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Effects of telomerase inhibitor on epigenetic chromatin modification enzymes in malignancies

机译:端粒酶抑制剂对恶性肿瘤中表观癌染色质修饰酶的影响

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Abstract Telomerase has a critical role in cell proliferation, tumor maintaining, and therapy resistance, which act by modifying many signaling pathways. 2‐[(E)‐3‐Naphtalen‐2‐yl‐but‐2‐enoylamino]‐benzoic acid (BIBR1532) is one of the most studied telomerase inhibitors, and it targets telomerase components TERC and TERT. In this novel study, we aimed to investigate the epigenetic effects of BIBR1532 on both hematologic malignancies and solid tumors. K‐562 human chronic myeloid leukemia cell line and U87MG glioblastoma cell line were compared with control groups without BIBR1532 treatment. Cytotoxic effects of BIBR1532 were determined by using WST‐1 assay. Apoptotic effects of BIBR1532 were detected by using annexin V method. To assess expression changes in the human epigenetic chromatin modification enzyme genes, total RNA was isolated from K‐562 and U87MG cells treated with BIBR1532 and untreated control cells. BIBR1532 induced 2.41‐fold apoptotic cell death in U87MG cell lines compared with control groups. Apoptosis was slightly induced in K‐562 cells with BIBR1532 treatment compared with control cells. We observed that BIBR1532 also regulates similar genes in both cell lines, and it is useful on epigenetic mechanisms. As a result, telomerase inhibitor BIBR1532 has a significant effect on both hematological malignancies and solid tumors.
机译:摘要端粒酶在细胞增殖,肿瘤维持和治疗抵抗中具有关键作用,通过改变许多信号通路来解决这些作用。 2 - [(e)-3-萘-2-烯-2- eNoylamino] - 苯甲酸(BIBR1532)是研究最多的端粒酶抑制剂之一,并且它靶向端粒酶组分Terc和Tert。在这项新的研究中,我们旨在探讨BIBR1532对血液学恶性肿瘤和实体瘤的表观遗传效应。将K-562人慢性骨髓白血病细胞系和U87MG胶质母细胞系与无BIBR1532处理的对照组进行比较。通过使用WST-1测定法测定BIBR1532的细胞毒性效应。使用膜蛋白V法检测BIBR1532的凋亡效应。为了评估人表表带染色质修饰酶基因的表达变化,从K-562和用BIBR1532处理的k-562和U87mg细胞分离总RNA和未处理的对照细胞。与对照组相比,BIBR1532在U87MG细胞系中诱导2.41倍的凋亡细胞死亡。与对照细胞相比,具有BIBR1532治疗的K-562细胞中略微诱导细胞凋亡。我们观察到BIBR1532还调节两种细胞系中的类似基因,并且可用于表观遗传机制。结果,端粒酶抑制剂BIBR1532对血液恶性恶性肿瘤和实体瘤具有显着影响。

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