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plc prf 5 cell line  (ATCC)


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    Structured Review

    ATCC plc prf 5 cell line
    Plc Prf 5 Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1253 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/plc+prf+5+cell+lines/PLC%2FPRF%2F5/pm42243436-83-1-8
    Average 96 stars, based on 1253 article reviews
    plc prf 5 cell line - by Bioz Stars, 2026-10
    96/100 stars

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    Planar Chromatography:

    Article Title: Identification of a cancer stem cell-like subpopulation that promotes HCC metastasis
    Article Snippet: .. The THP-1, Jurkat, HEK293, and PLC/PRF/5 cell lines were obtained from the American Type Culture Collection. ..

    Article Title: METTL16 promotes liver cancer stem cell self-renewal via controlling ribosome biogenesis and mRNA translation.
    Article Snippet: .. Human HepG2, HEK293T, CL-48, THLE-2, Hep3B, SNU449, PLC/PRF/5 cell lines were obtained from American Type Culture Collection (ATCC), Huh7 and MHCC97H cell lines were given from Professor Wendong Huang (City of Hope, Duarte, CA). .. HepG2, HEK293T, Huh7 and MHCC97H were all cultured in DMEM medium (Thermo Fisher Scientific), SNU449 were all cultured in RPMI-1640 medium (Thermo Fisher Scientific), Hep3B, CL-48 and PLC/PRF/5 were all cultured in EMEM medium (ATCC), THLE-2 were all cultured in BEGM Bullet Kit (Lonza), supplemented with 10% fetal bovine serum (Gemini Bio-Products) and 1% penicillin/streptomycin (Thermo Fisher Scientific) at 37 °C in a 5% CO2 humidified incubator.

    Article Title: Identification of a cancer stem cell-like subpopulation that promotes HCC metastasis
    Article Snippet: .. Cell lines The THP-1, Jurkat, HEK293, and PLC/PRF/5 cell lines were obtained from the American Type Culture Collection. ..

    Article Title: MicroRNA-142-3p Overcomes Drug Resistance in Hepatocellular Carcinoma by Targeting YES1 and TWF1
    Article Snippet: Additionally, the correlation between the TWF1 mRNA expression levels and patient survival was examined using data from The Human Protein Atlas (HPA) database ( https://www.proteinatlas.org/ ). .. SNU475, SNU423, and PLC/PRF/5 cell lines were sourced from the American Type Culture Collection (ATCC, Manassas, VA, USA). ..

    Article Title: ACSS2-mediated acetyl-CoA accumulation promotes mitophagy and tumor growth via increased H3K27ac in HBV-related HCC.
    Article Snippet: .. Cell lines and cell culture HepAD38 and PLC/PRF/5 cell lines were obtained from the American Type Culture Collection (Manassas, VA, USA). ..

    Article Title: Delactylation diminished the growth inhibitory role of CA3 by restoring DUOX2 expression in hepatocellular carcinoma.
    Article Snippet: Lactylation is an emerging pathogenesis of hepatocellular carcinoma (HCC).. However, the underlying mechanisms and biological significance remain poorly understood.. The Carbonic anhydrase III (CA3) gene, previously defined as a binding protein of SQLE and involved in the NAFLD disease, has now been identified as a novel tumor suppressor in HCC. mRNA expression of CA3 is associated with a favorable prognosis and negatively correlated with serum lactate levels, whereas CA3 protein expression does not correlate with patient prognosis or serum lactate levels, suggested there has lactate-related post-translational modification of CA3 in HCC.

    Article Title: MicroRNA-142-3p Overcomes Drug Resistance in Hepatocellular Carcinoma by Targeting YES1 and TWF1.
    Article Snippet: Additionally, the correlation between the TWF1 mRNA expression levels and patient survival was examined using data from The Human Protein Atlas (HPA) database (https://www.proteinatlas.org/). .. SNU475, SNU423, and PLC/PRF/5 cell lines were sourced from the American Type Culture Collection (ATCC, Manassas, VA, USA). ..

    Article Title: Pseudouridine synthase 1 promotes progression of hepatocellular carcinoma via mTOR and MYC signaling pathways
    Article Snippet: .. LO2, SNU449, HepG2, and PLC/PRF/5 cell lines were purchased from the American Type Culture Collection (ATCC; Manassas, VA, USA). ..

