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human colorectal cancer cell lines  (ATCC)


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    ATCC human colorectal cancer cell lines
    Human Colorectal Cancer Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 4444 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/sw620+human+colorectal+cancer+cell+line/SW620/pm42250753-47-0-35
    Average 98 stars, based on 4444 article reviews
    human colorectal cancer cell lines - by Bioz Stars, 2026-09
    98/100 stars

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    Related Articles

    MTS Assay:

    Article Title: Characterization of nano oxaliplatin prepared by novel Fat Employing Supercritical Nano System, the FESNS®.
    Article Snippet: Background: Oxaliplatin has long been used for the treatment of colorectal cancer via intra-venous infusion.. In order to improve patient compliance, a solid dosage form for oral administration of oxaliplatin was prepared as nano-sized particles.. Method: Nano oxaliplatin was prepared employing Fat Employing Supercritical Nano System (FESNS®) with Supercritical Fluid (SCF) apparatus by using myristyl alcohol as solvent.



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    sw620 human colorectal cancer cell line  (ATCC)
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    Oxidative stress markers in nude mice colon treated with <t>SW620,</t> AD, ADNPs1, and ADNPs2. A significant change at p < 0.05 in MDA and a non-significant change at p > 0.05 in SOD and catalase activity. Values presented as mean ± S.E., a, b different superscripts within columns are significantly different ( P < 0.05).
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    human colorectal cancer cell line sw620  (European Collection of Authenticated Cell Cultures)
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    European Collection of Authenticated Cell Cultures human colorectal cancer cell line sw620
    CS-6-mediated <t>colorectal</t> cancer suppression in vivo is associated with DNA damage and autophagy. (a) Tumor weight of SW620 cells in vivo. (b) Tumor volume of SW620 cells in vivo. (c) Body weight change of BALB/C nude mice. (d) Histological changes of liver and kidney in BALB/C nude mice treated with CS-6. (e) Expression of γH2AX and p62 was determined by immunohistochemistry (IHC). Data are presented as the mean ± SD from three independent experiments. (f) Expression of p-ATM, ATM, γH2AX, LC3 I/II and p62 in xenograft tumor at protein levels was detected by western blotting. *P < 0.05;; **P < 0.01; ***P < 0.001 compared with model group.
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    Oxidative stress markers in nude mice colon treated with SW620, AD, ADNPs1, and ADNPs2. A significant change at p < 0.05 in MDA and a non-significant change at p > 0.05 in SOD and catalase activity. Values presented as mean ± S.E., a, b different superscripts within columns are significantly different ( P < 0.05).

    Journal: Journal of Genetic Engineering & Biotechnology

    Article Title: Potential role of Adansonia digitata nanoparticles on colorectal cancer induced by colorectal cancer cells (SW620) in nude mice

    doi: 10.1016/j.jgeb.2026.100659

    Figure Lengend Snippet: Oxidative stress markers in nude mice colon treated with SW620, AD, ADNPs1, and ADNPs2. A significant change at p < 0.05 in MDA and a non-significant change at p > 0.05 in SOD and catalase activity. Values presented as mean ± S.E., a, b different superscripts within columns are significantly different ( P < 0.05).

    Article Snippet: The SW620 human colorectal cancer cell line was obtained from the American Type Culture Collection (ATCC, Rockville, MD, USA).

    Techniques: Activity Assay

    Anti-apoptotic/pro-apoptotic protein level markers in nude mice colon treated with SW620, AD, ADNPs1, and ADNPs2. A significant change at p < 0.05 compared to the SW620 group in cytochrome c and a non-significant change at p > 0.05 in caspase3, BAX, and BCL-2. Values presented as mean ± S.E., a, b different superscripts within columns are significantly different ( P < 0.05).

    Journal: Journal of Genetic Engineering & Biotechnology

    Article Title: Potential role of Adansonia digitata nanoparticles on colorectal cancer induced by colorectal cancer cells (SW620) in nude mice

    doi: 10.1016/j.jgeb.2026.100659

    Figure Lengend Snippet: Anti-apoptotic/pro-apoptotic protein level markers in nude mice colon treated with SW620, AD, ADNPs1, and ADNPs2. A significant change at p < 0.05 compared to the SW620 group in cytochrome c and a non-significant change at p > 0.05 in caspase3, BAX, and BCL-2. Values presented as mean ± S.E., a, b different superscripts within columns are significantly different ( P < 0.05).

