نتایج جستجو برای: سلول nb4

تعداد نتایج: 15514  

2006
Duo Chen Rosemarie Chan Samuel Waxman Yongkui Jing

The mechanism of apoptosis induced by treatment with As2O3 alone or in combination with buthionine sulfoximine (BSO) was studied in NB4, U937, Namalwa, and Jurkat cells. As2O3 at concentrations <2 Mmol/L induced apoptosis in NB4 cells and Namalwa cells but not in U937 and Jurkat cells. As2O3-induced apoptosis in NB4 cells and Namalwa cells correlated with increase of H2O2 and caspase activation...

Journal: :Blood 2008
Jianchang Yang Li Chai Chong Gao Taylor C Fowles Zaida Alipio Hien Dang Dan Xu Louis M Fink David C Ward Yupo Ma

Increasing studies suggest that SALL4 may play vital roles in leukemogenesis and stem cell phenotypes. We have mapped the global gene targets of SALL4 using chromatin immunoprecipitation followed by microarray hybridization and identified more than 2000 high-confidence, SALL4-binding genes in the human acute promyelocytic leukemic cell line, NB4. Analysis of SALL4-binding sites reveals that gen...

Journal: :Journal of the National Cancer Institute 2002
Yuji Mishima Yuko Matsumoto-Mishima Yasuhito Terui Misa Katsuyama Muneo Yamada Masaki Mori Yukihito Ishizaka Kazuma Ikeda Jun-ichiro Watanabe Nobuyuki Mizunuma Hirotoshi Hayasawa Kiyohiko Hatake

BACKGROUND Attachment of leukemic cells to vascular endothelial cells induces the vascular endothelial cells to release endothelial cell-derived interleukin 8 (endothelial IL-8), which then induces leukemic cells to undergo apoptosis. NB4, a human promyelocytic leukemic cell line that expresses high levels of cell-surface CD13/aminopeptidase N, does not undergo endothelial IL-8-induced apoptosi...

ژورنال: :مجله دانشگاه علوم پزشکی اراک 0
داود بشّاش davood bashash department of hematology, faculty of allied medicine, shahid beheshti university of medical sciences, darband st, tajrish, tehran, iran.تهران، تجریش، ابتدای خیابان دربند، دانشکده پیراپزشکی، دانشگاه علوم پزشکی شهید بهشتی. سید حمید الله غفاری seyed h. ghaffari hematology, oncology and stem cell transplantation research center, tehran university of medical sciences, amirabad, tehran, iran.تهران، امیر آباد، بخش خون و آنکولوژی بیمارستان دکتر شریعتی، دانشگاه علوم پزشکی تهران.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) مریم کازرانی maryam kazerani hematology, oncology and stem cell transplantation research center, tehran university of medical sciences, amirabad, tehran, iran.تهران، امیر آباد، بخش خون و آنکولوژی بیمارستان دکتر شریعتی، دانشگاه علوم پزشکی تهران.سازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) کبریا هزاوه kebria hezaveh hematology, oncology and stem cell transplantation research center, tehran university of medical sciences, amirabad, tehran, iran.تهران، امیر آباد، بخش خون و آنکولوژی بیمارستان دکتر شریعتی، دانشگاه علوم پزشکی تهران.سازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) کامران علی مقدم kamran alimoghaddam hematology, oncology and stem cell transplantation research center, tehran university of medical sciences, amirabad, tehran, iran.تهران، امیر آباد، بخش خون و آنکولوژی بیمارستان دکتر شریعتی، دانشگاه علوم پزشکی تهران.سازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) اردشیر قوام زاده ardeshir ghavamzadeh hematology, oncology and stem cell transplantation research center, tehran university of medical sciences, amirabad, tehran, iran.تهران، امیر آباد، بخش خون و آنکولوژی بیمارستان دکتر شریعتی، دانشگاه علوم پزشکی تهران.سازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences)

زمینه و هدف: با توجه به آن که حدود 90 درصد بیماران مبتلا به لوسمی پرومیلوسیتیک حاد دارای تلومرهای با طول کوتاه و فعالیت تلومراز بالا می‎باشند، لذا این بیماران کاندید مناسب برای درمان با مهارکنندگان تلومراز می‎باشند. برای بررسی کارآیی استفاده از استراتژی آنتی تلومراز در بیماری لوسمی پرومیلوسیتیک حاد، سلول‎های رده nb4 با غلظت‎های متفاوت از داروی bibr1532 که یک مهار کننده غیرنوکلئوزیدیکی تلومراز م...

2015
Tony Ly Aki Endo Angus I Lamond

Previously, we analyzed protein abundance changes across a 'minimally perturbed' cell cycle by using centrifugal elutriation to differentially enrich distinct cell cycle phases in human NB4 cells (Ly et al., 2014). In this study, we compare data from elutriated cells with NB4 cells arrested at comparable phases using serum starvation, hydroxyurea, or RO-3306. While elutriated and arrested cells...

Journal: :Molecules 2017
Yongbin Song Yihui Yang Lijun Wu Naiwei Dong Shang Gao Hongrui Ji Xia Du Bo Liu Guoyou Chen

In order to study the structure-activity relationships of xanthene derivatives, four series of N-substituted 14-aryl-14H-dibenzo[a,j]xanthene-3,11-dicarboxamide derivatives were synthesized. The structures of all compounds were identified by ¹H-NMR, HR-MS and IR spectra, in which compounds 6a-h were further identified by 13C-NMR spectra. The in vitro antitumor activity of the synthesized compou...

2014
Dong-zheng Ge Yan Sheng Xun Cai

All-trans retinoic acid (ATRA) resistance has been a critical problem in acute promyelocytic leukemia (APL) relapsed patients. In ATRA resistant APL cell lines NB4-R1 and NB4-R2, the combination of staurosporine and ATRA synergized to trigger differentiation accompanied by significantly enhanced protein level of CCAAT/enhancer binding protein ε (C/EBPε) and C/EBPβ as well as the phosphorylation...

Journal: :International journal of oncology 2014
Noriyoshi Iriyama Bo Yuan Yuta Yoshino Yoshihiro Hatta Akira Horikoshi Shin Aizawa Masami Takei Jin Takeuchi Norio Takagi Hiroo Toyoda

The effects of all-trans retinoic acid (ATRA) and valproic acid (VPA), alone and in combination, on the human acute promyelocytic leukemia (APL) cell line NB4 were investigated in view of differentiation induction and growth inhibition. After 48 h of treatment, not only ATRA but also VPA induced differentiation in NB4 cells, and their combination further augmented the differentiation activity. ...

Journal: :Blood 2004
Takayuki Ikezoe Sakae Tanosaki Utz Krug Bingrong Liu Pinchas Cohen Hirokuni Taguchi H Phillip Koeffler

Insulin-like growth factor binding protein-3 (IGFBP-3) can cause growth suppressive and proapoptotic effects on retinoids in many types of cancer cells. However, the expression and effects of IGFBP-3 in myeloid leukemia cells have not been elucidated. In this study, we found no IGFBP-3 expression in the human myeloid leukemia cell lines either at baseline or after stimulation with all-trans ret...

2015
Holly A. Jensen Harmony B. Yourish Rodica P. Bunaciu Jeffrey D. Varner Andrew Yen

Transcription factors that drive non-neoplastic myelomonocytic differentiation are well characterized but have not been systematically analyzed in the leukemic context. We investigated widely used, patient-derived myeloid leukemia cell lines with proclivity for differentiation into granulocytes by retinoic acid (RA) and/or monocytes by 1,25-dihyrdroxyvitamin D3 (D3). Using K562 (FAB M1), HL60 (...

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