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Published in: European Archives of Oto-Rhino-Laryngology 1/2013

01-01-2013 | Head and Neck

Polymorphisms of DNA repair genes and risk of squamous cell carcinoma of the head and neck in young adults

Authors: M. Kostrzewska-Poczekaj, W. Gawęcki, J. Illmer, M. Rydzanicz, M. Gajecka, W. Szyfter, K. Szyfter

Published in: European Archives of Oto-Rhino-Laryngology | Issue 1/2013

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Abstract

Squamous cell carcinoma of the head and neck (HNSCC) most frequently arise in the epithelial tissues of the upper aerodigestive tract. Patients with HNSCC, aged <45 years are categorized as young adults (YA). They are characterized by more severe form of this disease and often lack of classical, causative risk factors (tobacco smoking, alcohol abusing) in comparison to older (typical) patients (OP). The study purpose was to establish an anticipated protective role of DNA repair genes polymorphisms against cancer-causing agents. It was assumed that the polymorphisms in these genes may have a significant role in the etiology of HNSCC in YA. Studies were carried out on three groups: YA group with HNSCC (n = 90), young healthy group without cancer (YH, n = 160) and OP with HNSCC (n = 205). Three polymorphisms in DNA repair genes were analyzed: XPD ex23: A35931C, XRCC1 ex10: G28152A, and XRCC3 ex7: C18067T. The choice of these genes was connected with their involvement in three different DNA repair pathways. Genotyping was carried out by polymerase chain reaction with restriction fragment length polymorphism (PCR–RFLP) technique. Statistical analysis included: calculation of odds ratio (ORs), 95 % confidence intervals (CIs) and p value. There was no significant difference in the distribution of XPD genotypes in YA compared to OP or YH. The XRCC1 AA genotype variant was observed less frequently in HNSCC YA (4.7 %) than in YH and in OP group (17.1 and 10.8 %, respectively). XRCC3 CT genotype variant was observed more frequently in HNSCC YA (61.8 %) than in YH (36.3 %) and this result is statistically significant. This variant was associated with the borderline increased risk of HNSCC development in an early age, however, a similar tendency was not observed in case of double mutated TT variant. The established differences of genotypes distribution do not seem to differentiate substantially YA and OP in head and neck cancer risk.
Literature
1.
go back to reference Islami F, Fedirko V, Tramacere I, Bagnardi V, Jenab M, Scotti L, Rota M, Corrao G, Garavello W, Schuz J, Straif K, Negri E, Boffetta P, La Vecchia C (2011) Alcohol drinking and esophageal squamous cell carcinoma with focus on light-drinkers and never-smokers—a systematic review and meta-analysis. Int J Cancer 129:2473–2484PubMedCrossRef Islami F, Fedirko V, Tramacere I, Bagnardi V, Jenab M, Scotti L, Rota M, Corrao G, Garavello W, Schuz J, Straif K, Negri E, Boffetta P, La Vecchia C (2011) Alcohol drinking and esophageal squamous cell carcinoma with focus on light-drinkers and never-smokers—a systematic review and meta-analysis. Int J Cancer 129:2473–2484PubMedCrossRef
2.
go back to reference Verschuur HP, Irish JC, O’Sullivan B, Goh C, Gullane PJ, Pintilie M (1999) A matched control study of treatment outcome in young patients with squamous cell carcinoma of the head and neck. Laryngoscope 109:249–258PubMedCrossRef Verschuur HP, Irish JC, O’Sullivan B, Goh C, Gullane PJ, Pintilie M (1999) A matched control study of treatment outcome in young patients with squamous cell carcinoma of the head and neck. Laryngoscope 109:249–258PubMedCrossRef
3.
