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非小细胞肺癌中谷胱甘肽S-转移酶M1和T1的多态性与蛋白表达

Polymorphisms and Protein Expressions of Glutathione S-Transferase M1 and T1 in Non-Small Cell Lung Cancer.

作者信息

Kiliç Murat, Ada Ahmet Oğuz, Oğuztüzün Serpil, Demirağ Funda, Çelik Sezgin, Biçakçioğlu Pınar, Işcan Mümtaz

机构信息

Ankara University, Vocational School of Health Services, Department of Pharmacy Services, Ankara, Turkey.

Ankara University, Faculty of Pharmacy, Department of Pharmaceutical Toxicology, Ankara, Turkey.

出版信息

Turk J Pharm Sci. 2017 Dec;14(3):237-242. doi: 10.4274/tjps.74745. Epub 2017 Nov 20.

Abstract

OBJECTIVES

The deletion polymorphisms of glutathione S-transferase (GST) and genes result in the absence of the corresponding protein, which decreases the detoxification of carcinogens. Studies evaluating polymorphisms and protein expressions in the same patients are limited. Therefore, in this study, we aimed to investigate the association between polymorphisms and protein expressions of and in lung tissues of patients with non-small cell lung cancer (NSCLC).

MATERIALS AND METHODS

For protein expression and gene deletion studies, tumor and surrounding tumor free (normal) tissue of 33 patients with NSCLC were used. In paraffin-embedded tissues, immunohistochemistry was used to detect protein expressions, and multiplex polymerase chain reaction amplification was used to identify gene deletions.

RESULTS

and protein expressions were not detected in patients with and gene deletions, whereas protein expressions were detected in lung tissues of all patients carrying and genes. The protein expression level of was 2.0-fold higher in tumors of patients lacking genes than those with genes (p=0.018). Protein expression of was statistically higher in tumor tissues than in normal tissues of patients with genes (p=0.001).

CONCLUSION

These results show that a) there is an association between gene deletions and protein expressions of and in patients with NSCLC, b) in the absence of genes, enhancement of expression of in tumors is likely to show that increases its capacity to detoxify the toxic electrophiles in tumors, and c) protein expression is higher in tumors compared with normal lung tissues of patients with NSCLC.

摘要

目的

谷胱甘肽S-转移酶(GST)及相关基因的缺失多态性导致相应蛋白质缺失,从而降低致癌物的解毒作用。评估同一患者多态性和蛋白质表达的研究有限。因此,在本研究中,我们旨在探讨非小细胞肺癌(NSCLC)患者肺组织中相关基因多态性与蛋白质表达之间的关联。

材料与方法

为进行蛋白质表达和基因缺失研究,使用了33例NSCLC患者的肿瘤组织及肿瘤周围无瘤(正常)组织。在石蜡包埋组织中,采用免疫组织化学检测蛋白质表达,采用多重聚合酶链反应扩增鉴定基因缺失。

结果

在存在相关基因缺失的患者中未检测到相应蛋白质表达,而在所有携带相关基因的患者肺组织中检测到了蛋白质表达。缺乏相关基因的患者肿瘤中该蛋白质表达水平比携带相关基因的患者高2.0倍(p = 0.018)。在携带相关基因的患者中,肿瘤组织中的蛋白质表达在统计学上高于正常组织(p = 0.001)。

结论

这些结果表明,a)NSCLC患者中相关基因缺失与蛋白质表达之间存在关联;b)在缺乏相关基因的情况下,肿瘤中该蛋白质表达增强可能表明其增加了对肿瘤中毒性亲电试剂的解毒能力;c)NSCLC患者肿瘤中的该蛋白质表达高于正常肺组织。

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