    Cell Culture:

    Article Title: ACSS2-mediated acetyl-CoA accumulation promotes mitophagy and tumor growth via increased H3K27ac in HBV-related HCC.
    Article Snippet: .. Cell lines and cell culture HepAD38 and PLC/PRF/5 cell lines were obtained from the American Type Culture Collection (Manassas, VA, USA). ..



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    In vitro evaluation of molnupiravir in HEV cell culture models. (A) Cytotoxicity of molnupiravir, ribavirin, and <t>sofosbuvir</t> <t>in</t> <t>PLC/PRF/5</t> cells and PRH. Three replicates per concentration. Bars represent the mean and SEM. Mean viability at each concentration was compared with the no-drug control group using the Student t test; ** indicates statistically significant difference ( p <0.05). (B) PRH infected with rHEV and treated with either PBS, varying concentrations of molnupiravir, ribavirin, and sofosbuvir, as well as combinations. (C) Immunofluorescence staining for rHEV-infected PRH with/without antivirals: uninfected cells (negative control), rHEV-infected cells treated with either PBS (no drug control), sofosbuvir 10 μM, ribavirin 200 μM, or molnupiravir 100 μM. Cells were stained with polyclonal anti-rHEV sera and counterstained with DAPI. (D) PLC/PRF/5 cells infected with HEV infectious clone Kernow-p6, (E) PLC/PRF/5 cells infected with human-derived HEV. Cells were treated with either PBS, varying concentrations of molnupiravir, ribavirin, and sofosbuvir, as well as combinations. Error bars represent SEM (n=3 replicates per concentration). Mean viral loads at each concentration were compared with the no-drug control group using the Student t test; * indicates statistically significant difference ( p <0.05) from the untreated mean. ** indicates an extremely statistically significant difference ( p <0.01) from the untreated mean. Abbreviations: HEV, hepatitis E virus; PRH, primary rat hepatocytes; SEM, standard error of the mean; PBS, phosphate-buffered saline; rHEV, Rocahepevirus ratti genotype 1; DAPI, 4′,6-diamidino-2-phenylindole.
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    In vitro evaluation of molnupiravir in HEV cell culture models. (A) Cytotoxicity of molnupiravir, ribavirin, and <t>sofosbuvir</t> <t>in</t> <t>PLC/PRF/5</t> cells and PRH. Three replicates per concentration. Bars represent the mean and SEM. Mean viability at each concentration was compared with the no-drug control group using the Student t test; ** indicates statistically significant difference ( p <0.05). (B) PRH infected with rHEV and treated with either PBS, varying concentrations of molnupiravir, ribavirin, and sofosbuvir, as well as combinations. (C) Immunofluorescence staining for rHEV-infected PRH with/without antivirals: uninfected cells (negative control), rHEV-infected cells treated with either PBS (no drug control), sofosbuvir 10 μM, ribavirin 200 μM, or molnupiravir 100 μM. Cells were stained with polyclonal anti-rHEV sera and counterstained with DAPI. (D) PLC/PRF/5 cells infected with HEV infectious clone Kernow-p6, (E) PLC/PRF/5 cells infected with human-derived HEV. Cells were treated with either PBS, varying concentrations of molnupiravir, ribavirin, and sofosbuvir, as well as combinations. Error bars represent SEM (n=3 replicates per concentration). Mean viral loads at each concentration were compared with the no-drug control group using the Student t test; * indicates statistically significant difference ( p <0.05) from the untreated mean. ** indicates an extremely statistically significant difference ( p <0.01) from the untreated mean. Abbreviations: HEV, hepatitis E virus; PRH, primary rat hepatocytes; SEM, standard error of the mean; PBS, phosphate-buffered saline; rHEV, Rocahepevirus ratti genotype 1; DAPI, 4′,6-diamidino-2-phenylindole.
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    In vitro evaluation of molnupiravir in HEV cell culture models. (A) Cytotoxicity of molnupiravir, ribavirin, and <t>sofosbuvir</t> <t>in</t> <t>PLC/PRF/5</t> cells and PRH. Three replicates per concentration. Bars represent the mean and SEM. Mean viability at each concentration was compared with the no-drug control group using the Student t test; ** indicates statistically significant difference ( p <0.05). (B) PRH infected with rHEV and treated with either PBS, varying concentrations of molnupiravir, ribavirin, and sofosbuvir, as well as combinations. (C) Immunofluorescence staining for rHEV-infected PRH with/without antivirals: uninfected cells (negative control), rHEV-infected cells treated with either PBS (no drug control), sofosbuvir 10 μM, ribavirin 200 μM, or molnupiravir 100 μM. Cells were stained with polyclonal anti-rHEV sera and counterstained with DAPI. (D) PLC/PRF/5 cells infected with HEV infectious clone Kernow-p6, (E) PLC/PRF/5 cells infected with human-derived HEV. Cells were treated with either PBS, varying concentrations of molnupiravir, ribavirin, and sofosbuvir, as well as combinations. Error bars represent SEM (n=3 replicates per concentration). Mean viral loads at each concentration were compared with the no-drug control group using the Student t test; * indicates statistically significant difference ( p <0.05) from the untreated mean. ** indicates an extremely statistically significant difference ( p <0.01) from the untreated mean. Abbreviations: HEV, hepatitis E virus; PRH, primary rat hepatocytes; SEM, standard error of the mean; PBS, phosphate-buffered saline; rHEV, Rocahepevirus ratti genotype 1; DAPI, 4′,6-diamidino-2-phenylindole.
    Antivirals Human Hepatoma Cell Line Plc Prf 5, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    In vitro evaluation of molnupiravir in HEV cell culture models. (A) Cytotoxicity of molnupiravir, ribavirin, and <t>sofosbuvir</t> <t>in</t> <t>PLC/PRF/5</t> cells and PRH. Three replicates per concentration. Bars represent the mean and SEM. Mean viability at each concentration was compared with the no-drug control group using the Student t test; ** indicates statistically significant difference ( p <0.05). (B) PRH infected with rHEV and treated with either PBS, varying concentrations of molnupiravir, ribavirin, and sofosbuvir, as well as combinations. (C) Immunofluorescence staining for rHEV-infected PRH with/without antivirals: uninfected cells (negative control), rHEV-infected cells treated with either PBS (no drug control), sofosbuvir 10 μM, ribavirin 200 μM, or molnupiravir 100 μM. Cells were stained with polyclonal anti-rHEV sera and counterstained with DAPI. (D) PLC/PRF/5 cells infected with HEV infectious clone Kernow-p6, (E) PLC/PRF/5 cells infected with human-derived HEV. Cells were treated with either PBS, varying concentrations of molnupiravir, ribavirin, and sofosbuvir, as well as combinations. Error bars represent SEM (n=3 replicates per concentration). Mean viral loads at each concentration were compared with the no-drug control group using the Student t test; * indicates statistically significant difference ( p <0.05) from the untreated mean. ** indicates an extremely statistically significant difference ( p <0.01) from the untreated mean. Abbreviations: HEV, hepatitis E virus; PRH, primary rat hepatocytes; SEM, standard error of the mean; PBS, phosphate-buffered saline; rHEV, Rocahepevirus ratti genotype 1; DAPI, 4′,6-diamidino-2-phenylindole.
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    Nucleolar factors associated with FC/DFC are upregulated at both mRNA and protein level in HCC. Relative mRNA levels of ( A ) TCOF1 (Treacle), ( B ) UBF, ( C ) FBL (Fibrillarin), ( D ) NCL (nucleolin), and ( E ) NPM1 (nucleophosmin) measured by qPCR in HCC cells <t>(PLC/PRF/5</t> and SNU-449) and control cells (THLE-3). GAPDH was used as the housekeeping gene, and fold change was determined relative to mRNA levels in THLE-3 cells. Individual points in the graph represent biological replicates ( n = 3). The graph depicts the mean ± SD, with statistical significance assessed by one-way ANOVA and indicated with numerical P -values. Protein levels of ( F ) Treacle, ( G ) UBF, ( H ) Fibrillarin, ( I ) nucleolin, and ( J ) nucleophosmin measured by WB in HCC cells (PLC/PRF/5 and SNU-449) and control cells (THLE-3). α-tubulin was used as a loading control (LC). The molecular weight in kDa is listed on the left side of the blots (left panel), and protein signals were determined in each cell line relative to the loading control (right panel). Individual points in the graphs represent biological replicates ( n = 3). The graph depicts the mean ± SD, with statistical significance assessed by one-way ANOVA and indicated by numerical P -values.
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    Nucleolar factors associated with FC/DFC are upregulated at both mRNA and protein level in HCC. Relative mRNA levels of ( A ) TCOF1 (Treacle), ( B ) UBF, ( C ) FBL (Fibrillarin), ( D ) NCL (nucleolin), and ( E ) NPM1 (nucleophosmin) measured by qPCR in HCC cells <t>(PLC/PRF/5</t> and SNU-449) and control cells (THLE-3). GAPDH was used as the housekeeping gene, and fold change was determined relative to mRNA levels in THLE-3 cells. Individual points in the graph represent biological replicates ( n = 3). The graph depicts the mean ± SD, with statistical significance assessed by one-way ANOVA and indicated with numerical P -values. Protein levels of ( F ) Treacle, ( G ) UBF, ( H ) Fibrillarin, ( I ) nucleolin, and ( J ) nucleophosmin measured by WB in HCC cells (PLC/PRF/5 and SNU-449) and control cells (THLE-3). α-tubulin was used as a loading control (LC). The molecular weight in kDa is listed on the left side of the blots (left panel), and protein signals were determined in each cell line relative to the loading control (right panel). Individual points in the graphs represent biological replicates ( n = 3). The graph depicts the mean ± SD, with statistical significance assessed by one-way ANOVA and indicated by numerical P -values.
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    Image Search Results


