نتایج جستجو برای: mir 7

تعداد نتایج: 686546  

2017
Liangyu Lei Chao Chen Juanjuan Zhao HaiRong Wang Mengmeng Guo Ya Zhou Junming Luo Jidong Zhang Lin Xu

Targeted expression of gene technique is an important therapeutic strategy for lung cancer. MicroRNA-7 has been well documented as a promising tumor suppressor but never been test in specific gene-promoter-targeted expression in cancer gene therapy. Here, we first evaluated the efficacy of miR-7 expression operated by the promoter of TTF-1, a lineage-specific oncogene in lung cancer, in vitro u...

Journal: :The Journal of biological chemistry 2009
Rebecca J Webster Keith M Giles Karina J Price Priscilla M Zhang John S Mattick Peter J Leedman

The epidermal growth factor receptor (EGFR) is frequently overexpressed in cancer and is an important therapeutic target. Aberrant expression and function of microRNAs have been associated with tumorigenesis. Bioinformatic predictions suggest that the human EGFR mRNA 3'-untranslated region contains three microRNA-7 (miR-7) target sites, which are not conserved across mammals. We found that miR-...

Journal: :Biochemical and biophysical research communications 2008
Valia Bravo-Egana Samuel Rosero R Damaris Molano Antonello Pileggi Camillo Ricordi Juan Domínguez-Bendala Ricardo L Pastori

MicroRNAs (miRNAs) are non-coding gene products that regulate gene expression through specific binding to target mRNAs. Cell-specific patterns of miRNAs are associated with the acquisition and maintenance of a given phenotype, such as endocrine pancreas (islets). We hypothesized that a subset of miRNAs could be differentially expressed in the islets. Using miRNA microarray technology and quanti...

Journal: :Clinical science 2013
Xiao-Ming Meng Arthur C K Chung Hui Y Lan

TGF-β (transforming growth factor-β) and BMP-7 (bone morphogenetic protein-7), two key members in the TGF-β superfamily, play important but diverse roles in CKDs (chronic kidney diseases). Both TGF-β and BMP-7 share similar downstream Smad signalling pathways, but counter-regulate each other to maintain the balance of their biological activities. During renal injury in CKDs, this balance is sig...

2017
Chun-Mei Wang Bao-Hua Cheng Qing-jie Xue Jing Chen Bo Bai

Our previous high-throughput sequencing indicated that rno-miR-1298 was down-regulated in ischemia-reperfusion model of rat. However, little is known about the function and molecular mechanism of rno-miR-1298 in rat tumor cell. In this study, rno-miR-1298 was detected to be significantly down-regulated in rat tumor C6 cells. Moreover, overexpression of rno-miR-1298 obviously inhibited the proli...

2015
Jun-gang Zhao Wan-fu Men Jun Tang

Gefitinib is a tyrosine kinase inhibitor that has been used for the treatment of non-small-cell lung carcinoma (NSCLC). The ability of miR-7 to enhance gefitinib-induced cytotoxicity in NSCLC cells was evaluated in this study. We found that miR-7 significantly decreased the IC50 of gefitinib and inhibited cell growth. G0/G1 cell cycle arrest and cell apoptosis were increased after the treatment...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس - دانشکده علوم پایه 1391

ژن های mirna ، بیان ژن های دیگر را با ممانعت از ترجمه و یا تجزیه رونوشت های هدف تنظیم می کنند و بیان غیرعادی آن ها در بدخیمی های مختلف گزارش شده است. ازطرفی، نقش اعضای خانواده گیرنده تیروزین کینازی نوروتروفینی همانند trka در سرطان های مختلف ازجمله در نوروبلاستوما شناخته شده است. در این تحقیق، به منظور شناسایی mirnaهای جدید که ممکن است رونوشت ژن trka را هدف قرار دهند و در پیش آگهی مبتلایان به سر...

Journal: :Journal of Cell Biology 2015

2009
Brian D. Adams Danielle M. Cowee Bruce A. White

Epidermal growth factor (EGF) receptor (EGFR)/MAPK signaling can induce a switch in MCF-7 breast cancer cells, from an estrogen receptor (ER) -positive, Luminal-A phenotype, to an ER negative, Basal-like phenotype. Although mechanisms for this switch remain obscure, Basal-like cancers are typically high grade and confer a poorer clinical prognosis. We previously reported that miR-206 and ER rep...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید