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primary human uterine fibroblast normal cells huf  (ATCC)


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    ATCC primary human uterine fibroblast normal cells huf
    Effects of Pituranthos chloranthus (PC) and Teucrium ramosissimum Desf. (TR) extracts on normal primary human uterine <t>fibroblast</t> cells <t>(HUF)</t> and primary murine Bone Marrow-Derived Macrophages (BMDM) viability. After treatment of primary HUF and murine BMDM with increasing concentrations (0–100 µg/mL) of PC and TR for 72 h, the percentage of viable cells was assessed using the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. ( A ) Dose–response curves of PC-treated HUF (left panel) and TR-treated HUF (right panel). ( B ) Dose–response curves of PC-treated BMDM (left panel) and TR-treated BMDM (right panel). Data are expressed as a mean percentage of control growth ± Standard Deviation (SD) of two representative experiments ( n = 6 replicates per concentration).
    Primary Human Uterine Fibroblast Normal Cells Huf, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 63 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primary+human+uterine+fibroblast+normal+cells+huf/Primary+Uterine+Fibroblast+Cells%3B+Normal%2C+Human/pmc08160977-180-0-11
    Average 99 stars, based on 63 article reviews
    primary human uterine fibroblast normal cells huf - by Bioz Stars, 2026-09
    99/100 stars

    Images

    1) Product Images from "Essential Oils, Pituranthos chloranthus and Teucrium ramosissimum , Chemosensitize Resistant Human Uterine Sarcoma MES-SA/Dx5 Cells to Doxorubicin by Inducing Apoptosis and Targeting P-Glycoprotein"

    Article Title: Essential Oils, Pituranthos chloranthus and Teucrium ramosissimum , Chemosensitize Resistant Human Uterine Sarcoma MES-SA/Dx5 Cells to Doxorubicin by Inducing Apoptosis and Targeting P-Glycoprotein

    Journal: Nutrients

    doi: 10.3390/nu13051719

    Effects of Pituranthos chloranthus (PC) and Teucrium ramosissimum Desf. (TR) extracts on normal primary human uterine fibroblast cells (HUF) and primary murine Bone Marrow-Derived Macrophages (BMDM) viability. After treatment of primary HUF and murine BMDM with increasing concentrations (0–100 µg/mL) of PC and TR for 72 h, the percentage of viable cells was assessed using the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. ( A ) Dose–response curves of PC-treated HUF (left panel) and TR-treated HUF (right panel). ( B ) Dose–response curves of PC-treated BMDM (left panel) and TR-treated BMDM (right panel). Data are expressed as a mean percentage of control growth ± Standard Deviation (SD) of two representative experiments ( n = 6 replicates per concentration).
    Figure Legend Snippet: Effects of Pituranthos chloranthus (PC) and Teucrium ramosissimum Desf. (TR) extracts on normal primary human uterine fibroblast cells (HUF) and primary murine Bone Marrow-Derived Macrophages (BMDM) viability. After treatment of primary HUF and murine BMDM with increasing concentrations (0–100 µg/mL) of PC and TR for 72 h, the percentage of viable cells was assessed using the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. ( A ) Dose–response curves of PC-treated HUF (left panel) and TR-treated HUF (right panel). ( B ) Dose–response curves of PC-treated BMDM (left panel) and TR-treated BMDM (right panel). Data are expressed as a mean percentage of control growth ± Standard Deviation (SD) of two representative experiments ( n = 6 replicates per concentration).

    Techniques Used: Derivative Assay, MTT Assay, Control, Standard Deviation, Concentration Assay

    Related Articles

    Derivative Assay:

    Article Title: Essential Oils, Pituranthos chloranthus and Teucrium ramosissimum , Chemosensitize Resistant Human Uterine Sarcoma MES-SA/Dx5 Cells to Doxorubicin by Inducing Apoptosis and Targeting P-Glycoprotein
    Article Snippet: Cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium containing L-glutamine supplemented with 10% fetal bovine serum (FBS) (Dutscher, Brumath, France).Cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium containing L-glutamine supplemented with 10% fetal bovine serum (FBS) (Dutscher, Brumath, France).. Primary human uterine fibroblast normal cells (HUF) were obtained from the ATCC.. HUF cells were cultured in Fibroblast Basal Medium supplemented with Fibroblast Growth Kit-Low Serum (ATCC, Molsheim, France).HUF cells were cultured in Fibroblast Basal Medium supplemented with Fibroblast Growth Kit-Low Serum (ATCC, Molsheim, France).