go back to reference Gawecki W, Kostrzewska-Poczekaj M, Gajecka M, Milecki P, Szyfter K, Szyfter W (2007) The role of genetic factor in etiopathogenesis of squamous cell carcinoma of the head and neck in young adults. Eur Arch Otorhinolaryngol 264:1459–1465PubMedCrossRef Gawecki W, Kostrzewska-Poczekaj M, Gajecka M, Milecki P, Szyfter K, Szyfter W (2007) The role of genetic factor in etiopathogenesis of squamous cell carcinoma of the head and neck in young adults. Eur Arch Otorhinolaryngol 264:1459–1465PubMedCrossRef
4.
go back to reference Schantz SP, Liu FJ (1989) An immunologic profile of young adults with head and neck cancer. Cancer 64:1232–1237PubMedCrossRef Schantz SP, Liu FJ (1989) An immunologic profile of young adults with head and neck cancer. Cancer 64:1232–1237PubMedCrossRef
5.
go back to reference Donald PJ (1986) Marijuana smoking—possible cause of head and neck carcinoma in young patients. Otolaryngol Head Neck Surg 94:517–521PubMed Donald PJ (1986) Marijuana smoking—possible cause of head and neck carcinoma in young patients. Otolaryngol Head Neck Surg 94:517–521PubMed
6.
go back to reference Lefebvre JL, Vankemmel B, Adenis L, Buisset E, Demaille A (1987) Carcinomas of the upper aerodigestive tract before age 40 (excluding children). Apropos of 100 cases. Ann Otolaryngol Chir Cervicofac 104:89–92PubMed Lefebvre JL, Vankemmel B, Adenis L, Buisset E, Demaille A (1987) Carcinomas of the upper aerodigestive tract before age 40 (excluding children). Apropos of 100 cases. Ann Otolaryngol Chir Cervicofac 104:89–92PubMed
7.
go back to reference Papworth R, Slevin N, Roberts SA, Scott D (2001) Sensitivity to radiation-induced chromosome damage may be a marker of genetic predisposition in young head and neck cancer patients. Br J Cancer 84:776–782PubMedCrossRef Papworth R, Slevin N, Roberts SA, Scott D (2001) Sensitivity to radiation-induced chromosome damage may be a marker of genetic predisposition in young head and neck cancer patients. Br J Cancer 84:776–782PubMedCrossRef
8.
go back to reference Lingen MW, Chang KW, McMurray SJ, Solt DB, Kies MS, Mittal BB, Haines GK, Pelzer HJ (2000) Overexpression of p53 in squamous cell carcinoma of the tongue in young patients with no known risk factors is not associated with mutations in exons 5–9. Head Neck 22:328–335PubMedCrossRef Lingen MW, Chang KW, McMurray SJ, Solt DB, Kies MS, Mittal BB, Haines GK, Pelzer HJ (2000) Overexpression of p53 in squamous cell carcinoma of the tongue in young patients with no known risk factors is not associated with mutations in exons 5–9. Head Neck 22:328–335PubMedCrossRef
9.
go back to reference Shiboski CH, Schmidt BL, Jordan RC (2005) Tongue and tonsil carcinoma: increasing trends in the US population ages 20–44 years. Cancer 103:1843–1849PubMedCrossRef Shiboski CH, Schmidt BL, Jordan RC (2005) Tongue and tonsil carcinoma: increasing trends in the US population ages 20–44 years. Cancer 103:1843–1849PubMedCrossRef
10.
go back to reference Jin YT, Myers J, Tsai ST, Goepfert H, Batsakis JG, el-Naggar AK (1999) Genetic alterations in oral squamous cell carcinoma of young adults. Oral Oncol 35:251–256PubMedCrossRef Jin YT, Myers J, Tsai ST, Goepfert H, Batsakis JG, el-Naggar AK (1999) Genetic alterations in oral squamous cell carcinoma of young adults. Oral Oncol 35:251–256PubMedCrossRef
11.
go back to reference Conde L, Moyano S, Vilaseca I, Moragas M, Cardesa A, Nadal A (2011) Role of microsatellite instability in young patients with laryngeal carcinoma. Anal Quant Cytol Histol 33:111–118PubMed Conde L, Moyano S, Vilaseca I, Moragas M, Cardesa A, Nadal A (2011) Role of microsatellite instability in young patients with laryngeal carcinoma. Anal Quant Cytol Histol 33:111–118PubMed
12.
