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normal prostatic stromal cell line wpmy  (ATCC)


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    ATCC normal prostatic stromal cell line wpmy
    Normal Prostatic Stromal Cell Line Wpmy, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 323 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/normal+prostatic+stromal+cell+line+wpmy/WPMY-1/pm38050650-256-21-30
    Average 96 stars, based on 323 article reviews
    normal prostatic stromal cell line wpmy - by Bioz Stars, 2026-10
    96/100 stars

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    other:

    Article Title: YAP1 Recognizes Inflammatory and Mechanical Cues to Exacerbate Benign Prostatic Hyperplasia via Promoting Cell Survival and Fibrosis.
    Article Snippet: Cell Lines and Treatments: The human prostatic hyperplasia epithelial cell line BPH-1 was acquired from Leibniz Institute DSMZ, while the human normal prostatic stromal cell line WPMY-1 was acquired from American Type Culture Collection (ATCC).



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    FIGURE 1 Yuanhuacine selectively kills PCa cells. (A) Chemical structure of yuanhuacine (YC) (2D structure). (B) Normal prostate stromal <t>immortalized</t> cell line (WPMY‐1) was stimulated with the indicated doses of yuanhuacine (1–50 μM) for 24 h. Then, cell toxicity was determined by a CCK‐8 assay. (C, D) After treatment with yuanhuacine for 24 h, cell viability of LNCaP (C) and PC‐3 (D) were analyzed. (E) Following the exposure to 20 µM yuanhuacine, cells were then stained with Annexin V‐FITC and PI. Flow cytometry was used to evaluate cell apoptosis. CCK‐8, Cell Counting Kit‐8; PCa, prostate cancer; PI, propidium iodide. *p < 0.05 versus control group.
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    FIGURE 1 Yuanhuacine selectively kills PCa cells. (A) Chemical structure of yuanhuacine (YC) (2D structure). (B) Normal prostate stromal <t>immortalized</t> cell line (WPMY‐1) was stimulated with the indicated doses of yuanhuacine (1–50 μM) for 24 h. Then, cell toxicity was determined by a CCK‐8 assay. (C, D) After treatment with yuanhuacine for 24 h, cell viability of LNCaP (C) and PC‐3 (D) were analyzed. (E) Following the exposure to 20 µM yuanhuacine, cells were then stained with Annexin V‐FITC and PI. Flow cytometry was used to evaluate cell apoptosis. CCK‐8, Cell Counting Kit‐8; PCa, prostate cancer; PI, propidium iodide. *p < 0.05 versus control group.
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    FIGURE 1 Yuanhuacine selectively kills PCa cells. (A) Chemical structure of yuanhuacine (YC) (2D structure). (B) Normal prostate stromal <t>immortalized</t> cell line (WPMY‐1) was stimulated with the indicated doses of yuanhuacine (1–50 μM) for 24 h. Then, cell toxicity was determined by a CCK‐8 assay. (C, D) After treatment with yuanhuacine for 24 h, cell viability of LNCaP (C) and PC‐3 (D) were analyzed. (E) Following the exposure to 20 µM yuanhuacine, cells were then stained with Annexin V‐FITC and PI. Flow cytometry was used to evaluate cell apoptosis. CCK‐8, Cell Counting Kit‐8; PCa, prostate cancer; PI, propidium iodide. *p < 0.05 versus control group.
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    FIGURE 1 Yuanhuacine selectively kills PCa cells. (A) Chemical structure of yuanhuacine (YC) (2D structure). (B) Normal prostate stromal <t>immortalized</t> cell line (WPMY‐1) was stimulated with the indicated doses of yuanhuacine (1–50 μM) for 24 h. Then, cell toxicity was determined by a CCK‐8 assay. (C, D) After treatment with yuanhuacine for 24 h, cell viability of LNCaP (C) and PC‐3 (D) were analyzed. (E) Following the exposure to 20 µM yuanhuacine, cells were then stained with Annexin V‐FITC and PI. Flow cytometry was used to evaluate cell apoptosis. CCK‐8, Cell Counting Kit‐8; PCa, prostate cancer; PI, propidium iodide. *p < 0.05 versus control group.
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    FIGURE 1 Yuanhuacine selectively kills PCa cells. (A) Chemical structure of yuanhuacine (YC) (2D structure). (B) Normal prostate stromal <t>immortalized</t> cell line (WPMY‐1) was stimulated with the indicated doses of yuanhuacine (1–50 μM) for 24 h. Then, cell toxicity was determined by a CCK‐8 assay. (C, D) After treatment with yuanhuacine for 24 h, cell viability of LNCaP (C) and PC‐3 (D) were analyzed. (E) Following the exposure to 20 µM yuanhuacine, cells were then stained with Annexin V‐FITC and PI. Flow cytometry was used to evaluate cell apoptosis. CCK‐8, Cell Counting Kit‐8; PCa, prostate cancer; PI, propidium iodide. *p < 0.05 versus control group.
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    FIGURE 1 Yuanhuacine selectively kills PCa cells. (A) Chemical structure of yuanhuacine (YC) (2D structure). (B) Normal prostate stromal immortalized cell line (WPMY‐1) was stimulated with the indicated doses of yuanhuacine (1–50 μM) for 24 h. Then, cell toxicity was determined by a CCK‐8 assay. (C, D) After treatment with yuanhuacine for 24 h, cell viability of LNCaP (C) and PC‐3 (D) were analyzed. (E) Following the exposure to 20 µM yuanhuacine, cells were then stained with Annexin V‐FITC and PI. Flow cytometry was used to evaluate cell apoptosis. CCK‐8, Cell Counting Kit‐8; PCa, prostate cancer; PI, propidium iodide. *p < 0.05 versus control group.

    Journal: Journal of biochemical and molecular toxicology

    Article Title: Blockage of MDM2-mediated p53 ubiquitination by yuanhuacine restrains the carcinogenesis of prostate carcinoma cells by suppressing LncRNA LINC00665.

    doi: 10.1002/jbt.23265

    Figure Lengend Snippet: FIGURE 1 Yuanhuacine selectively kills PCa cells. (A) Chemical structure of yuanhuacine (YC) (2D structure). (B) Normal prostate stromal immortalized cell line (WPMY‐1) was stimulated with the indicated doses of yuanhuacine (1–50 μM) for 24 h. Then, cell toxicity was determined by a CCK‐8 assay. (C, D) After treatment with yuanhuacine for 24 h, cell viability of LNCaP (C) and PC‐3 (D) were analyzed. (E) Following the exposure to 20 µM yuanhuacine, cells were then stained with Annexin V‐FITC and PI. Flow cytometry was used to evaluate cell apoptosis. CCK‐8, Cell Counting Kit‐8; PCa, prostate cancer; PI, propidium iodide. *p < 0.05 versus control group.

    Article Snippet: The human normal prostate stromal immortalized cell line (WPMY‐1) and two PCa cell lines (LNCaP and PC‐3) were purchased from the American Type Culture Collection (ATCC).

    Techniques: CCK-8 Assay, Staining, Flow Cytometry, Cell Counting, Control