- Research article
- Open Access
Analysis of colorectal cancers for human cytomegalovirus presence
© Bender et al; licensee BioMed Central Ltd. 2009
- Received: 18 December 2008
- Accepted: 16 April 2009
- Published: 16 April 2009
A possible association between human cytomegalovirus (HCMV) infection and colorectal cancer progression has been inferred by the identification in tumour tissues of HCMV antigens and specific viral DNA or RNA sequences. To further investigate the relationship between HCMV and colorectal cancers we developed qualitative and quantitative PCR assay to detect HCMV DNA in 56 formalin-fixed paraffin-embedded (FFPE) tissue samples from patients belonging to 4 different histological phenotypes: adenoma; poorly, moderately and well differentiated adenocarcinomas.
Of the 56 FFPE tested tissue samples, 6 (11%) were positive for HCMV nested PCR amplification, and more precisely 1 (5%) of 20 cases of adenoma and 5 (21%) of 24 cases of moderately differentiated adenocarcinoma. No PCR positivity was obtained in samples from well and poorly differentiated adenocarcinomas.
Our observations suggest that there is no evidence of a direct association between HCMV and colorectal cancer. Moreover, the results obtained are not supportive of a causal role of HCMV in the processes of carcinogenesis and/or progression of colorectal cancer. However, the fact that the virus may present a "hit and run" like-mechanism and HCMV can thus only be detectable at a particular stage of a processing adenocarcinoma, suggests that a significant number of colorectal cancers might have been the subject of HCMV infection that could contribute to trigger the oncogenic differentiation. Our analysis does not exclude the possibility of HCMV infection subsequent viral clearance.
- Colorectal Cancer
- FFPE Tissue
- HCMV Infection
- Albumin Gene
HCMV is a member of the herpesvirus family and constitutes a major public health problem. HCMV infection is lifelong, and it manifests differently depending on the patient's underlying condition and immunological status. Healthy young people with primary HCMV infection are often asymptomatic but the latent virus can reactivate to cause severe diseases in immunocompromised individuals .
Evidence has already been obtained that HCMV gene products are capable of transforming cells in vitro and of regulating the expression of important host genes, thus inducing a deregulation of cellular pathways relevant to colon adenocarcinoma pathogenesis [1–6].
Furthermore, the identification of HCMV nucleic acids and antigens in tumour tissues, combined with serological evidence, has led to a suggestion of a possible association between HCMV infection and the progression of certain malignancies. Indeed, HCMV infection has been associated with colon adenocarcinoma by several authors [7–11]. However, other studies have found no evidence of a direct association between HCMV infection and adenocarcinoma malignancy [12–17].
The possible contribution of HCMV in the development and progression of colorectal cancer is thus still controversial. To further investigate whether HCMV infection could be responsible for the induction of colorectal cancers and to obtain a precise assessment of the presence of viral DNA in tissue samples, we have performed qualitative and quantitative PCR analyses for HCMV. We have analysed samples obtained from 58 different patients, including 20 adenomas and 38 adenocarcinomas. In order to study the possible relationship between HCMV infection and cancer differentiation we have compared adenomas with adenocarcinomas belonging to 3 different histological phenotypes (poorly, moderately and well differentiated).
Genomic DNA quality control
Nested PCR analysis of HCMV in adenomas and adenocarcinomas
Phenotype and PCR results for FFPE samples of colorectal cancer
number of samples
HCMV PCR positive samples
poorly differentiated adenocarcinomas
moderately differentiated adenocarcinomas
well differentiated adenocarcinomas
Since the presence of HCMV DNA was found only in a reduced subset of colorectal cancers, these results suggest that there is no evidence of a direct causal association between HCMV infection and induction of poorly or well-differentiated adenocarcinomas. However, viral DNA was found in approximately 21% of moderately differentiated adenocarcinomas, suggesting that the virus, although not essential to progression towards the transforming phenotype, could conceivably have a role in the initiation of the tumorigenic event.
Quantitative PCR analysis
We developed a real-time PCR quantitative analysis using SYBR® Green I to quantify the viral load in the nested PCR-HCMV positive samples. A standard curve was generated by 10 fold serial dilutions (8 × 105 – 8 copies) of a plasmid containing a single copy of HCMV US28 gene. The regression curve analysis consisting of 5 points tested in triplicate gave a reaction with an efficiency of 100% and a Spearmann's correlation coefficient (R2) of 0.99. Quantitative PCR analysis of DNA extracts from FFPE tissues did not allow to obtain reproducible data since the efficiency of PCR was lower (60%, R2 = 0.82) than the 100% standard required. Also the replicate values, from a paraffin-embedded tissue, were discordant (Ct standard deviation ≥ 1) and the dissociation curve highlighted the presence of non specific amplified products in target samples.
