Radiobiological response of human hepatoma and normal liver cells exposed to carbon ions generated by Heavy Ion Research Facility in Lanzhou

2006 ◽  
Vol 49 (1) ◽  
pp. 72-76 ◽  
Author(s):  
Jianshe Yang ◽  
Wenjian Li ◽  
Xiaodong Jin ◽  
Xigang Jing ◽  
Chuanling Guo ◽  
...  
Keyword(s):  
Normal Liver ◽  
Heavy Ion ◽  
Liver Cells ◽  
Human Hepatoma ◽  
Carbon Ions ◽  
Research Facility

Introduction of the Heavy Ion Research Facility in Lanzhou (HIRFL)

2020 ◽  
Vol 15 (12) ◽  
pp. T12015-T12015
Author(s):  
L.J. Mao ◽  
J.C. Yang ◽  
W.Q. Yang ◽  
J.W. Xia ◽  
Y.J. Yuan ◽  
...  
Keyword(s):  
Heavy Ion ◽  
Research Facility

scholarly journals Investigating Pathogenic and Hepatocarcinogenic Mechanisms from Normal Liver to HCC by Constructing Genetic and Epigenetic Networks via Big Genetic and Epigenetic Data Mining and Genome-Wide NGS Data Identification

2018 ◽  
Vol 2018 ◽  
pp. 1-22 ◽  
Author(s):  
Cheng-Wei Li ◽  
Yu-Kai Chiu ◽  
Bor-Sen Chen
Keyword(s):  
Data Mining ◽  
Dna Methylation ◽  
Normal Liver ◽  
Liver Cells ◽  
Next Generation Sequencing Data ◽  
Valuable Insight ◽  
Biliary Cirrhosis ◽  
Sequencing Data ◽  
Cellular Mechanisms ◽  
Genome Wide

The prevalence of hepatocellular carcinoma (HCC) is still high worldwide because liver diseases could develop into HCC. Recent reports indicate nonalcoholic fatty liver disease and nonalcoholic steatohepatitis (NAFLD&NASH) and primary biliary cirrhosis and primary sclerosing cholangitis (PBC&PSC) are significant of HCC. Therefore, understanding the cellular mechanisms of the pathogenesis and hepatocarcinogenesis from normal liver cells to HCC through NAFLD&NASH or PBC&PSC is a priority to prevent the progression of liver damage and reduce the risk of further complications. By the genetic and epigenetic data mining and the system identification through next-generation sequencing data and its corresponding DNA methylation profiles of liver cells in normal, NAFLD&NASH, PBC&PSC, and HCC patients, we identified the genome-wide real genetic and epigenetic networks (GENs) of normal, NAFLD&NASH, PBC&PSC, and HCC patients. In order to get valuable insight into these identified genome-wide GENs, we then applied a principal network projection method to extract the corresponding core GENs for normal liver cells, NAFLD&NASH, PBC&PSC, and HCC. By comparing the signal transduction pathways involved in the identified core GENs, we found that the hepatocarcinogenesis through NAFLD&NASH was induced through DNA methylation of HIST2H2BE, HSPB1, RPL30, and ALDOB and the regulation of miR-21 and miR-122, and the hepatocarcinogenesis through PBC&PSC was induced through DNA methylation of RPL23A, HIST2H2BE, TIMP1, IGF2, RPL30, and ALDOB and the regulation of miR-29a, miR-21, and miR-122. The genetic and epigenetic changes in the pathogenesis and hepatocarcinogenesis potentially serve as potential diagnostic biomarkers and/or therapeutic targets.

scholarly journals Coupled Operation Experience at the Holifield Heavy Ion Research Facility

1983 ◽  
Vol 30 (4) ◽  
pp. 2077-2079 ◽  
Author(s):  
R. S. Lord ◽  
J. B. Ball ◽  
E. D. Hudson ◽  
P. K. Kloeppel ◽  
C. A. Ludemann ◽  
...  
Keyword(s):  
Heavy Ion ◽  
Research Facility

scholarly journals The Radio-mitigative Effect of CpG-Oligodeoxynucleotides on Mice After Exposure to Carbon Ions Radiation.

2021 ◽  
Author(s):  
Chao Zhang ◽  
Hua Fu ◽  
Xiang-hui Zhu ◽  
Sha Li ◽  
Zhong-ze Tian ◽  
...  
Keyword(s):  
Bacterial Infections ◽  
Heavy Ion ◽  
Double Strand Breaks ◽  
Tunel Staining ◽  
Cpg Odn ◽  
Carbon Ions ◽  
Strand Breaks ◽  
Cpg Oligodeoxynucleotides ◽  
Tnf Α ◽  
Immune Tissues

Abstract Background: Heavy ion radiation constitutes a major health risk for astronaut in space flight, potential damage to healthy tissues surrounding the tumor target along its penetrating path should still be considered in hydrotherapy. Therefore, there is a demand for reliable countermeasure against heavy ions radiation. In this study, we will estimate the radiomitigative effect of CpG-ODN on immune tissues after carbon ions radiation (CIR). Methods: Firstly, the 30 days’ survival of mice was observed, peripheral blood cell was counted, the injury of three principal immune tissues (including bone marrow, thymus and spleen) was evaluated by histological examination, apoptosis and double strand breaks (DSB) were detected by TUNEL staining and γ-H2AX immunohistochemistry respectively, and cytokine (G-CSF, IL-6 and TNF-α) was measured by ELISA assay. Results: the 30 days’ survival improved, the injury of three principal immune tissues were obviously ameliorated, the number of γ-H2AX foci and TUNEL-positive nuclei decreased, and G-CSF, IL-6 and TNF-α expression increased by CpG-ODN treatment after CIR. Conclusion: CpG-ODN could enhanced mice survival, and ameliorate immune tissues injury, the mechanism may be that CpG-ODN induced cytokines production and inhibited the double strand breaks (DSB) and apoptosis in order to stimulate the generation and mobilization of the immune cells and reestablish immune system to combat bacterial infections.

