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human uterine leiomyosarcoma cell line sk ut 1  (ATCC)


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    Structured Review

    ATCC human uterine leiomyosarcoma cell line sk ut 1
    In vitro antiproliferative activity of Peptides 1–4 and control peptides in <t> SK-UT-1 </t> and HUtSMC cells after 48 h of treatment.
    Human Uterine Leiomyosarcoma Cell Line Sk Ut 1, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 151 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/leiomyosarcoma+sk+ut+1+htb+114+human+cell+lines/SK-UT-1/pmc13637783-78-1-37
    Average 95 stars, based on 151 article reviews
    human uterine leiomyosarcoma cell line sk ut 1 - by Bioz Stars, 2026-10
    95/100 stars

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    1) Product Images from "Structure-guided discovery of novel ERα-binding peptides with in vitro antiproliferative activity"

    Article Title: Structure-guided discovery of novel ERα-binding peptides with in vitro antiproliferative activity

    Journal: Journal of Enzyme Inhibition and Medicinal Chemistry

    doi: 10.1080/14756366.2026.2713724

    In vitro antiproliferative activity of Peptides 1–4 and control peptides in  SK-UT-1  and HUtSMC cells after 48 h of treatment.
    Figure Legend Snippet: In vitro antiproliferative activity of Peptides 1–4 and control peptides in SK-UT-1 and HUtSMC cells after 48 h of treatment.

    Techniques Used: In Vitro, Activity Assay, Control

    Five-day in vitro antiproliferative assessment of Peptide-4 and control peptides in SK-UT-1 and tested normal human cell lines.
    Figure Legend Snippet: Five-day in vitro antiproliferative assessment of Peptide-4 and control peptides in SK-UT-1 and tested normal human cell lines.

    Techniques Used: In Vitro, Control

    ERα knockdown attenuates the antiproliferative activity of Peptide-4 in  SK-UT-1  cells.
    Figure Legend Snippet: ERα knockdown attenuates the antiproliferative activity of Peptide-4 in SK-UT-1 cells.

    Techniques Used: Knockdown, Activity Assay

    Effects of Peptide-4 and anti-miR-149G on c-Myc and Cyclin D1 mRNA expression in SK-UT-1 cells. (A) Peptide-4 treatment decreased the relative mRNA levels of c-Myc and Cyclin D1 at 1 and 5 μM, with a greater reduction observed at 5 μM. (B) Anti-miR-149G treatment produced a similar concentration-associated decrease in c-Myc and Cyclin D1 mRNA expression. mRNA levels were determined by RT-qPCR and normalised to the control group. Data are presented as mean ± SD ( n = 3). *** P < 0.001 vs control. Corresponding Hedges’ g standardised effect sizes and their 95% confidence intervals are summarised in Table S3 .
    Figure Legend Snippet: Effects of Peptide-4 and anti-miR-149G on c-Myc and Cyclin D1 mRNA expression in SK-UT-1 cells. (A) Peptide-4 treatment decreased the relative mRNA levels of c-Myc and Cyclin D1 at 1 and 5 μM, with a greater reduction observed at 5 μM. (B) Anti-miR-149G treatment produced a similar concentration-associated decrease in c-Myc and Cyclin D1 mRNA expression. mRNA levels were determined by RT-qPCR and normalised to the control group. Data are presented as mean ± SD ( n = 3). *** P < 0.001 vs control. Corresponding Hedges’ g standardised effect sizes and their 95% confidence intervals are summarised in Table S3 .

