نتایج جستجو برای: beta particle k562 cell

تعداد نتایج: 1971489  

Journal: :iranian biomedical journal 0
ali bazi mohammad reza keramati mehran gholamin

background: recently, it has been revealed that tyrosine kinase inhibitors (tkis) act through inducing both oxidative and endoplasmic reticulum (er) stress in chronic myeloid leukemia cells. however, er stress signaling triggers both apoptotic and survival processes within cells. nevertheless, mechanisms by which tkis avoid the pro-survival effects are not clear. the aim of this study was to ev...

Journal: :Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques 2007
Jun Wu Yanhui Lu Alice Lee Xiaogang Pan Xiaojuan Yang Xiaobin Zhao Robert J Lee

PURPOSE Liposomes co-encapsulating doxorubicin (DOX) and verapamil (VER), and conjugated to transferrin (Tf-L-DOX/VER) were synthesized and evaluated in K562 leukemia cells. The design of this formulation was aimed at selective targeting of tumor cells, reducing cardiotoxicity of DOX and VER, as well as overcoming P-glycoprotein (Pgp)-mediated multidrug resistance (MDR) phenotype. METHODS The...

2016
WEN-JUN LIU TENG ZHANG QU-LIAN GUO CHUN-YAN LIU YONG-QI BAI

Leukemia is the most common malignant disease in children with high incidence and mortality rates, and a poor treatment effect. The aim of the present study was to examine the changes in the expression of homeobox (Hox) A5 gene and its relationship with cell cycle and apoptosis through the intervention of human K562 myeloid leukemia cell line by all-trans retinoic acid (ATRA), to analyze the ro...

2017
Rungkarn Sangkaruk Methee Rungrojsakul Singkome Tima Songyot Anuchapreeda

BACKGROUND Saraphi (Mammea siamensis) is a Thai traditional herb. In this study, the cytotoxic effects of crude ethanolic and fractional extracts including hexane, ethyl acetate, and methanol fractions from M. siamensis flowers were investigated in order to determine their effect on WT1 expression in Molt4 and K562 cells and Bcr/Abl expression in K562 cells. MATERIALS AND METHODS The flowers ...

Journal: :Journal of Experimental & Clinical Cancer Research : CR 2009
Yuxia Guo Gaihuan Zheng Xianqing Jin Youhua Xu Qing Luo Xiaomei Liu Zhenzhen Zhao Yong Chen

OBJECTIVE A novel multi-drug resistance gene named as HA117 has been screened and cloned in multidrug resisitant leukemia cell lines in our previous research, but its function is still unknown. In this study, HA117 gene was investigated whether it could increase the drug resistance in chronic myelogenous myeloid leukemia cell line K562. METHODS HA117 was cloned and adenovirus vectors were con...

Journal: :Iranian journal of allergy, asthma, and immunology 2005
Mohsen Hamedani Abbas Mirshafiey Hossein Vatanpour Mohammad Reza Khorramizadeh Farshid Saadat Azar Berahmeh Fatemeh Hadji-Ghasemi

Controversial immunomodulatory properties of bee venom (BV) have provided an appropriate field for more investigation. The aim of present research was to verify the effects of honeybee venom on matrix metalloproteinase activity and interferon production as well as cell proliferation in monocyte and fibroblast cell lines.The monocyte and fibroblast cell lines (K562, HT-1080, WEHI-164) were used ...

2017
Roslina Husaini Munirah Ahmad Zubaidah Zakaria

Chronic myeloid leukaemia (CML) is a form of leukaemia derived from the myeloid cell lineage. Imatinib mesylate, the breakpoint cluster region-abelson murine leukeamia kinase inhibitor, is a specific reagent used in the clinical treatment of CML. The DNA topoisomerase II inhibitor, etoposide, is also employed as a therapeutic, though it is used to a lesser extent. The present study aims to eval...

2013
Jian Ma Youtian Hu Mingxiong Guo Zan Huang Wenxin Li Yingliang Wu

BACKGROUND The hERG potassium channel can modulate the proliferation of the chronic myelogenous leukemic K562 cells, and its role in the erythroid differentiation of K562 cells still remains unclear. PRINCIPAL FINDINGS The hERG potassium channel blockage by a new 36-residue scorpion toxin BmKKx2, a potent hERG channel blocker with IC50 of 6.7 ± 1.7 nM, enhanced the erythroid differentiation o...

Journal: :Cancer research 1989
Y Ohe K Nakagawa Y Fujiwara Y Sasaki K Minato M Bungo S Niimi N Horichi M Fukuda N Saijo

A new model to predict antitumor activity of new analogues was developed, and the cross-resistance against cisplatin (CDDP) and Adriamycin (ADM) was examined. A preclinical evaluation of various new analogues using this new model was performed. The antitumor activities of KT6149, MX-2 (KRN8602), SM5887, menogaril (TUT-7), and liblomycin (NK313) were evaluated against four non-small cell lung ca...

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