检索结果-南通市图书馆

Interplay between micro RNA-17-5p, insulin-like growth factor-Ⅱ through binding protein-3 in hepatocellular carcinoma

引用

World Journal of Hepatology 2016年第23期8卷 976-984页

作者： Danira Ashraf Habashy Hend Mohamed El Tayebi injie omar fawzy Karim Adel Hosny Gamal Esmat Ahmed Ihab Abdelaziz Department of Pharmacology and Toxicology German University in Cairo Main Entrance Al Tagamoa Al Khames Department of General Surgery Faculty of Medicine Cairo University Department of Endemic Medicine and Hepatology Cairo University Department of Biology American University in Cairo

AIM: To investigate the effect of microR NA on insulinlike growth factor binding protein-3(IGFBP-3) and hence on insulin-like growth factor-Ⅱ(IGF-Ⅱ) bioavailability in hepatocellular carcinoma(HCC).METHODS: Bioinformatic analysis was performed using ***, DIANA lab and Segal lab softwares. Total RNA was extracted from 23 HCC and 10 healthy liver tissues using mir Vana mi RNA Isolation Kit. microR NA-17-5p(miR-17-5p) expression was mimicked and antagonized in Hu H-7 cell lines using Hi Per Fect Transfection Reagent, then total RNA was extracted using Biozol reagent then reverse transcribed into cD NA followed by quantification of mi R-17-5p and IGFBP-3 expression using Taq Man real-time quantitative PCR. Luciferase reporter assay was performed to validate the binding of miR-17-5p to the 3'UTR of IGFBP-3. Free IGF-Ⅱ protein was measured in transfected Hu H-7 cells using IGF-Ⅱ ELISA kit. RESULTS: Bioinformatic analysis revealed IGFBP-3 as a potential target for miR-17-5p. Screening of miR-17-5p and IGFBP-3 revealed a moderate negative correlation in HCC patients, where mi R-17-5p was extensively underexpressed in HCC tissues(P = 0.0012), while IGFBP-3 showed significant upregulation in the same set of patients(P = 0.0041) compared to healthy donors. Forcing mi R-17-5p expression in Hu H-7 cell lines showed a significant downregulation of IGFBP-3 mR NA expression(P = 0.0267) and a significant increase in free IGF-Ⅱ protein(P = 0.0339) compared to mock untransfected cells using unpaired t-test. Luciferase assay validated IGFBP-3 as a direct target of mi R-17-5p; luciferase activity was inhibited by 27.5% in cells co-transfected with miR-17-5p mimics and the construct harboring the wild-type binding region 2 of IGFBP-3 compared to cells transfected with this construct alone(P = 0.0474).CONCLUSION: These data suggest that regulating IGF-Ⅱ bioavailability and hence HCC progression can be achieved through targeting IGFBP-3 via manipulating the expression of miR NAs.

关键词： Insulin-like growth factor binding protein-3 Insulin-like growth factor signaling pathway MicroR NA Insulin-like growth factor-Ⅱ Hepatocellular carcinoma

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

miR-34a: Multiple Opposing Targets and One Destiny in Hepatocellular Carcinoma

引用

Journal of Clinical and Translational Hepatology 2016年第4期4卷 300-305页

作者： Radwa Alaa Yacoub injie omar fawzy Reem Amr Assal Karim Adel Hosny Abdel-Rahman Nabawy Zekri Gamal Esmat Hend Mohamed El Tayebi Ahmed Ihab Abdelaziz Pharmaceutical Biology Department Faculty of Pharmacy and Biotechnology German University in Cairo Cairo Egypt pharmacology and Toxicology Department Faculty of Pharmacy and Biotechnology German University in Cairo Cairo Egypt Department of General Surgery Faculty of Medicine Cairo University Cairo Egypt Virology and Immunology Cancer Biology Department National Cancer Institute Cairo University Cairo Egypt Department of Endemic Medicine and Hepatology Cairo University Cairo Egypt pharmacology and Toxicology Department Faculty of Pharmacy and Biotechnology German University in Cairo Cairo Egypt School of Medicine New Giza University Cairo Egypt

Background and Aims:The role of miR-34a in hepatocellular carcinoma (HCC) is controversial and several unresolved issues remain,including its expression pattern and relevance to tumor etiology,tumor stage and prognosis,and finally,its impact on ***:miR-34a expression was assessed in hepatitis C virus (HCV)-induced non-metastatic HCC tissues by ***-7 cells were transfected with miR-34a mimics and the impact of miR-34a was examined on 84 pro-apoptotic/anti-apoptotic genes using PCR array;its net effect was tested on cell viability via ***:miR-34a expression was up-regulated in HCC ***,miR-34a induced a large set of pro-apoptotic/anti-apoptotic genes,with a net result of triggering apoptosis and repressing cell ***:HCC-related differential expression of miR-34a could be etiology-based or stage-specific,and low expression of miR-34a may predict poor *** study's findings also emphasize the role of miR-34a in apoptosis.

关键词： MicroRNA Hepatocellular carcinoma Apoptosis PCR array.

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

欢迎您,

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

请选择保存的检索档案：

请选择收藏分类：

通借通还

欢迎您,

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：