Suppr超能文献

凋亡蛋白在 REC-2006 介导的肝癌细胞系辐射防护中的作用。

Role of Apoptotic Proteins in REC-2006 Mediated Radiation Protection in Hepatoma Cell Lines.

机构信息

Institute of Nuclear Medicine and Allied Sciences, Delhi, India.

出版信息

Evid Based Complement Alternat Med. 2011;2011:758326. doi: 10.1093/ecam/neq059. Epub 2011 Mar 20.

Abstract

The present study was carried out to evaluate the role of apoptotic proteins in REC-2006-mediated radiation protection in hepatoma cell lines. REC-2006 treatment 2 h before irradiation strongly inhibited the cleavage of ATM and PARP-1 in HepG2 cells. The expression of nuclear apoptosis inducing factor (AIF) was found to be more inhibited (17%) in HepG2 cells in REC-2006 + radiation-treated group. More inhibition (33%) of cytochrome c was observed in HepG2 cells upon REC-2006 treatment 2 h prior irradiation. Similarly, significantly more (P<.05) inhibition of Apaf-1, caspase-9 and caspase-3 was observed in REC-2006 + radition-treated group in HepG2 cells. REC-2006 treatment restored the expression of ICAD in HepG2 cells; however, no restoration was observed in Hep3B cells. Lower nuclear to cytoplasmic CAD ratio was observed in HepG2 cells (0.6) as compared with Hep3B cells (1.2) in REC-2006 + radiation-treated group. In conclusion, REC-2006 rendered higher protection in HepG2 cells by inhibiting the expression and translocation of AIF, inhibiting the cleavage of ATM and PARP-1, restoring the expression of ICAD, inhibiting the release of cytochrome c and thus modulating the expression of Apaf-1 caspase-9 and activity of caspase-3.

摘要

本研究旨在评估凋亡蛋白在 REC-2006 介导的肝癌细胞系辐射防护中的作用。REC-2006 在照射前 2 小时处理强烈抑制了 HepG2 细胞中 ATM 和 PARP-1 的裂解。发现核凋亡诱导因子(AIF)的表达在 REC-2006 + 辐射处理组中的 HepG2 细胞中受到更强的抑制(约 17%)。在 REC-2006 处理 2 小时后照射时,在 HepG2 细胞中观察到细胞色素 c 的抑制更为明显(约 33%)。同样,在 HepG2 细胞中,REC-2006 + 辐射处理组中 Apaf-1、caspase-9 和 caspase-3 的抑制更为显著(P<.05)。REC-2006 处理恢复了 HepG2 细胞中 ICAD 的表达;然而,在 Hep3B 细胞中未观察到恢复。与 Hep3B 细胞(1.2)相比,在 REC-2006 + 辐射处理组中,HepG2 细胞中的核质 CAD 比值较低(0.6)。总之,REC-2006 通过抑制 AIF 的表达和易位、抑制 ATM 和 PARP-1 的裂解、恢复 ICAD 的表达、抑制细胞色素 c 的释放,从而调节 Apaf-1 caspase-9 的表达和活性,在 HepG2 细胞中提供更高的保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b236/3137560/94ec980e2cc7/ECAM2011-758326.001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验