go back to reference Matullo G, Peluso M, Polidoro S, Guarrera S, Munnia A, Krogh V, Masala G, Berrino F, Panico S, Tumino R, Vineis P, Palli D (2003) Combination of DNA repair gene single nucleotide polymorphisms and increased levels of DNA adducts in a population-based study. Cancer Epidemiol Biomarkers Prev 12:674–677PubMed Matullo G, Peluso M, Polidoro S, Guarrera S, Munnia A, Krogh V, Masala G, Berrino F, Panico S, Tumino R, Vineis P, Palli D (2003) Combination of DNA repair gene single nucleotide polymorphisms and increased levels of DNA adducts in a population-based study. Cancer Epidemiol Biomarkers Prev 12:674–677PubMed
13.
go back to reference Vogel U, Hedayati M, Dybdahl M, Grossman L, Nexo BA (2001) Polymorphisms of the DNA repair gene XPD: correlations with risk of basal cell carcinoma revisited. Carcinogenesis 22:899–904PubMedCrossRef Vogel U, Hedayati M, Dybdahl M, Grossman L, Nexo BA (2001) Polymorphisms of the DNA repair gene XPD: correlations with risk of basal cell carcinoma revisited. Carcinogenesis 22:899–904PubMedCrossRef
14.
go back to reference Sturgis EM, Zheng R, Li L, Castillo EJ, Eicher SA, Chen M, Strom SS, Spitz MR, Wei Q (2000) XPD/ERCC2 polymorphisms and risk of head and neck cancer: a case-control analysis. Carcinogenesis 21:2219–2223PubMedCrossRef Sturgis EM, Zheng R, Li L, Castillo EJ, Eicher SA, Chen M, Strom SS, Spitz MR, Wei Q (2000) XPD/ERCC2 polymorphisms and risk of head and neck cancer: a case-control analysis. Carcinogenesis 21:2219–2223PubMedCrossRef
15.
go back to reference de Laat WL, Jaspers NG, Hoeijmakers JH (1999) Molecular mechanism of nucleotide excision repair. Genes Dev 13:768–785PubMedCrossRef de Laat WL, Jaspers NG, Hoeijmakers JH (1999) Molecular mechanism of nucleotide excision repair. Genes Dev 13:768–785PubMedCrossRef
16.
go back to reference Braithwaite E, Wu X, Wang Z (1999) Repair of DNA lesions: mechanisms and relative repair efficiencies. Mutat Res 424:207–219PubMedCrossRef Braithwaite E, Wu X, Wang Z (1999) Repair of DNA lesions: mechanisms and relative repair efficiencies. Mutat Res 424:207–219PubMedCrossRef
17.
go back to reference Flejter WL, McDaniel LD, Johns D, Friedberg EC, Schultz RA (1992) Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene. Proc Natl Acad Sci U S A 89:261–265PubMedCrossRef Flejter WL, McDaniel LD, Johns D, Friedberg EC, Schultz RA (1992) Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene. Proc Natl Acad Sci U S A 89:261–265PubMedCrossRef
18.
go back to reference Matullo G, Palli D, Peluso M, Guarrera S, Carturan S, Celentano E, Krogh V, Munnia A, Tumino R, Polidoro S, Piazza A, Vineis P (2001) XRCC1, XRCC3, XPD gene polymorphisms, smoking and (32)P-DNA adducts in a sample of healthy subjects. Carcinogenesis 22:1437–1445PubMedCrossRef Matullo G, Palli D, Peluso M, Guarrera S, Carturan S, Celentano E, Krogh V, Munnia A, Tumino R, Polidoro S, Piazza A, Vineis P (2001) XRCC1, XRCC3, XPD gene polymorphisms, smoking and (32)P-DNA adducts in a sample of healthy subjects. Carcinogenesis 22:1437–1445PubMedCrossRef
19.
