转染β -抑制素1对HGG细胞增殖和替莫唑胺治疗反应的影响

Cristina Horescu, S. Artene
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引用次数: 1

摘要

虽然有几项研究表明-抑制蛋白家族在几种癌症的发展中起着重要作用,但它对恶性胶质瘤的影响却几乎没有任何信息。在我们的研究中,我们用-1抑制蛋白质粒转染了已建立的高级别胶质瘤细胞系11hgg,以观察-1过表达如何影响增殖和对标准护理治疗的反应。24h后,转染的细胞与未转染的细胞相比,增殖能力下降。在治疗反应方面,与未转染的细胞相比,转染的细胞表现出明显升高的细胞毒性作用。然而,转染48h和72h后,细胞的增殖仅略有增加,而对TMZ的处理反应受到-1阻滞蛋白过表达的轻微影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
THE EFFECT OF BETA - ARRESTIN 1 TRANSFECTION ON PROLIFERATION AND TEMOZOLOMIDE TREATMENT RESPONSE IN HGG CELLS
While several studies have indicated a major role of the ?-arrestin family in the development of several types of cancer, little to no information is available on its influence in malignant gliomas. In our study we transfected an established high-grade glioma cell line, 11 HGG with a ?-1 arrestin plasmid in order to observe how ?-1 overexpression influences proliferation and response to standard of care treatment. After 24h, the transfected cells presented a drop in proliferation when compared to untransfected cells. In terms of treatment response, transfected cells presented a markedly elevated cytotoxic effect when compared to untransfected cells. However, after 48h and 72h transfected cells presented only a minor increase in proliferation while treatments responses to TMZ were modestly influenced by ?-1 arrestin overexpression.
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