Liver-specific RNA metabolism in hepatoma cells: variations in transcription rates and mRNA levels

1985 ◽  
Vol 5 (10) ◽  
pp. 2633-2641
Author(s):  
D F Clayton ◽  
M Weiss ◽  
J E Darnell
Keyword(s):  
Cell Lines ◽  
Transcriptional Control ◽  
Hepatoma Cell ◽  
Primary Cultures ◽  
Normal Liver ◽  
Liver Cells ◽  
Hepatoma Cell Line ◽  
Mrna Levels ◽  
Tissue Specific ◽  
Specific Mrnas

The transcription rate and abundance of several liver-specific mRNAs as well as mRNAs common to many cell types were compared in a series of rodent hepatoma cell lines, normal liver cells, and primary hepatocyte cultures. The rat hepatoma cell line, Fao, which displays a liver-specific phenotype, contained eight of eight liver-specific mRNAs examined. However, the transcription rates of most liver-specific mRNAs were found to be low (1 to 30%) compared with normal liver in this and other differentiated cell lines. This low rate is similar to the transcription rates of liver-specific mRNA sequences measured in primary cultures of hepatocytes. Several variant cell lines that had lost differentiated traits contained few or none of the liver-specific mRNAs; clonal descendents which had regained differentiated function regained the tissue-specific mRNAs as a group, but at various concentrations. Because all of the changes observed in mRNA levels were not accompanied by parallel changes in transcription of the same sequences, differential posttranscriptional stabilization of the liver-specific mRNAs must also occur in the different cell lines. These results qualify the utility of cultured cell lines in the study of tissue-specific transcriptional control, but raise the possibility that posttranscriptional mechanisms act in cooperation with transcriptional controls to bring the level of tissue-specific mRNAs closer to those found in liver cells.

scholarly journals Carbon Ion Radiobiology

Cancers ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 3022 ◽  
Author(s):  
Walter Tinganelli ◽  
Marco Durante
Keyword(s):  
Normal Tissue ◽  
Biological Response ◽  
Metastatic Potential ◽  
Clinical Results ◽  
Heavy Ion ◽  
Particle Therapy ◽  
X Rays ◽  
Carbon Ions ◽  
Treatment Protocols ◽  
Target Region

Radiotherapy using accelerated charged particles is rapidly growing worldwide. About 85% of the cancer patients receiving particle therapy are irradiated with protons, which have physical advantages compared to X-rays but a similar biological response. In addition to the ballistic advantages, heavy ions present specific radiobiological features that can make them attractive for treating radioresistant, hypoxic tumors. An ideal heavy ion should have lower toxicity in the entrance channel (normal tissue) and be exquisitely effective in the target region (tumor). Carbon ions have been chosen because they represent the best combination in this direction. Normal tissue toxicities and second cancer risk are similar to those observed in conventional radiotherapy. In the target region, they have increased relative biological effectiveness and a reduced oxygen enhancement ratio compared to X-rays. Some radiobiological properties of densely ionizing carbon ions are so distinct from X-rays and protons that they can be considered as a different “drug” in oncology, and may elicit favorable responses such as an increased immune response and reduced angiogenesis and metastatic potential. The radiobiological properties of carbon ions should guide patient selection and treatment protocols to achieve optimal clinical results.

Antimalarial agent artesunate induces G0/G1 cell cycle arrest and apoptosis via increasing intracellular ROS levels in normal liver cells

2020 ◽  
Vol 39 (12) ◽  
pp. 1681-1689
Author(s):  
S Yin ◽  
H Yang ◽  
X Zhao ◽  
S Wei ◽  
Y Tao ◽  
...  
Keyword(s):  
Cell Cycle ◽  
Cell Proliferation ◽  
Cell Cycle Arrest ◽  
Normal Liver ◽  
Liver Cells ◽  
Phase Cell ◽  
Normal Cells ◽  
Cycle Arrest ◽  
Intracellular Ros ◽  
G1 Cell Cycle Arrest

Artesunate (ARS) has been shown to be highly effective against chloroquine-resistant malaria. In vitro studies reported that ARS has anticancer effects; however, its detrimental action on cancer cells may also play a role in its toxicity toward normal cells and its potential toxicity has not been sufficiently researched. In this study, we investigated the possible cytotoxic effects using normal BRL-3A and AML12 liver cells. The results showed that ARS dose-dependently inhibited cell proliferation and arrested the G0/G1 phase cell cycle in both BRL-3A and AML12 liver cells. Western blotting demonstrated that ARS induced a significant downregulation of cyclin-dependent kinase-2 (CDK2), CDK4, cyclin D1, and cyclin E1 in various levels and then caused apoptosis when the Bcl-2/Bax ratio decreased. Conversely, the levels of intracellular reactive oxygen species (ROS) were increased. The ROS scavenger N-acetylcysteine can significantly inhibit cell cycle arrest and apoptosis induced by ARS. Thus, the data confirmed that ARS exposure impairs normal liver cell proliferation by inducing G0/G1 cell cycle arrest and apoptosis, and this detrimental action may be associated with intracellular ROS accumulation. Collectively, the possible side effects of ARS on healthy normal cells cannot be neglected when developing therapies.

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