- Research article
- Open Access
Increased mRNA expression levels of ERCC1, OGG1 and RAIin colorectal adenomas and carcinomas
BMC Cancer volume 6, Article number: 208 (2006)
The majority of colorectal cancer (CRC) cases develop through the adenoma-carcinoma pathway. If an increase in DNA repair expression is detected in both early adenomas and carcinomas it may indicate that low repair capacity in the normal mucosa is a risk factor for adenoma formation.
We have examined mRNA expression of two DNA repair genes, ERCC1 and OGG1 as well as the putative apoptosis controlling gene RAI, in normal tissues and lesions from 36 cases with adenomas (mild/moderat n = 21 and severe n = 15, dysplasia) and 9 with carcinomas.
Comparing expression levels of ERCC1, OGG1 and RAI between normal tissue and all lesions combined yielded higher expression levels in lesions, 3.3-fold higher (P = 0.005), 5.6-fold higher(P < 3·10-5) and 7.7-fold higher (P = 0.0005), respectively. The levels of ERCC1, OGG1 and RAI expressions when comparing lesions, did not differ between adenomas and CRC cases, P = 0.836, P = 0.341 and P = 0.909, respectively. When comparing expression levels in normal tissue, the levels for OGG1 and RAI from CRC cases were significantly lower compared to the cases with adenomas, P = 0.012 and P = 0.011, respectively.
Our results suggest that increased expression of defense genes is an early event in the progression of colorectal adenomas to carcinomas.
Most colorectal cancers (CRC) develop through multiple mutations in the normal colonic mucosa, and evolve through the adenoma-carcinoma sequence [1, 2]. Various endogenous and exogenous agents from environmental exposures are constantly damaging DNA, and in combination with low DNA repair capacity this have been interpreted as increasing the likelihood of cancer development [3–7].
The range of different DNA lesions is broad and there are different repair pathways depending on the nature of the damage. Nucleotide excision repair (NER) will repair bulky adducts  while base excision repair (BER) is responsible for the repair of base damage and single strand breaks . Only a few studies have to our knowledge studied DNA repair expression of nucleotide excision repair (NER) and base excision repair (BER) genes in CRC. Even less is known about the level and significance of DNA repair expression during the formation of adenomas and the transition period in the adenoma-carcinoma sequence. Previous studies have indicated that the NER gene excision repair cross-complementation group1 (ERCC1) and BER gene 8-oxoguanine glycosylase 1 (OGG1) may be inducible  and they have also been shown to correlate with enhanced DNA repair activities [11–15]. DNA repair mechanisms are complex and involve several genes. OGG1 and ERCC1 are among the few for which it has been shown that mRNA levels and repair activity correlate. The ERCC1 gene encodes a subunit of the nucleotide excision repair complex required for the incision step of NER [16, 17]. Several factors indicate that the ERCC1 mRNA levels can be used as a proxy for DNA repair capacity. The mRNA levels of ERCC1 may correlate with DNA repair capacity in various tissues [11–13, 15], and also predict the response to chemotherapy (high ERCC1 levels have been associated with tumor growth and lower levels have been associated with improved disease response) [15, 18–21]. In addition, inter-individual variation of ERCC1 mRNA levels is much larger than the intra-individual variation , indicating that the mRNA level of ERCC1 may be used as a biomarker for NER.
The enzymes responsible for the BER process which repair damaged bases, abasic sites and single-strand breaks are initiated by specific DNA glycosylases. The DNA glycosylase OGG1 removes 8-oxo-guanine (8-oxoG) directly from damaged DNA [23, 24]. Kondo et al concluded that there is a correlation between 8-OHdG levels and hOGG1 expression in CRC tissue . Kondo et al also concluded that colorectal carcinoma cells but not adenoma cells are exposed to more oxidative stress than corresponding normal tissue . Previous studies have shown that oxidative stress is generally proportional to OGG1 mRNA expression and activity [10, 26, 27]. To the best of our knowledge, it has not been investigated if increased OGG1 expression is an early or late event in the adenoma-carcinoma sequence. It is therefore of interest to study and compare the expression of OGG1 in adenoma and carcinoma tissues.