go back to reference Hu JJ, Smith TR, Miller MS, Mohrenweiser HW, Golden A, Case LD (2001) Amino acid substitution variants of APE1 and XRCC1 genes associated with ionizing radiation sensitivity. Carcinogenesis 22:917–922PubMedCrossRef Hu JJ, Smith TR, Miller MS, Mohrenweiser HW, Golden A, Case LD (2001) Amino acid substitution variants of APE1 and XRCC1 genes associated with ionizing radiation sensitivity. Carcinogenesis 22:917–922PubMedCrossRef
20.
go back to reference Nash RA, Caldecott KW, Barnes DE, Lindahl T (1997) XRCC1 protein interacts with one of two distinct forms of DNA ligase III. Biochemistry 36:5207–5211PubMedCrossRef Nash RA, Caldecott KW, Barnes DE, Lindahl T (1997) XRCC1 protein interacts with one of two distinct forms of DNA ligase III. Biochemistry 36:5207–5211PubMedCrossRef
21.
go back to reference Kubota Y, Nash RA, Klungland A, Schar P, Barnes DE, Lindahl T (1996) Reconstitution of DNA base excision-repair with purified human proteins: interaction between DNA polymerase beta and the XRCC1 protein. EMBO J 15:6662–6670PubMed Kubota Y, Nash RA, Klungland A, Schar P, Barnes DE, Lindahl T (1996) Reconstitution of DNA base excision-repair with purified human proteins: interaction between DNA polymerase beta and the XRCC1 protein. EMBO J 15:6662–6670PubMed
22.
go back to reference Masson M, Niedergang C, Schreiber V, Muller S, Menissier-de Murcia J, de Murcia G (1998) XRCC1 is specifically associated with poly(ADP-ribose) polymerase and negatively regulates its activity following DNA damage. Mol Cell Biol 18:3563–3571PubMed Masson M, Niedergang C, Schreiber V, Muller S, Menissier-de Murcia J, de Murcia G (1998) XRCC1 is specifically associated with poly(ADP-ribose) polymerase and negatively regulates its activity following DNA damage. Mol Cell Biol 18:3563–3571PubMed
23.
go back to reference Liu N, Lamerdin JE, Tebbs RS, Schild D, Tucker JD, Shen MR, Brookman KW, Siciliano MJ, Walter CA, Fan W, Narayana LS, Zhou ZQ, Adamson AW, Sorensen KJ, Chen DJ, Jones NJ, Thompson LH (1998) XRCC2 and XRCC3, new human Rad51-family members, promote chromosome stability and protect against DNA cross-links and other damages. Mol Cell 1:783–793PubMedCrossRef Liu N, Lamerdin JE, Tebbs RS, Schild D, Tucker JD, Shen MR, Brookman KW, Siciliano MJ, Walter CA, Fan W, Narayana LS, Zhou ZQ, Adamson AW, Sorensen KJ, Chen DJ, Jones NJ, Thompson LH (1998) XRCC2 and XRCC3, new human Rad51-family members, promote chromosome stability and protect against DNA cross-links and other damages. Mol Cell 1:783–793PubMedCrossRef
24.
go back to reference Winsey SL, Haldar NA, Marsh HP, Bunce M, Marshall SE, Harris AL, Wojnarowska F, Welsh KI (2000) A variant within the DNA repair gene XRCC3 is associated with the development of melanoma skin cancer. Cancer Res 60:5612–5616PubMed Winsey SL, Haldar NA, Marsh HP, Bunce M, Marshall SE, Harris AL, Wojnarowska F, Welsh KI (2000) A variant within the DNA repair gene XRCC3 is associated with the development of melanoma skin cancer. Cancer Res 60:5612–5616PubMed
25.
go back to reference Kanaar R, Hoeijmakers JH, van Gent DC (1998) Molecular mechanisms of DNA double strand break repair. Trends Cell Biol 8:483–489PubMedCrossRef Kanaar R, Hoeijmakers JH, van Gent DC (1998) Molecular mechanisms of DNA double strand break repair. Trends Cell Biol 8:483–489PubMedCrossRef
26.
