首页> 外文期刊>Hematology. >Morpholino Oligo Antisense efficiently suppresses BCR/ABL and cell proliferation in CML: specific inhibition of BCR-ABL gene expression by Morpholino Oligo Antisense in BCR-ABL(+) cells.
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Morpholino Oligo Antisense efficiently suppresses BCR/ABL and cell proliferation in CML: specific inhibition of BCR-ABL gene expression by Morpholino Oligo Antisense in BCR-ABL(+) cells.

机译:Morpholino Oligo反义有效地抑制了CML中的BCR / ABL和细胞增殖:Morpholino Oligo反义在BCR-ABL(+)细胞中对BCR-ABL基因表达的特异性抑制。

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摘要

Chronic myeloid leukemia is a disorder that develops when a hematopoietic stem cell acquires the Philadelphia chromosome carrying the chimeric BCR/ABL oncogene leading to a deregulated cell proliferation and a decreased apoptosis in response to mutagenic stimuli. Therefore, it has been considered that BCR/ABL oncogene is a potential attractive target for anticancer agents. Antisense strategies aiming to suppress the expression of BCR/ABL in chronic myeloid leukemia cells have been studied by several research groups over the last decade. In the present study, the effect of Morpholino Oligo Antisense in BCR/ABL oncogene silencing was evaluated. To examine the hypothesis, K562 was used as a BCR/ABL fusion gene positive cell line using a Jurkat cell line as a control. The capacity of Morpholino Oligo Antisense in inhibiting the translation of p210(bcr-abl) protein by a western blotting technique, inhibition of cell proliferation, and stimulation of apoptosis by flow cytometric analysis after 24 and 48 hours was studied. Prolonged exposure of K562 cell line to Morpholino Oligo Antisense targeted against BCR-ABL showed proliferation inhibition as the main feature. Following western blotting, we found that complete silencing of BCR-ABL had been achieved but flow cytometric analysis showed no significant apoptosis. The results indicate that Morpholino Oligo Antisense was able to inhibit p210(bcr-abl), but did not induce apoptosis due to co-silencing of BCR.
机译:慢性髓细胞性白血病是当造血干细胞获得携带嵌合BCR / ABL致癌基因的费城染色体后,导致细胞增殖失调并响应诱变刺激而减少的细胞凋亡时所形成的疾病。因此,已经认为BCR / ABL癌基因是抗癌剂的潜在诱人靶标。在过去的十年中,一些研究小组已经研究了旨在抑制慢性髓样白血病细胞中BCR / ABL表达的反义策略。在本研究中,评估了吗啉代寡核苷酸在BCR / ABL致癌基因沉默中的作用。为了检验该假设,使用Jurkat细胞系作为对照,将K562用作BCR / ABL融合基因阳性细胞系。通过蛋白质印迹技术研究了24和48小时后吗啉寡核苷酸反义抑制p210(bcr-abl)蛋白翻译,抑制细胞增殖和刺激细胞凋亡的能力。 K562细胞系长时间暴露于针对BCR-ABL的Morpholino Oligo Antisense中,其增殖抑制是其主要特征。 Western印迹后,我们发现已经实现了BCR-ABL的完全沉默,但流式细胞仪分析显示没有明显的细胞凋亡。结果表明,Morpholino Oligo Antisense能够抑制p210(bcr-abl),但不会由于BCR的共沉默而诱导细胞凋亡。

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