نتایج جستجو برای: runx2

تعداد نتایج: 2482  

Journal: :Circulation research 2015
Uwe Raaz Isabel N Schellinger Ekaterina Chernogubova Christina Warnecke Yosuke Kayama Kiril Penov Jan K Hennigs Florian Salomons Suzanne Eken Fabian C Emrich Wei H Zheng Matti Adam Ann Jagger Futoshi Nakagami Ryuji Toh Kensuke Toyama Alicia Deng Michael Buerke Lars Maegdefessel Gerd Hasenfuß Joshua M Spin Philip S Tsao

RATIONALE Accelerated arterial stiffening is a major complication of diabetes mellitus with no specific therapy available to date. OBJECTIVE The present study investigates the role of the osteogenic transcription factor runt-related transcription factor 2 (Runx2) as a potential mediator and therapeutic target of aortic fibrosis and aortic stiffening in diabetes mellitus. METHODS AND RESULTS...

2017
Wei-Min Chang Yuan-Feng Lin Chia-Yi Su Hsuan-Yu Peng Yu-Chan Chang Jenn-Ren Hsiao Chi-Long Chen Jang-Yang Chang Yi-Shing Shieh Michael Hsiao Shine-Gwo Shiah

Parathyroid Hormone-Like Hormone (PTHLH) is an autocrine/paracrine ligand that is up-regulated in head and neck squamous cell carcinoma (HNSCC). However, the cellular function and regulatory mechanism in HNSCC remains obscure. We investigated the clinical significance of PTHLH in HNSCC patients, and verified the role of RUNX2/PTHLH axis, which is stimulated HNSCC cell growth. In patients, PTHLH...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2010
Mohammad Q Hassan Jonathan A R Gordon Marcio M Beloti Carlo M Croce Andre J van Wijnen Janet L Stein Gary S Stein Jane B Lian

Induced osteogenesis includes a program of microRNAs (miRs) to repress the translation of genes that act as inhibitors of bone formation. How expression of bone-related miRs is regulated remains a compelling question. Here we report that Runx2, a transcription factor essential for osteoblastogenesis, negatively regulates expression of the miR cluster 23a∼27a∼24-2. Overexpression, reporter, and ...

Journal: :Genetics and molecular research : GMR 2010
G X Wang R P Sun F L Song

Cleidocranial dysplasia (CCD) is an autosomal-dominant heritable skeletal disease caused by heterozygous mutations in the RUNX2 gene. We studied a Chinese family that included three affected individuals with CCD phenotypes; the clinical features of patients with CCD include delayed closure of fontanelles, frontal bossing, dysplasia of clavicles, late tooth eruption, and other skeletal anomalies...

2017
Xiao-Dong Wu Ting Guo Li Liu Chao Wang Kun Zhang Han-Qiang Liu Feng Wang Wen-Dong Bai Meng-Yao Zhang

Rg1 is a predominant protopanaxatriol-type of ginsenoside found in Panax ginseng, and it has been shown to have anti-cancer effects in multiple types of cancer cells. However, Rg1 also induces the expression of proangiogenic factors, such as vascular endothelial growth factor (VEGF-A), in endothelial cells. Unfortunately, angiogenesis positively correlates with cancer development. In this study...

Journal: :European journal of medical research 2006
Takako Shimizu

OBJECTIVE The purpose of this study was to investigate the expression pattern of Runx2 in mandibular condylar cartilage, a type of secondary cartilage. METHODS Mandibular condyle of ddY mice were fixed from embryonic day 14 (E14) through just after birth (equivalent to E19). Samples were cut into 4 micro m serial sections through the central area of the mandibular condyle at the sagittal plan...

2015
Nicola Ferrari Alessandra I. Riggio Susan Mason Laura McDonald Ayala King Theresa Higgins Ian Rosewell James C. Neil Matthew J. Smalley Owen J. Sansom Joanna Morris Ewan R. Cameron Karen Blyth

Although best known for its role in bone development and associated structures the transcription factor RUNX2 is expressed in a wide range of lineages, including those of the mammary gland. Previous studies have indicated that Runx2 can regulate aspects of mammary cell function and influence the properties of cancer cells. In this study we investigate the role of Runx2 in the mammary stem/proge...

Journal: :Cells, tissues, organs 2007
Renny T Franceschi Chunxi Ge Guozhi Xiao Hernan Roca Di Jiang

The differentiation of osteoblasts from mesenchymal precursors requires a series of cell fate decisions controlled by a hierarchy of transcription factors. Among these are RUNX2, Osterix (OSX), ATF4, and a large number of nuclear coregulators. During bone development, initial RUNX2 expression coincides with the formation of mesenchymal condensations well before the branching of chondrogenic and...

Journal: :Cancer research 2010
Kyle C Kurek Sara Del Mare Zaidoun Salah Suhaib Abdeen Hussain Sadiq Suk-Hee Lee Eugenio Gaudio Nicola Zanesi Kevin B Jones Barry DeYoung Gail Amir Mark Gebhardt Matthew Warman Gary S Stein Janet L Stein Jane B Lian Rami I Aqeilan

The WW domain-containing oxidoreductase (WWOX) is a tumor suppressor that is deleted or attenuated in most human tumors. Wwox-deficient mice develop osteosarcoma (OS), an aggressive bone tumor with poor prognosis that often metastasizes to lung. On the basis of these observations, we examined the status of WWOX in human OS specimens and cell lines. In human OS clinical samples, WWOX expression ...

Journal: :The EMBO journal 2004
Sayyed K Zaidi Andrew J Sullivan Ricardo Medina Yoshiaki Ito Andre J van Wijnen Janet L Stein Jane B Lian Gary S Stein

Src/Yes tyrosine kinase signaling contributes to the regulation of bone homeostasis and inhibits osteoblast activity. Here we show that the endogenous Yes-associated protein (YAP), a mediator of Src/Yes signaling, interacts with the native Runx2 protein, an osteoblast-related transcription factor, and suppresses Runx2 transcriptional activity in a dose-dependent manner. Runx2, through its PY mo...

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