    MTT Assay:

    Article Title: Essential Oils, Pituranthos chloranthus and Teucrium ramosissimum , Chemosensitize Resistant Human Uterine Sarcoma MES-SA/Dx5 Cells to Doxorubicin by Inducing Apoptosis and Targeting P-Glycoprotein
    Article Snippet: Cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium containing L-glutamine supplemented with 10% fetal bovine serum (FBS) (Dutscher, Brumath, France).Cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium containing L-glutamine supplemented with 10% fetal bovine serum (FBS) (Dutscher, Brumath, France).. Primary human uterine fibroblast normal cells (HUF) were obtained from the ATCC.. HUF cells were cultured in Fibroblast Basal Medium supplemented with Fibroblast Growth Kit-Low Serum (ATCC, Molsheim, France).HUF cells were cultured in Fibroblast Basal Medium supplemented with Fibroblast Growth Kit-Low Serum (ATCC, Molsheim, France).

    Control:

    Article Title: Essential Oils, Pituranthos chloranthus and Teucrium ramosissimum , Chemosensitize Resistant Human Uterine Sarcoma MES-SA/Dx5 Cells to Doxorubicin by Inducing Apoptosis and Targeting P-Glycoprotein
    Article Snippet: Cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium containing L-glutamine supplemented with 10% fetal bovine serum (FBS) (Dutscher, Brumath, France).Cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium containing L-glutamine supplemented with 10% fetal bovine serum (FBS) (Dutscher, Brumath, France).. Primary human uterine fibroblast normal cells (HUF) were obtained from the ATCC.. HUF cells were cultured in Fibroblast Basal Medium supplemented with Fibroblast Growth Kit-Low Serum (ATCC, Molsheim, France).HUF cells were cultured in Fibroblast Basal Medium supplemented with Fibroblast Growth Kit-Low Serum (ATCC, Molsheim, France).

    Standard Deviation:

    Article Title: Essential Oils, Pituranthos chloranthus and Teucrium ramosissimum , Chemosensitize Resistant Human Uterine Sarcoma MES-SA/Dx5 Cells to Doxorubicin by Inducing Apoptosis and Targeting P-Glycoprotein
    Article Snippet: Cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium containing L-glutamine supplemented with 10% fetal bovine serum (FBS) (Dutscher, Brumath, France).Cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium containing L-glutamine supplemented with 10% fetal bovine serum (FBS) (Dutscher, Brumath, France).. Primary human uterine fibroblast normal cells (HUF) were obtained from the ATCC.. HUF cells were cultured in Fibroblast Basal Medium supplemented with Fibroblast Growth Kit-Low Serum (ATCC, Molsheim, France).HUF cells were cultured in Fibroblast Basal Medium supplemented with Fibroblast Growth Kit-Low Serum (ATCC, Molsheim, France).

    Concentration Assay:

    Article Title: Essential Oils, Pituranthos chloranthus and Teucrium ramosissimum , Chemosensitize Resistant Human Uterine Sarcoma MES-SA/Dx5 Cells to Doxorubicin by Inducing Apoptosis and Targeting P-Glycoprotein
    Article Snippet: Cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium containing L-glutamine supplemented with 10% fetal bovine serum (FBS) (Dutscher, Brumath, France).Cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium containing L-glutamine supplemented with 10% fetal bovine serum (FBS) (Dutscher, Brumath, France).. Primary human uterine fibroblast normal cells (HUF) were obtained from the ATCC.. HUF cells were cultured in Fibroblast Basal Medium supplemented with Fibroblast Growth Kit-Low Serum (ATCC, Molsheim, France).HUF cells were cultured in Fibroblast Basal Medium supplemented with Fibroblast Growth Kit-Low Serum (ATCC, Molsheim, France).



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    ATCC primary human uterine fibroblast normal cells huf
    Effects of Pituranthos chloranthus (PC) and Teucrium ramosissimum Desf. (TR) extracts on normal primary human uterine <t>fibroblast</t> cells <t>(HUF)</t> and primary murine Bone Marrow-Derived Macrophages (BMDM) viability. After treatment of primary HUF and murine BMDM with increasing concentrations (0–100 µg/mL) of PC and TR for 72 h, the percentage of viable cells was assessed using the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. ( A ) Dose–response curves of PC-treated HUF (left panel) and TR-treated HUF (right panel). ( B ) Dose–response curves of PC-treated BMDM (left panel) and TR-treated BMDM (right panel). Data are expressed as a mean percentage of control growth ± Standard Deviation (SD) of two representative experiments ( n = 6 replicates per concentration).
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    https://www.bioz.com/product/primary+human+uterine+fibroblast+normal+cells+huf/Primary+Uterine+Fibroblast+Cells%3B+Normal%2C+Human/pmc08160977-180-0-11
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    huf  (ATCC)
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    ATCC huf
    Effects of Pituranthos chloranthus (PC) and Teucrium ramosissimum Desf. (TR) extracts on normal primary human uterine <t>fibroblast</t> cells <t>(HUF)</t> and primary murine Bone Marrow-Derived Macrophages (BMDM) viability. After treatment of primary HUF and murine BMDM with increasing concentrations (0–100 µg/mL) of PC and TR for 72 h, the percentage of viable cells was assessed using the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. ( A ) Dose–response curves of PC-treated HUF (left panel) and TR-treated HUF (right panel). ( B ) Dose–response curves of PC-treated BMDM (left panel) and TR-treated BMDM (right panel). Data are expressed as a mean percentage of control growth ± Standard Deviation (SD) of two representative experiments ( n = 6 replicates per concentration).
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    ATCC human primary uterine fibroblast huf cells
    Effects of Pituranthos chloranthus (PC) and Teucrium ramosissimum Desf. (TR) extracts on normal primary human uterine <t>fibroblast</t> cells <t>(HUF)</t> and primary murine Bone Marrow-Derived Macrophages (BMDM) viability. After treatment of primary HUF and murine BMDM with increasing concentrations (0–100 µg/mL) of PC and TR for 72 h, the percentage of viable cells was assessed using the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. ( A ) Dose–response curves of PC-treated HUF (left panel) and TR-treated HUF (right panel). ( B ) Dose–response curves of PC-treated BMDM (left panel) and TR-treated BMDM (right panel). Data are expressed as a mean percentage of control growth ± Standard Deviation (SD) of two representative experiments ( n = 6 replicates per concentration).
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    https://www.bioz.com/product/primary+human+uterine+fibroblast+normal+cells+huf/Primary+Uterine+Fibroblast+Cells%3B+Normal%2C+Human/pmc12274959-51-0-16
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    ATCC human uterine fibroblast cells huf
    Effects of Pituranthos chloranthus (PC) and Teucrium ramosissimum Desf. (TR) extracts on normal primary human uterine <t>fibroblast</t> cells <t>(HUF)</t> and primary murine Bone Marrow-Derived Macrophages (BMDM) viability. After treatment of primary HUF and murine BMDM with increasing concentrations (0–100 µg/mL) of PC and TR for 72 h, the percentage of viable cells was assessed using the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. ( A ) Dose–response curves of PC-treated HUF (left panel) and TR-treated HUF (right panel). ( B ) Dose–response curves of PC-treated BMDM (left panel) and TR-treated BMDM (right panel). Data are expressed as a mean percentage of control growth ± Standard Deviation (SD) of two representative experiments ( n = 6 replicates per concentration).
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    ATCC primary human uterine fibroblast huf
    Metformin induces ZFP36 expression in cervical cancer-derived-cell lines. HeLa and CaSki cells were treated with metformin 20mM for 24 hours, then RNA was extracted for analysis by RT-qPCR. RT-qPCR of ZFP36 after metformin treatment in ( A ) HeLa and ( B ) CaSki. Representative Western Blot of ZFP36 and densitometric analysis in ( C ) HeLa and ( D ) CaSki, ( E ) HaCaT and ( F ) Human Uterine <t>Fibroblast</t> <t>(HUF).</t> Results are shown as means ± SD of at least three independent experiments. * p <0.05 **, p <0.01
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    ATCC human primary uterine fibroblast cells huf
    Metformin induces ZFP36 expression in cervical cancer-derived-cell lines. HeLa and CaSki cells were treated with metformin 20mM for 24 hours, then RNA was extracted for analysis by RT-qPCR. RT-qPCR of ZFP36 after metformin treatment in ( A ) HeLa and ( B ) CaSki. Representative Western Blot of ZFP36 and densitometric analysis in ( C ) HeLa and ( D ) CaSki, ( E ) HaCaT and ( F ) Human Uterine <t>Fibroblast</t> <t>(HUF).</t> Results are shown as means ± SD of at least three independent experiments. * p <0.05 **, p <0.01
    Human Primary Uterine Fibroblast Cells Huf, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC huf cells
    Figure 5. A comparison of NCAF with TCAF in terms of the alterations in genes and expression of protein markers: A comprehensive cancer panel report on all exon coverage on 409 genes involved in some of the most common known cancers shows the alteration of genes in aggressive TCAFs and NCAFs from the same patient compared to <t>HUF</t> <t>cells</t> (A). The pathway-based gene selection profiled the mutational spectrum in known cancer driver genes and drug targets along with signaling cascades, apoptosis genes, DNA repair genes, transcription regulators, inflammatory response genes, and growth factor genes. The panel covered both somatic and germline mutations. Heatmaps depicting the genetic alterations identified in NCAF, TCAF, or HUF samples are presented. The coding regions of 409 cancer-related genes are sequenced. Variants with a significant allele frequency difference between sample groups (n = 3) are summarized. Numbers of significantly altered variants of those genes are plotted. A 3-color scale-based conditionally formatted expression (% of expression by ICC) of CAF markers in aggressive TCAFs, and NCAFs from 29 representative patients sorted on the basis of CAFs with corresponding histologies, grades/stages (as presented with color codes, and numbers) is presented in a heatmap (B).
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    https://www.bioz.com/product/primary+human+uterine+fibroblast+normal+cells+huf/Primary+Uterine+Fibroblast+Cells%3B+Normal%2C+Human/pm37047422-354-4-11
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    Image Search Results