    In vitro evaluation of molnupiravir in HEV cell culture models. (A) Cytotoxicity of molnupiravir, ribavirin, and sofosbuvir in PLC/PRF/5 cells and PRH. Three replicates per concentration. Bars represent the mean and SEM. Mean viability at each concentration was compared with the no-drug control group using the Student t test; ** indicates statistically significant difference ( p <0.05). (B) PRH infected with rHEV and treated with either PBS, varying concentrations of molnupiravir, ribavirin, and sofosbuvir, as well as combinations. (C) Immunofluorescence staining for rHEV-infected PRH with/without antivirals: uninfected cells (negative control), rHEV-infected cells treated with either PBS (no drug control), sofosbuvir 10 μM, ribavirin 200 μM, or molnupiravir 100 μM. Cells were stained with polyclonal anti-rHEV sera and counterstained with DAPI. (D) PLC/PRF/5 cells infected with HEV infectious clone Kernow-p6, (E) PLC/PRF/5 cells infected with human-derived HEV. Cells were treated with either PBS, varying concentrations of molnupiravir, ribavirin, and sofosbuvir, as well as combinations. Error bars represent SEM (n=3 replicates per concentration). Mean viral loads at each concentration were compared with the no-drug control group using the Student t test; * indicates statistically significant difference ( p <0.05) from the untreated mean. ** indicates an extremely statistically significant difference ( p <0.01) from the untreated mean. Abbreviations: HEV, hepatitis E virus; PRH, primary rat hepatocytes; SEM, standard error of the mean; PBS, phosphate-buffered saline; rHEV, Rocahepevirus ratti genotype 1; DAPI, 4′,6-diamidino-2-phenylindole.

    Journal: Hepatology Communications

    Article Title: Molnupiravir is effective against hepatitis E virus infection in an animal model

    doi: 10.1097/HC9.0000000000000944

    Figure Lengend Snippet: In vitro evaluation of molnupiravir in HEV cell culture models. (A) Cytotoxicity of molnupiravir, ribavirin, and sofosbuvir in PLC/PRF/5 cells and PRH. Three replicates per concentration. Bars represent the mean and SEM. Mean viability at each concentration was compared with the no-drug control group using the Student t test; ** indicates statistically significant difference ( p <0.05). (B) PRH infected with rHEV and treated with either PBS, varying concentrations of molnupiravir, ribavirin, and sofosbuvir, as well as combinations. (C) Immunofluorescence staining for rHEV-infected PRH with/without antivirals: uninfected cells (negative control), rHEV-infected cells treated with either PBS (no drug control), sofosbuvir 10 μM, ribavirin 200 μM, or molnupiravir 100 μM. Cells were stained with polyclonal anti-rHEV sera and counterstained with DAPI. (D) PLC/PRF/5 cells infected with HEV infectious clone Kernow-p6, (E) PLC/PRF/5 cells infected with human-derived HEV. Cells were treated with either PBS, varying concentrations of molnupiravir, ribavirin, and sofosbuvir, as well as combinations. Error bars represent SEM (n=3 replicates per concentration). Mean viral loads at each concentration were compared with the no-drug control group using the Student t test; * indicates statistically significant difference ( p <0.05) from the untreated mean. ** indicates an extremely statistically significant difference ( p <0.01) from the untreated mean. Abbreviations: HEV, hepatitis E virus; PRH, primary rat hepatocytes; SEM, standard error of the mean; PBS, phosphate-buffered saline; rHEV, Rocahepevirus ratti genotype 1; DAPI, 4′,6-diamidino-2-phenylindole.

    Article Snippet: Human hepatoma cell line PLC/PRF/5 (ATCC CRL-8024, LGC Standards, Wesel, Germany) and primary rat hepatocytes (PRH) were used in this study.

    Techniques: In Vitro, Cell Culture, Concentration Assay, Control, Infection, Immunofluorescence, Staining, Negative Control, Derivative Assay, Virus, Saline

    Nucleolar factors associated with FC/DFC are upregulated at both mRNA and protein level in HCC. Relative mRNA levels of ( A ) TCOF1 (Treacle), ( B ) UBF, ( C ) FBL (Fibrillarin), ( D ) NCL (nucleolin), and ( E ) NPM1 (nucleophosmin) measured by qPCR in HCC cells (PLC/PRF/5 and SNU-449) and control cells (THLE-3). GAPDH was used as the housekeeping gene, and fold change was determined relative to mRNA levels in THLE-3 cells. Individual points in the graph represent biological replicates ( n = 3). The graph depicts the mean ± SD, with statistical significance assessed by one-way ANOVA and indicated with numerical P -values. Protein levels of ( F ) Treacle, ( G ) UBF, ( H ) Fibrillarin, ( I ) nucleolin, and ( J ) nucleophosmin measured by WB in HCC cells (PLC/PRF/5 and SNU-449) and control cells (THLE-3). α-tubulin was used as a loading control (LC). The molecular weight in kDa is listed on the left side of the blots (left panel), and protein signals were determined in each cell line relative to the loading control (right panel). Individual points in the graphs represent biological replicates ( n = 3). The graph depicts the mean ± SD, with statistical significance assessed by one-way ANOVA and indicated by numerical P -values.

    Journal: NAR Cancer

    Article Title: Ribosome biogenesis is increased in hepatocellular carcinoma and represents a potential therapeutic target

    doi: 10.1093/narcan/zcaf058

    Figure Lengend Snippet: Nucleolar factors associated with FC/DFC are upregulated at both mRNA and protein level in HCC. Relative mRNA levels of ( A ) TCOF1 (Treacle), ( B ) UBF, ( C ) FBL (Fibrillarin), ( D ) NCL (nucleolin), and ( E ) NPM1 (nucleophosmin) measured by qPCR in HCC cells (PLC/PRF/5 and SNU-449) and control cells (THLE-3). GAPDH was used as the housekeeping gene, and fold change was determined relative to mRNA levels in THLE-3 cells. Individual points in the graph represent biological replicates ( n = 3). The graph depicts the mean ± SD, with statistical significance assessed by one-way ANOVA and indicated with numerical P -values. Protein levels of ( F ) Treacle, ( G ) UBF, ( H ) Fibrillarin, ( I ) nucleolin, and ( J ) nucleophosmin measured by WB in HCC cells (PLC/PRF/5 and SNU-449) and control cells (THLE-3). α-tubulin was used as a loading control (LC). The molecular weight in kDa is listed on the left side of the blots (left panel), and protein signals were determined in each cell line relative to the loading control (right panel). Individual points in the graphs represent biological replicates ( n = 3). The graph depicts the mean ± SD, with statistical significance assessed by one-way ANOVA and indicated by numerical P -values.

    Article Snippet: Human osteosarcoma U2OS cells (#HTB-96), HCC cell lines PLC/PRF/5 (#CRL-8024), SNU-449 (#CRL-2234), and normal liver epithelial cells THLE-3 (#CRL-3583) were purchased from the American Type Culture Collection.

    Techniques: Control, Molecular Weight

    Nucleolar expression of FC/DFC-associated factors is upregulated in HCC. Representative images of ( A ) Treacle (green), ( B ) UBF (green), ( C ) Fibrillarin (green), and ( D ) nucleolin (green) and nucleophosmin (magenta), and Pol II (yellow) in THLE-3, PLC/PRF/5, and SNU-449 cells. ( E ) Total nucleolar Treacle intensity per nucleus. Graphs depict one representative replicate ( n = 3) with data points representing individual cells and the median indicated by the red line. A Kruskal–Wallis test was applied to assess differences between groups for all three biological replicates combined, and statistical significance is indicated by numerical P -values. ( F ) Total nucleolar UBF intensity per nucleus otherwise as in panel (E). ( G ) Total nucleolar Fibrillarin intensity per nucleus, otherwise as in panel (E). ( H ) Total nucleolar nucleolin intensity per nucleus otherwise as in panel (E). (I) Total nucleolar nucleophosmin intensity per nucleus otherwise as in panel (E).

    Journal: NAR Cancer

    Article Title: Ribosome biogenesis is increased in hepatocellular carcinoma and represents a potential therapeutic target

    doi: 10.1093/narcan/zcaf058

    Figure Lengend Snippet: Nucleolar expression of FC/DFC-associated factors is upregulated in HCC. Representative images of ( A ) Treacle (green), ( B ) UBF (green), ( C ) Fibrillarin (green), and ( D ) nucleolin (green) and nucleophosmin (magenta), and Pol II (yellow) in THLE-3, PLC/PRF/5, and SNU-449 cells. ( E ) Total nucleolar Treacle intensity per nucleus. Graphs depict one representative replicate ( n = 3) with data points representing individual cells and the median indicated by the red line. A Kruskal–Wallis test was applied to assess differences between groups for all three biological replicates combined, and statistical significance is indicated by numerical P -values. ( F ) Total nucleolar UBF intensity per nucleus otherwise as in panel (E). ( G ) Total nucleolar Fibrillarin intensity per nucleus, otherwise as in panel (E). ( H ) Total nucleolar nucleolin intensity per nucleus otherwise as in panel (E). (I) Total nucleolar nucleophosmin intensity per nucleus otherwise as in panel (E).

    Article Snippet: Human osteosarcoma U2OS cells (#HTB-96), HCC cell lines PLC/PRF/5 (#CRL-8024), SNU-449 (#CRL-2234), and normal liver epithelial cells THLE-3 (#CRL-3583) were purchased from the American Type Culture Collection.

    Techniques: Expressing

    rDNA transcription is increased in HCC. ( A ) Representative images of EU incorporation (green). THLE-3, PLC/PRF/5, and SNU-449 cells were stained with DAPI (blue) and an antibody against Pol II (yellow). ( B ) Total nucleolar EU intensity per nucleus as a readout for rDNA transcription in THLE-3, PLC/PRF/5, and SNU-449 cells. The graph depicts one representative biological replicate ( n = 3), with data points representing individual cells, and the median indicated by the red line. A Kruskal–Wallis test was applied to assess differences between groups for the replicates combined, and statistical significance is indicated by numerical P -values. ( C ) Nucleolar size measured through an inverse intensity-based mask of Pol II in THLE-3, PLC/PRF/5, and SNU-449 cells. Individual points in the graph represent biological replicates ( n = 3). The graph depicts the mean ± SD, and statistical significance assessed by one-way ANOVA is indicated with numerical P -values. ( D ) Number of nucleoli per nucleus in THLE-3, PLC/PRF/5, and SNU-449 cells measured through an inverse intensity-based mask of Pol II. Individual points in the graph represent biological replicates ( n = 3). The graph depicts the mean ± SD, and statistical significance assessed by one-way ANOVA is indicated with numerical P -values. ( E ) Total nucleolar area otherwise as in panel (C).

