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XRCC1单核苷酸多态性与鼻咽癌患者晚期放射性损伤的相关性 被引量:1

The Clinical Relevance between Single Nucleotide Polymorphisms of XRCC1 Codon399 and Chronic Irradiation-induced Injury of Normal Tissue in Patients with Nasopharyngeal Carcinoma
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摘要 目的分析XRCC1 Codon399单核苷酸多态性与鼻咽癌患者正常组织晚期放射性损伤的相关性。方法经病理学检查确诊的60例鼻咽癌患者,放疗前提取全血基因组DNA,进行PCR扩增及LDP连接检测反应扩增,得出XRCC1 Codon399的3种基因型。随访至放疗结束后3个月,对晚期放射性损伤进行评价,比较XRCC1 Codon399不同基因型与正常组织晚期放射性损伤的相关性。结果 60例患者中,XRCC1 Codon399 Gln/Gln基因型6例,Arg/Gln基因型21例,Arg/Arg基因型33例,不同性别之间无明显差异。Gln/Gln基因型者1、2、3级皮肤晚期放射性损伤发生率分别为33.3%、66.7%、0,Arg/Gln基因型者为52.4%、42.9%、4.7%,Arg/Arg基因型者为63.6%、36.4%、0;Gln/Gln基因型患者1、2、3级皮下组织晚期放射性损伤发生率分别为33.3%、66.7%、0,Arg/Gln基因型者为38.1%、57.2%、4.7%,Arg/Arg基因型者为42.4%、57.6%、0;Gln/Gln基因型患者1、2、3级黏膜晚期放射性损伤发生率分别为100.0%、0、0,Arg/Gln基因型者分别为80.9%、14.3%4.7%,Arg/Arg基因型者分别为93.9%、6.1%、0;Gln/Gln基因型患者1、2、3级涎腺晚期放射性损伤发生率分别为100.0%、0、0,Arg/Gln基因型者分别为80.9%、14.3%、4.7%,Arg/Arg基因型者分别为93.9%、6.1%、0。经统计分析,不同基因型患者间晚期放射性损伤发生率无明显差异(P>0.05)。结论 XRCC1 Co-don399单核苷酸多态性与鼻咽癌患者皮肤、皮下组织、黏膜、涎腺晚期放射性损伤程度无明显相关性,尚不能将其应用于对鼻咽癌患者正常组织晚期放射性损伤程度的预测。 Objective By detecting the single nucleotide polymorphisms(SNPs) of XRCC1 Codon399 of peripheral blood of patients suffering from nasopharyngeal carcinoma(NPC),the relationshipship between SNPs of XRCC1 Codon399 and radiation injury in normal tissues was analysed.Methods 60 patients with pathologically confirmed low differentiated squamous cell carcinoma of the nasopharynx were included in the study.Genome DNA was extracted from whole blood cells before radiotherapy and the PCR products were amplified by ligase detection reaction(LDR).The LDR products were put on sequencer to carry out electrophoresis,get the genotype of XRCC1 Codon399,evaluate the clinical effect in three months after radiotherapy and compare the chronic radiation reactions of normal tissue in the different genotypes.Results Of the 60 cases,the number of XRCC1 Codon399 Gln/Gln,Arg/Gln and Arg/Arg was 6,21 and 33,respectively.The incidence of grade Ⅰ,Ⅱ and Ⅲ chronic irradiation-induced injury of skin was 33.3%,66.7% and 0 with Gln/Gln,52.4%,42.9% and 4.7% with Arg/Gln,63.6%,36.4% and 0 with Arg/Arg.The rate of grade Ⅰ,Ⅱ and Ⅲchronic irradiation-induced injury of subcutaneous tissues was 33.3%,66.7% and 0 with Gln/Gln;42.4%,57.6% and 0 with Arg/Gln;38.1%,57.2% and 4.7% with Arg/Arg genotype.The rate of grade Ⅰ,Ⅱ and Ⅲchronic irradiation-induced injury of mucosa was 100.0%,0,0 with Gln/Gln;93.9%,6.1%,0 with Arg/Gln;80.9%,14.3%,4.7% with Arg/Arg genotype respectively.The rate of the grade Ⅰ,Ⅱ and Ⅲchronic irradiation-induced injury of parotid gland was 100.0%,0,0 with Gln/Gln,93.9%,6.1%,0 with Arg/Gln,80.9%,14.3%,4.7% with Arg/Arg genotype respectively.There were no significant differences among the three genotypes(P0.05).Conclusion There was no relationship between the SNPs of XRCC1 Codon399 and chronic irradiation-induced injury of normal tissues in NPC patients.
出处 《实用癌症杂志》 2011年第6期596-599,共4页 The Practical Journal of Cancer
关键词 XRCC1单核苷酸多态性 鼻咽癌 放射损伤 XRCC1 single nucleotide polymorphisms Nasopharyngeal carcinoma Chronic irradiation-induced injury
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参考文献9

