نتایج جستجو برای: sox2

تعداد نتایج: 3695  

Journal: :Oncology reports 2011
Yi-Ran Cai Hai-Qing Zhang Yang Qu Jing Mu Dan Zhao Li-Juan Zhou Hong Yan Jian-Wei Ye Yan Liu

Non-small cell lung carcinoma (NSCLC) is a leading cause of cancer-related deaths. Aberrance of the two oncogenes MET and SOX2 are frequently encountered in NSCLC. Exons 18 through 21 of the EGFR gene were screened and MET and SOX2 immunostaining was conducted to analyze the immunohistological staining of MET and SOX2 and the EGFR mutation status. One hundred and fifty tissue samples were exami...

2016
David S. Moura Isabel F. Fernández Gema Marín-Royo Inmaculada López-Sánchez Elena Martín-Doncel Francisco M. Vega Pedro A. Lazo

Sox2 is a pluripotency transcription factor that as an oncogene can also regulate cell proliferation. Therefore, genes implicated in several different aspects of cell proliferation, such as the VRK1 chromatin-kinase, are candidates to be targets of Sox2. Sox 2 and VRK1 colocalize in nuclei of proliferating cells forming a stable complex. Sox2 knockdown abrogates VRK1 gene expression. Depletion ...

Journal: :Cell reports 2013
Eunjeong Seo Upal Basu-Roy Preethi H Gunaratne Cristian Coarfa Dae-Sik Lim Claudio Basilico Alka Mansukhani

The osteoblastic and adipocytic lineages arise from mesenchymal stem cells (MSCs), but few regulators of self-renewal and early cell-fate decisions are known. Here, we show that the Hippo pathway effector YAP1 is a direct target of SOX2 and can compensate for the self-renewal defect caused by SOX2 inactivation in osteoprogenitors and MSCs. Osteogenesis is blocked by high SOX2 or YAP1, accelerat...

2012
Han Li Manuel Collado Aranzazu Villasante Ander Matheu Cian J. Lynch Marta Cañamero Karine Rizzoti Carmen Carneiro Gloria Martínez Anxo Vidal Robin Lovell-Badge Manuel Serrano

The mechanisms responsible for the transcriptional silencing of pluripotency genes in differentiated cells are poorly understood. We have observed that cells lacking the tumor suppressor p27 can be reprogrammed into induced pluripotent stem cells (iPSCs) in the absence of ectopic Sox2. Interestingly, cells and tissues from p27 null mice, including brain, lung, and retina, present an elevated ba...

Journal: :Cell stem cell 2013
Kuancan Liu Ming Jiang Yun Lu Hao Chen Jun Sun Shaoping Wu Wei-Yao Ku Hiroshi Nakagawa Yoshiaki Kita Shoji Natsugoe Jeffrey H Peters Anil Rustgi Mark W Onaitis Amy Kiernan Xiaoxin Chen Jianwen Que

Sox2 regulates the self-renewal of multiple types of stem cells. Recent studies suggest it also plays oncogenic roles in the formation of squamous carcinoma in several organs, including the esophagus where Sox2 is predominantly expressed in the basal progenitor cells of the stratified epithelium. Here, we use mouse genetic models to reveal a mechanism by which Sox2 cooperates with microenvironm...

Journal: :Journal of chemical neuroanatomy 2014
Sarah Hoefflin David A Carter

The transcription factor SOX2 has many established roles in neural development but is generally considered to have limited activity in the adult brain. As part of a study of neuronal phenotypes in the adult rodent hypothalamus, we have now used immunohistochemical analysis to investigate the expression of SOX2 in the adult rat and mouse hypothalamus. Our analysis has revealed that SOX2 protein ...

Journal: :American journal of physiology. Lung cellular and molecular physiology 2014
Weiliang Xie Thomas J Lynch Xiaoming Liu Scott R Tyler Shuyang Yu Xinyuan Zhou Meihui Luo David M Kusner Xingshen Sun Yaling Yi Yulong Zhang Michael J Goodheart Kalpaj R Parekh James M Wells Hai-Hui Xue Larysa H Pevny John F Engelhardt

Tracheobronchial submucosal glands (SMGs) are derived from one or more multipotent glandular stem cells that coalesce to form a placode in surface airway epithelium (SAE). Wnt/β-catenin-dependent induction of lymphoid enhancer factor (Lef-1) gene expression during placode formation is an early event required for SMG morphogenesis. We discovered that Sox2 expression is repressed as Lef-1 is indu...

2015
Natalia Tapia Caitlin MacCarthy Daniel Esch Adele Gabriele Marthaler Ulf Tiemann Marcos J. Araúzo-Bravo Ralf Jauch Vlad Cojocaru Hans R. Schöler

The transcription factors OCT4 and SOX2 are required for generating induced pluripotent stem cells (iPSCs) and for maintaining embryonic stem cells (ESCs). OCT4 and SOX2 associate and bind to DNA in different configurations depending on the arrangement of their individual DNA binding elements. Here we have investigated the role of the different OCT4-SOX2-DNA assemblies in regulating and inducin...

2015
Hui Gao Chunyuan Teng Wenjing Huang Jianjun Peng Chunbo Wang William Chi-shing Cho

UNLABELLED The transcription factor sex determining region (Y SRY)-box 2 (SOX2) is known to play a crucial role in the maintenance of self renewal or pluripotency of undifferentiated embryonic and neuronal stem cells. An elevated expression of SOX2 has been correlated with poor prognosis of esophageal squamous cell carcinoma (ESCC). We sought to investigate the mechanism(s) by which SOX2 modula...

2015
YOSHIHITO IIJIMA MASAHIRO SEIKE RINTARO NORO TAKAYUKI IBI SHINGO TAKEUCHI IWAO MIKAMI KIYOSHI KOIZUMI JITSUO USUDA AKIHIKO GEMMA

The recent development of human genome studies has demonstrated the possibility of alteration of several genes as oncogenic driver mutations of lung squamous cell carcinoma (SQCC). FGFR1, PIK3CA and SOX2 genes have been recognized as candidate driver genes of SQCC. The aim of the present study was to evaluate FGFR1, PIK3CA and SOX2 protein expression in SQCC and determine whether the expression...

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