نتایج جستجو برای: 29b

تعداد نتایج: 670  

2017
Fu Wang Hui Ma Wen-Jing Liang Jing-Jing Yang Xue-Qing Wang Mei-Rong Shan Yuan Chen Min Jia Ya-Ling Yin Xue-Ying Sun Jia-Ning Zhang Qi-Sheng Peng Yu-Guo Chen Li-Ying Liu Peng Li Tao Guo Shuang-Xi Wang

AIMS Proteasome-linked oxidative stress is believed to cause endothelial dysfunction, an early event in cardiovascular diseases (CVD). Statin, as HMG-CoA reductase inhibitor, prevents endothelial dysfunction in CVD. However, the molecular mechanism of statin-mediated normalization of endothelial function is not completely elucidated. METHODS AND RESULTS Lovastatin time/dose-dependently increa...

2012
Denis R. Merk Jocelyn T. Chin Benjamin A. Dake Lars Maegdefessel Miquell O. Miller Naoyuki Kimura Philip S. Tsao Cristiana Iosef Gerald J. Berry Friedrich W. Mohr Joshua M. Spin Cristina M. Alvira Robert C. Robbins Michael P. Fischbein

Rationale: Marfan syndrome (MFS) is a systemic connective tissue disorder notable for the development of aortic root aneurysms and the subsequent life-threatening complications of aortic dissection and rupture. Underlying fibrillin-1 gene mutations cause increased transforming growth factor(TGF) signaling. Although TGFblockade prevents aneurysms in MFS mouse models, the mechanisms through which...

Journal: :Circulation research 2012
Denis R Merk Jocelyn T Chin Benjamin A Dake Lars Maegdefessel Miquell O Miller Naoyuki Kimura Philip S Tsao Cristiana Iosef Gerald J Berry Friedrich W Mohr Joshua M Spin Cristina M Alvira Robert C Robbins Michael P Fischbein

RATIONALE Marfan syndrome (MFS) is a systemic connective tissue disorder notable for the development of aortic root aneurysms and the subsequent life-threatening complications of aortic dissection and rupture. Underlying fibrillin-1 gene mutations cause increased transforming growth factor-β (TGF-β) signaling. Although TGF-β blockade prevents aneurysms in MFS mouse models, the mechanisms throug...

2015
Masanori Kawano Kazuhiro Tanaka Ichiro Itonaga Tatsuya Iwasaki Hiroshi Tsumura Andrei L. Gartel

Myc oncogenic transcription factor is known to inhibit tumor suppressive microRNAs (miRNAs), resulting in greater expression of their target protein related to cell cycle, invasion or anti-apoptotic factors in human cancer cells. To explore possible oncogenic factors in Ewing's sarcoma (ES), we conducted microarray-based approach to profile the changes in the expression of miRNAs and its downst...

Journal: :The Journal of clinical investigation 2012
Lars Maegdefessel Junya Azuma Ryuji Toh Denis R Merk Alicia Deng Jocelyn T Chin Uwe Raaz Anke M Schoelmerich Azad Raiesdana Nicholas J Leeper Michael V McConnell Ronald L Dalman Joshua M Spin Philip S Tsao

MicroRNAs (miRs) regulate gene expression at the posttranscriptional level and play crucial roles in vascular integrity. As such, they may have a role in modifying abdominal aortic aneurysm (AAA) expansion, the pathophysiological mechanisms of which remain incompletely explored. Here, we investigate the role of miRs in 2 murine models of experimental AAA: the porcine pancreatic elastase (PPE) i...

Journal: :American journal of physiology. Cell physiology 2015
Tongtong Zou Jaladanki N Rao Lan Liu Lan Xiao Hee Kyoung Chung Yanwu Li Gang Chen Myriam Gorospe Jian-Ying Wang

Through its actions as component of the activating protein-1 (AP-1) transcription factor, JunD potently represses cell proliferation. Here we report a novel function of JunD in the regulation of microRNA expression in intestinal epithelial cells (IECs). Ectopically expressed JunD specifically increased the expression of primary and mature forms of miR-29b, whereas JunD silencing inhibited miR-2...

2017
Yonglei Liu Jingling Zhang Xiangjun Sun Quanping Su Cuiping You

Carcinoma associated fibroblasts (CAFs) play important roles in breast cancer development and progression. Recent studies show that microRNAs (miRNAs) are the main regulators in CAFs. MiR-29b is one of the significant down-regulated miRNAs in CAFs from the miRNA screening. The role of miR-29b in the interaction between CAFs and breast cancer is still unclear. In the present study, we investigat...

2017
Shilpa Thakur Charles Brenner

KRAS activation drives DNA methylation and silencing of specific tumor suppressor genes (TSGs). We previously showed that the ERK pathway induces transcriptional repression of TET1, which results in conversion of TSG promoters from a hydroxymethylated, active state to a hypermethylated and silenced state. Here we identified miR-29b as a KRAS-induced molecule that represses TET1 expression. In K...

2014
Ling Xu Yan Xu Zhenyi Jing Xu Wang Xianfeng Zha Chengwu Zeng Shaohua Chen Lijian Yang Gengxin Luo Bo Li Yangqiu Li

OBJECTIVES The miR-29 family have been demonstrated acting as vital tumor suppressor in multiple cancers as well as regulators in the adaptive immune system. Little is known about their role in leukemogenesis. The purpose of this study is to analyze the expression pattern of miR-29a/29b and its target genes Mcl-1 (myeloid cell leukemia sequence 1) and B-cell lymphoma 2 (Bcl-2) in myeloid leukem...

2017
Ushasree Sunkavalli Carmen Aguilar Ricardo Jorge Silva Malvika Sharan Ana Rita Cruz Caroline Tawk Claire Maudet Miguel Mano Ana Eulalio

MicroRNAs play an important role in the interplay between bacterial pathogens and host cells, participating as host defense mechanisms, as well as exploited by bacteria to subvert host cellular functions. Here, we show that microRNAs modulate infection by Shigella flexneri, a major causative agent of bacillary dysentery in humans. Specifically, we characterize the dual regulatory role of miR-29...

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