The difficulty in obtaining reliable data from clinical samples is probably linked to the process of paraffin removal that may result in formation of inhibitory substances [18, 19] which interfere with the PCR reaction and reduce PCR efficiency .
Although this method did not allow quantitation in deparaffinised samples, the real time PCR assay confirmed the qualitative positivity obtained by nested PCR in 2 tested samples (data not shown).
The role of HCMV in the development and progression of colorectal cancers has not yet been clarified. The presence of HCMV antigens and nucleic acids in colorectal cancers has been obtained by means of molecular and virologic studies and a direct relationship between the virus and cancer was suggested [7–11]. However, in other studies, no evidence of a direct association between colorectal cancer and HCMV infection was found [12–17].
More specifically, Harkins et al.  have conducted a study on 29 specimens of colorectal polyps and adenocarcinomas from different patients using immunohistochemistry with two different antibodies, and reported the presence of HCMV proteins in about 80% of polyps and 85% of adenocarcinomas, but not in adjacent healthy tissues. In addition, by means of PCR and DNA sequencing, the presence of viral nucleic acids was detected in 6 tumours (5 adenocarcinomas and 1 polyp) that were immunoreactive for HCMV, whereas it was not detected in healthy tissues from 3 of the same 6 patients. These results suggested a possible causative association between HCMV and colorectal cancer. Akintola-Ogunremi et al.  examined 23 colorectal hyperplastic polyps, 65 colorectal adenomas and 51 colorectal adenocarcinomas by immunohistochemical analysis with two different antibodies. No nuclear HCMV antigen positivity was detectable in any of the studied cases. In addition, PCR analysis failed to detect viral DNA in 24 selected cases showing non-specific cytoplasmic immunostaining. These results are in stark contrast to those reported by Harkins et al , since no evidence of HCMV DNA and proteins in human colorectal adenocarcinomas and their precursor lesions was found.
Knösel et al  investigated the presence of HCMV DNA and antigens, by using PCR analysis and immunohistochemistry. Fifty seven primary tumours and 20 metastases of fresh colorectal cancer tissue were tested, including 13 tumour pairs (primary and metastases) from the same patient. Four (7%) of 57 primary tumours were found positive for HCMV DNA by PCR, whereas all metastases were negative. In addition, no specific staining was detected by immunohistochemistry analysis. Although these results confirmed the results of Akintola-Ogunremi et al  indicating that there is no direct association between HCMV infection and progression or formation of metastases in colorectal cancer, evidence of HCMV positivity in a small number of colorectal neoplasms was found in the primary tumours.
Given the controversial conclusions of the reported results, we further investigated the issue by establishing a specific qualitative PCR analysis and a quantitative PCR reaction for HCMV viral load determination.
The nested PCR analysis conducted in our laboratory allowed the identification of HCMV sequence in 6 (10.7%) of 56 tissue samples tested, and more precisely in 1 (5%) of 20 cases of adenoma and 5 (20.8%) of 24 cases of moderately differentiated adenocarcinomas. However, there was no evidence of HCMV DNA in any of 5 cases of well-differentiated adenocarcinoma nor in 7 cases of poorly differentiated adenocarcinoma, suggesting the lack of a causative association between virus infection and cancer development in these two groups of adenocarcinomas.
Of interest is the detection of HCMV DNA in 20.8% of moderately differentiated adenocarcinomas, whereas it was undetectable in poorly and well-differentiated carcinomas, similar to the findings of Knösel et al. . It has been reported, in transformed HCMV cells, that the HCMV infection could present a "hit and run" oncogenic-like mechanism [2, 21], though viral DNA is undetectable in metastases. It's presence in earlier histological stages may suggest that the presence of HCMV DNA might not be essential to progress toward the transforming phenotype. Following the "hit and run" like mechanism, the virus could mediate cellular transformation through an initial hit, while maintenance of the transformed state is compatible with the loss of viral molecules. Thus, the fact that we have detected viral DNA only in moderately differentiated carcinomas may reflect the inability of HCMV to infect poorly differentiated cancer cells .
The quantitative real time PCR analysis was validated on HCMV DNA strains, but could not give reproducible data on DNA extracted from paraffin embedded samples. This could potentially be due to the presence of inhibitors in biopsy samples that can interfere with the PCR. Quantification of HCMV viral load by real-time PCR can yield important information on the timing of HCMV infection. Therefore, validation of the real-time PCR protocol in non-paraffin embedded samples could represent a useful tool for the identification of HCMV in human cancer.
