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pyruvic acid and Carcinoma, Hepatocellular

pyruvic acid has been researched along with Carcinoma, Hepatocellular in 23 studies

Pyruvic Acid: An intermediate compound in the metabolism of carbohydrates, proteins, and fats. In thiamine deficiency, its oxidation is retarded and it accumulates in the tissues, especially in nervous structures. (From Stedman, 26th ed)
pyruvic acid : A 2-oxo monocarboxylic acid that is the 2-keto derivative of propionic acid. It is a metabolite obtained during glycolysis.

Carcinoma, Hepatocellular: A primary malignant neoplasm of epithelial liver cells. It ranges from a well-differentiated tumor with EPITHELIAL CELLS indistinguishable from normal HEPATOCYTES to a poorly differentiated neoplasm. The cells may be uniform or markedly pleomorphic, or form GIANT CELLS. Several classification schemes have been suggested.

Research Excerpts

ExcerptRelevanceReference
" Following hyperpolarized [1-(13)C]pyruvate injections, pyruvate and its metabolic products, alanine and lactate, were observed in the liver of five rats with hepatocellular carcinoma and five healthy control rats."3.76T(2) relaxation times of (13)C metabolites in a rat hepatocellular carcinoma model measured in vivo using (13)C-MRS of hyperpolarized [1-(13)C]pyruvate. ( Butts Pauly, K; Hurd, R; King, R; Le Roux, P; Mayer, D; Pfefferbaum, A; Spielman, D; Tropp, J; Vasanawala, S; Yen, YF, 2010)
" To investigate this hypothesis, we compared the response to an anticancer agent chloroethylnitrosourea (CENU) of two transformed cell lines: HepG2 (hepatocarcinoma) with a partially differentiated phenotype and 143B (osteosarcoma) with an undifferentiated one."3.75Mitochondrial bioenergetic background confers a survival advantage to HepG2 cells in response to chemotherapy. ( Chevrollier, A; Demidem, A; Douay, O; Loiseau, D; Morvan, D; Reynier, P; Stepien, G, 2009)
" In summary, the results demonstrate that pyruvate metabolism acts as novel targetable metabolic vulnerabilities for HCC treatment in combination with a glutamine-deficient diet."1.72Genome-Wide CRISPR/Cas9 Library Screening Revealed Dietary Restriction of Glutamine in Combination with Inhibition of Pyruvate Metabolism as Effective Liver Cancer Treatment. ( Bao, MH; Chan, CY; Chen, Y; Lee, D; Tse, AP; Wei, L; Wong, BP; Wong, CC; Yang, C; Yuen, VW; Zhang, MS, 2022)
"Follow-up screening was performed in hepatocellular carcinoma with a focused CRISPR library targeting imaging-related genes."1.56Functional Genetic Screening Enables Theranostic Molecular Imaging in Cancer. ( Ackerman, D; Gade, TPF; Johnson, O; Mercadante, M; Perkons, NR; Pilla, G; Profka, E, 2020)
"Human hepatocellular carcinoma cells Huh7 and alveolar epithelial cells A549 were stimulated with either interleukin (IL) IL-1β (1 ng/ml, 24 h) or tumor necrosis factor (TNF) (10 ng/ml, 4 h), and then treated with EtP (2."1.43Ethanol, ethyl and sodium pyruvate decrease the inflammatory responses of human lung epithelial cells via Akt and NF-κB in vitro but have a low impact on hepatocellular cells. ( Juengel, E; Marzi, I; Mörs, K; Omid, N; Perl, M; Relja, B; Wagner, N; Werner, I, 2016)
"These data indicated that AS-30D hepatoma cells had a predominantly oxidative and not a glycolytic type of metabolism."1.31Substrate oxidation and ATP supply in AS-30D hepatoma cells. ( Moreno-Sánchez, R; Rodríguez-Enríquez, S; Torres-Márquez, ME, 2000)
"We have shown previously that rat hepatoma FTO-2B cells express two mRNAs, called F (fetal) and L (liver), from distinct promoters of the same gene coding for 6-phosphofructo-2-kinase (PFK-2)."1.30Glucose response elements in a gene that codes for 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase. ( Dupriez, VJ; Rousseau, GG, 1997)

Research

Studies (23)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (13.04)18.2507
2000's5 (21.74)29.6817
2010's10 (43.48)24.3611
2020's5 (21.74)2.80

Authors

AuthorsStudies
Kim, H1
Lee, HJ1
Sim, DY1
Park, JE1
Ahn, CH1
Park, SY2
Jang, E1
Kim, B1
Kim, SH1
Gnocchi, D1
Kurzyk, A1
Mintrone, A1
Lentini, G1
Sabbà, C1
Mazzocca, A1
Yang, C1
Lee, D1
Zhang, MS1
Tse, AP1
Wei, L1
Bao, MH1
Wong, BP1
Chan, CY1
Yuen, VW1
Chen, Y1
Wong, CC1
Shi, Q1
Xue, C1
Zeng, Y1
Gu, X1
Wang, J1
Li, L1
Tompkins, SC1
Sheldon, RD1
Rauckhorst, AJ1
Noterman, MF1
Solst, SR1
Buchanan, JL1
Mapuskar, KA1
Pewa, AD1
Gray, LR1
Oonthonpan, L1
Sharma, A1
Scerbo, DA1
Dupuy, AJ2
Spitz, DR1
Taylor, EB1
Perkons, NR1
Johnson, O1
Pilla, G1
Profka, E1
Mercadante, M1
Ackerman, D1
Gade, TPF1
Kim, J1
Yu, L1
Chen, W1
Xu, Y2
Wu, M1
Todorova, D1
Tang, Q1
Feng, B1
Jiang, L1
He, J1
Chen, G1
Fu, X1
Cipolleschi, MG1
Marzi, I2
Santini, R1
Fredducci, D1
Vinci, MC1
D'Amico, M1
Rovida, E1
Stivarou, T1
Torre, E1
Dello Sbarba, P1
Stecca, B1
Olivotto, M1
Bard-Chapeau, EA1
Nguyen, AT1
Rust, AG1
Sayadi, A1
Lee, P1
Chua, BQ1
New, LS1
de Jong, J1
Ward, JM1
Chin, CK1
Chew, V1
Toh, HC1
Abastado, JP1
Benoukraf, T1
Soong, R1
Bard, FA1
Johnson, RL1
Radda, GK1
Chan, EC1
Wessels, LF1
Adams, DJ1
Jenkins, NA1
Copeland, NG1
Relja, B1
Omid, N1
Wagner, N1
Mörs, K1
Werner, I1
Juengel, E1
Perl, M1
Brandt, AP1
Gozzi, GJ1
Pires, Ado R1
Martinez, GR1
Dos Santos Canuto, AV1
Echevarria, A1
Di Pietro, A1
Cadena, SM1
Ho, HY1
Cheng, ML1
Chiu, HY1
Weng, SF1
Chiu, DT1
Loiseau, D1
Morvan, D1
Chevrollier, A1
Demidem, A1
Douay, O1
Reynier, P1
Stepien, G1
Yen, YF2
Le Roux, P1
Mayer, D2
King, R1
Spielman, D1
Tropp, J1
Butts Pauly, K1
Pfefferbaum, A2
Vasanawala, S1
Hurd, R1
Jung, SY1
Song, HS1
Chung, SH1
Kim, YJ1
Darpolor, MM1
Chua, MS1
Xing, L1
Clarke-Katzenberg, RH1
Shi, W1
Josan, S1
Hurd, RE1
Senadheera, L1
So, S1
Hofmann, LV1
Glazer, GM1
Spielman, DM1
Ouattara, DA1
Prot, JM1
Bunescu, A1
Dumas, ME1
Elena-Herrmann, B1
Leclerc, E1
Brochot, C1
Perrin, A2
Roudier, E2
Duborjal, H1
Bachelet, C2
Riva-Lavieille, C1
Leverve, X1
Massarelli, R1
Weiss, P1
Ashwell, G1
Morell, AG1
Stockert, RJ1
Dupriez, VJ1
Rousseau, GG1
Rodríguez-Enríquez, S1
Torres-Márquez, ME1
Moreno-Sánchez, R1
Mizobuchi, N1
Kuwao, F1
Takeda, I1
Takemura, T1
Morita, S1
Horimi, T1
Takahashi, I1

Other Studies

23 other studies available for pyruvic acid and Carcinoma, Hepatocellular

ArticleYear
The Antitumor Effect of Cinnamaldehyde Derivative CB-PIC in Hepatocellular Carcinoma Cells via Inhibition of Pyruvate and STAT3 Signaling.
    International journal of molecular sciences, 2022, Jun-09, Volume: 23, Issue:12

    Topics: Acrolein; Apoptosis; Carcinoma, Hepatocellular; Cell Line, Tumor; HCT116 Cells; Humans; Liver Neopla

2022
Inhibition of LPAR6 overcomes sorafenib resistance by switching glycolysis into oxidative phosphorylation in hepatocellular carcinoma.
    Biochimie, 2022, Volume: 202

    Topics: Carcinoma, Hepatocellular; Glycolysis; Humans; Lactic Acid; Liver Neoplasms; Oxidative Phosphorylati

2022
Genome-Wide CRISPR/Cas9 Library Screening Revealed Dietary Restriction of Glutamine in Combination with Inhibition of Pyruvate Metabolism as Effective Liver Cancer Treatment.
    Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2022, Volume: 9, Issue:34

    Topics: Animals; Carcinoma, Hepatocellular; CRISPR-Cas Systems; Early Detection of Cancer; Glutamine; Liver

2022
A novel prognostic model for hepatocellular carcinoma based on pyruvate metabolism-related genes.
    Scientific reports, 2023, 06-16, Volume: 13, Issue:1

    Topics: Carcinoma, Hepatocellular; DNA Copy Number Variations; Humans; Liver Neoplasms; Prognosis; Pyruvic A

2023
Disrupting Mitochondrial Pyruvate Uptake Directs Glutamine into the TCA Cycle away from Glutathione Synthesis and Impairs Hepatocellular Tumorigenesis.
    Cell reports, 2019, 09-03, Volume: 28, Issue:10

    Topics: Animals; Apoptosis; Carcinogenesis; Carcinoma, Hepatocellular; Cell Line, Tumor; Citric Acid Cycle;

2019
Functional Genetic Screening Enables Theranostic Molecular Imaging in Cancer.
    Clinical cancer research : an official journal of the American Association for Cancer Research, 2020, 09-01, Volume: 26, Issue:17

    Topics: Animals; Carbon-13 Magnetic Resonance Spectroscopy; Carcinoma, Hepatocellular; CRISPR-Cas Systems; D

2020
Wild-Type p53 Promotes Cancer Metabolic Switch by Inducing PUMA-Dependent Suppression of Oxidative Phosphorylation.
    Cancer cell, 2019, 02-11, Volume: 35, Issue:2

    Topics: A549 Cells; Animals; Apoptosis Regulatory Proteins; Carcinoma, Hepatocellular; Cell Proliferation; G

2019
Hypoxia-resistant profile implies vulnerability of cancer stem cells to physiological agents, which suggests new therapeutic targets.
    Cell cycle (Georgetown, Tex.), 2014, Volume: 13, Issue:2

    Topics: Animals; Antineoplastic Agents; Carcinoma, Hepatocellular; Cell Hypoxia; Cell Line, Tumor; Citric Ac

2014
Transposon mutagenesis identifies genes driving hepatocellular carcinoma in a chronic hepatitis B mouse model.
    Nature genetics, 2014, Volume: 46, Issue:1

    Topics: Animals; Carcinoma, Hepatocellular; Disease Models, Animal; DNA Transposable Elements; Gene Expressi

2014
Ethanol, ethyl and sodium pyruvate decrease the inflammatory responses of human lung epithelial cells via Akt and NF-κB in vitro but have a low impact on hepatocellular cells.
    International journal of molecular medicine, 2016, Volume: 37, Issue:2

    Topics: bcl-2-Associated X Protein; Carcinoma, Hepatocellular; Cell Line, Tumor; Epithelial Cells; Ethanol;

2016
Impairment of oxidative phosphorylation increases the toxicity of SYD-1 on hepatocarcinoma cells (HepG2).
    Chemico-biological interactions, 2016, Aug-25, Volume: 256

    Topics: Adenosine Triphosphate; Antineoplastic Agents; Carcinoma, Hepatocellular; Hep G2 Cells; Hepatocytes;

2016
Dehydroepiandrosterone induces growth arrest of hepatoma cells via alteration of mitochondrial gene expression and function.
    International journal of oncology, 2008, Volume: 33, Issue:5

    Topics: Adenosine Triphosphate; Carcinoma, Hepatocellular; Cell Proliferation; Dehydroepiandrosterone; DNA,

2008
Mitochondrial bioenergetic background confers a survival advantage to HepG2 cells in response to chemotherapy.
    Molecular carcinogenesis, 2009, Volume: 48, Issue:8

    Topics: Adenosine Triphosphate; Carcinoma, Hepatocellular; Cell Differentiation; Cell Proliferation; Cell Re

2009
T(2) relaxation times of (13)C metabolites in a rat hepatocellular carcinoma model measured in vivo using (13)C-MRS of hyperpolarized [1-(13)C]pyruvate.
    NMR in biomedicine, 2010, Volume: 23, Issue:4

    Topics: Alanine; Animals; Carbon Isotopes; Carcinoma, Hepatocellular; Disease Models, Animal; Liver Neoplasm

2010
Pyruvate promotes tumor angiogenesis through HIF-1-dependent PAI-1 expression.
    International journal of oncology, 2011, Volume: 38, Issue:2

    Topics: Blotting, Western; Carcinoma, Hepatocellular; Cells, Cultured; Electrophoretic Mobility Shift Assay;

2011
In vivo MRSI of hyperpolarized [1-(13)C]pyruvate metabolism in rat hepatocellular carcinoma.
    NMR in biomedicine, 2011, Volume: 24, Issue:5

    Topics: Alanine; Animals; Carbon Isotopes; Carcinoma, Hepatocellular; Gene Expression Regulation, Neoplastic

2011
Metabolomics-on-a-chip and metabolic flux analysis for label-free modeling of the internal metabolism of HepG2/C3A cells.
    Molecular bioSystems, 2012, Jul-06, Volume: 8, Issue:7

    Topics: Carcinoma, Hepatocellular; Cell Line; Cell Respiration; Citric Acid Cycle; Energy Metabolism; Glycol

2012
Pyruvate reverses metabolic effects produced by hypoxia in glioma and hepatoma cell cultures.
    Biochimie, 2002, Volume: 84, Issue:10

    Topics: Animals; Carcinoma, Hepatocellular; Cell Hypoxia; Cell Line, Tumor; Glioma; Glucose; Humans; Hypoxia

2002
Pyruvate reduces DNA damage during hypoxia and after reoxygenation in hepatocellular carcinoma cells.
    The FEBS journal, 2007, Volume: 274, Issue:19

    Topics: Carcinoma, Hepatocellular; Cell Hypoxia; Cell Line, Tumor; Comet Assay; DNA Damage; Glutathione; Hum

2007
Modulation of the asialoglycoprotein receptor in human hepatoma cells: effect of glucose.
    Hepatology (Baltimore, Md.), 1994, Volume: 19, Issue:2

    Topics: Asialoglycoprotein Receptor; Asialoglycoproteins; Binding Sites; Carcinoma, Hepatocellular; Culture

1994
Glucose response elements in a gene that codes for 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase.
    DNA and cell biology, 1997, Volume: 16, Issue:9

    Topics: Animals; Carcinoma, Hepatocellular; Dactinomycin; Enhancer Elements, Genetic; Enzyme Inhibitors; Gen

1997
Substrate oxidation and ATP supply in AS-30D hepatoma cells.
    Archives of biochemistry and biophysics, 2000, Mar-01, Volume: 375, Issue:1

    Topics: 3-Hydroxybutyric Acid; Acetoacetates; Adenosine Triphosphate; Animals; Carcinoma, Hepatocellular; Ce

2000
[Changes in ketone body ratio and levels of pyruvate and lactate in arterial blood of patients with hepatocellular carcinoma after transcatheter arterial embolization].
    Rinsho byori. The Japanese journal of clinical pathology, 1990, Volume: 38, Issue:7

    Topics: Carcinoma, Hepatocellular; Embolization, Therapeutic; Humans; Ketones; Lactates; Lactic Acid; Liver;

1990