نتایج جستجو برای: pdcd4

تعداد نتایج: 501  

2016
John Zeng Hong Li Wei Gao Wai-Kuen Ho Wen Bin Lei William Ignace Wei Jimmy Yu-Wai Chan Thian-Sze Wong

BACKGROUND Programmed cell death protein 4 (PDCD4) is a novel tumor suppressor protein involved in programmed cell death. Its association with cancer progression has been observed in multiple tumor models, but evidence supporting its association with solid tumors in humans remains controversial. This study aimed to determine the clinical significance and prognostic value of PDCD4 in solid tumor...

2014
Han Yu Jiping Zeng Xiuming Liang Wenfu Wang Yabin Zhou Yundong Sun Shili Liu Wenjuan Li Chunyan Chen Jihui Jia

Helicobacter pylori, a Gram-negative, microaerophilic bacterium found in the stomach, is assumed to be associated with carcinogenesis, invasion and metastasis in digestive diseases. Cytotoxin-associated gene A (CagA) is an oncogenic protein of H. pylori that is encoded by a Cag pathogenicity island related to the development of gastric cancer. The epithelial-mesenchymal transition (EMT) is the ...

2004
R. Göke P. Barth A. Schmidt B. Samans B. Lankat-Buttgereit

Göke, R., P. Barth, A. Schmidt, B. Samans, and B. LankatButtgereit. Programmed cell death protein 4 suppresses CDK1/cdc2 via induction of p21. Am J Physiol Cell Physiol 287: C1541– C1546, 2004. First published August 18, 2004; doi:10.1152/ajpcell. 00025.2004.—We show that the recently discovered tumor suppressor pdcd4 represses the transcription of the mitosis-promoting factor cyclin-dependent ...

Journal: :Scientific reports 2015
Pedro M Rodrigues Marta B Afonso André L Simão Pedro M Borralho Cecília M P Rodrigues Rui E Castro

MicroRNAs (miRNAs/miRs) are key regulators of liver metabolism, while toxic bile acids participate in the development of several liver diseases. We previously demonstrated that deoxycholic acid (DCA), a cytotoxic bile acid implicated in the pathogenesis of non-alcoholic fatty liver disease, inhibits miR-21 expression in hepatocytes. Here, we investigated the mechanisms by which DCA modulates mi...

Journal: :Journal of Immunology 2023

Abstract CD8+ T cell clonal expansion is critical for controlling intracellular infections and tumors. Thus, unravelling the mechanisms that regulate proliferation are imperative to improve vaccine design immunotherapy. However, molecular govern still not fully understood. PDCD4 (Programmed death 4) was shown inhibit translation by sequestering mRNA helicase eIF4A, which leads inhibition of gen...

2015
Minran Zhou Jiping Zeng Xiaoming Wang Xiangyu Wang Tao Huang Yue Fu Ting Sun Jihui Jia Chunyan Chen

Chronic myeloid leukemia in the blastic phase (CML-BP) responds poorly to clinical treatments and is usually fatal. In this study, we found that the histone H3 lysine 4 (H3K4) demethylase RBP2 (also called JARID1A and KDM5A) is underexpressed in CML-BP. The RBP2 histone demethylase stimulates leukemia cell differentiation and inhibits cell proliferation. We identified miR-21 was directly downre...

2017
Qiang Su Lang Li Jinmin Zhao Yuhan Sun Huafeng Yang

Objective Post-percutaneous coronary intervention (PCI) myocardial injury is related to the CD4+ T lymphocyte-mediated inflammatory response. microRNA-21 expression is associated with CD4+ T lymphocyte activation. The pre-PCI use of trimetazidine prevents periprocedural myocardial injury and reduces inflammatory cytokine levels. This study aimed to assess the effects of trimetazidine on peripro...

2013
Urszula Liwak Lindsay E. Jordan Sally Davidson Von-Holt Poonam Singh Jennifer E.L. Hanson Ian A. Lorimer Federico Roncaroli Martin Holcik

Glioblastoma multiforme (GBM) is the most common and aggressive form of tumor of the central nervous system. Despite significant efforts to improve treatments, patient survival rarely exceeds 18 months largely due to the highly chemoresistant nature of these tumors. Importantly, misregulation of the apoptotic machinery plays a key role in the development of drug resistance. We previously demons...

2014
James J. Steinhardt Raymond J. Peroutka Krystyna Mazan-Mamczarz Qing Chen Simone Houng Carol Robles Rolf N. Barth Joseph DuBose Brandon Bruns Ronald Tesoriero Deborah Stein Raymond Fang Nader Hanna Jason Pasley Carlos Rodriguez Mark D. Kligman Matthew Bradley Joseph Rabin Stacy Shackelford Bojie Dai Ari L. Landon Thomas Scalea Ferenc Livak Ronald B. Gartenhaus

Human diffuse large B-cell lymphomas (DLBCLs) often aberrantly express oncogenes that generally contain complex secondary structures in their 5’ untranslated region (UTR). Oncogenes with complex 5’UTRs require enhanced eIF4A RNA helicase activity for translation. PDCD4 inhibits eIF4A and PDCD4 knockout mice have a high penetrance for B-cell lymphomas. Here, we show that upon B-cell receptor (BC...

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