    Journal: NAR Cancer

    Article Title: Ribosome biogenesis is increased in hepatocellular carcinoma and represents a potential therapeutic target

    doi: 10.1093/narcan/zcaf058

    Figure Lengend Snippet: rDNA transcription is increased in HCC. ( A ) Representative images of EU incorporation (green). THLE-3, PLC/PRF/5, and SNU-449 cells were stained with DAPI (blue) and an antibody against Pol II (yellow). ( B ) Total nucleolar EU intensity per nucleus as a readout for rDNA transcription in THLE-3, PLC/PRF/5, and SNU-449 cells. The graph depicts one representative biological replicate ( n = 3), with data points representing individual cells, and the median indicated by the red line. A Kruskal–Wallis test was applied to assess differences between groups for the replicates combined, and statistical significance is indicated by numerical P -values. ( C ) Nucleolar size measured through an inverse intensity-based mask of Pol II in THLE-3, PLC/PRF/5, and SNU-449 cells. Individual points in the graph represent biological replicates ( n = 3). The graph depicts the mean ± SD, and statistical significance assessed by one-way ANOVA is indicated with numerical P -values. ( D ) Number of nucleoli per nucleus in THLE-3, PLC/PRF/5, and SNU-449 cells measured through an inverse intensity-based mask of Pol II. Individual points in the graph represent biological replicates ( n = 3). The graph depicts the mean ± SD, and statistical significance assessed by one-way ANOVA is indicated with numerical P -values. ( E ) Total nucleolar area otherwise as in panel (C).

    Article Snippet: Human osteosarcoma U2OS cells (#HTB-96), HCC cell lines PLC/PRF/5 (#CRL-8024), SNU-449 (#CRL-2234), and normal liver epithelial cells THLE-3 (#CRL-3583) were purchased from the American Type Culture Collection.

    Techniques: Staining

    Anti-cancer drugs targeting the nucleolus inhibit cell viability in HCC. Drug response curves with corresponding IC 50 values and 95% CIs. Drugs were applied for 72 h, after which cell viability was assessed in THLE-3, PLC/PRF/5, and SNU-449 cells. ( A ) Drug response curve for CX-5461 with obtained IC 50 values and 95% CI (left panel). The graph shows the obtained IC 50 values represented as the mean ± SD (right panel). Individual points in the graph represent biological replicates ( n = 3). Statistical significance was assessed by one-way ANOVA and are indicated with numerical P -values. ( B ) Drug response curve for BMH-21 otherwise as in panel (A). ( C ) Drug response curve for Oxaliplatin, otherwise as in panel (A). ( D ) Drug response curve for JP-1302 otherwise as in panel (A). ( E ) Drug response curve for Sorafenib otherwise as in panel (A).

    Journal: NAR Cancer

    Article Title: Ribosome biogenesis is increased in hepatocellular carcinoma and represents a potential therapeutic target

    doi: 10.1093/narcan/zcaf058

    Figure Lengend Snippet: Anti-cancer drugs targeting the nucleolus inhibit cell viability in HCC. Drug response curves with corresponding IC 50 values and 95% CIs. Drugs were applied for 72 h, after which cell viability was assessed in THLE-3, PLC/PRF/5, and SNU-449 cells. ( A ) Drug response curve for CX-5461 with obtained IC 50 values and 95% CI (left panel). The graph shows the obtained IC 50 values represented as the mean ± SD (right panel). Individual points in the graph represent biological replicates ( n = 3). Statistical significance was assessed by one-way ANOVA and are indicated with numerical P -values. ( B ) Drug response curve for BMH-21 otherwise as in panel (A). ( C ) Drug response curve for Oxaliplatin, otherwise as in panel (A). ( D ) Drug response curve for JP-1302 otherwise as in panel (A). ( E ) Drug response curve for Sorafenib otherwise as in panel (A).

    Article Snippet: Human osteosarcoma U2OS cells (#HTB-96), HCC cell lines PLC/PRF/5 (#CRL-8024), SNU-449 (#CRL-2234), and normal liver epithelial cells THLE-3 (#CRL-3583) were purchased from the American Type Culture Collection.