    Article Snippet: The SW620 human colorectal cancer cell line was obtained from the American Type Culture Collection (ATCC, Rockville, MD, USA).

    Techniques:

    TGF-β, TNF-α, INOS, and IL-1β mRNA expression in nude mice colon treated with SW620, AD, ADNPs1, and ADNPs2. A significant change at p < 0.05 compared to the SW620 group in TGF-β, and a non-significant change at p > 0.05 in TNF-α, IL-1β, and INOS. Values presented as mean ± S.E., a, b, c different superscripts within columns are significantly different ( P < 0.05).

    Journal: Journal of Genetic Engineering & Biotechnology

    Article Title: Potential role of Adansonia digitata nanoparticles on colorectal cancer induced by colorectal cancer cells (SW620) in nude mice

    doi: 10.1016/j.jgeb.2026.100659

    Figure Lengend Snippet: TGF-β, TNF-α, INOS, and IL-1β mRNA expression in nude mice colon treated with SW620, AD, ADNPs1, and ADNPs2. A significant change at p < 0.05 compared to the SW620 group in TGF-β, and a non-significant change at p > 0.05 in TNF-α, IL-1β, and INOS. Values presented as mean ± S.E., a, b, c different superscripts within columns are significantly different ( P < 0.05).

    Article Snippet: The SW620 human colorectal cancer cell line was obtained from the American Type Culture Collection (ATCC, Rockville, MD, USA).

    Techniques: Expressing

    CS-6-mediated colorectal cancer suppression in vivo is associated with DNA damage and autophagy. (a) Tumor weight of SW620 cells in vivo. (b) Tumor volume of SW620 cells in vivo. (c) Body weight change of BALB/C nude mice. (d) Histological changes of liver and kidney in BALB/C nude mice treated with CS-6. (e) Expression of γH2AX and p62 was determined by immunohistochemistry (IHC). Data are presented as the mean ± SD from three independent experiments. (f) Expression of p-ATM, ATM, γH2AX, LC3 I/II and p62 in xenograft tumor at protein levels was detected by western blotting. *P < 0.05;; **P < 0.01; ***P < 0.001 compared with model group.

    Journal: Frontiers in Pharmacology

    Article Title: CS-6-induced p62 accumulation exacerbates DNA damage in colorectal cancer

    doi: 10.3389/fphar.2025.1568339

    Figure Lengend Snippet: CS-6-mediated colorectal cancer suppression in vivo is associated with DNA damage and autophagy. (a) Tumor weight of SW620 cells in vivo. (b) Tumor volume of SW620 cells in vivo. (c) Body weight change of BALB/C nude mice. (d) Histological changes of liver and kidney in BALB/C nude mice treated with CS-6. (e) Expression of γH2AX and p62 was determined by immunohistochemistry (IHC). Data are presented as the mean ± SD from three independent experiments. (f) Expression of p-ATM, ATM, γH2AX, LC3 I/II and p62 in xenograft tumor at protein levels was detected by western blotting. *P < 0.05;; **P < 0.01; ***P < 0.001 compared with model group.

    Article Snippet: The human colorectal cancer (CRC) cell lines, SW620 (ECACC identifier: 87051203) and DLD1 (ECACC identifier: 90102540) were obtained from the European Collection of Authenticated Cell Cultures (ECACC).

    Techniques: In Vivo, Expressing, Immunohistochemistry, Western Blot

    Schematic representation of the anti-tumor effect of CS-6 in colorectal cancer.

    Journal: Frontiers in Pharmacology

    Article Title: CS-6-induced p62 accumulation exacerbates DNA damage in colorectal cancer

    doi: 10.3389/fphar.2025.1568339

    Figure Lengend Snippet: Schematic representation of the anti-tumor effect of CS-6 in colorectal cancer.

    Article Snippet: The human colorectal cancer (CRC) cell lines, SW620 (ECACC identifier: 87051203) and DLD1 (ECACC identifier: 90102540) were obtained from the European Collection of Authenticated Cell Cultures (ECACC).

    Techniques: