结直肠癌风险人群中谷胱甘肽S-转移酶活性及谷胱甘肽S-转移酶μ表达情况

Glutathione S-transferase activity and glutathione S-transferase mu expression in subjects with risk for colorectal cancer.

作者信息

Szarka C E, Pfeiffer G R, Hum S T, Everley L C, Balshem A M, Moore D F, Litwin S, Goosenberg E B, Frucht H, Engstrom P F

机构信息

Division of Population Science, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111, USA.

出版信息

Cancer Res. 1995 Jul 1;55(13):2789-93.

DOI:
PMID:7796404
Abstract

The glutathione S-transferases (alpha, mu, and pi), a family of Phase II detoxication enzymes, play a critical role in protecting the colon mucosa by catalyzing the conjugation of dietary carcinogens with glutathione. We investigated the efficacy of using the glutathione S-transferase (GST) activity of blood lymphocytes and GST-mu expression as biomarkers of risk for colorectal cancer. GST activity was measured in the blood lymphocytes of control individuals (n = 67) and in the blood lymphocytes (n = 60) and colon tissue (n = 34) of individuals at increased risk for colon cancer. Total GST activity was determined spectrophotometrically with the use of 1-chloro-2,4-dinitrobenzene as a substrate. The ability to express the um subclass of GST was determined with the use of an ELISA. Although interindividual variability in the GST activity of blood lymphocytes was greater than 8-fold (range, 16.7-146.8 nmol/min/mg), the GST activity of blood lymphocytes and colon tissue within an individual was constant over time and was unrelated to sex, age, or race. The GST activity of blood lymphocytes from high-risk individuals was significantly lower than that of blood lymphocytes from control individuals (P < or = 0.004). No association was observed between the frequency of GST-mu phenotype and risk for colorectal cancer. Blood lymphocytes from high-risk individuals unable to express GST-mu had lower levels of GST activity than did those from control subjects with the GST-mu null phenotype; however, this difference was significant in male subjects only (P < or = 0.006). Analysis of paired samples of blood lymphocytes and colon tissue indicated a strong correlation between the GST activity of the two tissue types (Spearman's rank correlation, r = 0.87; P < or = 0.0001). The GST activity of blood lymphocytes may be used to identify high-risk individuals with decreased protection from this Phase II detoxication enzyme who may benefit from clinical trials evaluating GST modulators as chemopreventive agents for colorectal cancer. The GST activity of blood lymphocytes may also be used in colorectal cancer chemoprevention trials to monitor the responsiveness of colon tissue to regimens that modify Phase II detoxication enzymes.

摘要

谷胱甘肽S-转移酶(α、μ和π)是一类Ⅱ相解毒酶,通过催化膳食致癌物与谷胱甘肽的结合,在保护结肠黏膜方面发挥关键作用。我们研究了将血液淋巴细胞的谷胱甘肽S-转移酶(GST)活性和GST-μ表达用作结直肠癌风险生物标志物的有效性。在对照个体(n = 67)的血液淋巴细胞中,以及在患结肠癌风险增加的个体的血液淋巴细胞(n = 60)和结肠组织(n = 34)中测量了GST活性。使用1-氯-2,4-二硝基苯作为底物,通过分光光度法测定总GST活性。使用酶联免疫吸附测定法确定表达GST μ亚类的能力。尽管血液淋巴细胞的GST活性个体间变异性大于8倍(范围为16.7 - 146.8 nmol/min/mg),但个体内血液淋巴细胞和结肠组织的GST活性随时间保持恒定,且与性别、年龄或种族无关。高危个体血液淋巴细胞的GST活性显著低于对照个体血液淋巴细胞的GST活性(P≤0.004)。未观察到GST-μ表型频率与结直肠癌风险之间存在关联。无法表达GST-μ的高危个体的血液淋巴细胞的GST活性水平低于具有GST-μ无效表型的对照受试者的血液淋巴细胞;然而,这种差异仅在男性受试者中显著(P≤0.006)。对血液淋巴细胞和结肠组织配对样本的分析表明,两种组织类型的GST活性之间存在强相关性(Spearman等级相关性,r = 0.87;P≤0.0001)。血液淋巴细胞的GST活性可用于识别对这种Ⅱ相解毒酶保护作用降低的高危个体,这些个体可能从评估GST调节剂作为结直肠癌化学预防剂的临床试验中受益。血液淋巴细胞的GST活性也可用于结直肠癌化学预防试验,以监测结肠组织对改变Ⅱ相解毒酶的方案的反应性。

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