Analysis of expression levels in carcinomas according to Dukes' staging
Expression patterns of NDRG2 between genders in colorectal cancer
In the present study we demonstrated that NDRG2 mRNA expression levels were lower in colonic tumors than in normal colon tissue from the same individual. This was observed using two distinct subject populations, one of which was a Norwegian cohort, the other a group of affected individuals based on a commercially available product. The difference in mRNA level is likely to be reflected at the level of NDRG2 protein, since NDRG2 mRNA levels have previously been shown to correlate well with protein levels .
In the Norwegian cohort, NDRG2 mRNA levels were statistically significantly reduced in colorectal carcinoma when compared to the healthy controls. In order to examine whether the risk of carcinoma is affected by changes in the microenvironment, expression levels of NDRG2 in the lesion were compared to normal adjacent tissue as well as to normal tissue distant from the tumor. NDRG2 mRNA was statistically significantly reduced in tumor compared to either normal tissue sample. No difference was observed between the adjacent and distant samples, suggesting that changes in NDRG2 expression in the carcinoma are not attributable to the microenvironment.
Recent studies have demonstrated that colorectal cancer is a heterogenous disease with distinct molecular components. Distinct genetic or epigenetic alterations have been identified which correlate with the location of the tumors . Although it was not investigated in this study, it could be interesting to compare NDRG2 expression in tumors located in either the proximal or distal colon.
There was a tendency for decreasing NDRG2 mRNA levels with increasing tumor stage according to Dukes' staging of the CRC samples, and this trend was found to be significant using linear regression (p < 0.05). Our results are in agreement with that observed for other cancer types where NDRG2 expression is reduced in high-grade compared to low-grade tumors [4, 10]. This trend indicates either that the loss of NDRG2 promotes tumor progression or that NDRG2 is inactivated by factor(s) present at advanced tumor stages. NDRG2 has previously been shown to be negatively regulated by the c-Myc oncoprotein  and it is possible that elevated levels of c-Myc would result in reduced expression of NDRG2. Thus, it could be interesting to elucidate whether or not an increased level of c-Myc, which is a frequent event in colorectal cancer , correlates with a decreased level of NDRG2. Measurement of c-Myc levels was not included in these studies. However, we have investigated a subset of the CRC samples (n = 54) from the KAM study for β-catenin expression by immunohistochemistry. All of the tested CRC samples are positive for cytoplasmic β-catenin and 72% are β-catenin positive in all nuclei (data not shown). The remaining samples contain nuclear β-catenin in occasional nuclei. This suggests that c-Myc levels are likely to be elevated since c-Myc is known to be positively regulated by nuclear β-catenin .
In order to determine the stage at which NDRG2 expression is down-regulated in the adenoma-carcinoma sequence we also examined normal and affected tissue from low- and high-risk adenomas. When comparing affected tissue with normal tissue from the same individual, we found a statistically significant difference for individuals with high-risk adenomas. However, when compared to the control group of healthy individuals, only the affected tissue from individuals with colorectal carcinoma shows a statistically significant reduction in NDRG2 mRNA levels. Our results suggest that down-regulation of NDRG2 expression occurs during the progression from adenoma to carcinoma.
Whether down-regulation of NDRG2 in colorectal carcinoma is a cause or a consequence of malignant progression is at present unclear. Although the structure of NDRG2 resembles that of a hydrolase , its ability to function as an enzyme is presently unknown. It has recently been shown that overexpression of NDRG2 in a glioblastoma cell-line inhibits cell proliferation  and that NDRG2 expression correlates positively with survival in high-grade glioma . NDRG2 levels are also reduced in several cancer types and cell-lines [4, 9–11]. Thus, NDRG2 may have a general function in diverse tissues as a tumor suppressor gene. Future studies will be needed to examine whether increased NDRG2 levels in colorectal carcinoma correlate with improved prognosis.
In conclusion, NDRG2 mRNA levels were decreased in both high-risk colorectal adenoma and in colorectal carcinoma compared to corresponding normal colonic mucosa from the same individual. Furthermore, NDRG2 expression was reduced in colorectal carcinoma compared to normal tissue from healthy individuals. Our results suggest that NDRG2 down-regulation correlates with the progression of dysplastic tissue to carcinoma. Future studies are needed to address whether NDRG2 down-regulation is a cause or consequence of colorectal carcinogenesis.
This work was supported by The Norwegian Cancer Society (Grant numbers 51024/001 and E01-0851001), Telemark University College (Grant number 22069), the Norwegian Colorectal Cancer Prevention (NORCCAP) study, grants from the Norwegian Cancer Society and the Department of Health and Social Affairs with the aid of EXTRA funds from the Norwegian Foundation for Health and Rehabilitation (2001/2/0110), Eastern Norway Regional Health Authority, the Danish Medical Research Council, Novo Nordisk Foundation and the Danish Cancer Society (DP05117).
We thank Dr. Gunter Bock and Dr. Egil Johnson for collecting tumor tissues and Dr. Steinar Aase for contributing to the pathology of the cancer cases.
We thank Christel A. Halberg for her excellent technical assistance.
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