There are several responses to DNA damage including induction of apoptose to eliminate damaged cells. The putative apoptosis controlling gene RAI was included to determine if the expression of RAI was coordinated with the expression of ERCC1. Both genes are located on chromosome 19q13.2. The RelA associated inhibitor (RAI) gene, encodes an inhibitor of the RelA subunit of the transcription factor NF-κB . The inclusion of this gene is more explorative but previous studies suggest that RAI is involved in carcinogenesis . High levels of RAI seem to promote apoptosis while low levels of RAI may inhibit apoptosis, although the literature is not clear on this issue [28, 30]. This is to the best of our knowledge the first study to investigate if increased RAI expression is an early or late event in the adenoma-carcinoma sequence.
In this study we have measured mRNA levels of ERCC1, OGG1 and RAI in patients with colorectal adenomas and carcinomas (normal colonic mucosa and lesions).
The main focus was to investigate if increased expression of DNA repair genes is an early or late event in the adenoma-carcinoma sequence. By studying repair genes in the various stages of the adenoma-carcinoma sequence, we may gain new information on the significance of repair capacity in normal and neoplastic tissues during transition.
The KAM biobank (Kolorektal cancer, Arv og Miljø) is based on the screening group of the Norwegian Colorectal Cancer Prevention study (The NORCCAP study) in the county of Telemark . The ID number for the NORCCAP study at clinicaltrials.gov is I NCT00119912 . The KAM biobank has previously been described by Hansen et al. . In the present study we have selected and analyzed cases with adenocarcinomas (9) and cases with adenomas (36). The sampling pool of cases contains tissue (normal colonic mucosa and lesion) from 180 CRC cases and 242 adenoma cases. The cases are matched for age and gender. The adenocarcinomas were collected prior to chemo- or radiotherapy treatment. The tumor histology of the adenomas was examined independently by two specialist histopathologists in order to determine the tumor stage as either mild/moderate (n = 21) or severe (n = 15) dysplasia (tumor cellularity 60–80%). They reached the same conclusion in all cases. All cases completed a questionnaire containing information on a family history of cancer and the included cases had no known personal history of cancer. The KAM cohort consists of an ethnic homogeneous group of Norwegian origin. The KAM study is approved by the Regional Ethics Committee and The Data Inspectorate.
Total RNA was purified from normal colonic mucosa and lesions as recommended by the manufacturers using NucleoSpin DNA II kit (Macherey Nagel). The tissue had been snap frozen in liquid N2 before RNA purification. RNA purification included a DNAse treatment. The cDNA synthesis was performed on ca. 200 ng RNA in a final volume of 10 μl using Gold RT-PCR kit (Applied Biosystems, Nærum, Denmark).
Quantitative PCR was performed on ABI 7500 sequence detection system (Applied Biosystems, Nærum, Denmark) in universal mastermix (Applied Biosystems, Nærum, Denmark) using 100 nM Taqman probe and 200 nM primers for ERCC1 and for OGG1, 100 nM probe and 600 nM primers for RAI. ERCC1, OGG1 and RAI primers and probes were obtained from TAG Copenhagen, Copenhagen, Denmark. The OGG1 probe recognizes all splice forms of OGG1. The expression was normalized to 18S rRNA. 18S primers and probes were commercially available from Applied Biosystems, Nærum, Denmark.
The quantification of mRNA levels has been described previously [22, 34]. The probes and primers have been validated, and the PCR was shown to be quantitative over a range of 130-fold dilution for ERCC1 and OGG1 and over a 32-fold range for RAI. mRNA measurements were excluded if the 18S content was below the detection level of the individual mRNA defined by the validation experiments. ERCC1, OGG1, RAI mRNA and 18S levels were quantified in triplicate in separate wells. The average mRNA level of the specific mRNAs was then normalized to the average 18S level. The average standard deviation on triplicates was 15 %. The standard deviations on repeated measurements of the same sample (the control) in separate experiments were 34%, 21% and 25% for ERCC1, OGG1 and RAI, respectively, indicating the day-to-day variation of the assay. Independent PCR reactions of the same samples yielded a correlation coefficient of 0.97. Negative controls (where the RNA was not converted to cDNA) and positive controls were included in all sets.
