Suppr超能文献

皮肤T细胞淋巴瘤细胞暴露于硼替佐米和甲氨蝶呤后的凋亡诱导及基因表达谱改变

Apoptosis Induction and Gene Expression Profile Alterations of Cutaneous T-Cell Lymphoma Cells following Their Exposure to Bortezomib and Methotrexate.

作者信息

Mpakou Vassiliki, Papadavid Evangelia, Kontsioti Frieda, Konsta Eugene, Vikentiou Miriam, Spathis Aris, Papageorgiou Sotiris, Vasilatou Diamantina, Gkontopoulos Konstantinos, Mpazani Efthimia, Karakitsos Petros, Rigopoulos Dimitrios, Dimitriadis George, Pappa Vasiliki

机构信息

Second Dept. of Internal Medicine and Research Institute, Attikon University General Hospital, Rimini 1, Haidari, Athens, Greece.

Second Department of Dermatology, Attikon University General Hospital, Rimini 1, Haidari, Athens, Greece.

出版信息

PLoS One. 2017 Jan 20;12(1):e0170186. doi: 10.1371/journal.pone.0170186. eCollection 2017.

Abstract

Mycosis fungoides (MF) and its leukemic variant Sézary syndrome (SS) comprise the majority of CTCL, a heterogenous group of non-Hodgkins lymphomas involving the skin. The CTCL's resistance to chemotherapy and the lack of full understanding of their pathogenesis request further investigation. With the view of a more targeted therapy, we evaluated in vitro the effectiveness of bortezomib and methotrexate, as well as their combination in CTCL cell lines, regarding apoptosis induction. Our data are of clinical value and indicate that the bortezomib/methotrexate combinational therapy has an inferior impact on the apoptosis of CTCL compared to monotherapy, with bortezomib presenting as the most efficient treatment option for SS and methotrexate for MF. Using PCR arrays technology, we also investigated the alterations in the expression profile of genes related to DNA repair pathways in CTCL cell lines after treatment with bortezomib or methotrexate. We found that both agents, but mostly bortezomib, significantly deregulate a large number of genes in SS and MF cell lines, suggesting another pathway through which these agents could induce apoptosis in CTCL. Finally, we show that SS and MF respond differently to treatment, verifying their distinct nature and further emphasizing the need for discrete treatment approaches.

摘要

蕈样肉芽肿(MF)及其白血病变体塞扎里综合征(SS)构成了皮肤T细胞淋巴瘤(CTCL)的大部分,CTCL是一组累及皮肤的异质性非霍奇金淋巴瘤。CTCL对化疗的耐药性以及对其发病机制缺乏全面了解,需要进一步研究。为了实现更有针对性的治疗,我们在体外评估了硼替佐米和甲氨蝶呤以及它们的组合在CTCL细胞系中诱导凋亡的有效性。我们的数据具有临床价值,表明与单一疗法相比,硼替佐米/甲氨蝶呤联合疗法对CTCL凋亡的影响较小,硼替佐米是治疗SS最有效的选择,甲氨蝶呤是治疗MF最有效的选择。使用PCR阵列技术,我们还研究了硼替佐米或甲氨蝶呤处理后CTCL细胞系中与DNA修复途径相关的基因表达谱的变化。我们发现这两种药物,尤其是硼替佐米,会显著失调SS和MF细胞系中的大量基因,这表明这些药物可能通过另一种途径诱导CTCL凋亡。最后,我们表明SS和MF对治疗的反应不同,证实了它们的不同性质,并进一步强调了采用不同治疗方法的必要性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验