    Techniques:

    Nucleolar-targeting compounds inhibit nucleolar activity and induce selective DNA damage. ( A ) Representative images of EU incorporation (green) in THLE-3, PLC/PRF/5, and SNU-449 cells 24 h after treatment with four anti-cancer drugs targeting the nucleolus: CX-5461, BMH-21, Oxaliplatin, and JP-1302, or targeted therapy Sorafenib. Cells were treated with DMSO as control and were stained with DAPI (blue) and Pol II (yellow). ( B ) Mean nucleolar EU intensity per nucleus as a readout for rDNA transcription in THLE-3, PLC/PRF/5, and SNU-449 cells 24 h after treatment with four anti-cancer drugs targeting the nucleolus: CX-5461, BMH-21, Oxaliplatin, and JP-1302, or targeted therapy Sorafenib. Cells were treated with DMSO as control. The graph depicts one representative biological replicate ( n = 3), with data points representing individual cells, and the median indicated by the red line. A Kruskal–Wallis test was applied to assess differences between groups for the replicates combined, and statistical significance is indicated by numerical P -values. ( C ) Representative images of nuclear 53BP1 and γH2AX foci accumulation in THLE-3, PLC/PRF/5, and SNU-449 cells 24 h after treatment with four anti-cancer drugs targeting the nucleolus: CX-5461, BMH-21, Oxaliplatin, and JP-1302, or targeted therapy Sorafenib. Cells were treated with DMSO as control, and stained with DAPI (blue), 53BP1 (yellow), and γH2AX (red). ( D ) Fold change of nuclear 53BP1 foci per cell relative to DMSO. Individual points in the graph represent biological replicates ( n = 3). The graph depicts the mean ± SD and statistical significance was assessed by one sample t test and indicated by numerical P -values. ( E ) Fold change of nuclear γH2AX foci per cell relative to DMSO otherwise as in panel (D).

    Journal: NAR Cancer

    Article Title: Ribosome biogenesis is increased in hepatocellular carcinoma and represents a potential therapeutic target

    doi: 10.1093/narcan/zcaf058

    Figure Lengend Snippet: Nucleolar-targeting compounds inhibit nucleolar activity and induce selective DNA damage. ( A ) Representative images of EU incorporation (green) in THLE-3, PLC/PRF/5, and SNU-449 cells 24 h after treatment with four anti-cancer drugs targeting the nucleolus: CX-5461, BMH-21, Oxaliplatin, and JP-1302, or targeted therapy Sorafenib. Cells were treated with DMSO as control and were stained with DAPI (blue) and Pol II (yellow). ( B ) Mean nucleolar EU intensity per nucleus as a readout for rDNA transcription in THLE-3, PLC/PRF/5, and SNU-449 cells 24 h after treatment with four anti-cancer drugs targeting the nucleolus: CX-5461, BMH-21, Oxaliplatin, and JP-1302, or targeted therapy Sorafenib. Cells were treated with DMSO as control. The graph depicts one representative biological replicate ( n = 3), with data points representing individual cells, and the median indicated by the red line. A Kruskal–Wallis test was applied to assess differences between groups for the replicates combined, and statistical significance is indicated by numerical P -values. ( C ) Representative images of nuclear 53BP1 and γH2AX foci accumulation in THLE-3, PLC/PRF/5, and SNU-449 cells 24 h after treatment with four anti-cancer drugs targeting the nucleolus: CX-5461, BMH-21, Oxaliplatin, and JP-1302, or targeted therapy Sorafenib. Cells were treated with DMSO as control, and stained with DAPI (blue), 53BP1 (yellow), and γH2AX (red). ( D ) Fold change of nuclear 53BP1 foci per cell relative to DMSO. Individual points in the graph represent biological replicates ( n = 3). The graph depicts the mean ± SD and statistical significance was assessed by one sample t test and indicated by numerical P -values. ( E ) Fold change of nuclear γH2AX foci per cell relative to DMSO otherwise as in panel (D).

    Article Snippet: Human osteosarcoma U2OS cells (#HTB-96), HCC cell lines PLC/PRF/5 (#CRL-8024), SNU-449 (#CRL-2234), and normal liver epithelial cells THLE-3 (#CRL-3583) were purchased from the American Type Culture Collection.

    Techniques: Activity Assay, Control, Staining