  • 1张莉,王绿化.单核苷酸多态性与放射性损伤[J].癌症进展,2008,6(2):141-146. 被引量:6
  • 2Walter CA, Trolian DA, McFarland MB, et al. Xrcc-1 expres- sion during male meiosis in the mouse [ J 1. Biol Reprod, 1996,55 (3) :630.
  • 3Thompson LH, West MG. XRCC1 keeps DNA from getting stranded [ J ]. Mutat Res, 2000,459 ( 1 ) : 1.
  • 4Siciliano M J, Carrano AV, Thompson LH. Assignment of a human DNA-repair gene associated with sister-chromatid ex- change to chromosome 19 [ J ]. Mutat Res, 1986,174 (4) : 303.
  • 5余红平,曾小云,仇小强,徐顺清,施侣元,张晓蓉,李媛媛.DNA修复基因XRCC1单核苷酸多态性与肺癌易感性[J].广西医科大学学报,2006,23(3):355-358. 被引量:7
  • 6Andreassen CN, Alsner J, Overgaard M, et al. Prediction of normal tissue radiosensitivity from polymorphisms in candi- date genes [J]. Radiother Oncol,2003,69 (2) : 127.
  • 7Park JY, Lee SY, Jeon HS, et al. Polymorphism of the DNA repair gene XRCC1 and risk of primary lung cancer [ J ]. Cancer Epidemiol Biomarkers Prey,2002,11 ( 1 ) :23.
  • 8Keam B, Im SA, Han SW, et al. Modified FOLFOX-6 chemo- therapy in advanced gastric cancer:Results of phase II study and comprehensive analysis of polymorphisms as a predictive and prognostic marker[J]. BMC Cancer,2008,8 ( 1 ) : 148.
  • 9Andreassen CN, Alsner J, Overgaard M, et al. Prediction of normal tissue radiosensitivity from polymorphisms in candi- date genes [J]. Radiother Oncol,2003,69 (2) : 127.

二级参考文献56

  • 1[1]Fernet,M,J.Hall.Genetic biomarkers of therapeutic radiation sensitivity.DNA Repair(Amst),2004,3:1237
  • 2[2]Awwad,H.K.Normal tissue radiosensitivity:Prediction on deterministic or stochastic basis?J Egypt Natl Canc Inst,2005,17:221
  • 3[3]Andreassen,C.N.,J.Alsner,J.Overgaard.Does variability in normal tissue reactions after radiotherapy have a genetic basis-where and how to look for it?Radiother Oncol,2002,64:131
  • 4[4]Bentzen,S.M,J.Overgaard.Patient-to-patient variability in the expression of radiation-induced normal tissue iniurv.Semin Radiat Oncol,1994,4:68
  • 5[5]Bentzen,S.M.,J.J.Christensen,J.Overgaard,et al.Some methodological problems in estimating radiobiological parameters from clinical data.Alpha/beta ratios and electron RBE for cutaneous reactions in patients treated with postmastectomy radiotherapy.Acta Oncol,1988,27:105
  • 6[6]Budach,W,J.Classen,C.Belka,et al.Clinical impact of predictive assays for acute and late radiation morbidity.Strablenther Onkol,1998,174(Suppl 3):20
  • 7[7]Alter,B.P.Radiosensitivity in Fanconi's anemia patients.Radiother Oneol,2002,62:345
  • 8[8]Rogers,P.B.,P.N.Plowman,S.J.Harris,et al.Four radiation hypersensitivity cases and their implications for clinical radiotherapy.Radiother Oncol,2000,57:143
  • 9[9]Gatti,R.A.The inherited basis of human radiosensitivity.Acta Oncol,2001,40:702
  • 10[10]Riballo,E.,S.E.Critchlow.S.H.Teo,et al.Identification of a defect in DNA ligase Ⅳ in a radiosensitive leukaemia patient.Curt Biol,1999,9:699

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