首页> 美国卫生研究院文献>BMC Immunology >The DNA methyltransferase inhibitor guadecitabine targets tumor-induced myelopoiesis and recovers T cell activity to slow tumor growth in combination with adoptive immunotherapy in a mouse model of breast cancer
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The DNA methyltransferase inhibitor guadecitabine targets tumor-induced myelopoiesis and recovers T cell activity to slow tumor growth in combination with adoptive immunotherapy in a mouse model of breast cancer

机译:DNA甲基转移酶抑制剂guadecitabine可靶向肿瘤诱导的骨髓生成并在乳腺癌小鼠模型中与过继免疫疗法相结合恢复T细胞活性以减缓肿瘤生长

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摘要

Guadecitabine treatment results in smaller tumors and a reduction in myeloid cells. 4 T1 tumor-bearing mice were untreated or treated with guadecitabine on days 10–13. Final volume of excised tumors on day 16. Representative images of frozen tumor sections stained with TUNEL to detect apoptotic cells. Total cellularity (top) and number of MDSCs (bottom) from spleen, bone marrow, and blood. Surface expression of APC costimulatory markers on splenic MDSCs. Significance determined using student’s unpaired T test (a), ANOVA with Tukey’s (c-e) or Sidak’s (f) multiple comparison tests. Error bars represent SD. ns = not significant; **: valuep valuep value
机译:瓜地西他滨治疗可导致较小的肿瘤并减少髓样细胞。在第10-13天未治疗或用瓜地他滨治疗4 T1荷瘤小鼠。在第16天切除的肿瘤的最终体积。用TUNEL染色的冷冻肿瘤切片的代表性图像以检测凋亡细胞。脾脏,骨髓和血液中的总细胞数(顶部)和MDSC数(底部)。 APC共刺激标记在脾脏MDSC上的表面表达。使用学生的未配对T检验(a),ANOVA与Tukey的(c-e)或Sidak的(f)多重比较检验确定显着性。误差棒代表SD。 ns =不重要; **:valuep valuep值

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