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头颈部癌症患者中致癌物质解毒基因(CYP1A1、GSTP1 和 GSTT1)的表达模式。

Expression patterns of carcinogen detoxifying genes (CYP1A1, GSTP1 & GSTT1) in HNC patients.

机构信息

Cancer Genetics Lab, Department of Biosciences, COMSATS Institute of Information Technology, Islamabad, Pakistan.

出版信息

Pathol Oncol Res. 2013 Jan;19(1):89-94. doi: 10.1007/s12253-012-9563-3. Epub 2012 Aug 25.

Abstract

Carcinogen detoxifying genes may be involved in pathogenesis of head and neck cancer (HNC). CYP1A1 is phase I enzyme that converts carcinogens into water soluble compounds which are easily excreted from body. GSTs constitute phase II detoxification enzymes that recognize these highly electrophilic compounds and detoxify them. Abnormal expression of these genes can potentially lead to cancer initiation. In present study, we analyzed protein expression of these genes in a total of 192 HNC patients and noncancerous healthy control serum samples screened for GSTs specific activity by ELISA. Furthermore, expression of these molecules was also determined in 49 HNC tissues/ adjacent control tissue by immunohistochemistry with specific antibodies. Mean serum GSTs specific activity was found to be 7.7 (+11.5)U/L in HNC patients and 11.4 (+7.5)U/L in controls. Significant decrease (P < 0.05) in GSTs specific activity was observed in HNC patients compared with controls (P < 0.001). Data for immunohistochemistry showed that CYP1A1 and GSTT1 was down expressed whereas GSTP1 was over expressed in HNC tissues compared with adjacent normal control tissues. Results of immunohistochemistry revealed 63 % HNC tissues had weak, 27 % moderate and 10 % strong staining for CYP1A1. For GSTT1, 27 % HNC tissues had no staining, 49 % weak staining, 16 % moderate and 8 % strong staining. Similarly for GSTP1, percentages for weak, moderate and strong staining were 6 %, 12 % and 82 % respectively. These reduced proteins observed in cancer patients highlight a potential breach on DNA repair mechanism when compared with control. Thus altered expression of these detoxifying molecules may collectively contribute to HNC development in Pakistani population.

摘要

致癌物质解毒基因可能参与头颈部癌症(HNC)的发病机制。CYP1A1 是一种 I 相酶,可将致癌物质转化为水溶性化合物,这些化合物很容易从体内排出。GSTs 构成 II 相解毒酶,可识别这些高亲电化合物并对其进行解毒。这些基因的异常表达可能导致癌症的发生。在本研究中,我们分析了总共 192 例 HNC 患者和通过 ELISA 筛选 GSTs 特异性活性的非癌健康对照血清样本中这些基因的蛋白表达。此外,还通过特异性抗体的免疫组织化学测定了这 49 例 HNC 组织/相邻对照组织中这些分子的表达。发现 HNC 患者的血清 GSTs 特异性活性平均值为 7.7(+11.5)U/L,对照组为 11.4(+7.5)U/L。与对照组相比,HNC 患者的 GSTs 特异性活性显著降低(P<0.05;P<0.001)。免疫组织化学数据显示,与相邻正常对照组织相比,CYP1A1 和 GSTT1 表达下调,而 GSTP1 表达上调。免疫组织化学结果显示,63%的 HNC 组织 CYP1A1 染色弱,27%中度,10%强。对于 GSTT1,27%的 HNC 组织无染色,49%弱染色,16%中度,8%强染色。同样,对于 GSTP1,弱、中、强染色的百分比分别为 6%、12%和 82%。与对照组相比,在癌症患者中观察到这些减少的蛋白质,突出了 DNA 修复机制的潜在破坏。因此,这些解毒分子的表达改变可能共同导致巴基斯坦人群中 HNC 的发生。

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