For comparison of different mRNA expression levels between normal tissue and lesions in cases we used paired t-test. When comparing expression levels in normal colonic mucosa from all cases, and lesions in all the cases separately, a one-way ANOVA test was used. P values < 0.05 were considered significant for all statistical tests. For trend analysis of normal colonic mucosa in OGG1 and RAI we used logistic regression after dividing cases in mild/moderate dysplasia (1), severe dysplasia (2) and CRC (3). MiniTab Statistical Software, Release 13.1 Xtra (Minitab Inc.) was used for statistical calculations.
The distributions of age and gender are described in Table 1. Cases are divided into three groups according to diagnosed degree of dysplasia; adenomas (mild/moderate or severe dysplasia) and carcinomas. mRNA expression in normal colonic mucosa and all lesions for the three genes, ERCC1, OGG1 and RAI are displayed separately in Figure 1 (A, B, C), and mean values are displayed in Table 2.
For all three genes, ERCC1, OGG1 and RAI, a comparison of expression levels between normal colonic mucosa and lesions in all cases combined (adenomas and CRC) yielded significantly higher expression levels in lesions, 3.3-fold P = 0.005, 5.6-fold P < 3*10-5 and 7.7-fold P = 0.0005, respectively. When comparing expression levels between normal colonic mucosa and lesions separately for each case group (mild/moderate dysplasia, severe dysplasia and CRC), we detected significantly higher expression levels for ERCC1 and RAI in cases with severe degree of dysplasia and for OGG1 we detected significantly higher expression levels in cases with severe degrees of dysplasia and CRC (Table 2).
When comparing expression levels of ERCC1 in lesions only, we detected no difference between the adenoma and CRC case groups, P = 0.836. This was also true for normal tissue, P = 0.291, (Fig 1A).
The level of OGG1 expression when comparing lesions did not differ between adenoma and CRC cases P = 0.34, (Fig 1B), but for normal colonic mucosa the OGG1 expression in CRC patients was statistically significantly lower than in normal colonic mucosa from adenoma cases with mild/moderate dysplasia, P = 0.012, (Fig 1B). A trend of lowered mRNA expression with increasing degree of dysplasia was also observed in normal colonic mucosa, P = 0.003.
The level of RAI expression when comparing lesions did not differ between adenoma and CRC cases, P = 0.909, (Fig 1C). The level of expression in normal colonic mucosa was however significantly lower in CRC cases compared to adenoma cases with mild/moderate dysplasia, P = 0.043, (Fig 1C). A trend of lowered mRNA expression with increasing degree of dysplasia was also observed in normal colonic mucosa, P = 0.011.
In this study we have measured mRNA levels of ERCC1, OGG1 and RAI in patients with colorectal adenomas and carcinomas (normal colonic mucosa and lesions). We have compared expression levels between corresponding normal colonic mucosa and lesions in both adenoma and CRC cases. In order to see if an increase in expression is an early or late event in the adenoma-carcinoma sequence we have also compared expression levels between case groups in normal colonic mucosa and lesions separately.
ERCC1 expression was statistically significantly higher in lesions than in the corresponding normal tissue when all cases were combined. For OGG1 and RAI, a similar increase in mRNA levels in lesions compared to the corresponding normal colonic mucosa was detected. Previous studies have shown that the mRNA levels of ERCC1 [11–13, 15, 35] and OGG1 [10, 14, 27] correlate with the DNA-repair capacity in various tissues. The increased mRNA level detected in lesions in this study may therefore be interpreted as enhanced DNA repair activity.
Low expression of DNA repair genes in lymphocytes have previously been shown in patients with breast cancer, lung cancer and cancer of the head and neck [4–7]. This has been interpreted as low DNA repair gene expression is a risk factor for cancer. For both OGG1 and RAI we found that the expression was lower in normal colonic mucosa from CRC patients than in normal colonic mucosa from persons with mild/moderate dysplasia. This lowered mRNA level can either be interpreted as a risk factor for adenoma and CRC development but it can also be a consequence of the same.