    Effects of Pituranthos chloranthus (PC) and Teucrium ramosissimum Desf. (TR) extracts on normal primary human uterine fibroblast cells (HUF) and primary murine Bone Marrow-Derived Macrophages (BMDM) viability. After treatment of primary HUF and murine BMDM with increasing concentrations (0–100 µg/mL) of PC and TR for 72 h, the percentage of viable cells was assessed using the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. ( A ) Dose–response curves of PC-treated HUF (left panel) and TR-treated HUF (right panel). ( B ) Dose–response curves of PC-treated BMDM (left panel) and TR-treated BMDM (right panel). Data are expressed as a mean percentage of control growth ± Standard Deviation (SD) of two representative experiments ( n = 6 replicates per concentration).

    Journal: Nutrients

    Article Title: Essential Oils, Pituranthos chloranthus and Teucrium ramosissimum , Chemosensitize Resistant Human Uterine Sarcoma MES-SA/Dx5 Cells to Doxorubicin by Inducing Apoptosis and Targeting P-Glycoprotein

    doi: 10.3390/nu13051719

    Figure Lengend Snippet: Effects of Pituranthos chloranthus (PC) and Teucrium ramosissimum Desf. (TR) extracts on normal primary human uterine fibroblast cells (HUF) and primary murine Bone Marrow-Derived Macrophages (BMDM) viability. After treatment of primary HUF and murine BMDM with increasing concentrations (0–100 µg/mL) of PC and TR for 72 h, the percentage of viable cells was assessed using the (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. ( A ) Dose–response curves of PC-treated HUF (left panel) and TR-treated HUF (right panel). ( B ) Dose–response curves of PC-treated BMDM (left panel) and TR-treated BMDM (right panel). Data are expressed as a mean percentage of control growth ± Standard Deviation (SD) of two representative experiments ( n = 6 replicates per concentration).

    Article Snippet: Primary human uterine fibroblast normal cells (HUF) were obtained from the ATCC.

