نتایج جستجو برای: hepatoma cells

تعداد نتایج: 1385970  

2006
Wei-Wei Zhang Ronald Lindahl Perry Churchill

The regulation of succinyl-CoA:acetoacetyI-CoA transferase (CoA transferase) has been studied in 8 rat hepatoma cell lines. Compared with normal rat hepatocytes, which have almost nondetectable activity of the enzyme, the hepatoma cell lines have a wide range of expression of CoA transferase activity, from as low as 45 nmol/min/mg to as high as 960 nmol/min/mg. \Yestern blotting showed that the...

Journal: :Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2014
Bao-Feng Wang Xi-Jing Wang Hua-Feng Kang Ming-Hua Bai Hai-Tao Guan Zhong-Wei Wang Ying Zan Ling-Qin Song Wei-Li Min Shuai Lin Yan-An Cheng

BACKGROUND Our previous study revealed that the combination of Saikosaponin-d ( SSd) and radiation is more effective in the treatment of liver cancer than the application of either of these monotherapeutic methods. However, the molecular mechanisms of the radiosensitizing effect of SSd on liver cancer remained ill defined. METHODS Cells were treated with different interventions; afterward, ce...

Journal: :Oncology reports 2012
Liqun Xie Yanmin Zheng Xuan Li Junyan Zhao Xiaoyi Chen Li Chen Jing Zhou Ou Hai Fei Li

To investigate the expression and role of PAR-2 in the proliferation of the human hepatoma cell line HepG2, PAR-2 protein and mRNA expression were evaluated by immuno-histochemistry, immunofluorescence and RT-PCR analysis. The signaling pathways downstream of PAR-2 activation that lead to hepatoma cell proliferation were analyzed. The results showed that PAR-2 is expressed in human hepatoma cel...

2015
Kai Liu Tao Jiang Yabo Ouyang Ying Shi Yunjin Zang Ning Li Shichun Lu Dexi Chen

ASPP2 can bind to p53 and enhance the apoptotic capabilities of p53 by guiding it to the promoters of pro-apoptotic genes. Here, ASPP2 overexpression for 24 hours transiently induced apoptosis in hepatoma cells by enhancing the transactivation of p53 on pro-apoptotic gene promoters. However, long-term ASPP2 overexpression (more than 48 hours) failed to induce apoptosis because p53 was released ...

Journal: :Journal of virology 2006
Bruno Sainz Francis V Chisari

Dimethyl sulfoxide (DMSO) has been shown to induce the differentiation of primary hepatocytes in vitro. When actively dividing poorly differentiated human hepatoma-derived (Huh7) cells were cultured in the presence of 1% DMSO, cells became cytologically differentiated and transitioned into a nondividing state, characterized by the induction of hepatocyte-specific genes. Moreover, these cells we...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2008
Sorin Armeanu Matthias Krusch Katrin M Baltz Thomas S Weiss Irina Smirnow Alexander Steinle Ulrich M Lauer Michael Bitzer Helmut R Salih

PURPOSE Hepatocellular carcinoma (HCC) displays particular resistance to conventional cytostatic agents. Alternative treatment strategies focus on novel substances exhibiting antineoplastic and/or immunomodulatory activity enhancing for example natural killer (NK) cell antitumor reactivity. However, tumor-associated ligands engaging activating NK cell receptors are largely unknown. Exceptions a...

Journal: :Cancer research 2002
Masumi Suzui Muneyuki Masuda Jin T E Lim Chris Albanese Richard G Pestell I Bernard Weinstein

Acyclic retinoid (ACR), a novel synthetic retinoid, can prevent the recurrence of human hepatoma after surgical resection of primary tumors, but the molecular mechanisms by which ACR exerts antitumor effects are not known. In this study, we found that ACR inhibited the growth of three human hepatoma cell lines. In HepG2 cells, this inhibition was associated with an arrest of the cell cycle in G...

2002
Masumi Suzui Muneyuki Masuda Jin T. E. Lim Chris Albanese Richard G. Pestell Bernard Weinstein Herbert Irving

Acyclic retinoid (ACR), a novel synthetic retinoid, can prevent the recurrence of human hepatoma after surgical resection of primary tumors, but the molecular mechanisms by which ACR exerts antitumor effects are not known. In this study, we found that ACR inhibited the growth of three human hepatoma cell lines. In HepG2 cells, this inhibition was associated with an arrest of the cell cycle in G...

Journal: :Cancer letters 2007
Song Zhang Ju-Hong Yang Chang-Kai Guo Peng-Cheng Cai

We detected a strong upregulation of the mutated transketolase transcript (TKTL1) in human hepatoma cell line HepG2, whereas transketolase (TKT) and transketolase-like-2 (TKTL2) transcripts were not upregulated. We inhibited the expression of TKTL1 by RNAi in HepG2 cells. It was found that total transketolase activity was dramatically downregulated and the proliferation of cancer cells was sign...

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