go back to reference Wang Y, Irish J, MacMillan C, Brown D, Xuan Y, Boyington C, Gullane P, Kamel-Reid S (2001) High frequency of microsatellite instability in young patients with head-and-neck squamous-cell carcinoma: lack of involvement of the mismatch repair genes hMLH1 AND hMSH2. Int J Cancer 93:353–360PubMedCrossRef Wang Y, Irish J, MacMillan C, Brown D, Xuan Y, Boyington C, Gullane P, Kamel-Reid S (2001) High frequency of microsatellite instability in young patients with head-and-neck squamous-cell carcinoma: lack of involvement of the mismatch repair genes hMLH1 AND hMSH2. Int J Cancer 93:353–360PubMedCrossRef
27.
go back to reference Rydzanicz M, Wierzbicka M, Gajecka M, Szyfter W, Szyfter K (2005) The impact of genetic factors on the incidence of multiple primary tumors (MPT) of the head and neck. Cancer Lett 224:263–278PubMedCrossRef Rydzanicz M, Wierzbicka M, Gajecka M, Szyfter W, Szyfter K (2005) The impact of genetic factors on the incidence of multiple primary tumors (MPT) of the head and neck. Cancer Lett 224:263–278PubMedCrossRef
28.
go back to reference Gao W, Romkes M, Zhong S, Nukui T, Persad RA, Smith PJ, Branch R, Keohavong P (2010) Genetic polymorphisms in the DNA repair genes XPD and XRCC1, p53 gene mutations and bladder cancer risk. Oncol Rep 24:257–262PubMed Gao W, Romkes M, Zhong S, Nukui T, Persad RA, Smith PJ, Branch R, Keohavong P (2010) Genetic polymorphisms in the DNA repair genes XPD and XRCC1, p53 gene mutations and bladder cancer risk. Oncol Rep 24:257–262PubMed
29.
go back to reference Jelonek K, Gdowicz-Klosok A, Pietrowska M, Borkowska M, Korfanty J, Rzeszowska-Wolny J, Widlak P (2010) Association between single-nucleotide polymorphisms of selected genes involved in the response to DNA damage and risk of colon, head and neck, and breast cancers in a Polish population. J Appl Genet 51:343–352PubMedCrossRef Jelonek K, Gdowicz-Klosok A, Pietrowska M, Borkowska M, Korfanty J, Rzeszowska-Wolny J, Widlak P (2010) Association between single-nucleotide polymorphisms of selected genes involved in the response to DNA damage and risk of colon, head and neck, and breast cancers in a Polish population. J Appl Genet 51:343–352PubMedCrossRef
30.
go back to reference Shall S, de Murcia G (2000) Poly(ADP-ribose) polymerase-1: what have we learned from the deficient mouse model? Mutat Res 460:1–15PubMedCrossRef Shall S, de Murcia G (2000) Poly(ADP-ribose) polymerase-1: what have we learned from the deficient mouse model? Mutat Res 460:1–15PubMedCrossRef
31.
go back to reference Lunn RM, Langlois RG, Hsieh LL, Thompson CL, Bell DA (1999) XRCC1 polymorphisms: effects on aflatoxin B1-DNA adducts and glycophorin A variant frequency. Cancer Res 59:2557–2561PubMed Lunn RM, Langlois RG, Hsieh LL, Thompson CL, Bell DA (1999) XRCC1 polymorphisms: effects on aflatoxin B1-DNA adducts and glycophorin A variant frequency. Cancer Res 59:2557–2561PubMed
32.
