Association between GSTM1 and CYP1A1 polymorphisms and survival in oral cancer patients

被引：11
|
作者：
Shukla, Deepika [1 ]
Kale, Alka Dinesh [2 ]
Hallikerimath, Seema [3 ]
Yerramalla, Venkatakanthaiah [4 ]
Subbiah, Vivekanandhan [4 ]
Mishra, Shashwat [5 ]
机构：
[1] Jamia Millia Islamia, Dept Oral Pathol & Microbiol, Fac Dent, Delhi, India
[2] KLE VK Inst Dent Sci & Hosp, Belgaum, Karnataka, India
[3] KLE VK Inst Dent Sci & Hosp, Dept Oral Pathol & Microbiol, Belgaum, Karnataka, India
[4] All India Inst Med Sci, Neurosci Ctr, New Delhi, India
[5] Ram Manohar Lohia Institte Med Sci, Dept Neurosurg, Lucknow, Uttar Pradesh, India
来源：
BIOMEDICAL PAPERS-OLOMOUC | 2013年 / 157卷 / 04期
关键词：
glutathione S transferase; cytochrome P450; polymorphism; oral squamous cell carcinoma; survival; GLUTATHIONE-S-TRANSFERASE; CELL LUNG-CANCER; ACUTE LYMPHOBLASTIC-LEUKEMIA; GERM-LINE POLYMORPHISMS; ACUTE MYELOID-LEUKEMIA; GENETIC-POLYMORPHISM; ALLELIC VARIANTS; BREAST-CANCER; PROGNOSTIC-SIGNIFICANCE; NULL GENOTYPE;
D O I：
10.5507/bp.2013.028
中图分类号：
R318 [生物医学工程];
学科分类号：
0831 ;
摘要：
Aims. Cancer patient's inherited genotype may influence his or her survival, but evidence for the role of these genetic differences in oral cancer survival has not yet been explored. Methods. The authors evaluated polymorphisms in the GSTM1 and CYP1A1 genes for associations with overall survival in 100 oral squamous cell carcinoma (OSCC) treated patients and 100 controls who were followed up for survival within 2 years of the date of completion of their treatment. Overall survival was evaluated in Kaplan-Meier survival functions and Cox proportional hazards models. Results. After adjustment for stage and histology, GSTM1null genotype was associated with shorter survival among OSCC patients, compared with GSTM1 present genotype. There was no association between CYP1A1 C genotype and survival in the overall study population. Conclusion. The study indicated a potential role for GSTM1 polymorphism in predicting the clinical outcomes of treated oral carcinoma patients.
引用
收藏
页码：304 / 310
页数：7
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