Oldenburg Jan, Kraggerud Sigrid M, Brydøy Marianne, Cvancarova Milada, Lothe Ragnhild A, Fossa Sophie D
Department of Clinical Cancer Research, The Norwegian Radiumhospital, Oslo, Norway.
J Transl Med. 2007 Dec 27;5:70. doi: 10.1186/1479-5876-5-70.
To assess the impact of polymorphisms in Glutathione S-transferase (GST) -P1, -M1, and -T1 on self-reported chemotherapy-induced long-term toxicities in testicular cancer survivors (TCSs).
A total of 238 TCSs, who had received cisplatin-based chemotherapy at median twelve years earlier, had participated in a long-term follow-up survey which assessed the prevalence of self-reported paresthesias in fingers/toes, Raynaud-like phenomena in fingers/toes, tinnitus, and hearing impairment. From all TCSs lymphocyte-derived DNA was analyzed for the functional A-->G polymorphism at bp 304 in GSTP1, and deletions in GST-M1 and GST-T1. Evaluation of associations between GST polymorphisms and self-reported toxicities included adjustment for prior treatment.
All six evaluated toxicities were significantly associated with the cumulative dose of cisplatin and/or bleomycin. Compared to TCSs with either GSTP1-AG or GSTP1-AA, the 37 TCSs with the genotype GSTP1-GG, were significantly less bothered by paresthesias in fingers and toes (p = 0.039, OR 0.46 [0.22-0.96] and p = 0.023, OR 0.42 [0.20-0.88], respectively), and tinnitus (p = 0.008, OR 0.33 [0.14-0.74]). Furthermore, absence of functional GSTM1 protected against hearing impairment (p = 0.025, OR 1.81 [1.08-3.03]).
In TCSs long-term self-reported chemotherapy-induced toxicities are associated with functional polymorphisms in GSTP1 and GSTM1. Hypothetically, absence of GST-M1 leaves more glutathione as substrate for the co-expressed GST-P1. Also intracellular inactivation of pro-apoptotic mediators represents a possible explanation of our findings. Genotyping of these GSTs might be a welcomed step towards a more individualized treatment of patients with metastatic testicular cancer.
评估谷胱甘肽S-转移酶(GST)-P1、-M1和-T1基因多态性对睾丸癌幸存者(TCS)自我报告的化疗所致长期毒性的影响。
共有238名TCS,他们在中位时间12年前接受了以顺铂为基础的化疗,参与了一项长期随访调查,该调查评估了自我报告的手指/脚趾感觉异常、手指/脚趾雷诺样现象、耳鸣和听力障碍的发生率。从所有TCS中提取淋巴细胞来源的DNA,分析GSTP1基因第304位碱基处的功能性A→G多态性,以及GST-M1和GST-T1基因的缺失情况。评估GST基因多态性与自我报告毒性之间的关联时对先前治疗进行了校正。
所有六种评估的毒性均与顺铂和/或博来霉素的累积剂量显著相关。与携带GSTP1-AG或GSTP1-AA基因型的TCS相比,37名携带GSTP1-GG基因型的TCS对手指和脚趾感觉异常(分别为p = 0.039,OR 0.46 [0.22 - 0.96]和p = 0.023,OR 0.42 [0.20 - 0.88])以及耳鸣(p = 0.008,OR 0.33 [0.14 - 0.74])的困扰明显更少。此外,功能性GSTM1缺失可预防听力障碍(p = 0.025,OR 1.81 [1.08 - 3.03])。
在TCS中,自我报告的长期化疗所致毒性与GSTP1和GSTM1的功能性基因多态性相关。假设GST-M1缺失会使更多谷胱甘肽作为共表达的GST-P1的底物。此外,促凋亡介质的细胞内失活可能是我们研究结果的一种解释。对这些GST进行基因分型可能是朝着转移性睾丸癌患者更个体化治疗迈出的受欢迎的一步。