go back to reference Kowalski M, Przybylowska K, Rusin P, Olszewski J, Morawiec-Sztandera A, Bielecka-Kowalska A, Pietruszewska W, Mlynarski W, Janusz S, Majsterek I (2009) Genetic polymorphisms in DNA base excision repair gene XRCC1 and the risk of squamous cell carcinoma of the head and neck. J Exp Clin Cancer Res 28:37PubMedCrossRef Kowalski M, Przybylowska K, Rusin P, Olszewski J, Morawiec-Sztandera A, Bielecka-Kowalska A, Pietruszewska W, Mlynarski W, Janusz S, Majsterek I (2009) Genetic polymorphisms in DNA base excision repair gene XRCC1 and the risk of squamous cell carcinoma of the head and neck. J Exp Clin Cancer Res 28:37PubMedCrossRef
33.
go back to reference Abdel-Rahman SZ, El-Zein RA (2000) The 399Gln polymorphism in the DNA repair gene XRCC1 modulates the genotoxic response induced in human lymphocytes by the tobacco-specific nitrosamine NNK. Cancer Lett 159:63–71PubMedCrossRef Abdel-Rahman SZ, El-Zein RA (2000) The 399Gln polymorphism in the DNA repair gene XRCC1 modulates the genotoxic response induced in human lymphocytes by the tobacco-specific nitrosamine NNK. Cancer Lett 159:63–71PubMedCrossRef
34.
go back to reference Duell EJ, Wiencke JK, Cheng TJ, Varkonyi A, Zuo ZF, Ashok TD, Mark EJ, Wain JC, Christiani DC, Kelsey KT (2000) Polymorphisms in the DNA repair genes XRCC1 and ERCC2 and biomarkers of DNA damage in human blood mononuclear cells. Carcinogenesis 21:965–971PubMedCrossRef Duell EJ, Wiencke JK, Cheng TJ, Varkonyi A, Zuo ZF, Ashok TD, Mark EJ, Wain JC, Christiani DC, Kelsey KT (2000) Polymorphisms in the DNA repair genes XRCC1 and ERCC2 and biomarkers of DNA damage in human blood mononuclear cells. Carcinogenesis 21:965–971PubMedCrossRef
35.
go back to reference Lei YC, Hwang SJ, Chang CC, Kuo HW, Luo JC, Chang MJ, Cheng TJ (2002) Effects on sister chromatid exchange frequency of polymorphisms in DNA repair gene XRCC1 in smokers. Mutat Res 519:93–101PubMedCrossRef Lei YC, Hwang SJ, Chang CC, Kuo HW, Luo JC, Chang MJ, Cheng TJ (2002) Effects on sister chromatid exchange frequency of polymorphisms in DNA repair gene XRCC1 in smokers. Mutat Res 519:93–101PubMedCrossRef
36.
go back to reference Gajecka M, Rydzanicz M, Jaskula-Sztul R, Wierzbicka M, Szyfter W, Szyfter K (2005) Reduced DNA repair capacity in laryngeal cancer subjects. A comparison of phenotypic and genotypic results. Adv Otorhinolaryngol 62:25–37PubMed Gajecka M, Rydzanicz M, Jaskula-Sztul R, Wierzbicka M, Szyfter W, Szyfter K (2005) Reduced DNA repair capacity in laryngeal cancer subjects. A comparison of phenotypic and genotypic results. Adv Otorhinolaryngol 62:25–37PubMed
37.
go back to reference Shen H, Sturgis EM, Dahlstrom KR, Zheng Y, Spitz MR, Wei Q (2002) A variant of the DNA repair gene XRCC3 and risk of squamous cell carcinoma of the head and neck: a case–control analysis. Int J Cancer 99:869–872PubMedCrossRef Shen H, Sturgis EM, Dahlstrom KR, Zheng Y, Spitz MR, Wei Q (2002) A variant of the DNA repair gene XRCC3 and risk of squamous cell carcinoma of the head and neck: a case–control analysis. Int J Cancer 99:869–872PubMedCrossRef
38.
go back to reference Le Marchand L (2005) The predominance of the environment over genes in cancer causation: implications for genetic epidemiology. Cancer Epidemiol Biomarkers Prev 14:1037–1039PubMedCrossRef Le Marchand L (2005) The predominance of the environment over genes in cancer causation: implications for genetic epidemiology. Cancer Epidemiol Biomarkers Prev 14:1037–1039PubMedCrossRef
39.
