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可溶性肿瘤坏死因子相关凋亡诱导配体(sTRAIL)及其受体sTRAIL-R1和sTRAIL-R2浓度的评估——监测凋亡诱导外源性途径进程的标志物:在卵巢癌诊断中的潜在应用

Assessment of concentrations of sTRAIL ligand and its receptors sTRAIL-R1 and sTRAIL-R2 - markers monitoring the course of the extrinsic pathway of apoptosis induction: potential application in ovarian cancer diagnostics.

作者信息

Mielczarek-Palacz Aleksandra, Sikora Justyna, Kondera-Anasz Zdzisława

机构信息

School of Pharmacy with the Division of Laboratory Medicine in Sosnowiec, Department of Immunology and Serology, Medical University of Silesia, Katowice, Sosnowiec, Poland.

出版信息

Arch Med Sci. 2017 Apr 1;13(3):624-628. doi: 10.5114/aoms.2015.53144. Epub 2015 Nov 17.

Abstract

INTRODUCTION

TNF-related apoptosis-inducing ligand (TRAIL) together with its receptors are involved in activation of the extrinsic pathway of apoptosis. Due to the special role of the apoptosis pathway in pathogenesis of ovarian cancers, the aim of the study was to assess concentrations of sTRAIL, sTRAIL-R1 and sTRAIL-R2 in serum of affected women.

MATERIAL AND METHODS

The study group included 85 women with diagnosed ovarian tumors: 35 women with ovarian serous cystadenoma, 15 women with ovarian teratoma and 35 women with serous cystadenocarcinoma. The control group consisted of 30 healthy women. Concentrations of studied parameters were measured by ELISA methods.

RESULTS

Serum levels of all studied parameters were higher in serum of women with ovarian tumors than in the controls, but their concentrations varied depending on the clinical diagnosis. The highest concentration of TRAIL was found in serum of women with ovarian cancer, the highest sTRAIL-R1 level in serum of women with ovarian mature teratoma, and the highest sTRAIL-R2 level in serum of women with ovarian serous cystadenoma.

CONCLUSIONS

The state of immunosuppression accompanying neoplastic disease depends on the extrinsic pathway of apoptosis induction in the TRAIL/TRAIL-R system. Determination of TRAIL-R1 and TRAIL-R2 levels may prove to be useful in ovarian tumor differential diagnostics, which requires further research.

摘要

引言

肿瘤坏死因子相关凋亡诱导配体(TRAIL)及其受体参与凋亡外源性途径的激活。由于凋亡途径在卵巢癌发病机制中的特殊作用,本研究旨在评估患病女性血清中可溶性TRAIL(sTRAIL)、可溶性TRAIL受体1(sTRAIL-R1)和可溶性TRAIL受体2(sTRAIL-R2)的浓度。

材料与方法

研究组包括85例确诊为卵巢肿瘤的女性:35例卵巢浆液性囊腺瘤患者、15例卵巢畸胎瘤患者和35例浆液性囊腺癌患者。对照组由30名健康女性组成。采用酶联免疫吸附测定(ELISA)法测量研究参数的浓度。

结果

卵巢肿瘤女性血清中所有研究参数的水平均高于对照组,但其浓度因临床诊断而异。卵巢癌女性血清中TRAIL浓度最高,卵巢成熟畸胎瘤女性血清中sTRAIL-R1水平最高,卵巢浆液性囊腺瘤女性血清中sTRAIL-R2水平最高。

结论

肿瘤性疾病伴随的免疫抑制状态取决于TRAIL/TRAIL-R系统中凋亡诱导的外源性途径。TRAIL-R1和TRAIL-R2水平的测定可能在卵巢肿瘤鉴别诊断中有用,这需要进一步研究。

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