In conclusion, our observations, together with those of other authors [16, 17] suggest that there is no evidence of a direct association between HCMV and colorectal cancer. Moreover, there is no evidence supporting that HCMV can fulfil the necessary criteria for defining a causative role in the process of carcinogenesis and or progression of colorectal cancer. One of these requirements is, in fact, the regular presence and persistence of the nucleic acid of the respective infectious agent in cells of the specific tumour type [23, 24].
However, the fact that the virus may present a "hit and run" like-mechanism and that it was found only in a particular stage of a processing adenocarcinomas, provides a useful indication that a certain type of adenocarcinoma have been infected by HCMV and that this could have contributed to trigger the oncogenic differentiation.
The specimens included in this study consisted of 10% FFPE tissue blocks of colorectal tumours from the archives of the Pathology section of the Department of Pathology, University of Verona, Italy. Samples of 58 biopsies were obtained from different patients of which 20 were adenomas and 38 adenocarcinomas. Of the 38 adenocarcinomas, 5 were well differentiated, 25 moderately differentiated and 8 poorly differentiated.
Biopsies and histology
Samples were independently reviewed by two pathologists (AZ and FM) and classified according to the WHO classification of tumours of the digestive system. In case of discrepancy, a consensus was reached by reviewing discordant cases at a multi-head microscope. Representative tissue blocks were selected for DNA extraction, selecting blocks with high tumour content.
Isolation of genomic DNA from paraffin-embedded tissues
Four 3 μm sections of each sample were deparaffinised with xylol/ethanol, collected into a 1.5 ml Eppendorf tube containing 100 μl of lysis solution: 0.1 M NaCl, 0.15 M EDTA pH 8.0, 0.1 M Tris-HCl pH 8.0, 1% SDS, 45.8 mM β-mercaptoethanol and 100 μg Proteinase K. The tubes were incubated at 55°C for 3 hours, followed by Proteinase K heat inactivation. Samples were centrifuged at room temperature at 10.000 g for 5 min. The supernatants were collected and stored at -20°C, prior to the PCR amplification procedure.
Polymerase chain reaction analysis
Since DNA extracted from paraffin-embedded tissue might be partially degraded during formalin fixation or paraffin embedding , DNA quality was tested using the following PCR primers specific for the human albumin gene: primer alb fw (5'gctgtcatctcttgtgggctgt 3') and primer alb rv (5'actcatgggagctgctggttc 3'). A total of 56 samples were considered suitable to be tested for the presence of HCMV viral DNA.
Primers used for HCMV DNA amplification by nested PCR
UL55 gene position
655 to 675
902 to 922
685 to 705
847 to 867
The first-round of PCR amplification was performed in a 20 μl reaction containing 2–5 μl of each genomic DNA sample. As positive controls for PCR reactions 3 different HCMV DNA samples were used: DNA extracted from human fibroblasts cultured in vitro and infected with an HCMV strain from a newborn baby with congenital infection and viral DNA of the two laboratory strains AD169 and Towne. Each experiment was conducted using positive and negative controls.
For the first amplification round, after an initial denaturing step at 94°C for 5 min, 35 cycles of denaturation at 94°C for 30 sec, annealing at 58°C for 30 sec, extension at 72°C for 30 sec, were made, followed by a final extension at 72°C for 6 min. The amplified products were subjected to the second round of PCR using the primer pair I-1/I-2 and 1 μl of the first round amplification product. Cycling program was performed as follows: 94°C for 5 min, 1 cycle; 94°C for 30 sec, 59°C for 30 sec, 72°C for 30 sec, 40 cycles; 72°C for 5 min, 1 cycle.
At the end of the amplification 15–20 μl of each product were analysed on 2.5% w/v agarose gels by electrophoresis.
Primers used for HCMV DNA amplification by real-time quantitative PCR
267671 to 267690
267718 to 267735
Reactions were performed under the following conditions: 95°C for 5 min, followed by 45 cycles at 95°C for 20 sec and 60°C for 1 min.
Data were collected and analysed by Sequence Detection System Software (Applied Biosystems).
We thank Dr. Sunwen Chou (Division of Infectious Diseases, Oregon Health Sciences University, Portland, USA) for providing AD169 and Towne laboratory HCMV strains. We also thank the Division of Microbiology, Immunology and Virology of the Ospedale Maggiore di Borgo Trento, Verona, Italy, for providing a sample of HCMV infected human fibroblasts. This study was supported in part by MIUR PRIN 2005 and Cariverona (to U. Bertazzoni).
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