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KDM4C Activity Modulates Cell Proliferation and Chromosome Segregation in Triple-Negative Breast Cancer

机译:KDM4C活性调节三阴性乳腺癌细胞增殖和染色体分离。

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The Jumonji-containing domain protein, KDM4C, is a histone demethylase associated with the development of several forms of human cancer. However, its specific function in the viability of tumoral lineages is yet to be determined. This work investigates the importance of KDM4C activity in cell proliferation and chromosome segregation of three triple-negative breast cancer cell lines using a specific demethylase inhibitor. Immunofluorescence assays show that KDM4C is recruited to mitotic chromosomes and that the modulation of its activity increases the number of mitotic segregation errors. However, 3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide (MTT) cell proliferation assays demonstrate that the demethylase activity is required for cell viability. These results suggest that the histone demethylase activity of KDM4C is essential for breast cancer progression given its role in the maintenance of chromosomal stability and cell growth, thus highlighting it as a potential therapeutic target.
机译:含有Jumonji的域蛋白KDM4C是一种组蛋白脱甲基酶,与多种形式的人类癌症的发展有关。然而,其在肿瘤谱系生存力中的特定功能尚待确定。这项工作调查了KDM4C活性在使用特定脱甲基酶抑制剂的三种三阴性乳腺癌细胞系的细胞增殖和染色体分离中的重要性。免疫荧光分析表明,KDM4C被募集到有丝分裂染色体上,其活性的调节增加了有丝分裂分离错误的数量。但是,3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化硼(MTT)细胞增殖试验表明,脱甲基酶活性是细胞活力所必需的。这些结果表明,KDM4C的组蛋白脱甲基酶活性对于乳腺癌的进展至关重要,因为它在维持染色体稳定性和细胞生长中具有重要作用,因此使其成为潜在的治疗靶标。

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