    Techniques: Derivative Assay, MTT Assay, Control, Standard Deviation, Concentration Assay

    Metformin induces ZFP36 expression in cervical cancer-derived-cell lines. HeLa and CaSki cells were treated with metformin 20mM for 24 hours, then RNA was extracted for analysis by RT-qPCR. RT-qPCR of ZFP36 after metformin treatment in ( A ) HeLa and ( B ) CaSki. Representative Western Blot of ZFP36 and densitometric analysis in ( C ) HeLa and ( D ) CaSki, ( E ) HaCaT and ( F ) Human Uterine Fibroblast (HUF). Results are shown as means ± SD of at least three independent experiments. * p <0.05 **, p <0.01

    Journal: BMC Cancer

    Article Title: Metformin induces ZFP36 by mTORC1 inhibition in cervical cancer-derived cell lines

    doi: 10.1186/s12885-024-12555-5

    Figure Lengend Snippet: Metformin induces ZFP36 expression in cervical cancer-derived-cell lines. HeLa and CaSki cells were treated with metformin 20mM for 24 hours, then RNA was extracted for analysis by RT-qPCR. RT-qPCR of ZFP36 after metformin treatment in ( A ) HeLa and ( B ) CaSki. Representative Western Blot of ZFP36 and densitometric analysis in ( C ) HeLa and ( D ) CaSki, ( E ) HaCaT and ( F ) Human Uterine Fibroblast (HUF). Results are shown as means ± SD of at least three independent experiments. * p <0.05 **, p <0.01

    Article Snippet: Primary Human Uterine Fibroblast (HUF) (PCS-460–010) and human cervical cancer-derived cell lines HeLa (RRID: CVCL_0030) and CaSki (RRID: CVCL_1100) were obtained from ATCC (Manassas, VA, USA).

    Techniques: Expressing, Derivative Assay, Quantitative RT-PCR, Western Blot

    Figure 5. A comparison of NCAF with TCAF in terms of the alterations in genes and expression of protein markers: A comprehensive cancer panel report on all exon coverage on 409 genes involved in some of the most common known cancers shows the alteration of genes in aggressive TCAFs and NCAFs from the same patient compared to HUF cells (A). The pathway-based gene selection profiled the mutational spectrum in known cancer driver genes and drug targets along with signaling cascades, apoptosis genes, DNA repair genes, transcription regulators, inflammatory response genes, and growth factor genes. The panel covered both somatic and germline mutations. Heatmaps depicting the genetic alterations identified in NCAF, TCAF, or HUF samples are presented. The coding regions of 409 cancer-related genes are sequenced. Variants with a significant allele frequency difference between sample groups (n = 3) are summarized. Numbers of significantly altered variants of those genes are plotted. A 3-color scale-based conditionally formatted expression (% of expression by ICC) of CAF markers in aggressive TCAFs, and NCAFs from 29 representative patients sorted on the basis of CAFs with corresponding histologies, grades/stages (as presented with color codes, and numbers) is presented in a heatmap (B).

    Journal: International journal of molecular sciences

    Article Title: Characterization and Clinical Relevance of Endometrial CAFs: Correlation between Post-Surgery Event and Resistance to Drugs.

    doi: 10.3390/ijms24076449

    Figure Lengend Snippet: Figure 5. A comparison of NCAF with TCAF in terms of the alterations in genes and expression of protein markers: A comprehensive cancer panel report on all exon coverage on 409 genes involved in some of the most common known cancers shows the alteration of genes in aggressive TCAFs and NCAFs from the same patient compared to HUF cells (A). The pathway-based gene selection profiled the mutational spectrum in known cancer driver genes and drug targets along with signaling cascades, apoptosis genes, DNA repair genes, transcription regulators, inflammatory response genes, and growth factor genes. The panel covered both somatic and germline mutations. Heatmaps depicting the genetic alterations identified in NCAF, TCAF, or HUF samples are presented. The coding regions of 409 cancer-related genes are sequenced. Variants with a significant allele frequency difference between sample groups (n = 3) are summarized. Numbers of significantly altered variants of those genes are plotted. A 3-color scale-based conditionally formatted expression (% of expression by ICC) of CAF markers in aggressive TCAFs, and NCAFs from 29 representative patients sorted on the basis of CAFs with corresponding histologies, grades/stages (as presented with color codes, and numbers) is presented in a heatmap (B).

    Article Snippet: The complete medium for HUF cells (Primary Uterine Fibroblasts; Normal, Human (ATCC PCS-460-010) consisted of the components of the growth kit with the Fibroblast Basal Medium-Low Serum (ATCC PCS-201-041), which were added to the basal medium (ATCC PCS-201-030).

    Techniques: Comparison, Expressing, Selection