    Techniques Used: Expressing, Produced, Concentration Assay, Quantitative RT-PCR, Control

    Effect of Peptide-4, anti-miR-149G, and their combination on SK-UT-1 cell inhibition. Peptide-4 and anti-miR-149G alone showed moderate inhibitory effects on SK-UT-1 cells, while the combined treatment resulted in a higher inhibition rate than either single treatment. The dashed line indicates the 60% inhibition reference level. Cell inhibition rates were determined by the MTT assay. Data are presented as mean ± SD ( n = 3). *** P < 0.001 vs either single-treatment group. Corresponding Hedges’ g standardised effect sizes and their 95% confidence intervals are summarised in Table S4 .
    Figure Legend Snippet: Effect of Peptide-4, anti-miR-149G, and their combination on SK-UT-1 cell inhibition. Peptide-4 and anti-miR-149G alone showed moderate inhibitory effects on SK-UT-1 cells, while the combined treatment resulted in a higher inhibition rate than either single treatment. The dashed line indicates the 60% inhibition reference level. Cell inhibition rates were determined by the MTT assay. Data are presented as mean ± SD ( n = 3). *** P < 0.001 vs either single-treatment group. Corresponding Hedges’ g standardised effect sizes and their 95% confidence intervals are summarised in Table S4 .

    Techniques Used: Inhibition, MTT Assay

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    Article Snippet: The synovial sarcoma SW982 (HTB-93), liposarcoma SW872 (HTB-92), and leiomyosarcoma SK-UT-1 (HTB-114) human cell lines were obtained from the ATCC.



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    In vitro antiproliferative activity of Peptides 1–4 and control peptides in  SK-UT-1  and HUtSMC cells after 48 h of treatment.

    Journal: Journal of Enzyme Inhibition and Medicinal Chemistry

    Article Title: Structure-guided discovery of novel ERα-binding peptides with in vitro antiproliferative activity

    doi: 10.1080/14756366.2026.2713724

    Figure Lengend Snippet: In vitro antiproliferative activity of Peptides 1–4 and control peptides in SK-UT-1 and HUtSMC cells after 48 h of treatment.

    Article Snippet: The human uterine leiomyosarcoma cell line SK-UT-1 (HTB-114), primary human uterine smooth muscle cells (HuTSMCs; PCS-460–011), human umbilical vein endothelial cells (HUVECs; PCS-100–010), human adult dermal fibroblasts (HDFa; PCS-201–012), and HK-2 cells (CRL-2190) were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: In Vitro, Activity Assay, Control

    Five-day in vitro antiproliferative assessment of Peptide-4 and control peptides in SK-UT-1 and tested normal human cell lines.

    Journal: Journal of Enzyme Inhibition and Medicinal Chemistry

    Article Title: Structure-guided discovery of novel ERα-binding peptides with in vitro antiproliferative activity

    doi: 10.1080/14756366.2026.2713724

    Figure Lengend Snippet: Five-day in vitro antiproliferative assessment of Peptide-4 and control peptides in SK-UT-1 and tested normal human cell lines.

    Article Snippet: The human uterine leiomyosarcoma cell line SK-UT-1 (HTB-114), primary human uterine smooth muscle cells (HuTSMCs; PCS-460–011), human umbilical vein endothelial cells (HUVECs; PCS-100–010), human adult dermal fibroblasts (HDFa; PCS-201–012), and HK-2 cells (CRL-2190) were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: In Vitro, Control

    ERα knockdown attenuates the antiproliferative activity of Peptide-4 in  SK-UT-1  cells.

    Journal: Journal of Enzyme Inhibition and Medicinal Chemistry

    Article Title: Structure-guided discovery of novel ERα-binding peptides with in vitro antiproliferative activity

    doi: 10.1080/14756366.2026.2713724

    Figure Lengend Snippet: ERα knockdown attenuates the antiproliferative activity of Peptide-4 in SK-UT-1 cells.

    Article Snippet: The human uterine leiomyosarcoma cell line SK-UT-1 (HTB-114), primary human uterine smooth muscle cells (HuTSMCs; PCS-460–011), human umbilical vein endothelial cells (HUVECs; PCS-100–010), human adult dermal fibroblasts (HDFa; PCS-201–012), and HK-2 cells (CRL-2190) were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Knockdown, Activity Assay

    Effects of Peptide-4 and anti-miR-149G on c-Myc and Cyclin D1 mRNA expression in SK-UT-1 cells. (A) Peptide-4 treatment decreased the relative mRNA levels of c-Myc and Cyclin D1 at 1 and 5 μM, with a greater reduction observed at 5 μM. (B) Anti-miR-149G treatment produced a similar concentration-associated decrease in c-Myc and Cyclin D1 mRNA expression. mRNA levels were determined by RT-qPCR and normalised to the control group. Data are presented as mean ± SD ( n = 3). *** P < 0.001 vs control. Corresponding Hedges’ g standardised effect sizes and their 95% confidence intervals are summarised in Table S3 .

    Journal: Journal of Enzyme Inhibition and Medicinal Chemistry

    Article Title: Structure-guided discovery of novel ERα-binding peptides with in vitro antiproliferative activity

    doi: 10.1080/14756366.2026.2713724

    Figure Lengend Snippet: Effects of Peptide-4 and anti-miR-149G on c-Myc and Cyclin D1 mRNA expression in SK-UT-1 cells. (A) Peptide-4 treatment decreased the relative mRNA levels of c-Myc and Cyclin D1 at 1 and 5 μM, with a greater reduction observed at 5 μM. (B) Anti-miR-149G treatment produced a similar concentration-associated decrease in c-Myc and Cyclin D1 mRNA expression. mRNA levels were determined by RT-qPCR and normalised to the control group. Data are presented as mean ± SD ( n = 3). *** P < 0.001 vs control. Corresponding Hedges’ g standardised effect sizes and their 95% confidence intervals are summarised in Table S3 .

    Article Snippet: The human uterine leiomyosarcoma cell line SK-UT-1 (HTB-114), primary human uterine smooth muscle cells (HuTSMCs; PCS-460–011), human umbilical vein endothelial cells (HUVECs; PCS-100–010), human adult dermal fibroblasts (HDFa; PCS-201–012), and HK-2 cells (CRL-2190) were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Expressing, Produced, Concentration Assay, Quantitative RT-PCR, Control

    Effect of Peptide-4, anti-miR-149G, and their combination on SK-UT-1 cell inhibition. Peptide-4 and anti-miR-149G alone showed moderate inhibitory effects on SK-UT-1 cells, while the combined treatment resulted in a higher inhibition rate than either single treatment. The dashed line indicates the 60% inhibition reference level. Cell inhibition rates were determined by the MTT assay. Data are presented as mean ± SD ( n = 3). *** P < 0.001 vs either single-treatment group. Corresponding Hedges’ g standardised effect sizes and their 95% confidence intervals are summarised in Table S4 .

    Journal: Journal of Enzyme Inhibition and Medicinal Chemistry

    Article Title: Structure-guided discovery of novel ERα-binding peptides with in vitro antiproliferative activity

    doi: 10.1080/14756366.2026.2713724

    Figure Lengend Snippet: Effect of Peptide-4, anti-miR-149G, and their combination on SK-UT-1 cell inhibition. Peptide-4 and anti-miR-149G alone showed moderate inhibitory effects on SK-UT-1 cells, while the combined treatment resulted in a higher inhibition rate than either single treatment. The dashed line indicates the 60% inhibition reference level. Cell inhibition rates were determined by the MTT assay. Data are presented as mean ± SD ( n = 3). *** P < 0.001 vs either single-treatment group. Corresponding Hedges’ g standardised effect sizes and their 95% confidence intervals are summarised in Table S4 .

    Article Snippet: The human uterine leiomyosarcoma cell line SK-UT-1 (HTB-114), primary human uterine smooth muscle cells (HuTSMCs; PCS-460–011), human umbilical vein endothelial cells (HUVECs; PCS-100–010), human adult dermal fibroblasts (HDFa; PCS-201–012), and HK-2 cells (CRL-2190) were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Inhibition, MTT Assay