When comparing different lesions in the adenoma-carcinoma sequence, we detected no significant difference in expression. This was true for all three genes, ERCC1, OGG1 and RAI. This may indicate that increased expression of DNA repair is an early event in the adenoma-carcinoma sequence. The result for RAI may be an indication that RAI and ERCC1 are coordinated as they both are located on chromosome 19q13.2. The NER gene XPD is also located on chromosome 19q13.2 and a previous study by Vogel et al concluded that ERCC1 and XPD mRNA quantities were highly correlated . The RAI mRNA is many-fold induced during apoptosis and the induction is essential to apoptosis (Magdalena Laska et al, manuscript in preparation). Increased RAI expression has previously been observed in acute leukaemia cells . We and others have found that RAI mRNA is also often increased in cancer cells (Bergamaschi et al  and this paper). We interpret this increase as an attempt on the part of the cancer cells to activate the apoptotic pathway. However, that attempt is presumably abortive as the cancer cells continue to multiply. Possibly, the well-known derangement of the intracellular control in cancer cells may have destroyed other essential factors and/or the downstream response.
Higher expression of DNA repair genes in lesions compared with normal colonic mucosa may indicate chemoresistance. The difference in expression levels between normal colonic mucosa and lesions for both ERCC1 and OGG1 could mean that lesions in general have a higher DNA repair capacity and therefore is less sensitive to DNA damaging agents such as chemotherapy. Shirota et al showed that CRC patients with low levels of intratumoral mRNA ERCC1 expression had significantly better survival than patients with high expression, when treated with 5-FU and oxaliplatin as second- or third-line chemotherapy .
Hereditary cancer predisposition syndromes have provided insight to the importance of DNA repair, but there are only limited data on inter-individual variation in DNA repair and susceptibility to sporadic cancer. Vogel et al detected an inter-individual mRNA variation for ERCC1 and OGG1 that was 5–10 fold in healthy volunteers , and a study by Paz-Elillzur et al concluded that low OGG1 activity was associated with an increased risk of lung cancer . However, in the only prospective study of mRNA levels of DNA repair genes and RAI, low expressions of ERCC1, XPD or RAI were not associated with increased risk of lung cancer . In a study by Hansen et al  the OGG1 Ser326Cys polymorphism, which has a reduced glycosylase activity , was not associated with an increased risk of colorectal adenomas or carcinomas.
In conclusion, mRNA levels of ERCC1 and OGG1 were up-regulated in both colorectal adenomas and carcinomas compared to corresponding normal colonic mucosa, indicating that increased expression of defense genes is an early event in the progression of colorectal adenomas to CRC. There are some issues that must be considered when evaluating our findings. The number of cases is relatively small, therefore there is a possibility that the reported findings are due to chance. Larger prospective studies would be required to clarify this issue.
Kinzler KW, Vogelstein B: Lessons from hereditary colorectal cancer. Cell. 1996, 87 (2): 159-170. 10.1016/S0092-8674(00)81333-1.
Fearon ER, Vogelstein B: A genetic model for colorectal tumorigenesis. Cell. 1990, 61 (5): 759-767. 10.1016/0092-8674(90)90186-I.
Dybdahl M, Frentz G, Vogel U, Wallin H, Nexo BA: Low DNA repair is a risk factor in skin carcinogenesis: a study of basal cell carcinoma in psoriasis patients. Mutat Res. 1999, 433 (1): 15-22.
Wei Q, Matanoski GM, Farmer ER, Hedayati MA, Grossman L: DNA repair capacity for ultraviolet light-induced damage is reduced in peripheral lymphocytes from patients with basal cell carcinoma. J Invest Dermatol. 1995, 104 (6): 933-936. 10.1111/1523-1747.ep12606207.
Wei Q, Cheng L, Hong WK, Spitz MR: Reduced DNA repair capacity in lung cancer patients. Cancer Res. 1996, 56 (18): 4103-4107.
