头颈部肿瘤患者GSTM1、GSTT1、GSTP1基因相关基因多态性及其与放疗毒性的相关性研究

Anand K Gudur, Rashmi A Gudur, Suresh J Bhosale, Kailas D Datkhile
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引用次数: 0

摘要

背景:本研究探讨谷胱甘肽转移酶基因GSTM1、GSTT1和GSTP1多态性与HNC患者放疗后急性正常组织不良反应的关系。我们评估了GSTM1和GSTT1零基因型以及GSTP1基因多态性5外显子Ile105Val和6外显子Ala114Val与HNC患者放疗后急性皮肤毒性反应风险的关系。方法:选取400例接受调强放疗的HNC患者,评价放疗相关毒性反应。采用聚合酶链反应(PCR)对GSTM1和GSTT1进行基因分型。采用PCR +限制性片段长度多态性(PCR- rflp)测定GSTP1外显子5的Ile/Val和外显子6的Ala/Val多态性。结果:单因素logistic回归分析显示,GSTM1和GSTT1零基因型与放疗后引起的皮肤反应和口腔黏膜炎均无相关性。我们研究GSTP1基因5外显子A313G多态性和6外显子C341T多态性,大多数基因型为野生型,5外显子A/A基因型与皮肤反应不显著相关,6外显子C/T基因型与皮肤反应显著负相关。结论:本研究结果表明,GSTM1和GSTT1基因多态性的零基因型与放疗引起的皮炎、口腔黏膜炎等急性毒性无关。结果显示GSTP1外显子6杂合C/T基因型与急性皮肤反应呈负相关。
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Investigation of Genetic Polymorphisms Related GSTM1, GSTT1, GSTP1 Genes and their Association with Radiotherapy Toxicity among Head and Neck Cancer Patients.

Background: In this study we explored the association of polymorphisms of glutathione s transferase gene including GSTM1, GSTT1 and GSTP1 with adverse acute normal tissue reactions resulted from radiotherapy in HNC patients. We assessed the association of GSTM1 and GSTT1 null genotypes and Ile105Val of exon-5 and Ala114Val of exon-6 of GSTP1 gene polymorphisms with the risk of acute skin toxicity reactions after therapeutic radiotherapy in HNC patients.

Methods: Four hundred HNC patients administered with Intensity modulated radiation therapy were enrolled in this study for the evaluation of radiotherapy associated toxicity reactions. The genotyping of GSTM1 and GSTT1 were performed by polymerase chain reaction (PCR). The GSTP1 Ile/Val of exon-5 and Ala/Val of exon-6 polymorphism was determined by PCR followed by restriction fragment length polymorphism (PCR-RFLP).

Results: The univariate logistic regression analysis showed that GSTM1 and GSTT1 null genotypes were not associated with either skin reaction or oral mucositis in response to radiotherapy induced after effects. When we studied, A313G polymorphism at exon 5 and C341T polymorphism at exon 6 of GSTP1 gene, majority of genotypes were wild type A/A genotype for exon 5 showed non-significant association with Skin reactions whereas, C/T genotype of exon-6 showed significant negative association with skin reactions.

Conclusion: The findings obtained from this study concluded that the null genotypes of GSTM1 and GSTT1 gene polymorphisms showed no association with radiotherapy induced acute toxicities such as dermatitis and oral mucositis. The results indicated negative association of heterozygous C/T genotype of exon-6 of GSTP1 with acute skin reactions.

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来源期刊
CiteScore
2.80
自引率
0.00%
发文量
779
审稿时长
3 months
期刊介绍: Cancer is a very complex disease. While many aspects of carcinoge-nesis and oncogenesis are known, cancer control and prevention at the community level is however still in its infancy. Much more work needs to be done and many more steps need to be taken before effective strategies are developed. The multidisciplinary approaches and efforts to understand and control cancer in an effective and efficient manner, require highly trained scientists in all branches of the cancer sciences, from cellular and molecular aspects to patient care and palliation. The Asia Pacific Organization for Cancer Prevention (APOCP) and its official publication, the Asia Pacific Journal of Cancer Prevention (APJCP), have served the community of cancer scientists very well and intends to continue to serve in this capacity to the best of its abilities. One of the objectives of the APOCP is to provide all relevant and current scientific information on the whole spectrum of cancer sciences. They aim to do this by providing a forum for communication and propagation of original and innovative research findings that have relevance to understanding the etiology, progression, treatment, and survival of patients, through their journal. The APJCP with its distinguished, diverse, and Asia-wide team of editors, reviewers, and readers, ensure the highest standards of research communication within the cancer sciences community across Asia as well as globally. The APJCP publishes original research results under the following categories: -Epidemiology, detection and screening. -Cellular research and bio-markers. -Identification of bio-targets and agents with novel mechanisms of action. -Optimal clinical use of existing anti-cancer agents, including combination therapies. -Radiation and surgery. -Palliative care. -Patient adherence, quality of life, satisfaction. -Health economic evaluations.
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