Glutathione S-Transferase Gene Polymorphisms and Treatment Outcome in Cervical Cancer Patients under Concomitant Chemoradiation

被引:11
作者
Abbas, Mohammad [1 ]
Kushwaha, Vandana Singh [2 ]
Srivastava, Kirti [2 ]
Banerjee, Monisha [1 ]
机构
[1] Univ Lucknow, Dept Zool, Mol & Human Genet Lab, Lucknow 226007, Uttar Pradesh, India
[2] King Georges Med Univ, Dept Radiotherapy, Lucknow 226003, Uttar Pradesh, India
来源
PLOS ONE | 2015年 / 10卷 / 11期
关键词
CELL LUNG-CANCER; P1; POLYMORPHISMS; GST-PI; SURVIVAL; ASSOCIATION; CHEMOTHERAPY; CISPLATIN; RISK; M1; T1;
D O I
10.1371/journal.pone.0142501
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Purpose Cisplatin based concomitant chemoradiation (CRT) is the standard treatment for locally advanced cervical cancer (CC). Glutathione S-transferase (GST), a phase II antioxidant enzyme is induced by oxidative stress generated by drugs and reactive oxidants. The present study was undertaken to evaluate the association of GSTM1, T1 and P1 polymorphisms with the outcome of CRT treatment in CC patients. Methods A total of 227 cervical cancer patients with stages IIB-IIIB treated with the same chemoradiotherapy regimen were enrolled and genotyped for GSTM1, T1 and P1 gene polymorphisms by multiplex polymerase chain reaction (mPCR) and PCR-restriction fragment length polymorphism (PCR-RFLP). Overall survival was evaluated using Kaplan-Meier survival function and Cox proportional hazards model. All data were analyzed using SPSS (version 21.0). Results Stratified analysis showed that GSTM1 null (M1-) genotype was associated with a significantly better survival among patients with stage IIB cervical cancer (log-rank P = 0.004) than cases with stage IIIA/IIIB. Death and recurrence were significantly higher in patients with GSTM1 present genotype (M1+) (P = 0.037 and P = 0.003 respectively) and those with M1-showed reduced hazard of death with an adjusted hazard ratio 'HR' of 0.47 (95% CI, 0.269-0.802, P = 0.006). Women with M1-genotype as well as in combination with GSTT1 null (T1-), GSTP1 (AG+GG) and GSTT1 null/GSTP1 (AG+GG) showed better survival and also reduced risk of death (HR = 0.31, P = 0.016; HR = 0.45, P = 0.013; HR = 0.31, P = 0.02 respectively). Conclusions To the best of our knowledge, this is the first study to correlate the association of GSTM1, T1 and P1 gene polymorphisms with treatment outcome of CRT treated CC patients. Our results suggested that individuals with GSTM1 null genotype and in combination with GSTT1 null and GSTP1 (AG+GG) had a survival advantage. Such genetic studies may provide prognostic information in CRT treated CC patients.
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页数:11
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共 41 条
  • [1] Abbas M, 2013, IJBR, V4, P1
  • [2] Association of CYP1A1 gene variants rs4646903 (T>C) and rs1048943 (A>G) with cervical cancer in a North Indian population
    Abbas, Mohammad
    Srivastava, Kirti
    Imran, Mohd
    Banerjee, Monisha
    [J]. EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2014, 176 : 68 - 74
  • [3] Ambrosone CB, 2001, CANCER RES, V61, P7130
  • [4] Genetic predictors of acute toxicities related to radiation therapy following lumpectomy for breast cancer: a case-series study
    Ambrosone, Christine B.
    Tian, Chunqiao
    Ahn, Jiyoung
    Kropp, Silke
    Helmbold, Irmgard
    von Fournier, Dietrich
    Haase, Wulf
    Sautter-Bihl, Marie Luise
    Wenz, Frederik
    Chang-Claude, Jenny
    [J]. BREAST CANCER RESEARCH, 2006, 8 (04)
  • [5] Ban N, 1996, CANCER RES, V56, P3577
  • [6] The association of XRCC1 gene single nucleotide polymorphisms with response to neoadjuvant chemotherapy in locally advanced cervical carcinoma
    Cheng, Xiao-Dong
    Lu, Wei-Guo
    Ye, Feng
    Wan, Xiao-Yun
    Xie, Xing
    [J]. JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2009, 28
  • [7] Glutathione S-transferase polymorphisms and outcome of chemotherapy in childhood acute myeloid leukemia
    Davies, SM
    Robison, LL
    Buckley, JD
    Tjoa, T
    Woods, WG
    Radloff, GA
    Ross, JA
    Perentesis, JP
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (05) : 1279 - 1287
  • [8] Duggan C, 2013, SPRINGERPLUS, V2, P1
  • [9] Glutathione S-transferase M1, T1, and P1 Polymorphisms and Ovarian Cancer Risk A Meta-Analysis
    Economopoulos, Konstantinos P.
    Sergentanis, Theodoros N.
    Vlahos, Nikos F.
    [J]. INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2010, 20 (05) : 732 - 737
  • [10] An overview of the relations between polymorphisms in drug metabolising enzymes and drug transporters and survival after cancer drug treatment
    Ekhart, Corine
    Rodenhuis, Sjoerd
    Smits, Paul H. M.
    Beijnen, Jos H.
    Huitema, Alwin D. R.
    [J]. CANCER TREATMENT REVIEWS, 2009, 35 (01) : 18 - 31