Cheng L, Eicher SA, Guo Z, Hong WK, Spitz MR, Wei Q: Reduced DNA repair capacity in head and neck cancer patients. Cancer Epidemiol Biomarkers Prev. 1998, 7 (6): 465-468.
Shi Q, Wang LE, Bondy ML, Brewster A, Singletary SE, Wei Q: Reduced DNA repair of benzo[a]pyrene diol epoxide-induced adducts and common XPD polymorphisms in breast cancer patients. Carcinogenesis. 2004, 25 (9): 1695-1700. 10.1093/carcin/bgh167.
Benhamou S, Sarasin A: Variability in nucleotide excision repair and cancer risk: a review. Mutat Res. 2000, 462 (2–3): 149-158.
Wilson DM, Thompson LH: Life without DNA repair. Proc Natl Acad Sci USA. 1997, 94 (24): 12754-12757. 10.1073/pnas.94.24.12754.
Tsurudome Y, Hirano T, Yamato H, Tanaka I, Sagai M, Hirano H, Nagata N, Itoh H, Kasai H: Changes in levels of 8-hydroxyguanine in DNA, its repair and OGG1 mRNA in rat lungs after intratracheal administration of diesel exhaust particles. Carcinogenesis. 1999, 20 (8): 1573-1576. 10.1093/carcin/20.8.1573.
Cheng L, Guan Y, Li L, Legerski RJ, Einspahr J, Bangert J, Alberts DS, Wei Q: Expression in normal human tissues of five nucleotide excision repair genes measured simultaneously by multiplex reverse transcription-polymerase chain reaction. Cancer Epidemiol Biomarkers Prev. 1999, 8 (9): 801-807.
Dabholkar M, Bostick-Bruton F, Weber C, Egwuagu C, Bohr VA, Reed E: Expression of excision repair genes in non-malignant bone marrow from cancer patients. Mutat Res. 1993, 293 (2): 151-160.
Vogel U, Dybdahl M, Frentz G, Nexo BA: DNA repair capacity: inconsistency between effect of over-expression of five NER genes and the correlation to mRNA levels in primary lymphocytes. Mutat Res. 2000, 461 (3): 197-210.
Kondo S, Toyokuni S, Tanaka T, Hiai H, Onodera H, Kasai H, Imamura M: Overexpression of the hOGG1 gene and high 8-hydroxy-2'-deoxyguanosine (8-OHdG) lyase activity in human colorectal carcinoma: regulation mechanism of the 8-OHdG level in DNA. Clin Cancer Res. 2000, 6 (4): 1394-1400.
Li Q, Yu JJ, Mu C, Yunmbam MK, Slavsky D, Cross CL, Bostick-Bruton F, Reed E: Association between the level of ERCC-1 expression and the repair of cisplatin-induced DNA damage in human ovarian cancer cells. Anticancer Res. 2000, 20 (2A): 645-652.
van Duin M, de Wit J, Odijk H, Westerveld A, Yasui A, Koken HM, Hoeijmakers JH, Bootsma D: Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10. Cell. 1986, 44 (6): 913-923. 10.1016/0092-8674(86)90014-0.
Wood RD: Nucleotide excision repair in mammalian cells. J Biol Chem. 1997, 272 (38): 23465-23468. 10.1074/jbc.272.38.23465.
Metzger R, Leichman CG, Danenberg KD, Danenberg PV, Lenz HJ, Hayashi K, Groshen S, Salonga D, Cohen H, Laine L, et al: ERCC1 mRNA levels complement thymidylate synthase mRNA levels in predicting response and survival for gastric cancer patients receiving combination cisplatin and fluorouracil chemotherapy. J Clin Oncol. 1998, 16 (1): 309-316.
Lord RV, Brabender J, Gandara D, Alberola V, Camps C, Domine M, Cardenal F, Sanchez JM, Gumerlock PH, Taron M, et al: Low ERCC1 expression correlates with prolonged survival after cisplatin plus gemcitabine chemotherapy in non-small cell lung cancer. Clin Cancer Res. 2002, 8 (7): 2286-2291.
