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谷胱甘肽S-转移酶的基因变异性会影响乳腺癌的治疗结果。

Genetic variability of glutathione S-transferases influences treatment outcome of breast cancer.

作者信息

Zhou Liang, Huang Anzhong, Zhang Dawei, Yao Junliang, Zhang Yong, Li Xuejiao

机构信息

Department of General Surgery, Jinshan Hospital, Fudan University, 1508 Longhang Road Jinshan District, Shanghai, 201508, China,

出版信息

Tumour Biol. 2015 Aug;36(8):5925-9. doi: 10.1007/s13277-015-3266-9. Epub 2015 Mar 14.

Abstract

We investigated the relationship between the clinical outcome and the GSTM1 null/present, GSTT1 null/present, and GSTP1 IIe105Val polymorphisms in breast cancer patients with chemotherapy. A total of 420 consecutive breast cancer patients diagnosed between January 2010 and December 2011 were eligible for inclusion in our retrospective study. The designs of the assay and SNP genotyping of GSTM1 null/present, GSTT1 null/present, and GSTP1 IIe105Val were performed using the Sequenom MassARRAY platform. In the univariate analysis, patients who carried TT genotype and CT + TT genotype of GSTP1 IIe105Val showed a significant poorer tumor response to chemotherapy when compared with CC genotype (for TT genotype, adjusted OR = 0.44, 95 % CI = 0.22-0.89; for CT + TT genotype, adjusted OR = 0.59, 95 % CI = 0.39-0.92). By Cox multivariate analysis, TT genotype and CT + TT genotype were associated with increased risk of death from breast cancer, and the relationship was more obvious after being adjusted by potential confounding factors (for TT genotype, adjusted OR = 4.23, 95 % CI = 2.33-8.76; for CT + TT genotype, adjusted OR = 2.53, 95% CI = 1.60-4.03). Polymorphism of GSTP1 IIe105Val might affect the clinical outcome in breast cancer patients.

摘要

我们研究了接受化疗的乳腺癌患者的临床结局与谷胱甘肽S-转移酶M1(GSTM1)缺失/存在、谷胱甘肽S-转移酶T1(GSTT1)缺失/存在以及谷胱甘肽S-转移酶P1(GSTP1)Ile105Val多态性之间的关系。2010年1月至2011年12月期间连续诊断的420例乳腺癌患者符合纳入我们的回顾性研究的条件。使用Sequenom MassARRAY平台进行GSTM1缺失/存在、GSTT1缺失/存在以及GSTP1 Ile105Val的检测设计和单核苷酸多态性(SNP)基因分型。在单变量分析中,与携带GSTP1 Ile105Val的CC基因型相比,携带TT基因型以及CT + TT基因型的患者对化疗的肿瘤反应明显较差(对于TT基因型,校正比值比(OR)= 0.44,95%置信区间(CI)= 0.22 - 0.89;对于CT + TT基因型,校正OR = 0.59,95% CI = 0.39 - 0.92)。通过Cox多变量分析,TT基因型和CT + TT基因型与乳腺癌死亡风险增加相关,并且在经过潜在混杂因素校正后这种关系更为明显(对于TT基因型,校正OR = 4.23,95% CI = 2.33 - 8.76;对于CT + TT基因型,校正OR = 2.53,95% CI = 1.60 - 4.03)。GSTP1 Ile105Val多态性可能会影响乳腺癌患者的临床结局。

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