Department of Molecular Biological, Genetics and Molecular Biology Research Unit - UPGEM, Faculty of Medicine of São José do Rio Preto - FAMERP, São José do Rio Preto, São Paulo, Brazil.
Department of Otolaryngology and Head and Neck Surgery, Sao Jose do Rio Preto Medical School, São José do Rio Preto, São Paulo, Brazil.
Asian Pac J Cancer Prev. 2020 Jun 1;21(6):1637-1644. doi: 10.31557/APJCP.2020.21.6.1637.
BACKGROUND/AIM: The Glutathione S-transferases (GSTs) are important carcinogen-metabolizing enzymes. Polymorphisms involved in these enzymes can modulate the development and treatment of head and neck cancer. To investigate the association of GSTs polymorphisms with head and neck cancer and risk factors, clinical-pathological features, and survival time of the patients treated with chemotherapy and/or radiotherapy.
The GST gene polymorphisms were evaluated in 197 cases and 514 controls by PCR-RFLP-Polymerase Chain Reaction Restriction Fragment Length Polymorphism.
The GSTP-313 was associated with a decreased risk for HNSCC (p=0.050). The GSTP1 haplotype analysis revealed a higher frequency of the AC and AT haplotypes in the case group than in the control group (p=0.013 and p=0.019, respectively), and the opposite for G-C haplotype (p = 0.015). Yet, the different combinations between the genotypes were associated with an increased risk of cancer. The study showed no association between the polymorphisms and primary tumor site, clinical-pathological characteristics, treatment (chemotherapy and/or radiotherapy) and survival time of the patients.
The GST polymorphisms combination showed an increased risk for carcinogenesis, and studies with larger casuistry can contribute to the clarification of the role in individual patient differences for the response to chemotherapy and/or radiotherapy and identify biomarkers of susceptibility.
背景/目的:谷胱甘肽 S-转移酶(GSTs)是重要的致癌物质代谢酶。这些酶的多态性可以调节头颈部癌症的发展和治疗。研究 GSTs 多态性与头颈部癌症以及患者的化疗和/或放疗的风险因素、临床病理特征和生存时间的关系。
通过 PCR-RFLP-聚合酶链反应限制性片段长度多态性,在 197 例病例和 514 例对照中评估 GST 基因多态性。
GSTP-313 与 HNSCC 的风险降低相关(p=0.050)。GSTP1 单倍型分析显示,病例组中 AC 和 AT 单倍型的频率高于对照组(p=0.013 和 p=0.019),而 GC 单倍型的频率则相反(p=0.015)。然而,不同基因型的组合与癌症风险增加有关。研究表明,多态性与原发肿瘤部位、临床病理特征、治疗(化疗和/或放疗)以及患者的生存时间之间无相关性。
GST 多态性组合显示出致癌作用的风险增加,更大病例数的研究可以有助于阐明对化疗和/或放疗反应的个体差异中的作用,并确定易感性的生物标志物。