Rosell R, Taron M, Ariza A, Barnadas A, Mate JL, Reguart N, Margel M, Felip E, Mendez P, Garcia-Campelo R: Molecular predictors of response to chemotherapy in lung cancer. Semin Oncol. 2004, 31 (1 Suppl 1): 20-27. 10.1053/j.seminoncol.2003.12.011.
Shirota Y, Stoehlmacher J, Brabender J, Xiong YP, Uetake H, Danenberg KD, Groshen S, Tsao-Wei DD, Danenberg PV, Lenz HJ: ERCC1 and thymidylate synthase mRNA levels predict survival for colorectal cancer patients receiving combination oxaliplatin and fluorouracil chemotherapy. J Clin Oncol. 2001, 19 (23): 4298-4304.
Vogel U, Moller P, Dragsted L, Loft S, Pedersen A, Sandstrom B: Inter-individual variation, seasonal variation and close correlation of OGG1 and ERCC1 mRNA levels in full blood from healthy volunteers. Carcinogenesis. 2002, 23 (9): 1505-1509. 10.1093/carcin/23.9.1505.
Radicella JP, Dherin C, Desmaze C, Fox MS, Boiteux S: Cloning and characterization of hOGG1, a human homolog of the OGG1 gene of Saccharomyces cerevisiae. Proc Natl Acad Sci USA. 1997, 94 (15): 8010-8015. 10.1073/pnas.94.15.8010.
Aburatani H, Hippo Y, Ishida T, Takashima R, Matsuba C, Kodama T, Takao M, Yasui A, Yamamoto K, Asano M: Cloning and characterization of mammalian 8-hydroxyguanine-specific DNA glycosylase/apurinic, apyrimidinic lyase, a functional mutM homologue. Cancer Res. 1997, 57 (11): 2151-2156.
Kondo S, Toyokuni S, Iwasa Y, Tanaka T, Onodera H, Hiai H, Imamura M: Persistent oxidative stress in human colorectal carcinoma, but not in adenoma. Free Radic Biol Med. 1999, 27 (3–4): 401-410. 10.1016/S0891-5849(99)00087-8.
Bancroft LK, Lupton JR, Davidson LA, Taddeo SS, Murphy ME, Carroll RJ, Chapkin RS: Dietary fish oil reduces oxidative DNA damage in rat colonocytes. Free Radic Biol Med. 2003, 35 (2): 149-159. 10.1016/S0891-5849(03)00240-5.
Kim HN, Morimoto Y, Tsuda T, Ootsuyama Y, Hirohashi M, Hirano T, Tanaka I, Lim Y, Yun IG, Kasai H: Changes in DNA 8-hydroxyguanine levels, 8-hydroxyguanine repair activity, and hOGG1 and hMTH1 mRNA expression in human lung alveolar epithelial cells induced by crocidolite asbestos. Carcinogenesis. 2001, 22 (2): 265-269. 10.1093/carcin/22.2.265.
Yang JP, Hori M, Sanda T, Okamoto T: Identification of a novel inhibitor of nuclear factor-kappaB, RelA-associated inhibitor. J Biol Chem. 1999, 274 (22): 15662-15670. 10.1074/jbc.274.22.15662.
Yin J, Rockenbauer E, Hedayati M, Jacobsen NR, Vogel U, Grossman L, Bolund L, Nexo BA: Multiple single nucleotide polymorphisms on human chromosome 19q13.2-3 associate with risk of Basal cell carcinoma. Cancer Epidemiol Biomarkers Prev. 2002, 11 (11): 1449-1453.
Bergamaschi D, Samuels Y, O'Neil NJ, Trigiante G, Crook T, Hsieh JK, O'Connor DJ, Zhong S, Campargue I, Tomlinson ML, et al: iASPP oncoprotein is a key inhibitor of p53 conserved from worm to human. Nat Genet. 2003, 33 (2): 162-167. 10.1038/ng1070.
Gondal G, Grotmol T, Hofstad B, Bretthauer M, Eide TJ, Hoff G: The Norwegian Colorectal Cancer Prevention (NORCCAP) screening study: baseline findings and implementations for clinical work-up in age groups 50–64 years. Scand J Gastroenterol. 2003, 38 (6): 635-642. 10.1080/00365520310003002.
Hansen R, Saebo M, Skjelbred CF, Nexo BA, Hagen PC, Bock G, Bowitz Lothe IM, Johnson E, Aase S, Hansteen IL, et al: GPX Pro198Leu and OGG1 Ser326Cys polymorphisms and risk of development of colorectal adenomas and colorectal cancer. Cancer Lett. 2005, 229 (1): 85-91. 10.1016/j.canlet.2005.04.019.
Vogel U, Nexo BA, Tjonneland A, Wallin H, Hertel O, Raaschou-Nielsen O: ERCC1, XPD and RAI mRNA levels in lymphocytes are not associated with lung cancer risk in a prospective study of Danes. Mutat Res. 2006, 593 (1–2): 88-96.
Wei Q, Xu X, Cheng L, Legerski RJ, Ali-Osman F: Simultaneous amplification of four DNA repair genes and beta-actin in human lymphocytes by multiplex reverse transcriptase-PCR. Cancer Res. 1995, 55 (21): 5025-5029.
Zhang X, Wang M, Zhou C, Chen S, Wang J: The expression of iASPP in acute leukemias. Leuk Res. 2005, 29 (2): 179-183. 10.1016/j.leukres.2004.07.001.
Paz-Elizur T, Krupsky M, Blumenstein S, Elinger D, Schechtman E, Livneh Z: DNA repair activity for oxidative damage and risk of lung cancer. J Natl Cancer Inst. 2003, 95 (17): 1312-1319.
Vogel U, Nexo BA, Tjonneland A, Wallin H, Hertel O, Raaschou-Nielsen O: ERCC1, XPD and RAI mRNA levels in lymphocytes are not associated with lung cancer risk in a prospective study of Danes. Mutat Res. 2005
Hansen R, Saebo M, Skjelbred CF, Nexo BA, Hagen PC, Bock G, Bowitz Lothe IM, Johnson E, Aase S, Hansteen IL, et al: GPX Pro198Leu and OGG1 Ser326Cys polymorphisms and risk of development of colorectal adenomas and colorectal cancer. Cancer Lett. 2005
Yamane A, Kohno T, Ito K, Sunaga N, Aoki K, Yoshimura K, Murakami H, Nojima Y, Yokota J: Differential ability of polymorphic OGG1 proteins to suppress mutagenesis induced by 8-hydroxyguanine in human cell in vivo. Carcinogenesis. 2004, 25 (9): 1689-1694. 10.1093/carcin/bgh166.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/6/208/prepub
Anne-Karin Jensen is thanked for her excellent technical assistance. We will also like to thank Lotte Vogel for making the figures used in this paper. This study 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 Research Agency (Grant numbers 22-02-0356 and 2052-03-0016) and DRAGE, a grant from Danish Ministry of Health, Research Centre for Environmental Health's Fund.
The author(s) declare that they have no competing interests.
MS prepared samples for analysis and contributed with the data analysis. She prepared the first draft of the paper.
CFS prepared samples for analysis and contributed with the data analysis. She also contributed to the manuscript.
ILH participated in collection and quality control of the questionnaires.
UBV, HW and BAN performed quantification of RAI and OGG1
EHK brought the idea of the KAM study and organized it.
All authors discussed the results, contributed to interpretation of the results and the final manuscript.
Mona Sæbø, Camilla Furu Skjelbred contributed equally to this work.
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Sæbø, M., Skjelbred, C.F., Nexø, B.A. et al. Increased mRNA expression levels of ERCC1, OGG1 and RAIin colorectal adenomas and carcinomas. BMC Cancer 6, 208 (2006). https://doi.org/10.1186/1471-2407-6-208
- Nucleotide Excision Repair
- Colorectal Adenoma
- Base Excision Repair
- Normal Colonic Mucosa