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正常人血清及乳腺癌患者血清中促凋亡性CD95L水平。

Proapoptotic CD95L levels in normal human serum and sera of breast cancer patients.

作者信息

Olimón-Andalón Vicente, Aguilar-Lemarroy Adriana, Ratkovich-González Sarah, Uribe-López Aida, Mariscal-Ramírez Ignacio, Delgadillo-Cristerna Raúl, Ortiz-Lazareno Pablo, Hernández-Flores Georgina, de Celis Ruth, Bravo-Cuellar Alejandro, Jave-Suárez Luis F

机构信息

Escuela de Biología, Universidad Autónoma de Sinaloa, Culiacán, Sinaloa, Mexico.

出版信息

Tumour Biol. 2015 May;36(5):3669-78. doi: 10.1007/s13277-014-3005-7. Epub 2015 Jan 4.

Abstract

The CD95 pathway is a critical apoptotic pathway used by immune cells to avoid cancer development. CD95 ligand (CD95L) is found in several forms, as a cell membrane-associated form, a soluble metalloprotease-cleaved form, and a soluble but membrane-bound CD95L released on cell-derived exosomes. In this study, we used a cell-based assay to evaluate the activity of proapoptotic CD95L in sera from healthy individuals and breast cancer patients. We confirmed that our cell-based assay using Jurkat cells was sensitive to the presence of proapoptotic CD95L in serum, and apoptosis induction by mechanisms other than CD95 was discriminated using apoptosis-resistant Jurkat subclones. Our results indicated a proapoptotic potential of normal serum that involved CD95L. Sera from breast cancer patients exhibited significantly decreased apoptosis induction, due to increased CD95 receptor levels compared with healthy women. Apoptotic potential tended to decrease as the Breast Imaging Reporting and Data System grade increased, and we observed restoration of proapoptotic potential after tumor removal. The CD95L in serum responsible for apoptotic induction was associated with high-molecular-weight particles, perhaps with exosomes. The sera of healthy individuals generally contain a proapoptotic environment, and this property is mainly maintained by the presence of CD95L. Furthermore, measurement of CD95L-mediated apoptosis induction by sera could be a useful parameter to be evaluated during cancer development and therapeutic response.

摘要

CD95途径是免疫细胞用于避免癌症发生的关键凋亡途径。CD95配体(CD95L)有多种形式,包括细胞膜相关形式、可溶性金属蛋白酶切割形式以及细胞来源外泌体上释放的可溶性但膜结合的CD95L。在本研究中,我们使用基于细胞的检测方法来评估健康个体和乳腺癌患者血清中促凋亡CD95L的活性。我们证实,使用Jurkat细胞的基于细胞的检测方法对血清中促凋亡CD95L的存在敏感,并且使用抗凋亡Jurkat亚克隆区分了CD95以外机制诱导的凋亡。我们的结果表明正常血清具有涉及CD95L的促凋亡潜力。与健康女性相比,乳腺癌患者的血清诱导凋亡显著减少,这是由于CD95受体水平升高。随着乳腺影像报告和数据系统(Breast Imaging Reporting and Data System)分级增加,凋亡潜力趋于降低,并且我们观察到肿瘤切除后促凋亡潜力恢复。血清中负责诱导凋亡的CD95L与高分子量颗粒有关,可能与外泌体有关。健康个体的血清通常含有促凋亡环境,并且这种特性主要由CD95L的存在维持。此外,测量血清中CD95L介导的凋亡诱导可能是癌症发生发展和治疗反应过程中一个有用的评估参数。

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