نتایج جستجو برای: aza

تعداد نتایج: 5249  

2016
Yi-Ting Chen Wei-Chih Chao Hsiou-Ting Kuo Jiun-Yi Shen I-Han Chen Hsiao-Ching Yang Jinn-Shyan Wang Jyh-Feng Lu Richard P. Cheng Pi-Tai Chou

7-Azatryptophan and 2,7-diazatryptophan are sensitive to polarity changes and water content, respectively, and should be ideal for studying protein-protein and protein-peptide interactions. In this study, we replaced the tryptophan in peptide Baa (LKWKKLLKLLKKLLKLG-NH2) with 7-azatryptophan or 2,7-diazatryptophan, forming (7-aza)Trp-Baa and (2,7-aza)Trp-Baa, to study the calmodulin (CaM)-peptid...

Journal: :Cancer research 2006
Carlo Stresemann Bodo Brueckner Tanja Musch Helga Stopper Frank Lyko

DNA methyltransferase inhibitors represent promising new drugs for cancer therapies. The first of these compounds (5-azacytidine, Vidaza) has recently been approved as an antitumor agent, and others are presently in various stages of their preclinical or clinical development. Most of the archetypal inhibitors have been established and characterized in different experimental systems, which has t...

Journal: :European journal of haematology 2016
Katsumichi Fujimaki Kazuho Miyashita Rika Kawasaki Naoto Tomita

Although a 7-day (d) regimen of azacitidine (AZA) is the standard treatment of high-risk myelodysplastic syndromes (MDS), AZA is difficult to administer during weekends in an outpatient setting. We retrospectively investigated the outcome of a 5-d regimen of AZA in patients with high-risk MDS. High-risk MDS was defined as MDS with intermediate-2- or high-risk MDS according to the International ...

Journal: :The Journal of biological chemistry 1985
S J Smith H D White

The fluorescence emission of 1-N6-etheno-2-aza-ATP (epsilon-aza-ATP) at 410-460 nm is enhanced approximately 8-fold upon mixing substoichiometric concentrations of epsilon-aza-ATP with bovine cardiac actomyosin-S1 or myofibrils. The time course of nucleotide fluorescence measured in a front face stopped flow cell upon mixing epsilon-aza-ATP with bovine cardiac myofibrils ([Ca2+] less than 10(-7...

Journal: :Molecular cancer therapeutics 2009
Francesco Crea Elisa Giovannetti Filippo Cortesi Valentina Mey Sara Nannizzi Marielle I Gallegos Ruiz Simona Ricciardi Mario Del Tacca Godefridus J Peters Romano Danesi

Irinotecan is a topoisomerase-I (Top-I) inhibitor used for the treatment of colorectal cancer. DNA demethylating agents, including 5-azacytidine (5-aza), display synergistic antitumor activity with several chemotherapy drugs. 5-Aza may enhance irinotecan cytotoxicity by at least one of the following mechanisms: (a) Top-I promoter demethylation, (b) activation of genes involved in Top-I transcri...

Journal: :Blood 2012
Oliver C Goodyear Mike Dennis Nadira Y Jilani Justin Loke Shamyla Siddique Gordon Ryan Jane Nunnick Rahela Khanum Manoj Raghavan Mark Cook John A Snowden Mike Griffiths Nigel Russell John Yin Charles Crawley Gordon Cook Paresh Vyas Paul Moss Ram Malladi Charles F Craddock

Strategies that augment a GVL effect without increasing the risk of GVHD are required to improve the outcome after allogeneic stem cell transplantation (SCT). Azacitidine (AZA) up-regulates the expression of tumor Ags on leukemic blasts in vitro and expands the numbers of immunomodulatory T regulatory cells (Tregs) in animal models. Reasoning that AZA might selectively augment a GVL effect, we ...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2017
Asel Biktasova Michael Hajek Andrew Sewell Cyril Gary Gary Bellinger Hari A Deshpande Aarti Bhatia Barbara Burtness Benjamin Judson Saral Mehra Wendell G Yarbrough Natalia Issaeva

Purpose: DNA methylation in human papillomavirus-associated (HPV+) head and neck squamous cell carcinoma (HNSCC) may have importance for continuous expression of HPV oncogenes, tumor cell proliferation, and survival. Here, we determined activity of a global DNA-demethylating agent, 5-azacytidine (5-aza), against HPV+ HNSCC in preclinical models and explored it as a targeted therapy in a window ...

2016
Gilles Fransolet Grégory Ehx Joan Somja Loïc Delens Muriel Hannon Joséphine Muller Sophie Dubois Pierre Drion Jo Caers Stéphanie Humblet-Baron Philippe Delvenne Yves Beguin Giuseppina Conteduca Frédéric Baron

BACKGROUND Previous studies have demonstrated that regulatory T cells (Tregs) play a protective role in the pathogenesis of chronic graft-versus-host disease (cGVHD). Tregs constitutively express the gene of the transcription factor Foxp3 whose CNS2 region is heavily methylated in conventional CD4(+) T cells (CD4(+)Tconvs) but demethylated in Tregs. METHODS Here, we assessed the impact of aza...

Journal: :Journal of gastrointestinal and liver diseases : JGLD 2011
William Zabala-Fernández Manuel Barreiro-de Acosta Ana Echarri Daniel Carpio Aurelio Lorenzo Javier Castro David Martínez-Ares Santos Pereira Ignacio Martin-Granizo Marta Corton Angel Carracedo Francisco Barros

BACKGROUND AND AIMS Pharmacogenetic studies in inflammatory bowel diseases (IBD) are mainly focused on genes involved in the metabolism of Azathioprine (AZA). Use of AZA is limited by its toxicity, which occurs in 20-30% of patients. Variants in the Thiopurine S-methyltransferase (TPMT) and Inosine triphosphate pyrophosphatase (ITPA) genes have been associated with AZA toxicity, but also can co...

Journal: :Cancer research 2007
Christine B Yoo Shinwu Jeong Gerda Egger Gangning Liang Pasit Phiasivongsa Chunlin Tang Sanjeev Redkar Peter A Jones

The major goal of epigenetic therapy is to reverse aberrant promoter hypermethylation and restore normal function of tumor suppressor genes by the use of chromatin-modifying drugs. Decitabine, or 5-aza-2'-deoxycytidine (5-aza-CdR), is a well-characterized drug that is now Food and Drug Administration approved for the treatment of myelodysplastic syndrome. Although 5-aza-CdR is an extremely pote...

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