go back to reference Canova C, Hashibe M, Simonato L, Nelis M, Metspalu A, Lagiou P, Trichopoulos D, Ahrens W, Pigeot I, Merletti F, Richiardi L, Talamini R, Barzan L, Macfarlane GJ, Macfarlane TV, Holcatova I, Bencko V, Benhamou S, Bouchardy C, Kjaerheim K, Lowry R, Agudo A, Castellsague X, Conway DI, McKinney PA, Znaor A, McCartan BE, Healy CM, Marron M, Brennan P (2009) Genetic associations of 115 polymorphisms with cancers of the upper aerodigestive tract across 10 European countries: the ARCAGE project. Cancer Res 69:2956–2965PubMedCrossRef Canova C, Hashibe M, Simonato L, Nelis M, Metspalu A, Lagiou P, Trichopoulos D, Ahrens W, Pigeot I, Merletti F, Richiardi L, Talamini R, Barzan L, Macfarlane GJ, Macfarlane TV, Holcatova I, Bencko V, Benhamou S, Bouchardy C, Kjaerheim K, Lowry R, Agudo A, Castellsague X, Conway DI, McKinney PA, Znaor A, McCartan BE, Healy CM, Marron M, Brennan P (2009) Genetic associations of 115 polymorphisms with cancers of the upper aerodigestive tract across 10 European countries: the ARCAGE project. Cancer Res 69:2956–2965PubMedCrossRef
40.
go back to reference Kutler DI, Auerbach AD, Satagopan J, Giampietro PF, Batish SD, Huvos AG, Goberdhan A, Shah JP, Singh B (2003) High incidence of head and neck squamous cell carcinoma in patients with Fanconi anemia. Arch Otolaryngol Head Neck Surg 129:106–112PubMedCrossRef Kutler DI, Auerbach AD, Satagopan J, Giampietro PF, Batish SD, Huvos AG, Goberdhan A, Shah JP, Singh B (2003) High incidence of head and neck squamous cell carcinoma in patients with Fanconi anemia. Arch Otolaryngol Head Neck Surg 129:106–112PubMedCrossRef
41.
go back to reference Lu WT, Lemonidis K, Drayton RM, Nouspikel T (2011) The Fanconi anemia pathway is downregulated upon macrophage differentiation through two distinct mechanisms. Cell Cycle 10:3300–3310PubMedCrossRef Lu WT, Lemonidis K, Drayton RM, Nouspikel T (2011) The Fanconi anemia pathway is downregulated upon macrophage differentiation through two distinct mechanisms. Cell Cycle 10:3300–3310PubMedCrossRef
42.
go back to reference Szaumkessel M, Richter J, Giefing M, Jarmuz M, Kiwerska K, Tonnies H, Grenman R, Heidemann S, Szyfter K, Siebert R (2011) Pyrosequencing-based DNA methylation profiling of Fanconi anemia/BRCA pathway genes in laryngeal squamous cell carcinoma. Int J Oncol 39:505–514PubMed Szaumkessel M, Richter J, Giefing M, Jarmuz M, Kiwerska K, Tonnies H, Grenman R, Heidemann S, Szyfter K, Siebert R (2011) Pyrosequencing-based DNA methylation profiling of Fanconi anemia/BRCA pathway genes in laryngeal squamous cell carcinoma. Int J Oncol 39:505–514PubMed
Metadata
Title
Polymorphisms of DNA repair genes and risk of squamous cell carcinoma of the head and neck in young adults
Authors
M. Kostrzewska-Poczekaj
W. Gawęcki
J. Illmer
M. Rydzanicz
M. Gajecka
W. Szyfter
K. Szyfter
Publication date
01-01-2013
Publisher
Springer-Verlag
Published in
European Archives of Oto-Rhino-Laryngology / Issue 1/2013
Print ISSN: 0937-4477
Electronic ISSN: 1434-4726
DOI
https://doi.org/10.1007/s00405-012-1993-8

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